Value histogram for hg38.gwasCatalog.title
 
valuecountgraph
A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry.3411************************************************************
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population.1006******************
Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers.948*****************
Genome-wide association study of schizophrenia in Ashkenazi Jews.713*************
Genetic studies of body mass index yield new insights for obesity biology.653***********
Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.518*********
Mercapturic Acids Derived from the Toxicants Acrolein and Crotonaldehyde in the Urine of Cigarette Smokers from Five Ethnic Groups with Differing Risks for Lung Cancer.503*********
New genetic loci link adipose and insulin biology to body fat distribution.342******
An atlas of genetic influences on human blood metabolites.317******
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.293*****
Genome-wide association analysis of actigraphic sleep phenotypes in the LIFE Adult Study.290*****
Discovery and refinement of loci associated with lipid levels.262*****
Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.242****
Hundreds of variants clustered in genomic loci and biological pathways affect human height.222****
Variations in the FRA10AC1 Fragile Site and 15q21 Are Associated with Cerebrospinal Fluid A?1-42 Level.213****
Family-based association analyses of imputed genotypes reveal genome-wide significant association of Alzheimer's disease with OSBPL6, PTPRG, and PDCL3.204****
Genome-wide association study identifies 74 loci associated with educational attainment.194***
Genome-wide association study identifies novel loci associated with diisocyanate-induced occupational asthma.193***
Biological, clinical and population relevance of 95 loci for blood lipids.192***
Defining the role of common variation in the genomic and biological architecture of adult human height.191***
Human longevity is influenced by many genetic variants: evidence from 75,000 UK Biobank participants.188***
Genetics of rheumatoid arthritis contributes to biology and drug discovery.187***
Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.179***
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture.178***
Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.178***
The impact of low-frequency and rare variants on lipid levels.174***
Genome-wide meta-analysis identifies new susceptibility loci for migraine.163***
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias.147***
Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci.144***
Modulation of Genetic Associations with Serum Urate Levels by Body-Mass-Index in Humans.143***
Genetic loci associated with circulating phospholipid trans fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.138**
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.131**
Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy.131**
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens.130**
Genome-wide Comparative Analysis of Atopic Dermatitis and Psoriasis Gives Insight into Opposing Genetic Mechanisms.124**
Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans.123**
Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus.122**
A genome-wide association study of n-3 and n-6 plasma fatty acids in a Singaporean Chinese population.115**
Bivariate genome-wide association study identifies novel pleiotropic loci for lipids and inflammation.113**
Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.112**
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.111**
No Major Host Genetic Risk Factor Contributed to A(H1N1)2009 Influenza Severity.108**
Common genetic variation and the control of HIV-1 in humans.107**
Genome-wide association study of hematological and biochemical traits in a Japanese population.107**
Identification of Four Novel Loci in Asthma in European and African American Populations.106**
A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder.106**
Genome-wide association study of chronic periodontitis in a general German population.105**
Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.104**
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.104**
Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.103**
Genome-wide analysis of polymorphisms associated with cytokine responses in smallpox vaccine recipients.101**
A Genome-wide Association Study of Emphysema and Airway Quantitative Imaging Phenotypes.101**
52 Genetic Loci Influencing Myocardial Mass.101**
Biological insights from 108 schizophrenia-associated genetic loci.99**
Genome-wide joint meta-analysis of SNP and SNP-by-smoking interaction identifies novel loci for pulmonary function.94**
Genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.92**
Genome-wide association study of d-amphetamine response in healthy volunteers identifies putative associations, including cadherin 13 (CDH13).91**
Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality.87**
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.85*
The genetic architecture of economic and political preferences.82*
A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease.81*
Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus.81*
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.81*
Genetic variants in five novel loci including CFB and CD40 predispose to chronic hepatitis B.79*
Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci.78*
GWAS of 89,283 individuals identifies genetic variants associated with self-reporting of being a morning person.78*
Genome-Wide Association Studies of the Human Gut Microbiota.77*
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.77*
The effect of host genetics on the gut microbiome.76*
Genetic Variants Associated with Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics) Consortium.76*
Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.75*
Forty-three loci associated with plasma lipoprotein size, concentration, and cholesterol content in genome-wide analysis.73*
Genome-wide association study on dimethylarginines reveals novel AGXT2 variants associated with heart rate variability but not with overall mortality.73*
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.73*
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA.72*
Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture.72*
Trans-ethnic meta-analysis of white blood cell phenotypes.72*
Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels.72*
Genome-wide association study of a heart failure related metabolomic profile among African Americans in the Atherosclerosis Risk in Communities (ARIC) study.72*
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.71*
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.70*
Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.70*
Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility.69*
Common genetic variation and performance on standardized cognitive tests.69*
Common genetic variants associated with cognitive performance identified using the proxy-phenotype method.69*
Genome-Wide Association Study of Loneliness Demonstrates a Role for Common Variation.68*
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.68*
Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits.68*
New gene functions in megakaryopoiesis and platelet formation.67*
Genome-wide association study in Chinese identifies novel loci for blood pressure and hypertension.67*
Association of chromosome 5q21.3 polymorphisms with the exploratory eye movement dysfunction in schizophrenia.66*
Genome-wide association analysis identifies variation in vitamin D receptor and other host factors influencing the gut microbiota.65*
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.64*
Genome-wide association study of virologic response with efavirenz-containing or abacavir-containing regimens in AIDS clinical trials group protocols.64*
Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.64*
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.64*
Large-scale genotyping identifies 41 new loci associated with breast cancer risk.63*
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population.63*
Analysis of 23andMe antidepressant efficacy survey data: implication of circadian rhythm and neuroplasticity in bupropion response.63*
A large multi-ethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences.62*
Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.61*
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.61*
Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies.61*
Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.61*
Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.60*
A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function.60*
Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer.60*
Many sequence variants affecting diversity of adult human height.59*
Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects.59*
Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative.58*
Genome-Wide Association and Trans-ethnic Meta-Analysis for Advanced Diabetic Kidney Disease: Family Investigation of Nephropathy and Diabetes (FIND).58*
A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.58*
A novel Alzheimer disease locus located near the gene encoding tau protein.58*
Genome-wide association meta-analysis identifies five modifier loci of lung disease severity in cystic fibrosis.57*
A genome-wide analysis of the response to inhaled ?2-agonists in chronic obstructive pulmonary disease.57*
Genome-wide association study of plasma levels of polychlorinated biphenyls disclose an association with the CYP2B6 gene in a population-based sample.57*
Genetic variants associated with disordered eating.57*
Genome-wide meta-analysis identifies variants associated with platinating agent susceptibility across populations56*
Genome-wide analyses of aggressiveness in attention-deficit hyperactivity disorder.56*
Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.56*
Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47.56*
GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.56*
A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features.56*
Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.55*
A genome-wide association study identifies protein quantitative trait loci (pQTLs).55*
Genome-wide association analyses identify new susceptibility loci for oral cavity and pharyngeal cancer.55*
Genome-wide association study of plasma N6 polyunsaturated fatty acids within the cohorts for heart and aging research in genomic epidemiology consortium.55*
Fine-mapping, Novel Loci Identification, and SNP Association Transferability in a Genome-Wide Association Study of QRS Duration in African Americans.54*
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.54*
Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production.54*
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium.54*
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance.54*
Genome-wide association analysis of blood biomarkers in chronic obstructive pulmonary disease.54*
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants.53*
Web-based, participant-driven studies yield novel genetic associations for common traits.52*
Genome wide identification of new genes and pathways in patients with both autoimmune thyroiditis and type 1 diabetes.52*
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.52*
Genome-wide association study of bipolar disorder accounting for effect of body mass index identifies a new risk allele in TCF7L2.52*
Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.52*
Genome-wide association study identifies 14 novel risk alleles associated with basal cell carcinoma.52*
Genetics of coronary artery calcification among African Americans, a meta-analysis.51*
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.51*
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine.50*
Multiple common variants for celiac disease influencing immune gene expression.50*
Genome-wide association study of caffeine metabolites provides new insights to caffeine metabolism and dietary caffeine-consumption behavior.49*
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.49*
Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.49*
GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.49*
Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus.48*
Genetic Susceptibility to Lipid Levels and Lipid Change Over Time and Risk of Incident Hyperlipidemia in Chinese Populations.48*
ARHGEF12 influences the risk of glaucoma by increasing intraocular pressure.48*
Genome-wide association study of smoking behaviours among Bangladeshi adults.47*
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk.47*
Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project.47*
A genome-wide association study of behavioral disinhibition.47*
Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.46*
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases.46*
Genome-wide association study of smoking behaviours in patients with COPD.46*
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.46*
A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci.45*
A genome-wide association study identified new variants associated with the risk of chronic hepatitis B.45*
Literature-Informed Analysis of a Genome-Wide Association Study of Gestational Age in Norwegian Women and Children Suggests Involvement of Inflammatory Pathways.45*
Seventy-five genetic loci influencing the human red blood cell.45*
Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans.45*
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.45*
Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.45*
Genome-wide association study of primary dentition pit-and-fissure and smooth surface caries.45*
Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes.45*
Discovery and fine mapping of serum protein loci through transethnic meta-analysis.44*
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis.44*
Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.44*
The major genetic determinants of HIV-1 control affect HLA class I peptide presentation.44*
Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.44*
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.43*
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.43*
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.42*
A genome wide association study on Newfoundland colorectal cancer patients' survival outcomes.42*
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.42*
Meta-analysis of Genome Wide Association Studies Identifies Genetic Markers of Late Toxicity Following Radiotherapy for Prostate Cancer.42*
Genome-wide association study identifies novel loci associated with circulating phospho- and sphingolipid concentrations.42*
Genome-wide association studies in East Asians identify new loci for waist-hip ratio and waist circumference.42*
Cross-cancer genome-wide analysis of lung, ovary, breast, prostate and colorectal cancer reveals novel pleiotropic associations.42*
A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.42*
A meta-analysis of 120,246 individuals identifies 18 new loci for fibrinogen concentration.41*
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.41*
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits.41*
Genome-wide association study of lung function decline in adults with and without asthma.40*
Genetic loci associated with renal function measures and chronic kidney disease in children: the Pediatric Investigation for Genetic Factors Linked with Renal Progression Consortium.40*
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits.40*
Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.40*
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.40*
A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.40*
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.40*
A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.40*
Genome-wide association study of peripheral neuropathy with D-drug-containing regimens in AIDS Clinical Trials Group protocol 384.39*
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.39*
Joint influence of small-effect genetic variants on human longevity.39*
Genome-wide Association Studies Identify Genetic Loci Associated with Albuminuria in Diabetes.39*
Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.39*
A genome-wide association study identifies multiple loci for variation in human ear morphology.39*
Genome-wide association study of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Europe.39*
Genome wide analysis of narcolepsy in China implicates novel immune loci and reveals changes in association prior to versus after the 2009 H1N1 influenza pandemic.38*
Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease.38*
Genome-wide association study identifies multiple loci influencing human serum metabolite levels.38*
Genome-wide association study identifies 8 novel loci associated with blood pressure responses to interventions in Han Chinese.38*
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.38*
The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.38*
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.37*
Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.37*
Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.37*
Gout and type 2 diabetes have a mutual inter-dependent effect on genetic risk factors and higher incidences.37*
Genetic contributions to variation in general cognitive function: a meta-analysis of genome-wide association studies in the CHARGE consortium (N=53 949).37*
Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs.37*
Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity.37*
Gene-Smoking Interactions Identify Several Novel Blood Pressure Loci in the Framingham Heart Study.37*
Human metabolic individuality in biomedical and pharmaceutical research.37*
Genome-wide association study of antibody response to smallpox vaccine.37*
A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer.37*
Genome-wide association study identified the human leukocyte antigen region as a novel locus for plasma beta-2 microglobulin.37*
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.37*
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways.36*
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity.36*
Genetic Loci Associated with Circulating Levels of Very Long-Chain Saturated Fatty Acids.36*
Gene network analysis in a pediatric cohort identifies novel lung function genes.36*
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk.36*
Common variants at 30 loci contribute to polygenic dyslipidemia.36*
Multiethnic genome-wide association study of cerebral white matter hyperintensities on MRI.36*
Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis.36*
Meta-Analysis of Genome-Wide Association Studies Identifies Genetic Risk Factors for Stroke in African Americans.36*
Genome-wide association study of metabolic traits reveals novel gene-metabolite-disease links.36*
Genome-wide association of lipid-lowering response to statins in combined study populations.36*
Integrated Genome-wide Association, Coexpression Network, and Expression Single Nucleotide Polymorphism Analysis Identifies Novel Pathway in Allergic Rhinitis.35*
Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.35*
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment.35*
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.35*
Heritability and Genome-Wide Association Studies for Hair Color in a Dutch Twin Family Based Sample.35*
Meta-analysis of genome-wide association studies discovers multiple loci for chronic lymphocytic leukemia.34*
Genome-wide association scan of dental caries in the permanent dentition.34*
Lupus nephritis susceptibility Loci in women with systemic lupus erythematosus.34*
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease.34*
A genome-wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus.34*
Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease.34*
Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci.34*
Genome-wide Meta-analysis on the Sense of Smell Among US Older Adults.34*
Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.33*
Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.33*
Identification of a New Susceptibility Locus for Systemic Lupus Erythematosus on Chromosome 12 in Individuals of European Ancestry.33*
Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis.33*
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.33*
Genetic variants associated with breast size also influence breast cancer risk.33*
A genome-wide association study identifies two new risk loci for Graves' disease.33*
Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry.33*
Genetic variants influencing circulating lipid levels and risk of coronary artery disease.33*
Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.33*
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.33*
Genome-wide association study identifies five new schizophrenia loci.33*
Common variants at PVT1, ATG13-AMBRA1, AHI1 and CLEC16A are associated with selective IgA deficiency.32*
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.32*
Genome-wide association studies identify several new loci associated with pigmentation traits and skin cancer risk in European Americans.32*
Genome-wide association study confirming association of HLA-DP with protection against chronic hepatitis B and viral clearance in Japanese and Korean.32*
A comprehensive family-based replication study of schizophrenia genes.32*
Discovery of genetic biomarkers contributing to variation in drug response of cytidine analogues using human lymphoblastoid cell lines.32*
Generalization of variants identified by genome-wide association studies for electrocardiographic traits in African Americans.32*
Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders.32*
A genome-wide association meta-analysis of circulating sex hormone-binding globulin reveals multiple Loci implicated in sex steroid hormone regulation.32*
Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.32*
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.32*
Novel associations for hypothyroidism include known autoimmune risk loci.32*
Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans.32*
GWAS identifies novel SLE susceptibility genes and explains the association of the HLA region.32*
GWAS of dental caries patterns in the permanent dentition.31*
Insights into the genetic architecture of early stage age-related macular degeneration: a genome-wide association study meta-analysis.31*
Genome-wide association study identifies loci affecting blood copper, selenium and zinc.31*
A genome-wide association study in multiple system atrophy.31*
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.31*
A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population.31*
Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.31*
Genome-wide association study of parity in bangladeshi women.31*
A genome-wide association study of plasma total IgE concentrations in the Framingham Heart Study.31*
Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.31*
Meta-analysis of genome-wide association studies in african americans provides insights into the genetic architecture of type 2 diabetes.30*
Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.30*
Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks.30*
Genome-wide association study of selenium concentrations.30*
Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease.30*
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.30*
Genome-wide association study of conduct disorder symptomatology.30*
Common variants associated with general and MMR vaccine-related febrile seizures.30*
A genome-wide association study for reading and language abilities in two population cohorts.30*
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.30*
Genome-wide association scan in north Indians reveals three novel HLA-independent risk loci for ulcerative colitis.30*
Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women.30*
GWAS in an Amerindian ancestry population reveals novel systemic lupus erythematosus risk loci and the role of European admixture.30*
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.30*
A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.29*
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits.29*
A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese.29*
A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.29*
Genome-wide analysis identifies 12 loci influencing human reproductive behavior.29*
Genome-wide association study identifies multiple susceptibility loci for glioma.29*
Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1.29*
Variants in ELL2 influencing immunoglobulin levels associate with multiple myeloma.29*
Genetic association with overall survival of taxane-treated lung cancer patients - A genome-wide association study in human lymphoblastoid cell lines followed by a clinical association study.29*
Identification of Susceptibility Loci and Genes for Colorectal Cancer Risk.29*
Novel HLA-DP region susceptibility loci associated with severe acute GvHD.29*
Impact of ancestry and common genetic variants on QT interval in African Americans.29*
Genome-wide association identifies multiple ulcerative colitis susceptibility loci.29*
Gene-environment interactions and obesity traits among postmenopausal African-American and Hispanic women in the Women's Health Initiative SHARe Study.29*
Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype.28 
Genome-wide association identifies ATOH7 as a major gene determining human optic disc size.28 
Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.28 
