Genome-Wide Association Study Concept

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• ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia  Journal Articles
• DCC gene network in the prefrontal cortex is associated with total brain volume in childhood  Journal Articles
• A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression  Journal Articles
• A Genome-Wide Association Study Identifies a Novel Major Locus for Glycemic Control in Type 1 Diabetes, as Measured by Both A1C and Glucose  Journal Articles
• A Genome-Wide Association Study for Coronary Artery Disease Identifies a Novel Susceptibility Locus in the Major Histocompatibility Complex  Journal Articles
• A Genome-Wide Association Study to Identify Single-Nucleotide Polymorphisms for Acute Kidney Injury  Journal Articles
• A Genome-wide Association Study Identifies Risk Alleles in Plasminogen and P4HA2 Associated with Giant Cell Arteritis  Journal Articles
• A Genome‐Wide Association Study for Venous Thromboembolism: The Extended Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium  Journal Articles
• A Mendelian Randomization-Based Approach to Identify Early and Sensitive Diagnostic Biomarkers of Disease  Journal Articles
• A Multivariate Genome-Wide Association Study of Wing Shape inDrosophila melanogaster  Journal Articles
• A coding and non-coding transcriptomic perspective on the genomics of human metabolic disease  Journal Articles
• A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease  Journal Articles
• A fast algorithm to optimize SNP prioritization for gene-gene and gene-environment interactions  Journal Articles
• A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease  Journal Articles
• A genome-wide association study suggests correlations of common genetic variants with peritoneal solute transfer rates in patients with kidney failure receiving peritoneal dialysis  Journal Articles
• A genome-wide association, polygenic risk score and sex study on opioid use disorder treatment outcomes  Journal Articles
• A genome-wide linkage and association scan reveals novel loci for autism  Journal Articles
• A genome-wide linkage study of autism spectrum disorder and the broad autism phenotype in extended pedigrees  Journal Articles
• A genome-wide scan for common alleles affecting risk for autism  Journal Articles
• A large-scale genome-wide association study meta-analysis of cannabis use disorder  Journal Articles
• A method to estimate the contribution of rare coding variants to complex trait heritability  Journal Articles
• A method to estimate the contribution of regional genetic associations to complex traits from summary association statistics  Journal Articles
• A new highly penetrant form of obesity due to deletions on chromosome 16p11.2  Journal Articles
• A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder  Journal Articles
• A novel multi-ancestry proteome-wide Mendelian randomization study implicates extracellular proteins, tubular cells, and fibroblasts in estimated glomerular filtration rate regulation  Journal Articles
• A phased SNP-based classification of sickle cell anemia HBB haplotypes  Journal Articles
• A polygenic basis for four classical Fredrickson hyperlipoproteinemia phenotypes that are characterized by hypertriglyceridemia  Journal Articles
• A principal component regression based genome wide analysis approach reveals the presence of a novel QTL on BTA7 for MAP resistance in holstein cattle  Journal Articles
• A robust method to estimate regional polygenic correlation under misspecified linkage disequilibrium structure  Journal Articles
• A systematic review of GWAS identified SNPs associated with outcomes of medications for opioid use disorder  Journal Articles
• A thymic stromal lymphopoietin polymorphism may provide protection from asthma by altering gene expression  Journal Articles
• A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesity  Journal Articles
• Abdominal Aortic Aneurysm Is Associated with a Variant in Low-Density Lipoprotein Receptor-Related Protein 1  Journal Articles
• Advances in Genomic Analysis of Stroke  Journal Articles
• Allelic and phenotypic spectrum of plasma triglycerides  Journal Articles
• Amplification of the prolactin receptor gene in mammary lobular neoplasia  Journal Articles
• An intron variant of the GLI family zinc finger 3 (GLI3) gene differentiates resistance training‐induced muscle fiber hypertrophy in younger men  Journal Articles
• Analysis of Genetic Association of Intestinal Permeability in Healthy First-degree Relatives of Patients with Crohn’s Disease  Journal Articles
• Analytical strategies to include the X‐chromosome in variance heterogeneity analyses: Evidence for trait‐specific polygenic variance structure  Journal Articles
• Anti-Epileptic Drug Target Perturbation and Intracranial Aneurysm Risk: Mendelian Randomization and Colocalization Study  Journal Articles
• Assessment of the genetic and clinical determinants of fracture risk: genome wide association and mendelian randomisation study  Journal Articles
