23andMe cohort

Aliases

23andMe, 23andMe cohort, 23andMe replication, 23andMe research participants, 23andMe sample, 23andMe, Inc.

Related entities (41)

Mentioned in (24)

Papers in which this entity is mentioned.

• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
• Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
• 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)
• A saturated map of common genetic variants associated with human height. (2022)
• Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. (2021)
• Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
• Genetics of substance use disorders in the era of big data. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (2020)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Polygenic risk for alcohol misuse is moderated by romantic partnerships. (2019)
• Identification of common genetic risk variants for autism spectrum disorder. (2019)
• Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. (2019)
• Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences. (2019)
• Genome-Wide Association Study Meta-Analysis of the Alcohol Use Disorders Identification Test (AUDIT) in Two Population-Based Cohorts. (2019)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• 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)
• Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)

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