CEU cohort

Aliases

CEPH collection, CEPH, Utah residents with ancestry from northern and western Europe, CEU, CEU HapMap, CEU reference panel, CEU reference panels, Central European, European, European (CEU), European ancestry (1KG Phase 1), European population, Europeans, HapMap 2 panel of Utah residents of Northern and Western European ancestry, HapMap CEU sample, HapMap European, HapMap European samples, U.S. Utah residents with ancestry from Northern and Western Europe, Utah Residents with Northern and Western European ancestry, Utah residents of Northern and Western European ancestry, Utah residents with Northern and Western European ancestry, Utah residents with ancestry from northern and western Europe, Utah residents with northern and western European ancestry, simulated CEU HapMap

Related entities (31)

Mentioned in (61)

Papers in which this entity is mentioned.

• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (2023)
• Human Retrotransposons and Effective Computational Detection Methods for Next-Generation Sequencing Data. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• 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)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Identification of common genetic risk variants for autism spectrum disorder. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• Genome-wide association study identifies a novel locus for cannabis dependence. (2018)
• 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)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (2015)
• A global reference for human genetic variation. (2015)
• Candidate gene-environment interaction research: reflections and recommendations. (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)
• The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
• 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)
• Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking. (2013)
• A cross-platform analysis of 14,177 expression quantitative trait loci derived from lymphoblastoid cell lines. (2013)
• Analysis of variation at transcription factor binding sites in Drosophila and humans. (2012)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• Population-specificity of human DNA methylation. (2012)
• Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (2012)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
• The genetics of the opioid system and specific drug addictions. (2012)
• HLA typing from RNA-Seq sequence reads. (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)
• A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
• Genome-wide association study identifies five new schizophrenia loci. (2011)
• The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• LocusZoom: regional visualization of genome-wide association scan results. (2010)
• Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
• A new statistic to evaluate imputation reliability. (2010)
• BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. (2009)
• Genome-wide association study of bipolar disorder in European American and African American individuals. (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)
• Marker selection for genetic case-control association studies. (2009)
• Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
• Analysis and application of European genetic substructure using 300 K SNP information. (2008)
• 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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