GWAS cohort

Aliases

12,111 GWS SNPs, EUR GWS SNPs, GWAS, GWAS SNPs, GWAS arrays, GWAS cohort, GWAS cohorts, GWAS data, GWAS findings, GWAS hit, GWAS i, GWAS k, GWAS meta-analysis, GWAS stage, GWASs, Genome-Wide Association Study, Genome-wide association study, NIH NHGRI catalog of published genome-wide association studies, SNP, SNPs, combined GWAS, discovery GWAS, discovery cohort, genome-wide association studies, genome-wide association study, genome-wide significant SNPs, genome‑wide significant SNPs, large-scale GWAS, locus, our GWAS, small P-value GWAS SNP, summary statistics, trait-associated SNPs

Related entities (92)

Mentioned in (102)

Papers in which this entity is mentioned.

• Mapping the genetic landscape across 14 psychiatric disorders. (2026)
• Specificity, length and luck drive gene rankings in association studies. (2026)
• Modeling heterogeneity in single-cell perturbation states enhances detection of response eQTLs. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
• Mutations in the bone morphogenetic protein signaling pathway sensitize zebrafish and humans to ethanol-induced jaw malformations. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
• MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
• Integrative polygenic risk score improves the prediction accuracy of complex traits and diseases. (2024)
• Principles and methods for transferring polygenic risk scores across global populations. (2024)
• Global impact of unproductive splicing on human gene expression. (2024)
• Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
• Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Pervasive Downward Bias in Estimates of Liability-Scale Heritability in Genome-wide Association Study Meta-analysis: A Simple Solution. (2023)
• Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
• Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
• A saturated map of common genetic variants associated with human height. (2022)
• Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
• Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. (2022)
• Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (2021)
• Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Genetic association study of childhood aggression across raters, instruments, and age. (2021)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
• Tutorial: a guide to performing polygenic risk score analyses. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Genomic structural equation modelling provides insights into the multivariate genetic architecture of complex traits. (2019)
• g:Profiler: a web server for functional enrichment analysis and conversions of gene lists (2019 update). (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Polygenic risk for alcohol misuse is moderated by romantic partnerships. (2019)
• Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. (2018)
• A Brief Critique of the TATES Procedure. (2018)
• Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
• Genetic effects on gene expression across human tissues. (2017)
• The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog). (2017)
• The impact of structural variation on human gene expression. (2017)
• LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis. (2017)
• Translating genome-wide association findings into new therapeutics for psychiatry. (2016)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• An introductory review of parallel independent component analysis (p-ICA) and a guide to applying p-ICA to genetic data and imaging phenotypes to identify disease-associated biological pathways and systems in common complex disorders. (2015)
• Candidate gene-environment interaction research: reflections and recommendations. (2015)
• The landscape of long noncoding RNAs in the human transcriptome. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• An atlas of active enhancers across human cell types and tissues. (2014)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
• A general approach for haplotype phasing across the full spectrum of relatedness. (2014)
• Visualizing genomic information across chromosomes with PhenoGram. (2013)
• Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
• Charting a dynamic DNA methylation landscape of the human genome. (2013)
• A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
• Charting a dynamic DNA methylation landscape of the human genome. (2013)
• Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• A better prognosis for genetic association studies in mice. (2012)
• Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (2012)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• Fast and accurate genotype imputation in genome-wide association studies through pre-phasing. (2012)
• Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
• An integrated encyclopedia of DNA elements in the human genome. (2012)
• Meta-analysis and genome-wide interpretation of genetic susceptibility to drug addiction. (2011)
• Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
• Gene set analysis of genome-wide association studies: methodological issues and perspectives. (2011)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Distribution of allele frequencies and effect sizes and their interrelationships for common genetic susceptibility variants. (2011)
• Liver and adipose expression associated SNPs are enriched for association to type 2 diabetes. (2010)
• Large copy-number variations are enriched in cases with moderate to extreme obesity. (2010)
• i-GSEA4GWAS: a web server for identification of pathways/gene sets associated with traits by applying an improved gene set enrichment analysis to genome-wide association study. (2010)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
• SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (2009)
• Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
• Finding the missing heritability of complex diseases. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Genome-wide association study of alcohol dependence. (2009)
• Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. (2008)

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