non-European ancestry cohort

Aliases

individuals of non-European ancestry, non-EUR, non-European, non-European individuals, non-European populations, non-Europeans

Related entities (10)

Mentioned in (38)

Papers in which this entity is mentioned.

• 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)
• Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. (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)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (2024)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (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)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (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)
• Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk. (2022)
• Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
• Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (2021)
• Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood. (2021)
• Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology. (2021)
• Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
• Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Review: Pharmacogenetics of alcoholism treatment: Implications of ethnic diversity. (2017)
• Genome-wide association analysis identifies common variants influencing infant brain volumes. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• 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)
• Fast and accurate long-range phasing in a UK Biobank cohort. (2016)
• Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (2015)
• Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
• Discovering genetic ancestry using spectral graph theory. (2010)
• A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. (2010)
• Genome-wide association studies in diverse populations. (2010)
• Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
• Finding the missing heritability of complex diseases. (2009)
• Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
• Common and rare variants in multifactorial susceptibility to common diseases. (2008)

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