Genome-wide association analysis implicates the involvement of eight loci with response to tocilizumab for the treatment of rheumatoid arthritis.28 
International GWAS Consortium Identifies Novel Loci Associated with Blood Pressure in Children and Adolescents.28 
Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women.28 
Genome-wide association analysis identifies 13 new risk loci for schizophrenia.28 
GWAS identifies two susceptibility loci for lamotrigine-induced skin rash in patients with epilepsy.28 
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1.28 
First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes.28 
Seven new loci associated with age-related macular degeneration.28 
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.27 
A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population.27 
Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.27 
Discovery of six new susceptibility loci and analysis of pleiotropic effects in leprosy.27 
A genome-wide association study (GWAS) for bronchopulmonary dysplasia.27 
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.27 
Propensity score-based nonparametric test revealing genetic variants underlying bipolar disorder.27 
Heritability and molecular-genetic basis of resting EEG activity: A genome-wide association study.27 
Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.27 
New loci associated with kidney function and chronic kidney disease.27 
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.27 
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci.27 
GWAS of DNA methylation variation within imprinting control regions suggests parent-of-origin association.26 
Genome-wide association study of ulcerative colitis in Koreans suggests extensive overlapping of genetic susceptibility with Caucasians.26 
Genome-wide association study and meta-analysis identify ISL1 as genome-wide significant susceptibility gene for bladder exstrophy.26 
Shared genetic susceptibility of vascular-related biomarkers with ischemic and recurrent stroke.26 
A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci.26 
A novel common variant in DCST2 is associated with length in early life and height in adulthood.26 
Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families.26 
Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.26 
Genome Wide Association Study Identifies Novel Loci Associated with Airway Responsiveness in COPD.26 
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.26 
Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index.26 
Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.26 
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.26 
Genetic factors in nonsmokers with age-related macular degeneration revealed through genome-wide gene-environment interaction analysis.26 
Genome-wide analysis links NFATC2 with asparaginase hypersensitivity.26 
Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study.26 
Identification of a novel Parkinson's disease locus via stratified genome-wide association study.26 
A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathy.26 
Genome-wide association scan for survival on dialysis in African-Americans with type 2 diabetes.26 
Genomewide association study for determinants of HIV-1 acquisition and viral set point in HIV-1 serodiscordant couples with quantified virus exposure.25 
An Extended Genome-Wide Association Study Identifies Novel Susceptibility Loci for Nasopharyngeal Carcinoma.25 
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.25 
Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.25 
Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk.25 
Identification of novel germline polymorphisms governing capecitabine sensitivity.25 
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants.25 
A genome-wide association study identifies new susceptibility loci for esophageal adenocarcinoma and Barrett's esophagus.25 
A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.25 
Genetic variants associated with antithyroid drug-induced agranulocytosis: a genome-wide association study in a European population.25 
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.25 
Novel loci affecting iron homeostasis and their effects in individuals at risk for hemochromatosis.25 
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population.25 
Whole genome association scan for genetic polymorphisms influencing information processing speed.25 
Heritability and genetic association analysis of cognition in the Diabetes Heart Study.25 
A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia.25 
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemia.24 
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.24 
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.24 
Genome-wide association with bone mass and geometry in the Framingham Heart Study.24 
Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women.24 
Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.24 
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population.24 
Genetically distinct subsets within ANCA-associated vasculitis.24 
Identification of new susceptibility loci for IgA nephropathy in Han Chinese.24 
GWAS of clinically defined gout and subtypes identifies multiple susceptibility loci that include urate transporter genes.24 
New suggestive genetic loci and biological pathways for attention function in adult attention-deficit/hyperactivity disorder.24 
A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications.24 
Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.24 
Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size.24 
A genome-wide association study of sleep habits and insomnia.24 
A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.24 
Genetics of long-term treatment outcome in bipolar disorder.24 
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution.24 
Multistage genome-wide association meta-analyses identified two new loci for bone mineral density.24 
A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis.24 
Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer.23 
Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.23 
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci.23 
Genome-wide association study identifies 8p21.3 associated with persistent hepatitis B virus infection among Chinese.23 
Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia.23 
Genome-wide association analysis identifies novel loci for chronotype in 100,420 individuals from the UK Biobank.23 
Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3.23 
Genome-wide association study of colorectal cancer identifies six new susceptibility loci.23 
Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.23 
Genome-Wide Association Studies of HIV-1 Host Control in Ethnically Diverse Chinese Populations.23 
A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.23 
Two susceptibility loci identified for prostate cancer aggressiveness.23 
Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency.23 
Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study.23 
Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus.23 
Genome-wide association analysis of autoantibody positivity in type 1 diabetes cases.23 
Heritability, SNP- and Gene-Based Analyses of Cannabis Use Initiation and Age at Onset.23 
Genome-wide association study identifies susceptibility loci for IgA nephropathy.23 
A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels.22 
Genome-wide association of serum bilirubin levels in Korean population.22 
Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk.22 
Genome-wide association study identifies peanut allergy-specific loci and evidence of epigenetic mediation in US children.22 
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans.22 
Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.22 
Pharmacogenomic study of side-effects for antidepressant treatment options in STAR*D.22 
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization.22 
Multiple loci are associated with white blood cell phenotypes.22 
Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan.22 
HLA-C*01 is a Risk Factor for Crohn's Disease.22 
Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.22 
Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder.22 
A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis.22 
Identification of six new susceptibility loci for invasive epithelial ovarian cancer.22 
Investigating the Genetics of Hippocampal Volume in Older Adults without Dementia.22 
Genome-wide association analysis to predict optimal antipsychotic dosage in schizophrenia: a pilot study.22 
Interaction between Common Genetic Variants and Total Fat Intake on Low-Density Lipoprotein Peak Particle Diameter: A Genome-Wide Association Study.22 
Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.21 
Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.21 
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.21 
Genome-Wide Association Identifies Regulatory Loci Associated with Distinct Local Histogram Emphysema Patterns.21 
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.21 
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.21 
A systemic sclerosis and systemic lupus erythematosus pan-meta-GWAS reveals new shared susceptibility loci.21 
A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region.21 
Genome-wide association study of Crohn's disease in Koreans revealed three new susceptibility loci and common attributes of genetic susceptibility across ethnic populations.21 
Identification of seven new prostate cancer susceptibility loci through a genome-wide association study.21 
Genome-wide association study of serum minerals levels in children of different ethnic background.21 
Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3.21 
Genome-wide Association Study of Late-Onset Myasthenia Gravis: Confirmation of TNFRSF11A, and Identification of ZBTB10 and Three Distinct HLA Associations.21 
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error.21 
Genome-wide and candidate gene association study of cigarette smoking behaviors.21 
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.21 
Genome-wide association study of proneness to anger.21 
Genome-wide association study of leukotriene modifier response in asthma.21 
The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response.21 
Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness.21 
A genome-wide approach to children's aggressive behavior: The EAGLE consortium.21 
Genome-Wide Association Study Identifies Novel Susceptibility Genes Associated with Coronary Artery Aneurysm Formation in Kawasaki Disease.21 
Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.21 
Germline genetic variation in an organic anion transporter polypeptide associated with methotrexate pharmacokinetics and clinical effects.21 
Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations.21 
Variants in WFS1 and other Mendelian deafness genes are associated with cisplatin-associated ototoxicity.20 
Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.20 
Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels.20 
Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study.20 
Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci.20 
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations.20 
Large-scale genetic study in East Asians identifies six new loci associated with colorectal cancer risk.20 
Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition.20 
Genome-wide association study of lymphoblast cell viability after clozapine exposure.20 
Genome-Wide Association Study with Targeted and Non-targeted NMR Metabolomics Identifies 15 Novel Loci of Urinary Human Metabolic Individuality.20 
Genome-wide association study of cognitive functions and educational attainment in UK Biobank (N=112 151).20 
Genome-wide association study of behavioural and psychiatric features in human prion disease.20 
Genome-wide association analysis identifies 20 loci that influence adult height.20 
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region.20 
Genome-wide meta-analysis for severe diabetic retinopathy.19 
Rank-based genome-wide analysis reveals the association of ryanodine receptor-2 gene variants with childhood asthma among human populations.19 
Voxelwise genome-wide association study (vGWAS).19 
A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects.19 
Genome-wide meta-analysis uncovers novel loci influencing circulating leptin levels.19 
Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists.19 
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study.19 
Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.19 
Five endometrial cancer risk loci identified through genome-wide association analysis.19 
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.19 
A new GWAS and meta-analysis with 1000Genomes imputation identifies novel risk variants for colorectal cancer.19 
Genome-Wide and Gene-Based Meta-Analyses Identify Novel Loci Influencing Blood Pressure Response to Hydrochlorothiazide.19 
Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene.19 
Novel Genes for Airway Wall Thickness Identified with Combined Genome Wide Association and Expression Analyses.19 
Genetic influences on political ideologies: twin analyses of 19 measures of political ideologies from five democracies and genome-wide findings from three populations.19 
A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.19 
Genome-wide association with select biomarker traits in the Framingham Heart Study.19 
Genetic determinants of swallowing impairments among community dwelling older population.19 
Genome-wide association study of liver enzymes in korean children.19 
Genome-wide association study of Alzheimer's disease with psychotic symptoms.19 
Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study.19 
Loci at chromosomes 13, 19 and 20 influence age at natural menopause.19 
A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network.19 
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.19 
Genome-wide association study identifies multiple loci associated with bladder cancer risk.19 
Genome-Wide Association and Exome Sequencing Study of Language Disorder in an Isolated Population.18 
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.18 
Novel loci associated with usual sleep duration: the CHARGE Consortium Genome-Wide Association Study.18 
Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies.18 
Genome-wide association studies and heritability estimates of body mass index related phenotypes in bangladeshi adults.18 
TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.18 
A genome-wide association meta-analysis of plasma Aβ peptides concentrations in the elderly.18 
A genome-wide association study reveals susceptibility loci for myocardial infarction/coronary artery disease in Saudi Arabs.18 
Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis.18 
Identification of ten loci associated with height highlights new biological pathways in human growth.18 
A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation.18 
Genome-wide association study of age at menarche in African-American women.18 
Genome-wide association study identifies three novel loci for type 2 diabetes.18 
A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.18 
Meta-analysis of genome-wide association studies identifies novel loci that influence cupping and the glaucomatous process.18 
Genome-wide association study in Han Chinese identifies three novel loci for human height.18 
The genetics of alcohol dependence: Twin and SNP-based heritability, and genome-wide association study based on AUDIT scores.18 
Genetic predictors of medically refractory ulcerative colitis.18 
GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.18 
Genome-wide association meta-analyses identified 1q43 and 2q32.2 for hip Ward's triangle areal bone mineral density.18 
Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity.18 
Genome-wide association studies suggest sex-specific loci associated with abdominal and visceral fat.18 
A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjogren's syndrome at 7q11.23.18 
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).18 
Genome-wide association study of blood pressure and hypertension.18 
Genetic variants in LPL, OASL and TOMM40/APOE-C1-C2-C4 genes are associated with multiple cardiovascular-related traits.18 
Multiple genetic loci for bone mineral density and fractures.18 
Identification of a Systemic Lupus Erythematosus Risk Locus Spanning ATG16L2, FCHSD2, and P2RY2 in Koreans.18 
Genome wide study of maternal and parent-of-origin effects on the etiology of orofacial clefts.18 
A genome-wide association study of the metabolic syndrome in Indian Asian men.18 
Identification of Susceptibility Loci for Cutaneous Squamous Cell Carcinoma.18 
Several common variants modulate heart rate, PR interval and QRS duration.18 
Genome-wide association studies identify four ER negative-specific breast cancer risk loci.18 
Genetic determinants influencing human serum metabolome among African Americans.18 
Genome-wide data reveal novel genes for methotrexate response in a large cohort of juvenile idiopathic arthritis cases.18 
Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease.18 
A genome-wide meta-analysis of association studies of Cloninger's Temperament Scales.17 
A genome-wide association study on a southern European population identifies a new Crohn's disease susceptibility locus at RBX1-EP300.17 
Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups.17 
Common variation at 2p13.3, 3q29, 7p13 and 17q25.1 associated with susceptibility to pancreatic cancer.17 
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility.17 
Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma.17 
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.17 
Identification of a candidate gene for astigmatism.17 
Genes linked to energy metabolism and immunoregulatory mechanisms are associated with subcutaneous adipose tissue distribution in HIV-infected men.17 
Common genetic loci influencing plasma homocysteine concentrations and their effect on risk of coronary artery disease.17 
Genome-wide association reveals genetic effects on human Aβ42 and τ protein levels in cerebrospinal fluids: a case control study.17 
Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia.17 
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.17 
Genome-wide association study of panic disorder in the Japanese population.17 
Genetic determinants of hair, eye and skin pigmentation in Europeans.17 
Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).17 
Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans.17 
Genome-wide association study of pancreatic cancer in Japanese population.17 
Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.17 
Variability in the common genetic architecture of social-communication spectrum phenotypes during childhood and adolescence.17 
Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians.17 
Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum.17 
Drug-gene interactions and the search for missing heritability: a cross-sectional pharmacogenomics study of the QT interval.17 
A genome-wide association study of brain lesion distribution in multiple sclerosis.17 
Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network.17 
Bivariate Genome-Wide Association Study Implicates ATP6V1G1 as a Novel Pleiotropic Locus Underlying Osteoporosis and Age at Menarche.17 
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.17 
Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India.17 
Genome-wide association study of susceptibility loci for cervical cancer.17 
Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.17 
A genome-wide association study identifies two new cervical cancer susceptibility loci at 4q12 and 17q12.17 
Genome-wide association study of biochemical traits in Korcula Island, Croatia.17 
Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study.17 
Genomewide association study of movement-related adverse antipsychotic effects.17 
Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.17 
Common genetic variants influence human subcortical brain structures.16 
A genome wide association study identifies common variants associated with lipid levels in the Chinese population.16 
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes.16 
Genome-wide association study of atypical psychosis.16 
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.16 
Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC.16 
Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.16 
Genome-wide association study of warfarin maintenance dose in a Brazilian sample.16 
Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility.16 
Genome-wide association of mood-incongruent psychotic bipolar disorder.16 
Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100.16 
A large-scale, consortium-based genomewide association study of asthma.16 
New loci associated with chronic hepatitis B virus infection in Han Chinese.16 
Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysis.16 
Genome-wide association study of periodontal pathogen colonization.16 
A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations.16 
New sequence variants associated with bone mineral density.16 
Genome-wide Association Study Identifies Five Susceptibility Loci for Follicular Lymphoma outside the HLA Region.16 
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking.16 
Genome-wide association study of the modified Stumvoll Insulin Sensitivity Index identifies BCL2 and FAM19A2 as novel insulin sensitivity loci.16 
Identification of 15 loci influencing height in a Korean population.16 
A genome-wide association study of marginal zone lymphoma shows association to the HLA region.16 
Genome-wide association study of retinopathy in individuals without diabetes.16 
Genome-wide association study identifies new prostate cancer susceptibility loci.16 
Genome-wide association study evaluating lipoprotein-associated phospholipase A2 mass and activity at baseline and after rosuvastatin therapy.16 
Genome-wide and gene-based association studies of anxiety disorders in European and african american samples.16 
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypes.15 
Common variants in the trichohyalin gene are associated with straight hair in Europeans.15 
Genome-wide association analysis identified splicing single nucleotide polymorphism in CFLAR predictive of triptolide chemo-sensitivity.15 
Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.15 
Genome-wide association study in Han Chinese identifies four new susceptibility loci for coronary artery disease.15 
A genome-wide association study of rheumatoid arthritis without antibodies against citrullinated peptides.15 
Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians.15 
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX.15 
Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.15 
A genome-wide association study on thyroid function and anti-thyroid peroxidase antibodies in Koreans.15 
Genome-wide association study of anthropometric traits in Korcula Island, Croatia.15 
Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans.15 
Genetic susceptibility for chronic bronchitis in chronic obstructive pulmonary disease.15 
Genome-wide association study of body mass index in 23 000 individuals with and without asthma.15 
Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density.15 
A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region.15 
Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.15 
Evidence for several independent genetic variants affecting lipoprotein (a) cholesterol levels.15 
Common variants on 2p16.1, 6p22.1 and 10q24.32 are associated with schizophrenia in Han Chinese population.15 
Cross-Disorder Genome-Wide Analyses Suggest a Complex Genetic Relationship Between Tourette's Syndrome and OCD.15 
Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations.15 
Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis.15 
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.15 
Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.15 
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.15 
Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2.15 
Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study.15 
Identification of nine new susceptibility loci for testicular cancer, including variants near DAZL and PRDM14.15 
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci.15 
Risk loci for chronic obstructive pulmonary disease: a genome-wide association study and meta-analysis.15 
Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.15 
Genome- and exome-wide association study of serum lipoprotein (a) in the Jackson Heart Study.15 
Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene.15 
Genome-wide association study identifies novel susceptibility loci for cutaneous squamous cell carcinoma.15 
Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer.15 
Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci.15 
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.15 
Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes.15 
Host determinants of HIV-1 control in African Americans.15 
A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks.15 
Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.15 
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.15 
A genome-wide association study on obesity and obesity-related traits.14 
Common genetic variation at the IL1RL1 locus regulates IL-33/ST2 signaling.14 
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos.14 
