Europeans cohort

Aliases

15 771 Europeans, EA, EAs, EUR GWAS, European, European American, European GWAS, European ancestry, European ancestry cohort, European population, European populations, European samples

Related entities (20)

Mentioned in (46)

Papers in which this entity is mentioned.

• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• OXSeg: Multidimensional Attention UNet-Based Lip Segmentation Using Semi-Supervised Lip Contours. (2025)
• KILDA: identifying KIV-2 repeats from kmers. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
• 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)
• A saturated map of common genetic variants associated with human height. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Cross-tissue transcriptome-wide association studies identify susceptibility genes shared between schizophrenia and inflammatory bowel disease. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (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)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
• Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations. (2017)
• Ancient DNA and the rewriting of human history: be sparing with Occam's razor. (2016)
• Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
• New insights into the generation and role of de novo mutations in health and disease. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Next-generation genotype imputation service and methods. (2016)
• RNA splicing is a primary link between genetic variation and disease. (2016)
• The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
• Pharmacogenetics of OPRM1. (2014)
• Face shape differs in phylogenetically related populations. (2014)
• Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
• Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (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)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
• 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)
• Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
• Genome-wide association studies in diverse populations. (2010)
• SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (2009)
• Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• A common genetic variant in the 15q24 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) is associated with a reduced ability of women to quit smoking in pregnancy. (2009)
• Genome-wide association study of alcohol dependence. (2009)
• Geographic patterns of genome admixture in Latin American Mestizos. (2008)

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