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 (1)

Mentioned in (29)

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)
• 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)
• 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)
• Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (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)
• A global reference for human genetic variation. (2015)
• A germline polymorphism of thymine DNA glycosylase induces genomic instability and cellular transformation. (2014)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

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