Genome-wide association study of temperament in bipolar disorder reveals significant associations with three novel Loci.14 
Genome-wide association study of antiphospholipid antibodies.14 
A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.14 
Genetic predictors of fibrin D-dimer levels in healthy adults.14 
Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.14 
Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols.14 
Common variants at 5q22 associate with pediatric eosinophilic esophagitis.14 
Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study.14 
Genome-wide association study in alopecia areata implicates both innate and adaptive immunity.14 
Multiple newly identified loci associated with prostate cancer susceptibility.14 
Genome-wide association study of blood lead shows multiple associations near ALAD.14 
Sequence variants in the PTCH1 gene associate with spine bone mineral density and osteoporotic fractures.14 
Genome-wide analysis of BMI in adolescents and young adults reveals additional insight into the effects of genetic loci over the life course.14 
Genome-wide association analysis identifies new lung cancer susceptibility loci in never-smoking women in Asia.14 
A genome-wide association study of host genetic determinants of the antibody response to Anthrax Vaccine Adsorbed.14 
Genetics of Plasma Soluble Receptor for Advanced Glycation End-Products and Cardiovascular Outcomes in a Community-based Population: Results from the Atherosclerosis Risk in Communities Study.14 
Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles.14 
Response to Intravenous Cyclophosphamide Treatment for Lupus Nephritis Associated with Polymorphisms in the FCGR2B-FCRLA Locus.14 
Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control.14 
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.14 
New basal cell carcinoma susceptibility loci.14 
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.14 
Genetic Factors of the Disease Course after Sepsis: A Genome-Wide Study for 28Day Mortality.14 
Genome-wide association study for biomarker identification of Rapamycin and Everolimus using a lymphoblastoid cell line system.14 
A genome-wide association study identifies polymorphisms in the HLA-DR region associated with non-response to hepatitis B vaccination in Chinese Han populations.14 
Germline genomic variants associated with childhood acute lymphoblastic leukemia.14 
Genome-wide association study reveals genetic risk underlying Parkinson's disease.14 
Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.14 
Polymorphisms In HLA Class II Genes Are Associated With Susceptibility To Staphylococcus aureus Infection In A Caucasian Population.14 
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.14 
Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics.14 
Genome-wide association of body fat distribution in African ancestry populations suggests new loci.14 
A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study.14 
Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.14 
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.14 
A genome-wide association study of early menopause and the combined impact of identified variants.14 
Novel Association of Genetic Markers Affecting CYP2A6 activity and Lung Cancer Risk.14 
Genome-wide association study of biologically-informed periodontal complex traits offers novel insights into the genetic basis of periodontal disease.13 
Genome-wide association analysis of age-at-onset in Alzheimer's disease.13 
A genome-wide association study of red blood cell traits using the electronic medical record.13 
Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia.13 
Heritability and molecular genetic basis of electrodermal activity: A genome-wide association study.13 
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.13 
Pharmacogenetic Discovery in CALGB (Alliance) 90401 and Mechanistic Validation of a VAC14 Polymorphism that Increases Risk of Docetaxel-Induced Neuropathy.13 
Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2.13 
Genome-wide association study of sex hormones, gonadotropins and sex hormone-binding protein in Chinese men.13 
Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL).13 
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.13 
Genetic variations affecting serum carcinoembryonic antigen levels and status of regional lymph nodes in patients with sporadic colorectal cancer from Southern China.13 
Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris.13 
Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci.13 
A genome-wide association meta-analysis of preschool internalizing problems.13 
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.13 
White Matter Lesion Progression: Genome-Wide Search for Genetic Influences.13 
Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma.13 
A longitudinal genome-wide association study of anti-tumor necrosis factor response among Japanese patients with rheumatoid arthritis.13 
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry.13 
Obsessive-compulsive symptoms in a large population-based twin-family sample are predicted by clinically based polygenic scores and by genome-wide SNPs.13 
Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.13 
Association of common variants in the calcium-sensing receptor gene with serum calcium levels in East Asians.13 
Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study.13 
White matter integrity as an intermediate phenotype: exploratory genome-wide association analysis in individuals at high risk of bipolar disorder.13 
Genome-wide diet-gene interaction analyses for risk of colorectal cancer.13 
Association of granulomatosis with polyangiitis (Wegener's) with HLA-DPB1*04 and SEMA6A gene variants: evidence from genome-wide analysis.13 
A genome-wide association study of saturated, mono- and polyunsaturated red blood cell fatty acids in the Framingham Heart Offspring Study.13 
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20.13 
The Contribution of Common Genetic Variation to Nicotine and Cotinine Glucuronidation in Multiple Ethnic/Racial Populations.13 
Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder.13 
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.13 
A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.13 
Common variants in left/right asymmetry genes and pathways are associated with relative hand skill.13 
Risk alleles for multiple sclerosis identified by a genomewide study.13 
Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.13 
Common body mass index-associated variants confer risk of extreme obesity.13 
Heritability and Genome-Wide Association Analyses of Human Gait Suggest Contribution of Common Variants.13 
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.13 
Genome-wide association study link novel loci to endometriosis.13 
Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption.13 
New loci and coding variants confer risk for age-related macular degeneration in East Asians.13 
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.13 
Genome-wide association study identifies five loci associated with lung function.13 
Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study.13 
Common variants at ten loci modulate the QT interval duration in the QTSCD Study.13 
Genome-wide association study identifies five new breast cancer susceptibility loci.13 
Common variants at ten loci influence QT interval duration in the QTGEN Study.13 
Common variants conferring risk of schizophrenia.13 
Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.13 
Prognostic implications of genetic variants in advanced non-small cell lung cancer: a genome-wide association study.13 
Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels.12 
A genome-wide association scan implicates DCHS2, RUNX2, GLI3, PAX1 and EDAR in human facial variation.12 
A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population.12 
Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.12 
Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.12 
Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines.12 
An association study revealed substantial effects of dominance, epistasis and substance dependence co-morbidity on alcohol dependence symptom count.12 
Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia.12 
Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.12 
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.12 
A genome-wide association study of serum uric acid in African Americans.12 
Genome wide association study identifies two loci associated with cadmium in erythrocytes among never-smokers.12 
Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium.12 
A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.12 
Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions.12 
Genome-wide association study on progression of carotid artery intima media thickness over 10 years in a Chinese cohort.12 
Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction.12 
Preliminary evidence of genetic determinants of adiponectin response to fenofibrate in the Genetics of Lipid Lowering Drugs and Diet Network.12 
Wnt signaling and Dupuytren's disease.12 
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.12 
Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes.12 
Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia.12 
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.12 
Genome-Wide Association Study of Staphylococcus aureus Carriage in a Community-Based Sample of Mexican-Americans in Starr County, Texas.12 
Genetic architecture of age-related cognitive decline in African Americans.12 
Genome-wide association study of hepatitis C virus- and cryoglobulin-related vasculitis.12 
Metformin pharmacogenomics: a genome-wide association study to identify genetic and epigenetic biomarkers involved in metformin anticancer response using human lymphoblastoid cell lines.12 
Framingham Heart Study genome-wide association: results for pulmonary function measures.12 
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.12 
Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways.12 
Genome-wide association study identifies three new melanoma susceptibility loci.12 
Genome-wide association study in essential tremor identifies three new loci.12 
Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort.12 
A genome-wide association study of optic disc parameters.12 
Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma.12 
Genome-wide association study identifies three susceptibility loci for laryngeal squamous cell carcinoma in the Chinese population.12 
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).12 
The Genetic Landscape of Renal Complications in Type 1 Diabetes.12 
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.12 
Genome-wide pathway analysis of genome-wide association studies on systemic lupus erythematosus and rheumatoid arthritis.12 
A genome-wide association study of suicidal behavior.12 
Genome-wide scan of healthy human connectome discovers SPON1 gene variant influencing dementia severity.12 
Clinical, serologic, and genetic factors associated with pyoderma gangrenosum and erythema nodosum in inflammatory bowel disease patients.12 
Genome-wide association study identifies common variants associated with pharmacokinetics of psychotropic drugs.12 
A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).12 
Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders.11 
Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.11 
Genomewide association study of leprosy.11 
APOE and BCHE as modulators of cerebral amyloid deposition: a florbetapir PET genome-wide association study.11 
Genome-wide association study of tanning phenotype in a population of European ancestry.11 
Genome-wide association with diabetes-related traits in the Framingham Heart Study.11 
A genome-wide association study of aging.11 
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.11 
Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome.11 
Genome-wide association scan of trait depression.11 
Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.11 
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.11 
Gene-set and multivariate genome-wide association analysis of oppositional defiant behavior subtypes in attention-deficit/hyperactivity disorder.11 
Genome-wide association study of maternal and inherited loci for conotruncal heart defects.11 
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.11 
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations.11 
Meta-analysis of genome-wide association studies identifies multiple lung cancer susceptibility loci in never-smoking Asian women.11 
Genome-wide association study of co-occurring anxiety in major depression.11 
A comprehensive genetic association study of Alzheimer disease in African Americans.11 
Genome-wide association study identifies susceptibility loci for dengue shock syndrome at MICB and PLCE1.11 
Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci.11 
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease.11 
Genome-wide association study identifies five loci associated with susceptibility to pancreatic cancer in Chinese populations.11 
Common variants at 1p36 are associated with superior frontal gyrus volume.11 
Identification of HKDC1 and BACE2 as genes influencing glycemic traits during pregnancy through genome-wide association studies.11 
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors.11 
Susceptible gene of stasis-stagnation constitution from genome-wide association study related to cardiovascular disturbance and possible regulated traditional Chinese medicine.11 
New susceptibility loci in MYL2, C12orf51 and OAS1 associated with 1-h plasma glucose as predisposing risk factors for type 2 diabetes in the Korean population.11 
Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.11 
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation.11 
Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.11 
A genome-wide association study of body mass index across early life and childhood.11 
Performance of genetic risk factors in prediction of trichloroethylene induced hypersensitivity syndrome.11 
Identification of four new susceptibility loci for testicular germ cell tumour.11 
A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci.11 
Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus.11 
Genome-wide association scan for variants associated with early-onset prostate cancer.11 
Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.11 
Genome-wide association study of multiplex schizophrenia pedigrees.11 
Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy.11 
A genome wide association study of genetic loci that influence tumour biomarkers cancer antigen 19-9, carcinoembryonic antigen and α fetoprotein and their associations with cancer risk.11 
A genome-wide association study identifies three new risk loci for Kawasaki disease.11 
Genome-wide association study of vitamin D levels in children: replication in the Western Australian Pregnancy Cohort (Raine) study.11 
Genetic susceptibility to accelerated cognitive decline in the US Health and Retirement Study.11 
A genome-wide association study of seasonal pattern mania identifies NF1A as a possible susceptibility gene for bipolar disorder.11 
Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study.11 
Genetic determinants of P wave duration and PR segment.11 
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.11 
Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder.11 
Meta-analysis identifies four new loci associated with testicular germ cell tumor.11 
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque.11 
Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.11 
New susceptibility loci associated with kidney disease in type 1 diabetes.11 
A common variant association study reveals novel susceptibility loci for low HDL-cholesterol levels in ethnic Arabs.11 
Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.10 
Genome-wide association study of periodontal health measured by probing depth in adults ages 18-49 years.10 
Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy.10 
Genome-wide association analysis identifies susceptibility loci for migraine without aura.10 
Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes.10 
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene.10 
A genome-wide association study for serum bilirubin levels and gene-environment interaction in a Chinese population.10 
Genome-wide common and rare variant analysis provides novel insights into clozapine-associated neutropenia.10 
Antiphospholipid antibodies in a large population-based cohort: genome-wide associations and effects on monocyte gene expression.10 
Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians.10 
A genome-wide association study of self-rated health.10 
Genome-wide association study identifies genetic loci associated with iron deficiency.10 
A genome-wide association study of DSM-IV cannabis dependence.10 
Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus.10 
Genome-wide association study in East Asians suggests UHMK1 as a novel bone mineral density susceptibility gene.10 
Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology.10 
Multiple loci influencing hippocampal degeneration identified by genome scan.10 
Genome-Wide Study of Response to Platinum, Taxane, and Combination Therapy in Ovarian Cancer: In vitro Phenotypes, Inherited Variation, and Disease Recurrence.10 
Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus.10 
Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.10 
Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data.10 
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study.10 
A meta-analysis of genome-wide association studies for adiponectin levels in East Asians identifies a novel locus near WDR11-FGFR2.10 
Genome-wide association study of height and body mass index in Australian twin families.10 
Genome-wide association of trajectories of systolic blood pressure change.10 
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.10 
Common 5p15.33 and 6p21.33 variants influence lung cancer risk.10 
Variation at HLA-DPB1 is associated with dermatomyositis in Chinese population.10 
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.10 
Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies.10 
Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis.10 
Genome-wide association study of HPV-associated cervical cancer in Japanese women.10 
Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption.10 
Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.10 
Identifying genetic loci associated with antidepressant drug response with drug-gene interaction models in a population-based study.10 
Genome-wide SNP associations with rubella-specific cytokine responses in measles-mumps-rubella vaccine recipients.10 
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.10 
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.10 
A genome-wide association study for coronary artery disease identifies a novel susceptibility locus in the major histocompatibility complex.10 
Novel loci and pathways significantly associated with longevity.10 
Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion.10 
Genome-wide association analysis identifies multiple loci related to resting heart rate.10 
Common variation contributes to the genetic architecture of social communication traits.10 
Genome-wide association studies of asthma in population-based cohorts confirm known and suggested loci and identify an additional association near HLA.10 
Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases.10 
A genome wide association study (GWAS) providing evidence of an association between common genetic variants and late radiotherapy toxicity.10 
Genome-wide association study and meta-analysis of intraocular pressure.10 
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.10 
Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.10 
Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility.10 
Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility.10 
Genetic variants near PDGFRA are associated with corneal curvature in Australians.10 
Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes.10 
Meta-analysis identifies six new susceptibility loci for atrial fibrillation.10 
Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction.10 
Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.3210 
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility.10 
A genome-wide investigation of food addiction.10 
PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease.10 
A genome-wide assessment of variability in human serum metabolism.9 
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.9 
Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2.9 
Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels.9 
Genetic correction of PSA values using sequence variants associated with PSA levels.9 
Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome.9 
Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients.9 
GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP.9 
A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis.9 
Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.9 
A Twin Study of Breastfeeding With a Preliminary Genome-Wide Association Scan.9 
A genome-wide association study of caffeine-related sleep disturbance: confirmation of a role for a common variant in the adenosine receptor.9 
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.9 
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.9 
Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility.9 
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.9 
Genome-wide association study of patient-rated and clinician-rated global impression of severity during antipsychotic treatment.9 
Genome-wide association study in NSAID-induced acute urticaria/angioedema in Spanish and Han Chinese populations.9 
Genetic associations with C-reactive protein level and white blood cell count in the KARE study.9 
UGT1A1 is a major locus influencing bilirubin levels in African Americans.9 
A genome-wide meta-analysis of six type 1 diabetes cohorts identifies multiple associated loci.9 
Genome-wide association study of PR interval.9 
Genome-wide significant predictors of metabolites in the one-carbon metabolism pathway.9 
Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies.9 
Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism.9 
Genome-wide association study confirms lung cancer susceptibility loci on chromosomes 5p15 and 15q25 in an African-American population.9 
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study.9 
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.9 
Multiple loci identified in a genome-wide association study of prostate cancer.9 
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.9 
Common variants near ABCA1, AFAP1 and GMDS confer risk of primary open-angle glaucoma.9 
Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations.9 
Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.9 
Genome-wide association study of endometrial cancer in E2C2.9 
Genome-wide association study indicates variants associated with insulin signaling and inflammation mediate lipoprotein responses to fenofibrate.9 
Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis.9 
Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis.9 
Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.9 
Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility.9 
Genome-wide association scans for idiopathic osteonecrosis of the femoral head in a Korean population.9 
Genetic determinants of plasma β₂-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.9 
Identification of genetic variants or genes that are associated with Homoharringtonine (HHT) response through a genome-wide association study in human lymphoblastoid cell lines (LCLs).9 
Genome-Wide Association Study of the Genetic Determinants of Emphysema Distribution.9 
Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.9 
New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study.9 
Genome-wide association study does not reveal major genetic determinants for anti-cytomegalovirus antibody response.9 
A combined large-scale meta-analysis identifies COG6 as a novel shared risk locus for rheumatoid arthritis and systemic lupus erythematosus.9 
Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels.9 
Genome-wide association study of posttraumatic stress disorder in a cohort of Iraq-Afghanistan era veterans.9 
Genome-wide association study of coronary artery disease in the Japanese.9 
Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.9 
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene.9 
Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid.9 
Two new loci and gene sets related to sex determination and cancer progression are associated with susceptibility to testicular germ cell tumor.9 
Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease.9 
Genome-wide association study of triglyceride response to a high-fat meal among participants of the NHLBI Genetics of Lipid Lowering Drugs and Diet Network (GOLDN).9 
Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.9 
Clinical and Genetic Risk Factors for Acute Pancreatitis in Patients With Acute Lymphoblastic Leukemia.9 
Genome-wide association study in East Asians identifies two novel breast cancer susceptibility loci.9 
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.9 
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.9 
Genome-wide association study of intelligence: additive effects of novel brain expressed genes.9 
Genome-wide association study identifies variants associated with autoimmune hepatitis type 1.9 
