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 (29)

Mentioned in (45)

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)
• Guidelines for Evaluating the Comparability of Down-Sampled GWAS Summary Statistics. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• 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)
• Genetic association study of childhood aggression across raters, instruments, and age. (2021)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Tutorial: a guide to performing polygenic risk score analyses. (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)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• A Brief Critique of the TATES Procedure. (2018)
• The impact of structural variation on human gene expression. (2017)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (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)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• An integrated encyclopedia of DNA elements in the human genome. (2012)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results. (2008)

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