replication sample cohort

Aliases

49,160 participants of the EBB, replication cohort, replication phase independent samples, replication sample

Related entities (8)

Mentioned in (29)

Papers in which this entity is mentioned.

• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Heritable defects in telomere and mitotic function selectively predispose to sarcomas. (2023)
• A saturated map of common genetic variants associated with human height. (2022)
• Reproducible brain-wide association studies require thousands of individuals. (2022)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Brain Volume Abnormalities in Youth at High Risk for Depression: Adolescent Brain and Cognitive Development Study. (2020)
• Association of a Schizophrenia-Risk Nonsynonymous Variant With Putamen Volume in Adolescents: A Voxelwise and Genome-Wide Association Study. (2019)
• Mega-Analysis of Gray Matter Volume in Substance Dependence: General and Substance-Specific Regional Effects. (2019)
• Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
• Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
• Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
• Genomic influences on alcohol problems in a population-based sample of young adults. (2015)
• 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (2014)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
• A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
• Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
• Neuronal calcium sensor-1 and cocaine addiction: a genetic association study in African-Americans and European Americans. (2012)
• Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (2012)
• Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
• The AVPR1A gene and substance use disorders: association, replication, and functional evidence. (2011)
• Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (2011)
• Genome-wide association study identifies five new schizophrenia loci. (2011)
• Trans-eQTLs reveal that independent genetic variants associated with a complex phenotype converge on intermediate genes, with a major role for the HLA. (2011)
• Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Genome-wide association study of alcohol dependence. (2009)

Merged raw entities (6)

All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.