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index  Journal Articles
• Association analyses of the autosomal genome and mitochondrial DNA with accelerometry-derived sleep parameters in depressed UK biobank subjects  Journal Articles
• Association of Granulomatosis With Polyangiitis (Wegener's) With HLA–DPB1*04 and SEMA6A Gene Variants: Evidence From Genome‐Wide Analysis  Journal Articles
• Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals  Journal Articles
• Association of common variants in the human eyes shut ortholog (EYS) with statin‐induced myopathy: Evidence for additional functions of EYS  Journal Articles
• Association of polymorphisms of the tryptophan hydroxylase 2 gene with risk for bipolar disorder or suicidal behavior  Journal Articles
• Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort  Journal Articles
• Benefits and limitations of genome-wide association studies  Journal Articles
• Big brown bats experience slower epigenetic ageing during hibernation  Journal Articles
• Biological, clinical and population relevance of 95 loci for blood lipids  Journal Articles
• Biomarkers Associated With Severe COVID-19 Among Populations With High Cardiometabolic Risk  Journal Articles
• Blood CSF1 and CXCL12 as Causal Mediators of Coronary Artery Disease  Journal Articles
• CADM2 is implicated in impulsive personality and numerous other traits by genome- and phenome-wide association studies in humans and mice  Journal Articles
• CRISPRi screens reveal a DNA methylation-mediated 3D genome dependent causal mechanism in prostate cancer  Journal Articles
• Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories  Journal Articles
• Can social support during pregnancy affect maternal DNA methylation? Findings from a cohort of African-Americans  Journal Articles
• Causal Effect of MMP-1 (Matrix Metalloproteinase-1), MMP-8, and MMP-12 Levels on Ischemic Stroke  Journal Articles
• Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)  Journal Articles
• Clinically detectable copy number variations in a Canadian catchment population of schizophrenia  Journal Articles
• Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease  Journal Articles
• Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus  Journal Articles
• Complexities of recapitulating polygenic effects in natural populations: replication of genetic effects on wing shape in artificially selected and wild-caught populations of Drosophila melanogaster  Journal Articles
• Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies  Journal Articles
• Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies  Journal Articles
• Consistent cord blood DNA methylation signatures of gestational age between South Asian and white European cohorts  Journal Articles
• Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke  Journal Articles
• Current State and Future of Polygenic Risk Scores in Cardiometabolic Disease: A Scoping Review  Journal Articles
• Cystic fibrosis–related diabetes onset can be predicted using biomarkers measured at birth  Journal Articles
• DNA Repair in Huntington’s Disease and Spinocerebellar Ataxias: Somatic Instability and Alternative Hypotheses  Journal Articles
• DNA methylation age calculators reveal association with diabetic neuropathy in type 1 diabetes  Journal Articles
• DNA methylation changes in cord blood and the developmental origins of health and disease – a systematic review and replication study  Journal Articles
• DNA methylation mediates the effect of maternal smoking on offspring birthweight: a birth cohort study of multi-ethnic US mother–newborn pairs  Journal Articles
• Defining the biological bases of individual differences in musicality  Journal Articles
• Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis  Journal Articles
• Developmental Origins for Kidney Disease Due to Shroom3 Deficiency  Journal Articles
• Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions  Journal Articles
• Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals  Journal Articles
• Does genetic heterogeneity account for the divergent risk of type 2 diabetes in South Asian and white European populations?  Journal Articles
• Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan  Journal Articles
• EGF Decreases the Abundance of MicroRNAs That Restrain Oncogenic Transcription Factors  Journal Articles
• Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease  Journal Articles
• Eight Common Genetic Variants Associated with Serum DHEAS Levels Suggest a Key Role in Ageing Mechanisms  Journal Articles
• Elevated Lipoprotein(a) and Risk of Atrial Fibrillation  Journal Articles
• Enabling the genomic revolution in Africa  Journal Articles
• Epigenetics, heritability and longitudinal analysis  Journal Articles
• Evidence of causal effect of major depression on alcohol dependence: findings from the psychiatric genomics consortium  Journal Articles
• Excess of Rare Variants in Non–Genome-Wide Association Study Candidate Genes in Patients With Hypertriglyceridemia  Journal Articles
• Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia  Journal Articles
• Extremes of Unexplained Variation as a Phenotype  Journal Articles
• Fetal Serotonin Reuptake Inhibitor Antidepressant Exposure: Maternal and Fetal Factors  Journal Articles
• Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster  Journal Articles
• Fine Mapping of the Insulin-Induced Gene 2 Identifies a Variant Associated With LDL Cholesterol and Total Apolipoprotein B Levels  Journal Articles
• Fine-Scale Patterns of Population Stratification Confound Rare Variant Association Tests  Journal Articles
• Fine-mapping of retinal vascular complexity loci identifies Notch regulation as a shared mechanism with myocardial infarction outcomes  Journal Articles
• Fine-tuning of Genome-Wide Polygenic Risk Scores and Prediction of Gestational Diabetes in South Asian Women  Journal Articles
• Forty-Three Loci Associated with Plasma Lipoprotein Size, Concentration, and Cholesterol Content in Genome-Wide Analysis  Journal Articles
• Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants  Journal Articles
• Functional impact of global rare copy number variation in autism spectrum disorders  Journal Articles
• GWAS and ExWAS of blood mitochondrial DNA copy number identifies 71 loci and highlights a potential causal role in dementia  Journal Articles
• GWAS of biological aging to find longevity genes in schizophrenia.  Journal Articles
• GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal effect of schizophrenia liability  Journal Articles
• GWAS-based machine learning approach to predict duloxetine response in major depressive disorder  Journal Articles
• GWAS-identified genetic variants associated with medication-assisted treatment outcomes in patients with opioid use disorder: a systematic review and meta-analysis protocol  Journal Articles
• Gene Expression Profiles for the Identification of Prevalent Atrial Fibrillation  Conferences
• Gene expression analysis in asthma using a targeted multiplex array  Journal Articles
• Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci  Journal Articles
• Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations  Journal Articles
• Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders  Journal Articles
• Genetic Determinants of Dabigatran Plasma Levels and Their Relation to Bleeding  Journal Articles
• Genetic Determinants of Vascular Dementia  Journal Articles
• Genetic Determinants of Warfarin Maintenance Dose and Time in Therapeutic Treatment Range: A RE-LY Genomics Substudy  Journal Articles
• Genetic Determinants of “Cognitive Impairment, No Dementia”  Journal Articles
• Genetic Interactions with Age, Sex, Body Mass Index, and Hypertension in Relation to Atrial Fibrillation: The AFGen Consortium  Journal Articles
• Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease  Journal Articles
• Genetic Loci Associated With Plasma Concentration of Low-Density Lipoprotein Cholesterol, High-Density Lipoprotein Cholesterol, Triglycerides, Apolipoprotein A1, and Apolipoprotein B Among 6382 White Women in Genome-Wide Analysis With Replication  Journal Articles
• Genetic Markers of Inflammation and Their Role in Cardiovascular Disease  Journal Articles
• Genetic Polymorphisms in the Long Noncoding RNA MIR2052HG Offer a Pharmacogenomic Basis for the Response of Breast Cancer Patients to Aromatase Inhibitor Therapy  Journal Articles
• Genetic Predictors of Cardiovascular Mortality During Intensive Glycemic Control in Type 2 Diabetes: Findings From the ACCORD Clinical Trial  Journal Articles
• Genetic Susceptibility to West Nile Virus and Dengue  Journal Articles
• Genetic analysis of impulsive personality traits: Examination of a priori candidates and genome-wide variation  Journal Articles
• Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits  Journal Articles
• Genetic and phenotypic determinants of blood pressure and other cardiovascular risk factors (GAPP)  Journal Articles
• Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease  Journal Articles
• Genetic association of the GDNF alpha-receptor genes with schizophrenia and clozapine response  Journal Articles
• Genetic bases of hypertriglyceridemic phenotypes  Journal Articles
• Genetic basis of cannabis use: a systematic review  Journal Articles
• Genetic determinants of cannabis use: a systematic review protocol  Journal Articles
• Genetic determinants of plasma triglycerides  Journal Articles
• Genetic drivers of heterogeneity in type 2 diabetes pathophysiology  Journal Articles
• Genetic influences on ADHD symptom dimensions: Examination of a priori candidates, gene‐based tests, genome‐wide variation, and SNP heritability  Journal Articles
• Genetic influences on delayed reward discounting: A genome-wide prioritized subset approach.  Journal Articles
• Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration  Journal Articles
• Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs  Journal Articles
• Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies  Journal Articles