A genome-wide association study of total serum and mite-specific IgEs in asthma patients.9 
Infection and inflammation in schizophrenia and bipolar disorder: a genome wide study for interactions with genetic variation.9 
Genome-wide association study of recurrent early-onset major depressive disorder.9 
Genome-wide association study of hepatitis in korean populations.9 
Association between single nucleotide polymorphism-genotype and outcome of patients with chronic lymphocytic leukemia in a randomized chemotherapy trial.9 
Genome-wide association study identifies eight loci associated with blood pressure.9 
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.9 
Genome-wide association study implicates HLA-C*01:02 as a risk factor at the major histocompatibility complex locus in schizophrenia.9 
Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 Loci.9 
Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21.9 
Serum ferritin levels are associated with a distinct phenotype of chronic hepatitis C poorly responding to pegylated interferon-alpha and ribavirin therapy.9 
Genome-wide association meta-analysis for total serum bilirubin levels.9 
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.9 
EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children.9 
Genome-wide association identifies three new susceptibility loci for Paget's disease of bone.9 
A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.9 
Frontotemporal dementia and its subtypes: a genome-wide association study.9 
IREB2 and GALC are Associated with Pulmonary Artery Enlargement in Chronic Obstructive Pulmonary Disease.8 
Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations.8 
Genome-wide association study of the five-factor model of personality in young Korean women.8 
Genome wide association and linkage analyses identified three loci-4q25, 17q23.2, and 10q11.21-associated with variation in leukocyte telomere length: the Long Life Family Study.8 
Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data.8 
Evaluating genetic risk for prostate cancer among Japanese and Latinos.8 
Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence.8 
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis.8 
ALDH2 is associated to alcohol dependence and is the major genetic determinant of "daily maximum drinks" in a GWAS study of an isolated rural Chinese sample.8 
HLA-DRB1*16: 01-DQB1*05: 02 is a novel genetic risk factor for flupirtine-induced liver injury.8 
Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke.8 
Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project.8 
Genome wide association study of age at menarche in the Japanese population.8 
A Genome-Wide Association Meta-Analysis of Attention-Deficit/Hyperactivity Disorder Symptoms in Population-Based Pediatric Cohorts.8 
Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation.8 
Genetic determinants of statin-induced low-density lipoprotein cholesterol reduction: the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial.8 
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study.8 
Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).8 
A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine.8 
A whole-genome association study of major determinants for allopurinol-related Stevens-Johnson syndrome and toxic epidermal necrolysis in Japanese patients.8 
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis.8 
Investigation of single nucleotide polymorphisms and biological pathways associated with response to TNFα inhibitors in patients with rheumatoid arthritis.8 
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.8 
Common variants on chromosome 6p22.1 are associated with schizophrenia.8 
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.8 
Loss-of-function variants in ATM confer risk of gastric cancer.8 
A genome-wide association study in progressive multiple sclerosis.8 
Genome-Wide Association Analysis of Young Onset Stroke Identifies a Locus on Chromosome 10q25 Near HABP2.8 
Common variation near ROBO2 is associated with expressive vocabulary in infancy.8 
Newly identified genetic risk variants for celiac disease related to the immune response.8 
Genome-wide association study of kidney function decline in individuals of European descent.8 
Genome-wide association study of spontaneous resolution of hepatitis C virus infection: data from multiple cohorts.8 
Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.8 
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms.8 
Heritability and genome-wide association analysis of renal sinus fat accumulation in the Framingham Heart Study.8 
Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men.8 
Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma.8 
A genome-wide association study of survival in small-cell lung cancer patients treated with irinotecan plus cisplatin chemotherapy.8 
C9orf72 and UNC13A are shared risk loci for ALS and FTD: A genome-wide meta-analysis.8 
Genome-wide association analysis of Vogt-Koyanagi-Harada syndrome identifies two new susceptibility loci at 1p31.2 and 10q21.3.8 
Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk.8 
Novel loci associated with PR interval in a genome-wide association study of 10 African American cohorts.8 
Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.8 
Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients.8 
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3.8 
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies.8 
Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21.8 
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.8 
Genome-wide association study of aspirin-exacerbated respiratory disease in a Korean population.8 
A Pooling Genome-Wide Association Study Combining a Pathway Analysis for Typical Sporadic Parkinson's Disease in the Han Population of Chinese Mainland.8 
Genetic risk variants for membranous nephropathy: extension of and association with other chronic kidney disease aetiologies.8 
Genome-wide association and admixture analysis of glaucoma in the Women's Health Initiative.8 
Genome-wide association study of diabetic retinopathy in a Taiwanese population.8 
Beyond single-marker analyses: mining whole genome scans for insights into treatment responses in severe sepsis.8 
Genetic Associations with Plasma B12, B6, and Folate Levels in an Ischemic Stroke Population from the Vitamin Intervention for Stroke Prevention (VISP) Trial.8 
A genome-wide association study of the Protein C anticoagulant pathway.8 
A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.8 
Genome-wide association study of electrocardiographic parameters identifies a new association for PR interval and confirms previously reported associations.8 
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.8 
A genome-wide study of lipid response to fenofibrate in Caucasians: a combined analysis of the GOLDN and ACCORD studies.8 
A Genome-wide Association Study of Myasthenia Gravis.8 
Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population.8 
Pharmacogenomic Study of Clozapine-Induced Agranulocytosis/Granulocytopenia in a Japanese Population.8 
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.8 
A genome-wide association study and biological pathway analysis of epilepsy prognosis in a prospective cohort of newly treated epilepsy.8 
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.8 
Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash.8 
Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.8 
Genetic association analyses highlight biological pathways underlying mitral valve prolapse.8 
Genome-wide association study implicates PARD3B-based AIDS restriction.8 
Genome-wide association analysis identifies three psoriasis susceptibility loci.8 
Genome-wide association study of lung function phenotypes in a founder population.8 
Effect of genetic variations on ticagrelor plasma levels and clinical outcomes.8 
A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury.8 
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.8 
Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma.8 
GWAS identifies novel susceptibility loci on 6p21.32 and 21q21.3 for hepatocellular carcinoma in chronic hepatitis B virus carriers.8 
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.8 
A genome-wide association study reveals that variants within the HLA region are associated with risk for nonobstructive azoospermia.8 
Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis.8 
A Genome-Wide Association Study in Caucasian Women suggests the involvement of HLA genes in the severity of facial solar lentigines.8 
Identification of a Novel Mucin Gene HCG22 Associated with Steroid-Induced Ocular Hypertension.8 
An association between anti-nuclear antibody and HLA class II locus and heterogeneous characteristics of staining patterns: The Nagahama Study.8 
Seasonality shows evidence for polygenic architecture and genetic correlation with schizophrenia and bipolar disorder.8 
A Genome-wide study of blood pressure in African Americans accounting for gene-smoking interaction.8 
Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene.8 
Family-based genome-wide association study of frontal θ oscillations identifies potassium channel gene KCNJ6.8 
Linkage and association of successful aging to the 6q25 region in large Amish kindreds.8 
A genome-wide association study reveals ARL15, a novel non-HLA susceptibility gene for rheumatoid arthritis in North Indians.8 
Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis.8 
Genome-wide association study of comorbid depressive syndrome and alcohol dependence.8 
A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.8 
Plasma Levels of Soluble Interleukin-2 Receptor ?: Associations With Clinical Cardiovascular Events and Genome-Wide Association Scan.7 
HLA-DQA1-HLA-DRB1 variants confer susceptibility to pancreatitis induced by thiopurine immunosuppressants.7 
Genome-wide association study of blood pressure response to methylphenidate treatment of attention-deficit/hyperactivity disorder.7 
Genome-wide association meta-analysis identifies new endometriosis risk loci.7 
Genome-wide association study of the child behavior checklist dysregulation profile.7 
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population.7 
Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.7 
Genome-wide association study of colorectal cancer in Hispanics.7 
Genome-wide association study of sensory disturbances in the inferior alveolar nerve after bilateral sagittal split ramus osteotomy.7 
Genome-wide meta-analysis of observational studies shows common genetic variants associated with macronutrient intake.7 
Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish.7 
Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood.7 
HLA-Cw*1202-B*5201-DRB1*1502 haplotype increases risk for ulcerative colitis but reduces risk for Crohn's disease.7 
Common variants at the promoter region of the APOM confer a risk of rheumatoid arthritis.7 
Genome-wide association study of new-onset atrial fibrillation after coronary artery bypass grafting surgery.7 
NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium.7 
GWAS of human bitter taste perception identifies new loci and reveals additional complexity of bitter taste genetics.7 
Genome-wide association study of personality traits in bipolar patients.7 
Genome-wide association study of survival in patients with pancreatic adenocarcinoma.7 
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.7 
A genome-wide association study identifies susceptibility loci for Wilms tumor.7 
Genome-wide association analysis of eating disorder-related symptoms, behaviors, and personality traits.7 
Ancestry and other genetic associations with plasma PCSK9 response to simvastatin.7 
Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset.7 
Genome-wide association study for levels of total serum IgE identifies HLA-C in a Japanese population.7 
Investigation of Genetic Variation Underlying Central Obesity amongst South Asians.7 
GWAS findings for human iris patterns: associations with variants in genes that influence normal neuronal pattern development.7 
The genetic aetiology of cannabis use initiation: a meta-analysis of genome-wide association studies and a SNP-based heritability estimation.7 
Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study.7 
A genomewide association study of citalopram response in major depressive disorder.7 
Common Genetic Variation and Survival after Colorectal Cancer Diagnosis: A Genome-Wide Analysis.7 
HLA-DQ strikes again: genome-wide association study further confirms HLA-DQ in the diagnosis of asthma among adults.7 
Genetic variants and environmental factors associated with hormonal markers of ovarian reserve in Caucasian and African American women.7 
Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study.7 
HLA-B*57:01 Confers Susceptibility to Pazopanib-Associated Liver Injury in Patients With Cancer.7 
Genome-wide association study in Chinese men identifies two new prostate cancer risk loci at 9q31.2 and 19q13.4.7 
HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans.7 
A genome-wide association study of clinical symptoms of dissociation in a trauma-exposed sample.7 
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.7 
Genetics of aging, health, and survival: dynamic regulation of human longevity related traits.7 
Chromosome 7p11.2 (EGFR) variation influences glioma risk.7 
Meta-analysis identifies seven susceptibility loci involved in the atopic march.7 
Epidemiological and genome-wide association study of gastritis or gastric ulcer in korean populations.7 
Identification of Risk Loci for Crohn's Disease Phenotypes Using a Genome-wide Association Study.7 
Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels.7 
GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma.7 
A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality.7 
Genomewide association analysis of coronary artery disease.7 
Genetic variants that confer resistance to malaria are associated with red blood cell traits in African-Americans: an electronic medical record-based genome-wide association study.7 
A meta-analysis of reflux genome-wide association studies in 6750 Northern Europeans from the general population.7 
Meta-analysis identifies common variants associated with body mass index in east Asians.7 
Genome-wide association study of Alzheimer's disease.7 
Genome-wide association study identifies five susceptibility loci for glioma.7 
A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.7 
Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies.7 
Genetic determinants of trabecular and cortical volumetric bone mineral densities and bone microstructure.7 
Genome-wide association study of HPV seropositivity.7 
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.7 
HLA has strongest association with IgA nephropathy in genome-wide analysis.7 
Genetic Determinants of Survival in Patients with Alzheimer's Disease.7 
A genome-wide association study of carotid atherosclerosis in HIV-infected men.7 
Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort.7 
Genome-wide association study of Tourette's syndrome.7 
An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits.7 
Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations.7 
Genome-wide association analysis identifies six new loci associated with forced vital capacity.7 
Genetic variants at 6p21.1 and 7p15.3 are associated with risk of multiple cancers in Han Chinese.7 
Genome-wide association study of gastric adenocarcinoma in Asia: a comparison of associations between cardia and non-cardia tumours.7 
Genome-wide association analyses in East Asians identify new susceptibility loci for colorectal cancer.7 
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study.7 
Genetic variants associated with vein graft stenosis after coronary artery bypass grafting.7 
Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.7 
Genome-wide association study on plasma levels of midregional-proadrenomedullin and C-terminal-pro-endothelin-1.7 
HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study.7 
Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae.7 
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.7 
Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease.7 
Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).7 
A new 3p25 locus is associated with liver fibrosis progression in HIV/HCV co-infected patients.7 
Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes.7 
Genome-wide interaction study of gene-by-occupational exposure and effects on FEV<sub>1</sub> levels.7 
GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy.7 
Variation at HLA-DRB1 is associated with resistance to enteric fever.7 
Chemerin, a novel adipokine in the regulation of angiogenesis.7 
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate.7 
Genome-wide association study identifies BICD1 as a susceptibility gene for emphysema.7 
Genome-wide genetic investigation of serological measures of common infections.7 
Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.7 
A genome-wide association study on amyotrophic lateral sclerosis in the Taiwanese Han population.7 
Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study.6 
A genome-wide association study of testicular germ cell tumor.6 
Genome-wide association study of intracranial aneurysm identifies three new risk loci.6 
A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?6 
Genetic variation associated with circulating monocyte count in the eMERGE Network.6 
Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia.6 
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.6 
Pooled analysis of genome-wide association studies of cervical intraepithelial neoplasia 3 (CIN3) identifies a new susceptibility locus.6 
Genome-wide significant risk associations for mucinous ovarian carcinoma.6 
THOC5: a novel gene involved in HDL-cholesterol metabolism.6 
Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene.6 
Childhood intelligence is heritable, highly polygenic and associated with FNBP1L.6 
Genome-wide association study reveals two new risk loci for bipolar disorder.6 
Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia.6 
Genome-wide interaction studies reveal sex-specific asthma risk alleles.6 
Genetic Variants Associated with Circulating Parathyroid Hormone.6 
Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.6 
A genome wide association study of plasma uric acid levels in obese cases and never-overweight controls.6 
Genome-wide association analysis identifies new susceptibility loci for Beh&#x000e7;et's disease and epistasis between HLA-B*51 and ERAP1.6 
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate.6 
Bivariate genome-wide association analyses identified genes with pleiotropic effects for femoral neck bone geometry and age at menarche.6 
Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study.6 
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.6 
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.6 
Genetic underpinnings of left superior temporal gyrus thickness in patients with schizophrenia.6 
Using multiple measures for quantitative trait association analyses: application to estimated glomerular filtration rate.6 
Imputation-based meta-analysis of severe malaria in three African populations.6 
A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3.6 
A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease.6 
Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population.6 
Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21.6 
Genome-wide association study to identify genetic determinants of severe asthma.6 
HLA-B*38:02:01 predicts carbimazole/methimazole-induced agranulocytosis.6 
From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases.6 
Genomewide association for schizophrenia in the CATIE study: results of stage 1.6 
Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.6 
GWAS identifies four novel eosinophilic esophagitis loci.6 
Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes.6 
A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation.6 
Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups.6 
Genome-wide association study identifies novel loci associated with serum level of vitamin B12 in Chinese men.6 
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.6 
Common variation at 6q16 within HACE1 and LIN28B influences susceptibility to neuroblastoma.6 
A Genome-Wide Association Study of Early Spontaneous Preterm Delivery.6 
A Genome-Wide Test of the Differential Susceptibility Hypothesis Reveals a Genetic Predictor of Differential Response to Psychological Treatments for Child Anxiety Disorders.6 
A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.6 
Pilot genome-wide association search identifies potential loci for risk of erectile dysfunction in type 1 diabetes using the DCCT/EDIC study cohort.6 
Genome-wide association study of alcohol dependence.6 
Genome-wide interaction study of smoking and bladder cancer risk.6 
GWAS meta analysis identifies TSNARE1 as a novel Schizophrenia / Bipolar susceptibility locus.6 
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.6 
Genome-wide association study of clinically defined gout identifies multiple risk loci and its association with clinical subtypes.6 
Genome-wide association study of severity in multiple sclerosis.6 
Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: A genome-wide association study.6 
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.6 
Genome-wide association study identifies novel loci association with fasting insulin and insulin resistance in African Americans.6 
A genome-wide association study reveals 2 new susceptibility loci for atopic dermatitis.6 
Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci.6 
Genome-wide Association Study of Radiographic Knee Osteoarthritis in North American Caucasians.6 
Genome-wide association study meta-analysis reveals transethnic replication of mean arterial and pulse pressure loci.6 
GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.6 
T2DM GWAS in the Lebanese population confirms the role of TCF7L2 and CDKAL1 in disease susceptibility.6 
Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas.6 
Genome-wide association study of serum lipids confirms previously reported associations as well as new associations of common SNPs within PCSK7 gene with triglyceride.6 
CKM and LILRB5 Are Associated with Serum Levels of Creatine Kinase.6 
Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study.6 
IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR.6 
Identification of a melanoma susceptibility locus and somatic mutation in TET2.6 
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip.6 
Sequence variants in three loci influence monocyte counts and erythrocyte volume.6 
Genome-wide association studies identify loci associated with age at menarche and age at natural menopause.6 
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins.6 
Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1.6 
Genome-wide Interrogation of Longitudinal FEV1 in Children with Asthma.6 
A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study.6 
Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer.6 
A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.6 
Genome-wide association analysis of pain severity in dysmenorrhea identifies association at chromosome 1p13.2, near the nerve growth factor locus.6 
Identification of new susceptibility loci for gastric non-cardia adenocarcinoma: pooled results from two Chinese genome-wide association studies.6 
Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies.6 
Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data.6 
Genetic association with lipids in Filipinos: waist circumference modifies an APOA5 effect on triglyceride levels.6 
Genome-wide association study identifies new susceptibility loci for epithelial ovarian cancer in Han Chinese women.6 
Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies.6 
Human genome-wide association and mouse knockout approaches identify platelet supervillin as an inhibitor of thrombus formation under shear stress.6 
Genome-wide association study of recalcitrant atopic dermatitis in Korean children.6 
Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium.6 
Genome-wide association study identifies novel breast cancer susceptibility loci.6 
A Common Variant in the SETD7 Gene Predicts Serum Lycopene Concentrations.6 
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.6 
Electronic medical records and genomics (eMERGE) network exploration in cataract: Several new potential susceptibility loci.6 
Two new susceptibility loci for Kawasaki disease identified through genome-wide association analysis.6 
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.6 
Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men.6 
Meta-analysis of new genome-wide association studies of colorectal cancer risk.6 
Genome-wide association study identifies two susceptibility loci for osteosarcoma.6 
Genome-wide association study identifies candidate genes for male fertility traits in humans.6 
Genome-wide association study of autistic-like traits in a general population study of young adults.6 
A genome-wide association study identifies potential susceptibility Loci for hirschsprung disease.6 
Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism.6 
Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia.6 
Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia.6 
Large-scale genome-wide association study of Asian population reveals genetic factors in FRMD4A and other loci influencing smoking initiation and nicotine dependence.6 
