East Asian cohort

Aliases

ASN, Asian, E. Asian, E. Asians, EAA, EAS, East Asian, East Asian ancestry, East Asian cohort, East Asian individuals, East Asian population, East Asian sample, East Asian samples, East Asians, people of East Asian origin

Related entities (27)

Mentioned in (69)

Papers in which this entity is mentioned.

• Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
• Functional analysis of cancer-associated germline risk variants. (2025)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (2025)
• 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)
• Principles and methods for transferring polygenic risk scores across global populations. (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)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• A harmonized public resource of deeply sequenced diverse human genomes. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (2024)
• Combination of genomic instability score and TP53 status for prognosis prediction in lung adenocarcinoma. (2023)
• Effect of schizophrenia common variants on infant brain volumes: cross-sectional study in 207 term neonates in developing Human Connectome Project. (2023)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
• Alcohol use polygenic risk score, social support, and alcohol use among European American and African American adults. (2023)
• Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
• Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
• Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (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)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
• Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Genetics of substance use disorders in the era of big data. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Klotho gene polymorphism, brain structure and cognition in early-life development. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
• Rare variant phasing using paired tumor:normal sequence data. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Review: Pharmacogenetics of alcoholism treatment: Implications of ethnic diversity. (2017)
• Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. (2017)
• Review: Prevalence and co-occurrence of addictions in US ethnic/racial groups: Implications for genetic research. (2017)
• Associations between cortical thickness and neurocognitive skills during childhood vary by family socioeconomic factors. (2017)
• Ancient DNA and the rewriting of human history: be sparing with Occam's razor. (2016)
• G = E: What GWAS Can Tell Us about the Environment. (2016)
• The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. (2016)
• Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (2015)
• Family income, parental education and brain structure in children and adolescents. (2015)
• What is the DNA repair defect underlying Fanconi anemia? (2015)
• A global reference for human genetic variation. (2015)
• ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy children. (2015)
• A global reference for human genetic variation. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• Face shape differs in phylogenetically related populations. (2014)
• Prevalence of amblyopia or strabismus in asian and non-Hispanic white preschool children: multi-ethnic pediatric eye disease study. (2013)
• Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. (2012)
• The genetic basis of addictive disorders. (2012)
• Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
• ADH1B*3 and response to alcohol in African-Americans. (2010)
• Discovering genetic ancestry using spectral graph theory. (2010)
• Mothers' maximum drinks ever consumed in 24 hours predicts mental health problems in adolescent offspring. (2010)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• The enrichment study of the Minnesota twin family study: increasing the yield of twin families at high risk for externalizing psychopathology. (2009)
• Genome-wide association study of alcohol dependence. (2009)
• Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
• Variations in alcohol-metabolizing enzymes in people of East Indian and African descent from Trinidad and Tobago. (2007)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

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