• Genetic risk for dengue hemorrhagic fever and dengue fever in multiple ancestries  Journal Articles
• Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema  Journal Articles
• Genetic variants associated with syncope implicate neural and autonomic processes  Journal Articles
• Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes  Journal Articles
• Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge  Journal Articles
• Genetically determined P2X7 receptor pore formation regulates variability in chronic pain sensitivity  Journal Articles
• Genetically proxied therapeutic inhibition of antihypertensive drug targets and risk of common cancers: A mendelian randomization analysis  Journal Articles
• Genetics of cannabis use in opioid use disorder: A genome-wide association and polygenic risk score study  Journal Articles
• Gene‐ or region‐based analysis of genome‐wide association studies  Journal Articles
• Genome Wide Association Identifies Common Variants at the SERPINA6/SERPINA1 Locus Influencing Plasma Cortisol and Corticosteroid Binding Globulin  Journal Articles
• Genome-Wide Association Analysis of Soluble ICAM-1 Concentration Reveals Novel Associations at the NFKBIK, PNPLA3, RELA, and SH2B3 Loci  Journal Articles
• Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias  Journal Articles
• Genome-Wide Association Studies across Environmental and Genetic Contexts Reveal Complex Genetic Architecture of Symbiotic Extended Phenotypes  Journal Articles
• Genome-Wide Association Studies of Hypertension: Have They Been Fruitful?  Journal Articles
• Genome-Wide Association Studies—Data Generation, Storage, Interpretation, and Bioinformatics  Journal Articles
• Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke  Journal Articles
• Genome-Wide Association Study of Diabetic Kidney Disease Highlights Biology Involved in Glomerular Basement Membrane Collagen  Journal Articles
• Genome-Wide Associations and Functional Genomic Studies of Musculoskeletal Adverse Events in Women Receiving Aromatase Inhibitors  Journal Articles
• Genome-Wide DNA Methylation Analysis of Chinese Patients with Systemic Lupus Erythematosus Identified Hypomethylation in Genes Related to the Type I Interferon Pathway  Journal Articles
• Genome-Wide Identification and Expression Analysis of Udp-Glucuronosyltransferases in the Whitefly Bemisia Tabaci (Gennadius) (HemipterA: Aleyrodidae)  Journal Articles
• Genome-wide Association Analysis of Blood-Pressure Traits in African-Ancestry Individuals Reveals Common Associated Genes in African and Non-African Populations  Journal Articles
• Genome-wide Association Study for AKI  Journal Articles
• Genome-wide Linkage Analyses of Quantitative and Categorical Autism Subphenotypes  Journal Articles
• Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits  Journal Articles
• Genome-wide analysis suggests the importance of vascular processes and neuroinflammation in late-life antidepressant response  Journal Articles
• Genome-wide association analyses for lung function and chronic obstructive pulmonary disease identify new loci and potential druggable targets  Journal Articles
• Genome-wide association analyses of physical activity and sedentary behavior provide insights into underlying mechanisms and roles in disease prevention  Journal Articles
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences  Journal Articles
• Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk  Journal Articles
• Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2  Journal Articles
• Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer  Journal Articles
• Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants  Journal Articles
• Genome-wide association studies identify loci associated with age at menarche and age at natural menopause  Journal Articles
• Genome-wide association studies in oesophageal adenocarcinoma and Barrett's oesophagus: a large-scale meta-analysis  Journal Articles
• Genome-wide association studies of impulsive personality traits (BIS-11 and UPPSP) and drug experimentation in up to 22,861 adult research participants identify loci in the CACNA1I and CADM2 genes  Journal Articles
• Genome-wide association studies of placebo and duloxetine response in major depressive disorder  Journal Articles
• Genome-wide association study identifies 48 common genetic variants associated with handedness  Journal Articles
• Genome-wide association study identifies a novel maternal gene × stress interaction associated with spontaneous preterm birth  Journal Articles
• Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity  Journal Articles
• Genome-wide association study of delay discounting in 23,217 adult research participants of European ancestry  Journal Articles
• Genome-wide association study of emotional empathy in children  Journal Articles
• Genome-wide association study of eosinophilic granulomatosis with polyangiitis reveals genomic loci stratified by ANCA status  Journal Articles
• Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder  Journal Articles