Genetic Contributions to Urgency Urinary Incontinence in Women.6 
A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations.6 
Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.6 
Genome-wide association study identifies variants associated with progression of liver fibrosis from HCV infection.6 
Genetic variants associated with glycine metabolism and their role in insulin sensitivity and type 2 diabetes.6 
Genome-wide association study identifies WNT7B as a novel locus for central corneal thickness in Latinos.6 
Genome-wide association study for the interaction between BMR and BMI in obese Korean women including overweight.6 
Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.6 
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.5 
Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.5 
Genome-wide meta-analysis of homocysteine and methionine metabolism identifies five one carbon metabolism loci and a novel association of ALDH1L1 with ischemic stroke.5 
Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.5 
Common variants at 12q14 and 12q24 are associated with hippocampal volume.5 
Common genetic variants associate with serum phosphorus concentration.5 
PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.5 
Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.5 
An integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri Lanka.5 
Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.5 
Novel Genetic Locus Implicated for HIV-1 Acquisition with Putative Regulatory Links to HIV Replication and Infectivity: A Genome-Wide Association Study.5 
Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes.5 
Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study.5 
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.5 
Genetic and clinical factors associated with obesity among adult survivors of childhood cancer: A report from the St. Jude Lifetime Cohort.5 
Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis.5 
New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.5 
Genome-wide association study of serum albumin:globulin ratio in Korean populations.5 
Identification of low-frequency variants associated with gout and serum uric acid levels.5 
Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.5 
Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer.5 
Genetic association and stress mediated down-regulation in trabecular meshwork implicates MPP7 as a novel candidate gene in primary open angle glaucoma.5 
Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption.5 
Genome-wide association study of perioperative myocardial infarction after coronary artery bypass surgery.5 
GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.5 
Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior.5 
Meta-analysis of genome-wide association studies for circulating phylloquinone concentrations.5 
Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.5 
Genome-wide association study of SSRI/SNRI-induced sexual dysfunction in a Japanese cohort with major depression.5 
Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science.5 
A genome-wide association study for diabetic nephropathy genes in African Americans.5 
The First Pilot Genome-Wide Gene-Environment Study of Depression in the Japanese Population.5 
Genome wide association study of uric acid in Indian population and interaction of identified variants with Type 2 diabetes.5 
Genome-wide meta-analysis points to CTC1 and ZNF676 as genes regulating telomere homeostasis in humans.5 
Genetic determinants of cardiovascular events among women with migraine: a genome-wide association study.5 
A Genome Wide Association Study of Fast Beta EEG in Families of European Ancestry.5 
Genome-wide association studies of the PR interval in African Americans.5 
Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese.5 
Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.5 
Common genetic variants and gene expression associated with white matter microstructure in the human brain.5 
A mega-analysis of genome-wide association studies for major depressive disorder.5 
Genetic Interactions Explain Variance in Cingulate Amyloid Burden: An AV-45 PET Genome-Wide Association and Interaction Study in the ADNI Cohort.5 
The landscape of recombination in African Americans.5 
Genome-wide association analysis identifies three new risk loci for gout arthritis in Han Chinese.5 
A genome-wide perspective of genetic variation in human metabolism.5 
Identification of inherited genetic variations influencing prognosis in early-onset breast cancer.5 
Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate.5 
Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study.5 
A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease.5 
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.5 
Genome-wide association study for serum urate concentrations and gout among African Americans identifies genomic risk loci and a novel URAT1 loss-of-function allele.5 
The chromosome 3q25 genomic region is associated with measures of adiposity in newborns in a multi-ethnic genome-wide association study.5 
Chronic Periodontitis Genome-wide Association Study in the Hispanic Community Health Study / Study of Latinos.5 
A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation.5 
Robust evidence for five new Graves' disease risk loci from a staged genome-wide association analysis.5 
Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples.5 
Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study.5 
Common variants at 12q15 and 12q24 are associated with infant head circumference.5 
Genomewide association study for onset age in Parkinson disease.5 
Genome-wide Association Studies in Women of African Ancestry Identified 3q26.21 as a Novel Susceptibility Locus for Estrogen Receptor Negative Breast Cancer.5 
Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.5 
Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.5 
Genome-wide meta-analyses identify multiple loci associated with smoking behavior.5 
Overrepresentation of glutamate signaling in Alzheimer's disease: network-based pathway enrichment using meta-analysis of genome-wide association studies.5 
Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics.5 
Genome-wide analysis of hepatic lipid content in extreme obesity.5 
Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma.5 
Common variants in the GDF5-UQCC region are associated with variation in human height.5 
Genome-wide association scan for five major dimensions of personality.5 
Genome-Wide Association Study of CSF Levels of 59 Alzheimer's Disease Candidate Proteins: Significant Associations with Proteins Involved in Amyloid Processing and Inflammation.5 
Genome-wide association study and gene expression analysis identifies CD84 as a predictor of response to etanercept therapy in rheumatoid arthritis.5 
Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation.5 
A genome-wide association study of metabolic traits in human urine.5 
Genome-wide scan for loci of adolescent obesity and their relationship with blood pressure.5 
The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease.5 
Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression.5 
Assessment of genetic determinants of the association of &#x003b3;' fibrinogen in relation to cardiovascular disease.5 
Genomic and transcriptomic predictors of triglyceride response to regular exercise.5 
A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids.5 
A genome-wide association meta-analysis identifies new childhood obesity loci.5 
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.5 
A genome-wide association study in Chinese men identifies three risk loci for non-obstructive azoospermia.5 
A genome-wide association study of a coronary artery disease risk variant.5 
Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.5 
Genetic variants at 1q32.1, 10q11.2 and 19q13.41 are associated with prostate-specific antigen for prostate cancer screening in two Korean population-based cohort studies.5 
Gene by stress genome-wide interaction analysis and path analysis identify EBF1 as a cardiovascular and metabolic risk gene.5 
Genome-wide association study (GWAS) for molar-incisor hypomineralization (MIH).5 
Weight loss after gastric bypass is associated with a variant at 15q26.1.5 
Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels.5 
Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.5 
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.5 
New variants including ARG1 polymorphisms associated with C-reactive protein levels identified by genome-wide association and pathway analysis.5 
Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels.5 
Genetic loci influencing kidney function and chronic kidney disease.5 
Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study.5 
A genome-wide association study identifies a potential novel gene locus for keratoconus, one of the commonest causes for corneal transplantation in developed countries.5 
Genome-wide association study of orthostatic hypotension and supine-standing blood pressure changes in two korean populations.5 
Novel locus FER is associated with serum HMW adiponectin levels.5 
A Genome-Wide Association Study of Cutaneous Squamous Cell Carcinoma among European Descendants.5 
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.5 
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations.5 
Variants in several genomic regions associated with asperger disorder.5 
Genetic analysis of advanced glycation end products in the DHS MIND study.5 
Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.5 
Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia.5 
Genome-wide scan of copy number variation in late-onset Alzheimer's disease.5 
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.5 
Genetic predictors of risk and resilience in psychiatric disorders: a cross-disorder genome-wide association study of functional impairment in major depressive disorder, bipolar disorder, and schizophrenia.5 
Genome-wide association study of prognosis in advanced non-small cell lung cancer patients receiving platinum-based chemotherapy.5 
Genome-wide association study of HLA-DQB1*06:02 negative essential hypersomnia.5 
Genome-wide association study identifies three loci associated with melanoma risk.5 
Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.5 
Genome-wide association of sleep and circadian phenotypes.5 
Genomic determinants of motor and cognitive outcomes in Parkinson's disease.5 
A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium.5 
Enhanced meta-analysis and replication studies identify five new psoriasis susceptibility loci.5 
Genome-wide association study identifies genetic risk underlying primary rhegmatogenous retinal detachment.5 
A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.5 
Genetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.5 
Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project.5 
Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.5 
Genome-wide association study of a quantitative disordered gambling trait.5 
A trans-ethnic genome-wide association study identifies gender-specific loci influencing pediatric aBMD and BMC at the distal radius.5 
Genetic determinants of circulating sphingolipid concentrations in European populations.5 
Genetic loci for serum magnesium among African-Americans and gene-environment interaction at MUC1 and TRPM6 in European-Americans: the Atherosclerosis Risk in Communities (ARIC) study.5 
Genome-wide association study of the age of onset of childhood asthma.5 
Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes.5 
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.5 
Genome wide association study identifies a novel putative mammographic density locus at 1q12-q21.5 
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1).5 
Genome-Wide Association of Heroin Dependence in Han Chinese.5 
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease.5 
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.5 
Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2.5 
Variation at 10p12.2 and 10p14 influences risk of childhood B-cell acute lymphoblastic leukemia and phenotype.5 
Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.5 
Candidate Loci are Revealed by an Initial Genome-wide Association Study of Juvenile Osteochondritis Dissecans.5 
Genome- and phenome-wide analyses of cardiac conduction identifies markers of arrhythmia risk.5 
Genome-wide meta-analyses of smoking behaviors in African Americans.5 
A genome-wide association study in Han Chinese identifies new susceptibility loci for ankylosing spondylitis.5 
Genome-wide association analysis in East Asians identifies breast cancer susceptibility loci at 1q32.1, 5q14.3 and 15q26.1.4 
Common genetic variation near MC4R is associated with waist circumference and insulin resistance.4 
Genome-wide association study identifies TH1 pathway genes associated with lung function in asthmatic patients.4 
A genome-wide association study of monozygotic twin-pairs suggests a locus related to variability of serum high-density lipoprotein cholesterol.4 
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.4 
Identification of genetic modifiers of age-at-onset for familial Parkinson's disease.4 
A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.4 
A genome-wide association study of suicide severity scores in bipolar disorder.4 
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.4 
Genome-wide association study of breast cancer in the Japanese population.4 
Genome-wide linkage and association scans for pulse pressure in Chinese twins.4 
Digital quantification of human eye color highlights genetic association of three new loci.4 
Association analyses identify three susceptibility Loci for vitiligo in the Chinese Han population.4 
Multiple loci associated with indices of renal function and chronic kidney disease.4 
Genetic variants in PLG, LPA and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels.4 
Genomewide association studies of stroke.4 
Identification of two new loci at IL23R and RAB32 that influence susceptibility to leprosy.4 
The National Longitudinal Study of Adolescent to Adult Health (Add Health) Sibling Pairs Genome-Wide Data.4 
Genome-wide association study of Parkinson's disease in East Asians.4 
Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci.4 
Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area.4 
Genome-wide association study identifies four loci associated with eruption of permanent teeth.4 
Susceptibility loci for intracranial aneurysm in European and Japanese populations.4 
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.4 
CMPK1 and RBP3 are associated with corneal curvature in Asian populations.4 
Genetic variants on chromosome 1q41 influence ocular axial length and high myopia.4 
Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned.4 
Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.4 
Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8.4 
Common and rare variants associated with kidney stones and biochemical traits.4 
Genetic variants in LEKR1 and GALNT10 modulate sex-difference in carotid intima-media thickness: A genome-wide interaction study.4 
Novel genetic variants modify the effect of smoking on carotid plaque burden in Hispanics.4 
Genome-Wide Association Study Identifies ZNF354C Variants Associated with Depression from Interferon-Based Therapy for Chronic Hepatitis C.4 
Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.4 
A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.4 
1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data.4 
Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations.4 
A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.4 
Genetic determinants of haemolysis in sickle cell anaemia.4 
Genome-wide association analysis of juvenile idiopathic arthritis identifies a new susceptibility locus at chromosomal region 3q13.4 
Genetic variation modifies risk for neurodegeneration based on biomarker status.4 
Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels.4 
Common variants at five new loci associated with early-onset inflammatory bowel disease.4 
Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.4 
Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM.4 
Meta-analysis identifies loci affecting levels of the potential osteoarthritis biomarkers sCOMP and uCTX-II with genome wide significance.4 
A combined analysis of genome-wide association studies in breast cancer.4 
Genetic relationships between suicide attempts, suicidal ideation and major psychiatric disorders: a genome-wide association and polygenic scoring study.4 
Common genetic variation in ETV6 is associated with colorectal cancer susceptibility.4 
Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men.4 
Genome-wide association study of serum selenium concentrations.4 
Identification of new genetic risk variants for type 2 diabetes.4 
A genomewide association study of skin pigmentation in a South Asian population.4 
A genome-wide association search for type 2 diabetes genes in African Americans.4 
Association between liver-specific gene polymorphisms and their expression levels with nonalcoholic fatty liver disease.4 
Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.4 
Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.4 
Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus.4 
Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL.4 
A genome-wide association study of recipient genotype and medium-term kidney allograft function.4 
GWAS for executive function and processing speed suggests involvement of the CADM2 gene.4 
A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer.4 
VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock.4 
A genome-wide association study identifies two new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese.4 
Genomics and metabolomics of muscular mass in community-based sample of UK females.4 
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.4 
Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases.4 
Genome-wide association study of N370S homozygous Gaucher disease reveals the candidacy of CLN8 gene as a genetic modifier contributing to extreme phenotypic variation.4 
Clinical, polysomnographic and genome-wide association analyses of narcolepsy with cataplexy: a European Narcolepsy Network study.4 
Genome-wide association study of neurocognitive impairment and dementia in HIV-infected adults.4 
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment.4 
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease.4 
Novel genetic predictors of venous thromboembolism risk in African Americans.4 
Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities.4 
Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C.4 
Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.4 
Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.4 
Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts.4 
Identification of IL6R and chromosome 11q13.5 as risk loci for asthma.4 
A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13.4 
Genome-wide association study of major recurrent depression in the U.K. population.4 
Drug-Gene Interactions of Antihypertensive Medications and Risk of Incident Cardiovascular Disease: A Pharmacogenomics Study from the CHARGE Consortium.4 
A Genome-Wide Association Study Identifies the Skin Color Genes IRF4, MC1R, ASIP, and BNC2 Influencing Facial Pigmented Spots.4 
Genetic Markers Associated With Plasma Protein C Level in African Americans: The Atherosclerosis Risk in Communities (ARIC) Study.4 
Association of 3q13.32 variants with hip trochanter and intertrochanter bone mineral density identified by a genome-wide association study.4 
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.4 
Loci affecting gamma-glutamyl transferase in adults and adolescents show age &#x000d7; SNP interaction and cardiometabolic disease associations.4 
Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.4 
Meta-analysis of two genome-wide association studies identifies four genetic loci associated with thyroid function.4 
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study.4 
GCKR and PPP1R3B identified as genome-wide significant loci for plasma lactate: the Atherosclerosis Risk in Communities (ARIC) study.4 
Multiethnic genome-wide association study identifies ethnic-specific associations with body mass index in Hispanics and African Americans.4 
Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study.4 
Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: a meta-analysis of three genome-wide association studies.4 
Genome wide association study of SNP-, gene-, and pathway-based approaches to identify genes influencing susceptibility to Staphylococcus aureus infections.4 
Genome wide association (GWA) predictors of anti-TNFalpha therapeutic responsiveness in pediatric inflammatory bowel disease.4 
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis.4 
Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humans.4 
A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.4 
Impact of four loci on serum tamsulosin hydrochloride concentration.4 
Genome-wide association study identifies three novel genetic markers associated with elite endurance performance.4 
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis.4 
Genome-wide association study of serious blistering skin rash caused by drugs.4 
Common variants at 10p12.31, 10q21.1 and 13q12.13 are associated with sporadic pituitary adenoma.4 
Genome-wide association study of suicide attempts in mood disorder patients.4 
A genome-wide association study of acenocoumarol maintenance dosage.4 
Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation.4 
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis.4 
Genome-Wide Association Study of Peripheral Arterial Disease in a Japanese Population.4 
Genome Wide Association Study for Predictors of Progression Free Survival in Patients on Capecitabine, Oxaliplatin, Bevacizumab and Cetuximab in First-Line Therapy of Metastatic Colorectal Cancer.4 
Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne.4 
A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.4 
Genetic determinants of dabigatran plasma levels and their relation to bleeding.4 
A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese.4 
A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.4 
Fasting glucose GWAS candidate region analysis across ethnic groups in the Multiethnic Study of Atherosclerosis (MESA).4 
Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study.4 
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.4 
A genome-wide association meta-analysis on apolipoprotein A-IV concentrations.4 
Genome-Wide Association Study of Intracranial Aneurysm Identifies a New Association on Chromosome 7.4 
Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.4 
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways.4 
Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population.4 
A genome-wide association study identifies four novel susceptibility loci underlying inguinal hernia.4 
A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33.4 
Are C-reactive protein associated genetic variants associated with serum levels and retinal markers of microvascular pathology in Asian populations from Singapore?4 
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder.4 
A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.4 
Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A.4 
SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.4 
Variants in MTNR1B influence fasting glucose levels.4 
Genome-wide association study identifies genetic determinants of urine PCA3 levels in men.4 
Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis.4 
ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology.4 
A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.4 
Meta-analysis of genome-wide association studies identifies two loci associated with circulating osteoprotegerin levels.4 
Dissecting the genetics of chronic mucus hypersecretion in smokers with and without COPD.4 
Genome-wide association study of maternal and inherited effects on left-sided cardiac malformations.4 
A genome-wide association study of third molar agenesis in Japanese and Korean populations.4 
Pooling-Based Genome-Wide Association Study Identifies Risk Loci in the Pathogenesis of Ovarian Endometrioma in Chinese Han Women.4 
Individual common variants exert weak effects on the risk for autism spectrum disorderspi.4 
Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project.4 
Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls.4 
Characteristics of Bipolar I patients grouped by externalizing disorders.4 
Genome-wide association study indicates two novel resistance loci for severe malaria.4 
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.4 
Association study of common genetic variants and HIV-1 acquisition in 6,300 infected cases and 7,200 controls.4 
Genetic variants, plasma lipoprotein(a) levels, and risk of cardiovascular morbidity and mortality among two prospective cohorts of type 2 diabetes.4 
A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential.4 
Identification of cis- and trans-acting genetic variants explaining up to half the variation in circulating vascular endothelial growth factor levels.4 
Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study.4 
A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma.4 
A genome-wide association study identifies common variants influencing serum uric acid concentrations in a Chinese population.4 
A genome-wide association study of female sexual dysfunction.4 
