YRI cohort

Aliases

African (YRI), Africans, HapMap African, HapMap YRI, YRI, YRI analysis panels, Yoruba, Yoruba in Ibadan, Nigeria, Yoruba people of Ibadan, Nigeria, Yoruba, Nigeria

Related entities (23)

Mentioned in (37)

Papers in which this entity is mentioned.

• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Global impact of unproductive splicing on human gene expression. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
• Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• DNA methylation signature of human fetal alcohol spectrum disorder. (2016)
• Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel). (2016)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
• A global reference for human genetic variation. (2015)
• A global reference for human genetic variation. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Inference of high resolution HLA types using genome-wide RNA or DNA sequencing reads. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013)
• Population-specificity of human DNA methylation. (2012)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• The genetics of the opioid system and specific drug addictions. (2012)
• A comparison of approaches to account for uncertainty in analysis of imputed genotypes. (2011)
• Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
• Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library. (2010)
• Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• Genetic structure of Europeans: a view from the North-East. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
• A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. (2006)

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