• Genome-wide association study of platelet factor 4/heparin antibodies in heparin-induced thrombocytopenia  Journal Articles
• Genome-wide association study of sepsis in extremely premature infants  Journal Articles
• Genome-wide meta-analyses identify multiple loci associated with smoking behavior  Journal Articles
• Genome-wide meta-analysis of cerebral white matter hyperintensities in patients with stroke  Journal Articles
• Genome-wide studies reveal factors associated with circulating uromodulin and its relationships to complex diseases  Journal Articles
• Genome-wide studies to identify risk factors for kidney disease with a focus on patients with diabetes  Journal Articles
• Genome-wide study investigating effector genes and polygenic prediction for kidney function in persons with ancestry from Africa and the Americas  Journal Articles
• Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis  Journal Articles
• Genome‐wide association study of alcohol use disorder identification test (AUDIT) scores in 20 328 research participants of European ancestry  Journal Articles
• Genome‐wide study identifies novel genes associated with bone toxicities in children with acute lymphoblastic leukaemia  Journal Articles
• Genomic atlas of the plasma metabolome prioritizes metabolites implicated in human diseases  Journal Articles
• Genomic basis of delayed reward discounting  Journal Articles
• Germline variation in inflammation-related pathways and risk of Barrett's oesophagus and oesophageal adenocarcinoma  Journal Articles
• Germline variation in the insulin-like growth factor pathway and risk of Barrett’s esophagus and esophageal adenocarcinoma  Journal Articles
• HDL Cholesterol, LDL Cholesterol, and Triglycerides as Risk Factors for CKD: A Mendelian Randomization Study  Journal Articles
• Hemochromatosis neural archetype reveals iron disruption in motor circuits.  Journal Articles
• Homozygosity for a haplotype in the HBG2‐OR51B4 region is exclusive to Arab‐Indian haplotype sickle cell anemia  Journal Articles
• Human milk oligosaccharides are associated with maternal genetics and respiratory health of human milk-fed children.  Journal Articles
• Hundreds of variants clustered in genomic loci and biological pathways affect human height  Journal Articles
• Identification of Circulating Proteins Associated With Blood Pressure Using Mendelian Randomization  Journal Articles
• Identification of Endocannabinoid Predictors of Treatment Outcomes in Major Depressive Disorder: A Secondary Analysis of the First Canadian Biomarker Integration Network in Depression (CAN-BIND 1) Study  Journal Articles
• Identification of Functional and Expression Polymorphisms Associated With Risk for Antineutrophil Cytoplasmic Autoantibody–Associated Vasculitis  Journal Articles
• Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders  Journal Articles
• Identification of Susceptibility Loci in IL6, RPS9/LILRB3, and an Intergenic Locus on Chromosome 21q22 in Takayasu Arteritis in a Genome‐Wide Association Study  Journal Articles
• Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy  Journal Articles
• Identification of genetic effects underlying type 2 diabetes in South Asian and European populations  Journal Articles
• Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease  Journal Articles
• Identification of susceptibility loci for Takayasu arteritis through a large multi-ancestral genome-wide association study  Journal Articles
• Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis  Journal Articles
• Impact of a Genetic Risk Score on Myocardial Infarction Risk Across Different Ethnic Populations  Journal Articles
• Imputation of missing genotypes: an empirical evaluation of IMPUTE  Journal Articles
• Incorporating Linear Mixed Models into GWAS of Kidney Function Decline  Journal Articles
• Individual common variants exert weak effects on the risk for autism spectrum disorders  Journal Articles
• Integrated genome-wide methylation and expression analyses reveal functional predictors of response to antidepressants  Journal Articles
• Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies  Journal Articles
• Large meta-analysis of genome-wide association studies identifies five loci for lean body mass  Journal Articles
• Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci  Journal Articles
• Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci  Journal Articles
• Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitness  Journal Articles
• Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation  Journal Articles
• Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease  Journal Articles
• Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility  Journal Articles
• Leveraging cell type specific regulatory regions to detect SNPs associated with tissue factor pathway inhibitor plasma levels  Journal Articles
• Leveraging related health phenotypes for polygenic prediction of impulsive choice, impulsive action, and impulsive personality traits in 1534 European ancestry community adults  Journal Articles