Common variants at 6q22 and 17q21 are associated with intracranial volume.4 
Genome-wide association analysis identifies TYW3/CRYZ and NDST4 loci associated with circulating resistin levels.4 
Genome-wide population-based association study of extremely overweight young adults--the GOYA study.4 
A polymorphism in CCR1/CCR3 is associated with narcolepsy.4 
Common variants in KCNN3 are associated with lone atrial fibrillation.3 
The CAPN2/CAPN8 Locus on Chromosome 1q Is Associated with Variation in Serum Alpha-Carotene Concentrations.3 
Genome-wide meta-analysis reveals common splice site acceptor variant in CHRNA4 associated with nicotine dependence.3 
Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.3 
Genome-wide association study identifies candidate Loci associated with platelet count in koreans.3 
Identification of regions associated with variation in sensitivity to food-related odors in the human genome.3 
Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A.3 
Genome-wide association and Mendelian randomization study of NT-proBNP in patients with acute coronary syndrome.3 
Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population.3 
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study.3 
Novel genetic risk factors for asthma in African American children: Precision Medicine and the SAGE II Study.3 
Novel genetic markers of breast cancer survival identified by a genome-wide association study.3 
A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23.3 
Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk.3 
Is the gene-environment interaction paradigm relevant to genome-wide studies? The case of education and body mass index.3 
Genome-wide association study of acute kidney injury after coronary bypass graft surgery identifies susceptibility loci.3 
A genome-wide metabolic QTL analysis in Europeans implicates two loci shaped by recent positive selection.3 
Genome-wide association study identifies pharmacogenomic loci linked with specific antihypertensive drug treatment and new-onset diabetes.3 
No evidence of gene-calcium interactions from genome-wide analysis of colorectal cancer risk.3 
Genetic variants in the ADAMTS13 and SUPT3H genes are associated with ADAMTS13 activity.3 
A common variant in SLC8A1 is associated with the duration of the electrocardiographic QT interval.3 
Multidimensional prognostic risk assessment identifies association between IL12B variation and surgery in Crohn's disease.3 
Thyroid cancer GWAS identifies 10q26.12 and 6q14.1 as novel susceptibility loci and reveals genetic heterogeneity among populations.3 
Genome-wide association study of antipsychotic-induced QTc interval prolongation.3 
Pharmacoethnicity in Paclitaxel-Induced Sensory Peripheral Neuropathy.3 
A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose.3 
Common Variation at 1q24.1 (ALDH9A1) Is a Potential Risk Factor for Renal Cancer.3 
Novel gene variants predict serum levels of the cytokines IL-18 and IL-1ra in older adults.3 
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.3 
Identification of a Hashimoto thyroiditis susceptibility locus via a genome-wide comparison with Graves' disease.3 
A genome wide meta-analysis study for identification of common variation associated with breast cancer prognosis.3 
Genome-wide association study identifies a common variant associated with risk of endometrial cancer.3 
Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus?3 
Systematic association mapping identifies NELL1 as a novel IBD disease gene.3 
The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study.3 
Genome-wide association study of pathological gambling.3 
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.3 
A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.3 
Genome-wide association study of alcohol dependence implicates KIAA0040 on chromosome 1q.3 
A novel locus of resistance to severe malaria in a region of ancient balancing selection.3 
Genome-wide study of percent emphysema on computed tomography in the general population. The Multi-Ethnic Study of Atherosclerosis Lung/SNP Health Association Resource Study.3 
Genome-wide association scan for childhood caries implicates novel genes.3 
Genome-wide association with C-reactive protein levels in CLHNS: evidence for the CRP and HNF1A loci and their interaction with exposure to a pathogenic environment.3 
Pharmacogenomics in Alzheimer's disease: a genome-wide association study of response to cholinesterase inhibitors.3 
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis.3 
A genome-wide association study of antidepressant response in Koreans.3 
Common genes underlying asthma and COPD? Genome-wide analysis on the Dutch hypothesis.3 
DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.3 
Bipolar disorder with comorbid binge eating history: A genome-wide association study implicates APOB.3 
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3.3 
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families.3 
Genome-wide association study of obsessive-compulsive disorder.3 
Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance.3 
A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer.3 
Genome-wide association study identifies common variants associated with circulating vitamin E levels.3 
Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia.3 
Combined linkage and association analyses identify a novel locus for obesity near PROX1 in Asians.3 
A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity.3 
A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.3 
A Large Genome-Wide Association Study of Age-Related Hearing Impairment Using Electronic Health Records.3 
Identification of seven loci affecting mean telomere length and their association with disease.3 
Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1.3 
Genetics of venous thrombosis: insights from a new genome wide association study.3 
Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample.3 
A Genome-Wide Association Study to Identify Single Nucleotide Polymorphisms for Acute Kidney Injury.3 
Genome-Wide Association Study of L-Arginine and Dimethylarginines Reveals Novel Metabolic Pathway for Symmetric Dimethylarginine.3 
Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.3 
Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome.3 
F-box/LRR-repeat protein 7 is genetically associated with Alzheimer's disease.3 
A genome-wide association study in American Indians implicates DNER as a susceptibility locus for type 2 diabetes.3 
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death.3 
A genome-wide association study identifies three loci associated with mean platelet volume.3 
A Genome-wide Association Study Provides Evidence of Sex-specific Involvement of Chr1p35.1 (ZSCAN20-TLR12P) and Chr8p23.1 (HMGB1P46) With Diabetic Neuropathic Pain.3 
Common genetic variants on 1p13.2 associate with risk of autism.3 
Genome-wide association study identified novel genetic variant on SLC45A3 gene associated with serum levels prostate-specific antigen (PSA) in a Chinese population.3 
Lung cancer susceptibility locus at 5p15.33.3 
Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data.3 
LDL-cholesterol concentrations: a genome-wide association study.3 
Discovery of common variants associated with low TSH levels and thyroid cancer risk.3 
Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations.3 
Exploring the genetic basis of chronic periodontitis: a genome-wide association study.3 
Integrative genomics identifies LMO1 as a neuroblastoma oncogene.3 
Variants near TERT and TERC influencing telomere length are associated with high-grade glioma risk.3 
A genome-wide association study of neuroticism in a population-based sample.3 
Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.3 
A Genome-Wide Association Study of Chronic Obstructive Pulmonary Disease in Hispanics.3 
GWAS of butyrylcholinesterase activity identifies four novel loci, independent effects within BCHE and secondary associations with metabolic risk factors.3 
Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits.3 
Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time.3 
Identification of novel genetic markers of breast cancer survival.3 
Genome-wide association study reveals three susceptibility loci for common migraine in the general population.3 
Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levels.3 
Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia.3 
Genome-wide and fine-resolution association analysis of malaria in West Africa.3 
Genome-wide association study of glioma and meta-analysis.3 
Genetics of callous-unemotional behavior in children.3 
Genome-wide association study of antibody responses to Plasmodium falciparum candidate vaccine antigens.3 
A genome-wide association study for age-related hearing impairment in the Saami.3 
Genome-wide association study on serum alkaline phosphatase levels in a Chinese population.3 
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.3 
Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk.3 
Genome-Wide Meta-Analyses of Plasma Renin Activity and Concentration Reveal Association with the Kininogen 1 and Prekallikrein Genes.3 
Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4.3 
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.3 
Genome-wide association study in east Asians identifies novel susceptibility loci for breast cancer.3 
Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis.3 
A genome-wide association and gene-environment interaction study for serum triglycerides levels in a healthy Chinese male population.3 
Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility.3 
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.3 
Identification of novel susceptibility Loci for kawasaki disease in a Han chinese population by a genome-wide association study.3 
Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ.3 
Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence.3 
A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.3 
Genome-wide association study of acute post-surgical pain in humans.3 
RTN4 and FBXL17 Genes are Associated with Coronary Heart Disease in Genome-Wide Association Analysis of Lithuanian Families.3 
Variants in FAM13A are associated with chronic obstructive pulmonary disease.3 
A genome-wide association study confirms previously reported loci for type 2 diabetes in Han Chinese.3 
A genome-wide association study of gestational diabetes mellitus in Korean women.3 
Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.3 
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.3 
Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study.3 
Genome-wide association replicates the association of Duffy antigen receptor for chemokines (DARC) polymorphisms with serum monocyte chemoattractant protein-1 (MCP-1) levels in Hispanic children.3 
Novel locus including FGF21 is associated with dietary macronutrient intake.3 
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.3 
A study assessing the association of glycated hemoglobin A1C (HbA1C) associated variants with HbA1C, chronic kidney disease and diabetic retinopathy in populations of Asian ancestry.3 
No Evidence of a Common DNA Variant Profile Specific to World Class Endurance Athletes.3 
A novel locus for body mass index on 5p15.2: a meta-analysis of two genome-wide association studies.3 
A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.3 
Genome-Wide Association Study for Endothelial Growth Factors.3 
Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein.3 
A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1.3 
Three new pancreatic cancer susceptibility signals identified on chromosomes 1q32.1, 5p15.33 and 8q24.21.3 
Genome-wide association study of circulating vitamin D-binding protein.3 
Parkinson disease loci in the mid-western Amish.3 
Genome-Wide Association Study of Prostate Cancer-Specific Survival.3 
Genome-wide association study of opioid dependence: multiple associations mapped to calcium and potassium pathways.3 
A genome-wide association study reveals variants in ARL15 that influence adiponectin levels.3 
A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population.3 
Genome-wide association study of exercise behavior in Dutch and American adults.3 
A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.3 
Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data.3 
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile.3 
Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions.3 
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes.3 
A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.3 
Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.3 
Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.3 
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.3 
Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma.3 
Genome-wide association study of hoarding traits.3 
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease.3 
A genome-wide association study identifies susceptibility loci of silica related pneumoconiosis in Han Chinese.3 
Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions.3 
A genome-wide association study of a sustained pattern of antidepressant response.3 
Pharmacogenetic study of long-term response to interferon-? treatment in multiple sclerosis.3 
Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.3 
Genome-wide scan identifies variant in TNFSF13 associated with serum IgM in a healthy Chinese male population.3 
A colorectal cancer genome-wide association study in a Spanish cohort identifies two variants associated with colorectal cancer risk at 1p33 and 8p12.3 
Genome-wide Association Study of Survival in Early-stage Non-Small Cell Lung Cancer.3 
Genetic variation in SCN10A influences cardiac conduction.3 
Genome-wide association study on bipolar disorder in the Bulgarian population.3 
Identification of loci associated with schizophrenia by genome-wide association and follow-up.3 
Polymorphic markers associated with severe oxaliplatin-induced, chronic peripheral neuropathy in colon cancer patients.3 
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects.3 
A genome-wide association study identifies novel risk loci for type 2 diabetes.3 
Genome-wide association study in bipolar patients stratified by co-morbidity.3 
Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.3 
Genome-wide association of implantable cardioverter-defibrillator activation with life-threatening arrhythmias.3 
Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.3 
Genome-wide association study to characterize serum bilirubin elevations in patients with HCV treated with GS-9256, an HCV NS3 serine protease inhibitor.3 
A genome-wide association study of amygdala activation in youths with and without bipolar disorder.3 
Genome-wide association analysis with gray matter volume as a quantitative phenotype in first-episode treatment-na&#x000ef;ve patients with schizophrenia.3 
Genetic association of short sleep duration with hypertension incidence--a 6-year follow-up in the Korean genome and epidemiology study.3 
BCL9 and C9orf5 are associated with negative symptoms in schizophrenia: meta-analysis of two genome-wide association studies.3 
African Ancestry-Specific Alleles and Kidney Disease Risk in Hispanics/Latinos.3 
Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.3 
Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster.3 
Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5' olfactory receptor gene cluster.3 
Genome-wide admixture and association study of serum iron, ferritin, transferrin saturation and total iron binding capacity in African Americans.3 
Genome-wide association study identifies a region on chromosome 11q14.3 associated with late rectal bleeding following radiation therapy for prostate cancer.3 
The Genetics of Hemoglobin A2 Regulation in Sickle Cell Anemia.3 
Implication of a Chromosome 15q15.2 Locus in Regulating UBR1 and Predisposing Smokers to MGMT Methylation in Lung.3 
Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel.3 
Results of a "GWAS Plus:" General Cognitive Ability Is Substantially Heritable and Massively Polygenic.3 
Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism.3 
Fucosyltransferase 2 (FUT2) non-secretor status and blood group B are associated with elevated serum lipase activity in asymptomatic subjects, and an increased risk for chronic pancreatitis: a genetic association study.3 
WNT16 influences bone mineral density, cortical bone thickness, bone strength, and osteoporotic fracture risk.3 
Genetic and clinical correlates of early-outgrowth colony-forming units.3 
Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis.3 
Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.3 
Common genetic determinants of vitamin D insufficiency: a genome-wide association study.3 
A genome-wide association study of attempted suicide.3 
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma.3 
A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern.3 
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease.2 
A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence.2 
Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease.2 
Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population.2 
Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population.2 
Common genetic variants associated with resting oxygenation in chronic obstructive pulmonary disease.2 
Genome-wide association analysis in primary sclerosing cholangitis and ulcerative colitis identifies risk loci at GPR35 and TCF4.2 
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study.2 
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosis.2 
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.2 
Meta-analysis of genome-wide association studies of HDL cholesterol response to statins.2 
Genome-wide association studies of cerebral white matter lesion burden: the CHARGE consortium.2 
Genome-wide meta-analysis of psoriatic arthritis identifies susceptibility locus at REL.2 
A genome-wide association study of hypertension and blood pressure in African Americans.2 
Common variants at 19p13 are associated with susceptibility to ovarian cancer.2 
Genome-wide association of BMI in African Americans.2 
Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels.2 
Susceptibility to tuberculosis is associated with variants in the ASAP1 gene encoding a regulator of dendritic cell migration.2 
Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore.2 
Genome-wide association study and targeted metabolomics identifies sex-specific association of CPS1 with coronary artery disease.2 
Pharmacodynamic genome-wide association study identifies new responsive loci for glucocorticoid intervention in asthma.2 
Familial young-onset diabetes, pre-diabetes and cardiovascular disease are associated with genetic variants of DACH1 in Chinese.2 
Genome-wide association study identifies variants at 16p13 associated with survival in multiple myeloma patients.2 
Genetic determinants of serum testosterone concentrations in men.2 
E2-2 protein and Fuchs's corneal dystrophy.2 
Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13.2 
Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium.2 
Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer.2 
A high-density genome-wide association screen of sporadic ALS in US veterans.2 
Male-pattern baldness susceptibility locus at 20p11.2 
Genome-Wide Association Analysis of Plasma B-Type Natriuretic Peptide in African Americans: The Jackson Heart Study.2 
Genome-wide association study identifies common loci influencing circulating glycated hemoglobin (HbA1c) levels in non-diabetic subjects: the Long Life Family Study (LLFS).2 
A genome-wide scan for common alleles affecting risk for autism.2 
Evidence for shared genetic risk between methamphetamine-induced psychosis and schizophrenia.2 
Genetic loci for retinal arteriolar microcirculation.2 
Genetic and methylation variation in the CYP2B6 gene is related to circulating p,p'-dde levels in a population-based sample.2 
A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease.2 
First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.2 
Genetic evidence that lower circulating FSH levels lengthen menstrual cycle, increase age at menopause and impact female reproductive health.2 
Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder.2 
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish.2 
A genome-wide association study of anorexia nervosa.2 
Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene.2 
Genome-wide association analysis accounting for environmental factors through propensity-score matching: application to stressful live events in major depressive disorder.2 
Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci.2 
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.2 
Discovery of Genetic Variation on Chromosome 5q22 Associated with Mortality in Heart Failure.2 
Genome-wide association study of survival from sepsis due to pneumonia: an observational cohort study.2 
Identification of a genetic variant at 2q12.1 associated with blood pressure in East-Asians by genome-wide scan including gene-environment interactions.2 
Identification of genetic loci associated with Helicobacter pylori serologic status.2 
A genome-wide association study identifies risk loci for childhood acute lymphoblastic leukemia at 10q26.13 and 12q23.1.2 
Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations.2 
Fine-scale recombination rate differences between sexes, populations and individuals.2 
Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia.2 
Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility.2 
A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels.2 
Common variation in GPC5 is associated with acquired nephrotic syndrome.2 
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.2 
Meta-analysis of genome-wide association for migraine in six population-based European cohorts.2 
Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer.2 
Genome wide association scan for chronic periodontitis implicates novel locus.2 
A genome-wide gene-environment interaction analysis for tobacco smoke and lung cancer susceptibility.2 
Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer.2 
Genetics of hand grip strength in mid to late life.2 
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.2 
Prediction of breast cancer survival using clinical and genetic markers by tumor subtypes.2 
Genome-wide environment interaction between depressive state and stressful life events.2 
Genome-wide association study in German patients with attention deficit/hyperactivity disorder.2 
SORL1 is genetically associated with late-onset Alzheimer's disease in Japanese, Koreans and Caucasians.2 
New susceptibility locus for coronary artery disease on chromosome 3q22.3.2 
Novel susceptibility genes associated with diabetic cataract in a Taiwanese population.2 
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.2 
Genetic regulation of serum phytosterol levels and risk of coronary artery disease.2 
Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.2 
Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS.2 
Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm.2 
Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.2 
Confirmation of Childhood Acute Lymphoblastic Leukemia Variants, ARID5B and IKZF1, and Interaction with Parental Environmental Exposures.2 
Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study.2 
Insight into genetic determinants of resting heart rate.2 
Identification of common variants associated with human hippocampal and intracranial volumes.2 
Genome-wide association study of circulating retinol levels.2 
Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels.2 
Associations of Sleep Apnea, NRG1 Polymorphisms, Alcohol Consumption, and Cerebral White Matter Hyperintensities: Analysis with Genome-Wide Association Data.2 
The correlation between reading and mathematics ability at age twelve has a substantial genetic component.2 
Genome-wide significant association signals in IPO11-HTR1A region specific for alcohol and nicotine codependence.2 
Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups.2 
Genome-wide association study of breast cancer in Latinas identifies novel protective variants on 6q25.2 
A coding variant in FTO confers susceptibility to thiopurine-induced leukopenia in East Asian patients with IBD.2 
Novel genes identified in a high-density genome wide association study for nicotine dependence.2 
A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility.2 
A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease.2 
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.2 
Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness.2 
Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.2 
A genome-wide association study for irinotecan-related severe toxicities in patients with advanced non-small-cell lung cancer.2 
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.2 
Genome-wide association study identifies variants in casein kinase II (CSNK2A2) to be associated with leukocyte telomere length in a Punjabi Sikh diabetic cohort.2 
Genome-wide association study identifies a susceptibility locus for thyrotoxic periodic paralysis at 17q24.3.2 
Meta-analysis of genome-wide association studies of anxiety disorders.2 
Sequence variant on 8q24 confers susceptibility to urinary bladder cancer.2 
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20.2 
Bivariate genome-wide association analyses of femoral neck bone geometry and appendicular lean mass.2 
Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population.2 