• Linkage and association analysis in pedigrees from different populations  Journal Articles
• Lipoprotein(a): An independent, genetic, and causal factor for cardiovascular disease and acute myocardial infarction  Journal Articles
• Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study  Journal Articles
• Loci influencing blood pressure identified using a cardiovascular gene-centric array  Journal Articles
• Longitudinal Data Analysis in Genome‐Wide Association Studies  Journal Articles
• Management of Menstrual Migraine  Journal Articles
• Mendelian Randomization Studies Do Not Support a Role for Vitamin D in Coronary Artery Disease  Journal Articles
• Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression  Journal Articles
• Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels  Journal Articles
• Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design?  Journal Articles
• Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin  Journal Articles
• Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways  Journal Articles
• Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution  Journal Articles
• Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12  Journal Articles
• Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease  Journal Articles
• Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height  Journal Articles
• Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia  Journal Articles
• Meta-analysis of genetic association studies under heterogeneity  Journal Articles
• Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetes  Journal Articles
• Metabolomic and Genome‐wide Association Studies Reveal Potential Endogenous Biomarkers for OATP1B1  Journal Articles
• Modulation of GLP-1 Levels by a Genetic Variant That Regulates the Cardiovascular Effects of Intensive Glycemic Control in ACCORD  Journal Articles
• Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction  Journal Articles
• Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation  Journal Articles
• Multi-ethnic genome-wide association study for atrial fibrillation  Journal Articles
• Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes  Journal Articles
• Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset  Journal Articles
• Multiple Genetic Loci Influence Serum Urate Levels and Their Relationship With Gout and Cardiovascular Disease Risk Factors  Journal Articles
• Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis  Journal Articles
• Multiple loci associated with indices of renal function and chronic kidney disease  Journal Articles
• Networks of human milk microbiota are associated with host genomics, childhood asthma, and allergic sensitization.  Journal Articles
• New Locus for Skin Intrinsic Fluorescence in Type 1 Diabetes Also Associated With Blood and Skin Glycated Proteins  Journal Articles
• New alcohol-related genes suggest shared genetic mechanisms with neuropsychiatric disorders  Journal Articles
• New loci associated with kidney function and chronic kidney disease  Journal Articles
• 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  Journal Articles
• Novel Associations of CPS1, MUT, NOX4, and DPEP1 With Plasma Homocysteine in a Healthy Population  Journal Articles
• Novel Drug Targets for Ischemic Stroke Identified Through Mendelian Randomization Analysis of the Blood Proteome  Journal Articles
• Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals  Journal Articles
• Novel Loci, Including Those Related to Crohn Disease, Psoriasis, and Inflammation, Identified in a Genome-Wide Association Study of Fibrinogen in 17 686 Women  Journal Articles
• Obesity and Multiple Sclerosis: A Mendelian Randomization Study  Journal Articles
• Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study  Journal Articles
• Patterns of allele distribution in a hybrid population of the Cryptococcus neoformans species complex  Journal Articles
• Personalized medicine - the promised land: are we there yet?  Journal Articles
• Pharmacogenomic study of heart failure and candesartan response from the CHARM programme  Journal Articles
• Phenome-wide association analysis of LDL-cholesterol lowering genetic variants in PCSK9  Journal Articles
• Plasma Ghrelin and Risks of Sex-Specific, Site-Specific, and Early-Onset Colorectal Cancer: A Mendelian Randomization Analysis.  Journal Articles
• Pleiotropy among Common Genetic Loci Identified for Cardiometabolic Disorders and C-Reactive Protein  Journal Articles
• Polygenic Risk Score for Low-Density Lipoprotein Cholesterol Is Associated With Risk of Ischemic Heart Disease and Enriches for Individuals With Familial Hypercholesterolemia  Journal Articles
• Polygenic contributions to performance on the Balloon Analogue Risk Task  Journal Articles
• Polygenic risk and the development and course of asthma: an analysis of data from a four-decade longitudinal study  Journal Articles
• Polymorphism in the CETP Gene Region, HDL Cholesterol, and Risk of Future Myocardial Infarction  Journal Articles