HbA2 levels in normal adults are influenced by two distinct genetic mechanisms.2 
A genome-wide association study identifies new susceptibility loci for non-cardia gastric cancer at 3q13.31 and 5p13.1.2 
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.2 
Genome-wide association study on antipsychotic-induced weight gain in the CATIE sample.2 
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.2 
Genome-wide association and functional follow-up reveals new loci for kidney function.2 
Genome-wide association analysis confirms and extends the association of SLC2A9 with serum uric acid levels to Mexican Americans.2 
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.2 
Variants of DENND1B associated with asthma in children.2 
A genome-wide association study of bronchodilator response in asthmatics.2 
Integrative genome-wide association analysis of cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.2 
Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males.2 
Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population.2 
Two independent alleles at 6q23 associated with risk of rheumatoid arthritis.2 
Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1.2 
Identification of myopia-associated WNT7B polymorphisms provides insights into the mechanism underlying the development of myopia.2 
Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease.2 
Genome-wide association study of handedness excludes simple genetic models.2 
Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.2 
Genome-Wide Association Study of Event-Free Survival in Diffuse Large B-Cell Lymphoma Treated With Immunochemotherapy.2 
A genome-wide association study identifies a locus on TERT for mean telomere length in Han Chinese.2 
Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate.2 
A genome-wide association study of serum levels of prostate-specific antigen in the Japanese population.2 
Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility.2 
Genome-wide association study on differentiated thyroid cancer.2 
THBS2 Is a Candidate Modifier of Liver Disease Severity in Alagille Syndrome.2 
A genome-wide search for genetic influences and biological pathways related to the brain's white matter integrity.2 
Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan.2 
Identification of additional risk loci for stroke and small vessel disease: a meta-analysis of genome-wide association studies.2 
Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count.2 
A genome-wide association study of plasma resistin levels identified rs1423096 and rs10401670 as possible functional variants in the Japanese population.2 
A genome-wide association study in Koreans identifies susceptibility loci for allergic nickel dermatitis.2 
A Genome-wide Association Study of Periodontitis in a Japanese Population.2 
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.2 
A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease.2 
A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.2 
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis.2 
Genome-Wide Association Study of Absolute QRS Voltage Identifies Common Variants of TBX3 as Genetic Determinants of Left Ventricular Mass in a Healthy Japanese Population.2 
Genome-Wide Association Study Identifies Novel Pharmacogenomic Loci For Therapeutic Response to Montelukast in Asthma.2 
Genome-wide association study of treatment refractory schizophrenia in Han Chinese.2 
Genetic associations with neuroendocrine tumor risk: results from a genome-wide association study.2 
A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis.2 
Benzene Uptake and Glutathione S-transferase T1 Status as Determinants of S-Phenylmercapturic Acid in Cigarette Smokers in the Multiethnic Cohort.2 
Genome-wide association study of circulating vitamin D levels.2 
Sequence variants at the TERT-CLPTM1L locus associate with many cancer types.2 
Genome-wide association study identifies loci at ATF7IP and KLK2 associated with percentage of circulating free PSA.2 
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis.2 
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.2 
Meta-analysis of genome-wide association studies for personality.2 
Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.2 
Genome-wide association study yields variants at 20p12.2 that associate with urinary bladder cancer.2 
A coding variant in RARG confers susceptibility to anthracycline-induced cardiotoxicity in childhood cancer.2 
Sequence variants in the RNF212 gene associate with genome-wide recombination rate.2 
Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study.2 
Common variants on 8p12 and 1q24.2 confer risk of schizophrenia.2 
A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia.2 
Genome-wide association study reveals novel genetic determinants of DNA repair capacity in lung cancer.2 
Genome-wide association study of height-adjusted BMI in childhood identifies functional variant in ADCY3.2 
New variants at 10q26 and 15q21 are associated with aggressive prostate cancer in a genome-wide association study from a prostate biopsy screening cohort.2 
Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study.2 
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling.2 
Genome-wide association analysis of age at onset in schizophrenia in a European-American sample2 
Genome wide association study: searching for genes underlying body mass index in the Chinese.2 
Genetic predictors associated with improvement of asthma symptoms in response to inhaled corticosteroids.2 
GWAS in the SIGNAL/PHARE clinical cohort restricts the association between the FGFR2 locus and estrogen receptor status to HER2-negative breast cancer patients.2 
Pathway Analysis of Metabolic Syndrome Using a Genome-Wide Association Study of Korea Associated Resource (KARE) Cohorts.2 
Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Beh&#x000e7;et's disease susceptibility loci.2 
Genome-wide gene-environment interaction analysis for asbestos exposure in lung cancer susceptibility.2 
Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children.2 
SUCLG2 identified as both a determinator of CSF Ass1-42-levels and an attenuator of cognitive decline in Alzheimer's disease.2 
Genome-wide association and network analysis of lung function in the Framingham Heart Study.2 
Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).2 
Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.2 
Variants conferring risk of atrial fibrillation on chromosome 4q25.2 
Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk.2 
Genome-wide association and replication study of anti-tuberculosis drugs-induced liver toxicity.2 
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.2 
Genome-wide association study supports the role of the immunological system and of the neurodevelopmental processes in response to haloperidol treatment.2 
A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24.2 
Bivariate genome-wide association study suggests fatty acid desaturase genes and cadherin DCHS2 for variation of both compressive strength index and appendicular lean mass in males.2 
Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci.2 
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese.2 
Two newly identified genetic determinants of pigmentation in Europeans.2 
Genome-wide association study of urinary albumin excretion rate in patients with type 1 diabetes.2 
Genome-wide association study of bipolar I disorder in the Han Chinese population.2 
The molecular genetic architecture of self-employment.2 
Genome-wide analysis of methotrexate pharmacogenomics in rheumatoid arthritis shows multiple novel risk variants and leads for TYMS regulation.2 
ITPA gene variants protect against anaemia in patients treated for chronic hepatitis C.2 
Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search.2 
A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci.2 
Genome-wide study identifies PTPRO and WDR72 and FOXQ1-SUMO1P1 interaction associated with neurocognitive function.2 
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.2 
Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Beh&#x000c3;&#x000a7;et's disease.2 
Common genetic determinants of intraocular pressure and primary open-angle glaucoma.2 
Genetic loci associated with ideal cardiovascular health: A meta-analysis of genome-wide association studies.2 
A genome-wide association study identifies four genetic markers for hematological toxicities in cancer patients receiving gemcitabine therapy.2 
A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.2 
Genome-wide association study of medication adherence in chronic diseases in the korean population.2 
Genome-wide association study identifies genetic loci associated with body mass index and high density lipoprotein-cholesterol levels during psychopharmacological treatment - a cross-sectional naturalistic study.2 
Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies.2 
Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction.2 
Genome wide association study of fetal hemoglobin in sickle cell anemia in Tanzania.2 
Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi.2 
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.2 
A genome-wide analysis in cluster headache points to neprilysin and PACAP receptor gene variants.2 
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-&#x003ba;B pathway are associated with rheumatoid arthritis in Japanese.2 
Common variants near MC4R are associated with fat mass, weight and risk of obesity.2 
Heritability of submaximal exercise heart rate response to exercise training is accounted for by nine SNPs.2 
Genome-wide association study of susceptibility loci for breast cancer in Sardinian population.2 
IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study.2 
Meta-analysis of genome-wide association data identifies two loci influencing age at menarche.2 
The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes.2 
Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis.2 
15q12 Variants, Sputum Gene Promoter Hypermethylation, and Lung Cancer Risk: A GWAS in Smokers.2 
A Pilot Genome-wide Association Study of Breast Cancer Susceptibility Loci in Indonesia.2 
A genome-wide association study of central corneal thickness in Latinos.2 
Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age.2 
Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE.2 
A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor.2 
Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis.2 
Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study.2 
Association of aspirin and NSAID use with risk of colorectal cancer according to genetic variants.2 
A genome-wide scan identifies variants in NFIB associated with metastasis in patients with osteosarcoma.2 
Common genetic variation near the connexin-43 gene is associated with resting heart rate in African Americans: a genome-wide association study of 13,372 participants.2 
Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.2 
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma.2 
Susceptibility variants on chromosome 7p21.1 suggest HDAC9 as a new candidate gene for male-pattern baldness.2 
Genome-wide association study identifies a susceptibility locus for schizophrenia in Han Chinese at 11p11.2.2 
Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight.2 
A genome-wide association study reveals association between common variants in an intergenic region of 4q25 and high-grade myopia in the Chinese Han population.2 
Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.2 
Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population.2 
A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.2 
Genome wide association study identifies KCNMA1 contributing to human obesity.2 
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.2 
Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium.2 
A Genome-Wide Association Study Uncovers a Genetic Locus Associated with Thoracic-to-Hip Ratio in Koreans.2 
Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.2 
A Common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults.2 
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium.2 
Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia.2 
Novel common variants and susceptible haplotype for exfoliation glaucoma specific to Asian population.2 
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.2 
Genome-wide association reveals that common genetic variation in the kallikrein-kinin system is associated with serum L-arginine levels.2 
A genome-wide association study suggests an association of Chr8p21.3 (GFRA2) with diabetic neuropathic pain.2 
Genome-wide association study of prostate cancer identifies a second risk locus at 8q24.2 
Genome-wide association analyses in Han Chinese identify two new susceptibility loci for amyotrophic lateral sclerosis.2 
Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus.2 
Genome-wide association study in Spanish identifies ADAM metallopeptidase with thrombospondin type 1 motif, 9 (ADAMTS9), as a novel asthma susceptibility gene.2 
A genome wide association study links glutamate receptor pathway to sporadic creutzfeldt-jakob disease risk.2 
Nine susceptibility loci for hepatitis B virus-related hepatocellular carcinoma identified by a pilot two-stage genome-wide association study.2 
Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data.2 
Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study.2 
A genome-wide linkage and association scan reveals novel loci for autism.2 
Meta-analysis of genome-wide scans for total body BMD in children and adults reveals allelic heterogeneity and age-specific effects at the WNT16 locus.2 
Genome-wide association study of epirubicin-induced leukopenia in Japanese patients.2 
A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese.2 
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.2 
Genome-wide association study for rotator cuff tears identifies two significant single-nucleotide polymorphisms.2 
Genome-wide association study identifies chromosome 10q24.32 variants associated with arsenic metabolism and toxicity phenotypes in Bangladesh.2 
Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder.2 
Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E &#x000cf;&#x000b5;4,and the risk of late-onset Alzheimer disease in African Americans.2 
Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.2 
A genome-wide association study of depressive symptoms.2 
NCK2 is significantly associated with opiates addiction in African-origin men.2 
Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study.2 
Clinical and genetic association of serum paraoxonase and arylesterase activities with cardiovascular risk.2 
Genome-wide Association Study of 25(OH) Vitamin D Concentrations in Punjabi Sikhs: Results of the Asian Indian Diabetic Heart Study.2 
Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response.1 
Genome-wide association study of B cell non-Hodgkin lymphoma identifies 3q27 as a susceptibility locus in the Chinese population.1 
Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.1 
Common variants on chromosome 9p21 are associated with normal tension glaucoma.1 
Genome-wide association study identifies 3 genomic loci significantly associated with serum levels of homoarginine: the AtheroRemo Consortium.1 
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals.1 
A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis.1 
A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females.1 
Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs.1 
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.1 
From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.1 
Genome-wide association study implicates NDST3 in schizophrenia and bipolar disorder.1 
Chromosome 6p22 locus associated with clinically aggressive neuroblastoma.1 
Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer.1 
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.1 
Genetic polymorphisms in the long noncoding RNA MIR2052HG offer a pharmacogenomic basis for the response of breast cancer patients to aromatase inhibitor therapy.1 
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.1 
Genome-wide association study of irritable vs. elated mania suggests genetic differences between clinical subtypes of bipolar disorder.1 
A pilot genome-wide association study of early-onset breast cancer.1 
A genome-wide association analysis of temozolomide response using lymphoblastoid cell lines shows a clinically relevant association with MGMT.1 
Association of SNPs in the UGT1A gene cluster with total bilirubin and mortality in the Diabetes Heart Study.1 
Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits.1 
Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers.1 
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study.1 
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.1 
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.1 
C-reactive protein (CRP) promoter polymorphisms influence circulating CRP levels in a genome-wide association study of African Americans.1 
Complement factor H polymorphism in age-related macular degeneration.1 
Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci.1 
Combining Genome Wide Association Study and lung eQTL analysis provides evidence for novel genes associated with asthma.1 
Genome-wide association and functional studies identify the DOT1L gene to be involved in cartilage thickness and hip osteoarthritis.1 
Genome-wide association of pericardial fat identifies a unique locus for ectopic fat.1 
Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density.1 
Somatic, positive and negative domains of the Center for Epidemiological Studies Depression (CES-D) scale: a meta-analysis of genome-wide association studies.1 
Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.1 
Genetic variation in LIN28B is associated with the timing of puberty.1 
Genome-wide association study identifies candidate loci associated with postoperative fentanyl requirements after laparoscopic-assisted colectomy.1 
PCSK6 is associated with handedness in individuals with dyslexia.1 
Genome-wide association study identifies common variants in SLC39A6 associated with length of survival in esophageal squamous-cell carcinoma.1 
Genome-wide analysis of genetic loci associated with Alzheimer disease.1 
Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans.1 
A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol.1 
Possible association of CUX1 gene polymorphisms with antidepressant response in major depressive disorder.1 
Genome-wide significant locus of beta-trace protein, a novel kidney function biomarker, identified in European and African Americans.1 
Meta-analysis and imputation refines the association of 15q25 with smoking quantity.1 
A genome-wide association study of emotion dysregulation: Evidence for interleukin 2 receptor alpha.1 
Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study.1 
The Interplay Between Risky Sexual Behaviors and Alcohol Dependence: Genome-Wide Association and Neuroimaging Support for LHPP as a Risk Gene.1 
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.1 
Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q.1 
Common variants in CDKN2B-AS1 associated with optic-nerve vulnerability of glaucoma identified by genome-wide association studies in Japanese.1 
A genome wide association study suggests the association of muskelin with early onset bipolar disorder: Implications for a GABAergic epileptogenic neurogenesis model.1 
A novel sarcoidosis risk locus for Europeans on chromosome 11q13.1.1 
Clinical and genetic association of serum ceruloplasmin with cardiovascular risk.1 
Comprehensive genome-wide evaluation of lapatinib-induced liver injury yields a single genetic signal centered on known risk allele HLA-DRB1*07:01.1 
Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis.1 
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.1 
A whole genome association study of neuroticism using DNA pooling.1 
Genome-wide association study identifies ITPR2 as a susceptibility gene for Kashin-Beck disease in Han Chinese.1 
Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population.1 
Severe osteoarthritis of the hand associates with common variants within the ALDH1A2 gene and with rare variants at 1p31.1 
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene.1 
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.1 
TMPRSS9 and GRIN2B are associated with neuroticism: a genome-wide association study in a European sample.1 
Genome-wide association analysis of body mass in chronic obstructive pulmonary disease.1 
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population.1 
Common genetic variants and modification of penetrance of BRCA2-associated breast cancer.1 
Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages.1 
A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer.1 
A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population.1 
Cerivastatin, genetic variants, and the risk of rhabdomyolysis.1 
A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length.1 
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease.1 
A genome-wide search for type 2 diabetes susceptibility genes in an extended Arab family.1 
Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women.1 
NKAIN1-SERINC2 is a functional, replicable and genome-wide significant risk gene region specific for alcohol dependence in subjects of European descent.1 
Common variants in DGKK are strongly associated with risk of hypospadias.1 
The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12.1 
A New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes also Associated with Blood and Skin Glycated Proteins.1 
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels.1 
A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease.1 
A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.1 
Genetic associations with valvular calcification and aortic stenosis.1 
Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk.1 
CDH13 and HCRTR2 May Be Associated with Hypersomnia Symptom of Bipolar Depression: A Genome-Wide Functional Enrichment Pathway Analysis.1 
A germline variant in the TP53 polyadenylation signal confers cancer susceptibility.1 
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.1 
A weighted false discovery rate control procedure reveals alleles at FOXA2 that influence fasting glucose levels.1 
Suggestion of GLYAT gene underlying variation of bone size and body lean mass as revealed by a bivariate genome-wide association study.1 
Novel loci involved in platelet function and platelet count identified by a genome-wide study performed in children.1 
CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk.1 
Influence of common genetic variation on lung cancer risk: meta-analysis of 14 900 cases and 29 485 controls.1 
Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians.1 
Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1.1 
C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies.1 
A genome-wide scan for breast cancer risk haplotypes among African American women.1 
A genome-wide association study identifies UGT1A1 as a regulator of serum cell-free DNA in young adults: The Cardiovascular Risk in Young Finns Study.1 
Variant between CPT1B and CHKB associated with susceptibility to narcolepsy.1 
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.1 
Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.1 
IKZF1, a new susceptibility gene for cold medicine-related Stevens-Johnson syndrome/toxic epidermal necrolysis with severe mucosal involvement.1 
The FOXE1 locus is a major genetic determinant for radiation-related thyroid carcinoma in Chernobyl.1 
Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease.1 
Genetic association suggests that SMOC1 mediates between prenatal sex hormones and digit ratio.1 
Genome wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population.1 
A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity.1 
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.1 
Genome-wide association study of dermatomyositis reveals genetic overlap with other autoimmune disorders.1 
A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass.1 
ABCC5, a gene that influences the anterior chamber depth, is associated with primary angle closure glaucoma.1 
Combinations of newly confirmed Glioma-Associated loci link regions on chromosomes 1 and 9 to increased disease risk.1 
Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy.1 
Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy.1 
Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer.1 
COL4A1 is associated with arterial stiffness by genome-wide association scan.1 
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.1 
Trans-ethnic genome-wide association study of colorectal cancer identifies a new susceptibility locus in VTI1A.1 
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.1 
Identification of a variant in KDR associated with serum VEGFR2 and pharmacodynamics of pazopanib.1 
Association study on long-living individuals from Southern Italy identifies rs10491334 in the CAMKIV gene that regulates survival proteins.1 
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.1 
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease.1 
DPP6 as a candidate gene for neuroleptic-induced tardive dyskinesia.1 
Evidence of CNIH3 involvement in opioid dependence.1 
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.1 
Common variations in BARD1 influence susceptibility to high-risk neuroblastoma.1 
Genome-wide association study of genetic determinants of LDL-c response to atorvastatin therapy: importance of Lp(a).1 
Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder.1 
Sorl1 as an Alzheimer's disease predisposition gene?1 
A three-stage genome-wide association study identifies a susceptibility locus for late radiotherapy toxicity at 2q24.1.1 
Extended genetic effects of ADH cluster genes on the risk of alcohol dependence: from GWAS to replication.1 
The nuclear transcription factor PKNOX2 is a candidate gene for substance dependence in European-origin women.1 
Polymorphism at 19q13.41 predicts breast cancer survival specifically after endocrine therapy.1 
Genomic association analysis of common variants influencing antihypertensive response to hydrochlorothiazide.1 
A genome-wide association study of pulmonary function measures in the Framingham Heart Study.1 
Genome-wide association of single-nucleotide polymorphisms with weight loss outcomes after Roux-en-Y gastric bypass surgery.1 
Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).1 
Genetic variants and risk of lung cancer in never smokers: a genome-wide association study.1 
Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes.1 
Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families.1 
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene.1 
A variant in the LRRFIP1 gene is associated with adiposity and inflammation.1 
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes.1 
The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts.1 
A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection.1 
A genetic locus in 7p12.2 associated with treatment resistant schizophrenia.1 
IgA measurements in over 12 000 Swedish twins reveal sex differential heritability and regulatory locus near CD30L.1 
Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population.1 
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.1 
Genome-wide association scan of Dupuytren's disease.1 
FTO genotype is associated with phenotypic variability of body mass index.1 
Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.1 
Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis.1 
Genome-wide association study pinpoints a new functional apolipoprotein B variant influencing oxidized low-density lipoprotein levels but not cardiovascular events: AtheroRemo Consortium.1 
Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study.1 
Genome-wide Association for Major Depression Through Age at Onset Stratification: Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium.1 
The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia.1 
Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33.1 
European genome-wide association study identifies SLC14A1 as a new urinary bladder cancer susceptibility gene.1 
Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor.1 
A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor &#x003b1; gene as a quantitative trait locus for eye size in white Europeans.1 
A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1.1 
Identification of KCNN2 as a susceptibility locus for coronary artery aneurysms in Kawasaki disease using genome-wide association analysis.1 
Common variants on Xq28 conferring risk of schizophrenia in Han Chinese.1 
Screening for replication of genome-wide SNP associations in sporadic ALS.1 
IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations.1 
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.1 
SLCO1B1 variants and statin-induced myopathy--a genomewide study.1 
Genome-wide association identifies the T gene as a novel asthma pharmacogenetic locus.1 
A common variant on chromosome 9p21 affects the risk of myocardial infarction.1 
Association between common variants near the melanocortin 4 receptor gene and severe antipsychotic drug-induced weight gain.1 
A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.1 
Identification of a sudden cardiac death susceptibility locus at 2q24.2 through genome-wide association in European ancestry individuals.1 
Common sequence variants on 20q11.22 confer melanoma susceptibility.1 
A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk.1 
Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus.1 
A genome-wide association study of chronic otitis media with effusion and recurrent otitis media identifies a novel susceptibility locus on chromosome 2.1 
Genome-Wide Association Study in an Admixed Case Series Reveals IL12A as a New Candidate in Behcet Disease.1 
Bivariate genome-wide association analyses identified genetic pleiotropic effects for bone mineral density and alcohol drinking in Caucasians.1 
Genome-wide association and replication studies identified TRHR as an important gene for lean body mass.1 
Association between a genetic variant related to glutamic acid metabolism and coronary heart disease in individuals with type 2 diabetes.1 
Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations.1 
BAIAP2 is related to emotional modulation of human memory strength.1 
SLC2A9 influences uric acid concentrations with pronounced sex-specific effects.1 
Genome-Wide Association Study of Bladder Cancer in a Chinese Cohort Reveals a New Susceptibility Locus at 5q12.3.1 
Identification of a novel percent mammographic density locus at 12q24.1 
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption.1 
Genome-wide association study with the risk of schizophrenia in a Korean population.1 
A genome-wide association study of intra-ocular pressure suggests a novel association in the gene FAM125B in the TwinsUK cohort.1 
A genome-wide association study of circulating galectin-3.1 
Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium.1 
Genome-wide association study on susceptibility genes associated with yang-deficiency constitution: A small sample case-control study.1 
Variant in the sequence of the LINGO1 gene confers risk of essential tremor.1 
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder.1 
SORBS1 gene, a new candidate for diabetic nephropathy: results from a multi-stage genome-wide association study in patients with type 1 diabetes.1 
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer.1 
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis.1 
A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms.1 
A variant in MCF2L is associated with osteoarthritis.1 
Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.1 
Pharmacogenomic Determinants of the Cardiovascular Effects of Dalcetrapib.1 
A genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3.1 
Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.1 
A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function.1 
A genome-wide association study of sporadic ALS in a homogenous Irish population.1 
A genome-wide association study identifies a LEPR gene as a novel predisposing factor for childhood fasting plasma glucose.1 
Genome-wide association study in a Chinese population with diabetic retinopathy.1 
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.1 
A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.1 
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study.1 
A genome-wide association analysis of serum iron concentrations.1 
A common variant on chromosome 11q13 is associated with atopic dermatitis.1 
Genomewide association study for susceptibility genes contributing to familial Parkinson disease.1 
Common genetic variants on 5p14.1 associate with autism spectrum disorders.1 
A 2-stage genome-wide association study to identify single nucleotide polymorphisms associated with development of urinary symptoms after radiotherapy for prostate cancer.1 
Bivariate genome-wide association study suggests that the DARC gene influences lean body mass and age at menarche.1 
Multistage genomewide association study identifies a locus at 1q41 associated with rate of HIV-1 disease progression to clinical AIDS.1 
Genome-wide association study identifies a susceptibility locus for thoracic aortic aneurysms and aortic dissections spanning FBN1 at 15q21.1.1 
Common variation at 10p12.31 near MLLT10 influences meningioma risk.1 
Genome-wide association study identifies common variants at TNFRSF13B associated with IgG level in a healthy Chinese male population.1 
A Common Variant Of Ubiquinol-Cytochrome c Reductase Complex Is Associated with DDH.1 
Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians.1 
Chromosome 2q31.1 associates with ESRD in women with type 1 diabetes.1 
Aspirin hydrolysis in plasma is a variable function of butyrylcholinesterase and platelet-activating factor acetylhydrolase 1b2 (PAFAH1b2).1 
Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients.1 
Adiponectin concentrations: a genome-wide association study.1 
A novel SNP associated with nighttime pulse pressure in young-onset hypertension patients could be a genetic prognostic factor for cardiovascular events in a general cohort in Taiwan.1 
Evidence of gene-environment interaction for two genes on chromosome 4 and environmental tobacco smoke in controlling the risk of nonsyndromic cleft palate.1 
Common Variants in the CRP Promoter are Associated with a High C-Reactive Protein Level in Kawasaki Disease.1 
ELF1 is associated with systemic lupus erythematosus in Asian populations.1 
A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.1 
Three new single nucleotide polymorphisms identified by a genome-wide association study in Korean patients with vitiligo.1 
Genome-wide association study reveals sex-specific selection signals against autosomal nucleotide variants.1 
Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement.1 
A variant in FTO shows association with melanoma risk not due to BMI.1 
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.1 
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.1 
A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium.1 
Genome-wide association analysis of circulating vitamin D levels in children with asthma.1 
Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis.1 
A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22.1 
A common variant of HMGA2 is associated with adult and childhood height in the general population.1 
Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.1 
Genome-wide Association Study of Postburn Scarring Identifies a Novel Protective Variant.1 
Genetic variation in the vaspin gene affects circulating serum vaspin concentrations.1 
Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3.1 
IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy.1 
Genome-wide Association Study of Short Acting ss2-agonists: A Novel Genome Wide Significant Locus on Chromosome 2 Near ASB3.1 
Genome-wide association study of three-dimensional facial morphology identifies a variant in PAX3 associated with nasion position.1 
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.1 
Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus.1 
Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.1 
A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis.1 
Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension.1 
Genome-wide association study identified UQCC locus for spine bone size in humans.1 
Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations.1 
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke.1 
Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23.1 
Common quantitative trait locus downstream of RETN gene identified by genome-wide association study is associated with risk of type 2 diabetes mellitus in Han Chinese: a Mendelian randomization effect.1 
Genome-Wide Association Study Identifies Variants in PMS1 Associated with Serum Ferritin in a Chinese Population.1 
Does metformin work for everyone? A genome-wide association study for metformin response.1 
A novel colorectal cancer risk locus at 4q32.2 identified from an international genome-wide association study.1 
Genome-wide association study of degenerative bony changes of the temporomandibular joint.1 
A genome-wide association study for diabetic retinopathy in a Japanese population: potential association with a long intergenic non-coding RNA.1 
A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer.1 
Genome Wide Association Study Identifies L3MBTL4 as a Novel Susceptibility Gene for Hypertension.1 
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.1 
ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients.1 
Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function.1 
TAOK3, a novel genome-wide association study locus associated with morphine requirement and postoperative pain in a retrospective pediatric day surgery population.1 
Identification of susceptibility gene associated with female primary Sjogren's syndrome in Han Chinese by genome-wide association study.1 
Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes.1 
A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder.1 
Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene.1 
A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.1 
Genome-Wide Association Study Identifies IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis.1 
Genome-wide scan of job-related exhaustion with three replication studies implicate a susceptibility variant at the UST gene locus.1 
Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals.1 
Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians.1 
Association of Polymorphisms in MACRO Domain Containing 2 With Thyroid-Associated Orbitopathy.1 
A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study.1 
Genome-wide association study identifies new disease loci for isolated clubfoot.1 
Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22.1 
A genetic risk factor for periodic limb movements in sleep.1 
A genome-wide association study for quantitative traits in schizophrenia in China.1 
Beyond cigarettes-per-day: A genome-wide association study of the biomarker carbon monoxide.1 
A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.1 
Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C.1 
Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study.1 
Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers.1 
Genome-wide study of methotrexate clearance replicates SLCO1B1.1 
A genome-wide association study of pulmonary tuberculosis in Morocco.1 
Variants close to NTRK2 gene are associated with birth weight in female twins.1 
Meta analysis identifies a novel susceptibility locus associated with heel bone strength in the Korean population.1 
Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes.1 
A genome-wide association study in Caucasian women points out a putative role of the STXBP5L gene in facial photoaging.1 
Replication of 13 obesity loci among Singaporean Chinese, Malay and Asian-Indian populations.1 
Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.1 
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes.1 
Genome-wide association study identifies a novel susceptibility locus at 12q23.1 for lung squamous cell carcinoma in han chinese.1 
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients.1 
Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24.1 
A genome-wide association study reveals a quantitative trait locus of adiponectin on CDH13 that predicts cardiometabolic outcomes.1 
Common variants at 11p13 are associated with susceptibility to tuberculosis.1 
The GRM7 gene, early response to risperidone, and schizophrenia: a genome-wide association study and a confirmatory pharmacogenetic analysis.1 
The genetics of antipsychotic induced tremors: a genome-wide pathway analysis on the STEP-BD SCP sample.1 
Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin.1 
Mutations in BRIP1 confer high risk of ovarian cancer.1 
Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels.1 
FASTKD2 is associated with memory and hippocampal structure in older adults.1 
Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.1 
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.1 
Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1.1 
Melanesian blond hair is caused by an amino acid change in TYRP1.1 
Narcolepsy is strongly associated with the T-cell receptor alpha locus.1 
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.1 
A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk.1 
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.1 
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma.1 
Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels.1 
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene.1 
A Genome-wide Approach Validates that Thiopurine Methyltransferase Activity is a Monogenic Pharmacogenomic Trait.1 
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity gene.1 
Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors.1 
A genome-wide association study identifies rs2000999 as a strong genetic determinant of circulating haptoglobin levels.1 
Shared genetic contribution to Ischaemic Stroke and Alzheimer's Disease.1 
A genome-wide association study identifies common variants near LBX1 associated with adolescent idiopathic scoliosis.1 
ITGB5 and AGFG1 variants are associated with severity of airway responsiveness.1 
GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.1 
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1.1 
Association of intronic sequence variant in the gene encoding spleen tyrosine kinase with susceptibility to vascular dementia.1 
Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension.1 
Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients.1 
Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.1 
Genome-wide association study of relative telomere length.1 
Genetic variations associated with postoperative recurrence in stage I non-small cell lung cancer.1 
Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts.1 
A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21.1 
CDH13 gene coding T-cadherin influences variations in plasma adiponectin levels in the Japanese population.1 
Examination of the current top candidate genes for AD in a genome-wide association study.1 
Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients.1 
Limited contribution of common genetic variants to risk for liver injury due to a variety of drugs.1 
A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough.1 
Genome-wide analyses of borderline personality features.1 
A genome-wide association study in 574 schizophrenia trios using DNA pooling.1 
A genome-wide association study of non-HPV-related head and neck squamous cell carcinoma identifies prognostic genetic sequence variants in the MAP-kinase and hormone pathways.1 
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.1 
Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function.1 
Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer.1 
Genome-wide association study of bipolar disorder in European American and African American individuals.1 
A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study.1 
HTRA1 promoter polymorphism in wet age-related macular degeneration.1 
Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA.1 
A Genome-Wide Screen for Large-Effect Alloimmunization Susceptibility Loci among Red Blood Cell Transfusion Recipients with Sickle Cell Disease.1 
Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals.1 
High-resolution whole-genome association study of Parkinson disease.1 
CUBN is a gene locus for albuminuria.1 
Genome-wide Association Study of Parental Life Span.1 
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.1 
The TCF7L2 diabetes risk variant is associated with HbA&#x02081;(C) levels: a genome-wide association meta-analysis.1 
MGAT5 alters the severity of multiple sclerosis.1 
Genetic variations in GRIA1 on chromosome 5q33 related to asparaginase hypersensitivity.1 
Abdominal aortic aneurysm is associated with a variant in low-density lipoprotein receptor-related protein 1.1 
Variant of TREM2 associated with the risk of Alzheimer's disease.1 
CHRNB3 is more strongly associated with Fagerstr&#x000c3;&#x000b6;m test for cigarette dependence-based nicotine dependence than cigarettes per day: phenotype definition changes genome-wide association studies results.1 
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects.1 
Mosaic loss of chromosome Y is associated with common variation near TCL1A.1 
A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults.1 
Genome-wide association study for sight-threatening diabetic retinopathy reveals association with genetic variation near the GRB2 gene.1 
Genetic Polymorphisms Associated with Hearing Threshold Shift in Subjects during First Encounter with Occupational Impulse Noise.1 
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke.1 
Genome-wide gene-environment interaction analysis of pesticide exposure and risk of Parkinson's disease.1 
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.1 
Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos.1 
Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2.1 
Common variants of FUT2 are associated with plasma vitamin B12 levels.1 
Genome-wide association study of myelosuppression in non-small-cell lung cancer patients with platinum-based chemotherapy.1 
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.1 
A variant in LDLR is associated with abdominal aortic aneurysm.1 
Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy.1 
Common variants near TERC are associated with mean telomere length.1 
A genome-wide association study identifies a region at chromosome 12 as a potential susceptibility locus for restenosis after percutaneous coronary intervention.1 
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.1 
Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage.1 
Association of genetic variants on 15q12 with cortical thickness and cognition in schizophrenia.1 
The 18p11.22 locus is associated with never smoker non-small cell lung cancer susceptibility in Korean populations.1 
A genome-wide association study implicates the APOE locus in nonpathological cognitive ageing.1 
Susceptibility to chronic mucus hypersecretion, a genome wide association study.1 
SSBP2 variants are associated with survival in glioblastoma patients.1 
Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts.1 
A genome-wide association study of basal transepidermal water loss finds variants at 9q34.3 to be associated with skin barrier function.1 
Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone.1 
A genome-wide association study of breast cancer in women of African ancestry.1 
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25.1 
Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study.1 
A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS).1 
Genome-wide association study identifies a potent locus associated with human opioid sensitivity.1 
A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9.1 
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.1 
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.1 
A genome-wide association study with DNA pooling identifies the variant rs11866328 in the GRIN2A gene that affects disease progression of chronic HBV infection.1 
Genome-wide association study identifies TNFSF13 as a susceptibility gene for IgA in a South Chinese population in smokers.1 
A genome-wide scan for common variants affecting the rate of age-related cognitive decline.1 
Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.1 
Susceptibility variants for male-pattern baldness on chromosome 20p11.1 
Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1.1 
Association of glycosylated hemoglobin with the gene encoding CDKAL1 in the Korean Association Resource (KARE) study.1 
The neuronal transporter gene SLC6A15 confers risk to major depression.1 
Genome-wide study of gene variants associated with differential cardiovascular event reduction by pravastatin therapy.1 
Genetic modifiers of cystic fibrosis-related diabetes.1 
Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium.1 
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.1 
Sequence variants at 22q13 are associated with prostate cancer risk.1 
Common variants at 12q24 are associated with drinking behavior in Han Chinese.1 
Genome-wide exploration identifies sex-specific genetic effects of alleles upstream NPY to increase the risk of severe periodontitis in men.1 
Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.1 
Common variants in ZNF365 are associated with both mammographic density and breast cancer risk.1 
Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.1 
Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.1 
The obesity-risk variant of FTO is inversely related with the So-Eum constitutional type: genome-wide association and replication analyses.1 
A novel interaction between the FLJ33534 locus and smoking in obesity: a genome-wide study of 14 131 Pakistani adults.1 
Genetic Factors for the Severity of ACPA-negative Rheumatoid Arthritis in 2 Cohorts of Early Disease: A Genome-wide Study.1 
A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk.1 
Common genetic variation near melatonin receptor 1A gene linked to job-related exhaustion in shift workers.1 
A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure.1 
Identification of PVT1 as a candidate gene for end-stage renal disease in type 2 diabetes using a pooling-based genome-wide single nucleotide polymorphism association study.1 
Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE.1 
Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes.1 
Genome-wide association study identifies a single major locus contributing to survival into old age; the APOE locus revisited.1 
KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex.1 
Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function.1 
Meta-analysis of genome-wide studies identifies MEF2C SNPs associated with bone mineral density at forearm.1 
A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis.1