• Polymorphisms Near TBX5 and GDF7 Are Associated With Increased Risk for Barrett’s Esophagus  Journal Articles
• Population genetics of chronic kidney disease: The evolving story of APOL1  Journal Articles
• Population genomic analyses reveal high diversity, recombination and nosocomial transmission among Candida glabrata (Nakaseomyces glabrata) isolates causing invasive infections  Journal Articles
• Population-Based Genomewide Genetic Analysis of Common Clinical Chemistry Analytes  Journal Articles
• Prostate Cancer Transcriptomic Regulation by the Interplay of Germline Risk Alleles, Somatic Mutations, and 3D Genomic Architecture  Journal Articles
• Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways  Journal Articles
• Rank-based genome-wide analysis reveals the association of Ryanodine receptor-2 gene variants with childhood asthma among human populations  Journal Articles
• Ranking and characterization of established BMI and lipid associated loci as candidates for gene-environment interactions  Journal Articles
• Rare DNA copy number variants in cardiovascular malformations with extracardiac abnormalities  Journal Articles
• Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes  Journal Articles
• Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Study†  Journal Articles
• Recent progress in genetics, epigenetics and metagenomics unveils the pathophysiology of human obesity  Journal Articles
• Regulation at Drosophila’s Malic Enzyme highlights the complexity of transvection and its sensitivity to genetic background  Journal Articles
• Replication of genetic associations with plasma lipoprotein traits in a multiethnic sample  Journal Articles
• Risk loci involved in giant cell arteritis susceptibility: a genome-wide association study  Journal Articles
• Segregating patterns of copy number variations in extended autism spectrum disorder (ASD) pedigrees  Journal Articles
• Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes: Evidence from genome‐wide association studies  Journal Articles
• Shroom3, a Gene Associated with CKD, Modulates Epithelial Recovery after AKI  Journal Articles
• Sortilin: An unusual suspect in cholesterol metabolism  Journal Articles
• Stroke genetics informs drug discovery and risk prediction across ancestries  Journal Articles
• TWIST1 DNA methylation is a cell marker of airway and parenchymal lung fibroblasts that are differentially methylated in asthma  Journal Articles
• Targeted exonic sequencing of GWAS loci in the high extremes of the plasma lipids distribution  Journal Articles
• Targeting a phospho-STAT3-miRNAs pathway improves vesicular hepatic steatosis in an in vitro and in vivo model  Journal Articles
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data  Journal Articles
• The Generation R study: a candidate gene study and genome-wide association study (GWAS) on health-related quality of life (HRQOL) of mothers and young children  Journal Articles
• The Genetic Factors of the Airway Epithelium Associated with the Pathology of Asthma  Journal Articles
• The Genetic Link Between Diabetes and Atherosclerosis  Journal Articles
• The Role of Airway Epithelial Cell Alarmins in Asthma  Journal Articles
• The genetic risk of gestational diabetes in South Asian women  Journal Articles
• The genetics of hemoglobin A₂ regulation in sickle cell anemia  Journal Articles
• The genetics of human personality  Journal Articles
• The genomics of heart failure: design and rationale of the HERMES consortium  Journal Articles
• The need for inclusion of sex and age of onset variables in genetic association studies of obsessive–compulsive disorder: Overview  Journal Articles
• Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies  Journal Articles
• Thrombocytopenic Platelet Disorders  Journal Articles
• Thymic stromal lymphopoietin (TSLP) secretion from human nasal epithelium is a function of TSLP genotype  Journal Articles
• Towards the genetic basis of cerebral venous thrombosis—the BEAST Consortium: a study protocol  Journal Articles
• Trans-ethnic association study of blood pressure determinants in over 750,000 individuals  Journal Articles
• Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders  Journal Articles
• Translating Genomic Analyses into Improved Management of Coronary Artery Disease  Journal Articles
• Understanding the population structure of North American patients with cystic fibrosis  Journal Articles
• Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes  Journal Articles
• Variability of polygenic prediction for body mass index in Africa  Journal Articles
• Vitamin D and Risk of Multiple Sclerosis: A Mendelian Randomization Study  Journal Articles
• Vitamin D levels and risk of type 1 diabetes: A Mendelian randomization study  Journal Articles
• What should the genome-wide significance threshold be? Empirical replication of borderline genetic associations  Journal Articles
• Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder  Journal Articles
• gJLS2: an R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies  Journal Articles