European population cohort

Aliases

6166 subjects of European descent, EA, EA controls, EA meta-analysis, EA participants, EA samples, EAs, EUR, EUR participants, EUR subjects, Europe, European, European American, European American sample, European Americans, European ancestry, European cohort, European countries, European decent, European descent, European focus, European genetic structure, European meta-analysis, European nations, European populations, European- sample, European-American, European-American "control", European-American Fast Track cohort, European-American ethnicity, European-American sample, European-American subset, European-Americans, European-ancestry individuals, European-descent populations, Europeans, European–Americans, individuals of European descent, mixed European population, participants of European ancestry, participants of European descent, populations of European descent, populations of European origin, samples with European ancestry, six independent European-ancestry cohorts

Related entities (25)

Mentioned in (70)

Papers in which this entity is mentioned.

• Whole-genome landscapes of 1,364 breast cancers. (2026)
• Associations between common genetic variants and income provide insights about the socio-economic health gradient. (2025)
• Trajectories of genetic risk across dimensions of alcohol use behaviors. (2025)
• Tumour-wide RNA splicing aberrations generate actionable public neoantigens. (2025)
• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (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)
• Nucleotide Transformer: building and evaluating robust foundation models for human genomics. (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)
• 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)
• Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
• Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
• A global multicohort study to map subcortical brain development and cognition in infancy and early childhood. (2024)
• Nanopore sequencing with unique molecular identifiers enables accurate mutation analysis and haplotyping in the complex lipoprotein(a) KIV-2 VNTR. (2024)
• Genome-wide association analyses identify 95 risk loci and provide insights into the neurobiology of post-traumatic stress disorder. (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)
• Pitfalls of predicting age-related traits by polygenic risk scores. (2023)
• Associations Between Cannabis Use, Polygenic Liability for Schizophrenia, and Cannabis-related Experiences in a Sample of Cannabis Users. (2023)
• Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. (2022)
• Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
• Using a developmental perspective to examine the moderating effects of marriage on heavy episodic drinking in a young adult sample enriched for risk. (2021)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Pan-cancer analysis of whole genomes. (2020)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Polygenic prediction via Bayesian regression and continuous shrinkage priors. (2019)
• Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria. (2019)
• RNA sequence analysis reveals macroscopic somatic clonal expansion across normal tissues. (2019)
• Genome-wide association analysis links multiple psychiatric liability genes to oscillatory brain activity. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Enter the Matrix: Factorization Uncovers Knowledge from Omics. (2018)
• Genome-wide association study identifies a novel locus for cannabis dependence. (2018)
• Combined Face-Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders. (2018)
• Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
• Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
• The Impact of Peer Substance Use and Polygenic Risk on Trajectories of Heavy Episodic Drinking Across Adolescence and Emerging Adulthood. (2017)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• Phenotypic and familial associations between childhood maltreatment and cannabis initiation and problems in young adult European-American and African-American women. (2017)
• 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)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Tools and best practices for data processing in allelic expression analysis. (2015)
• Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans. (2015)
• A global reference for human genetic variation. (2015)
• HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
• Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
• A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. (2013)
• A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
• Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• Prevalence of children with severe fetal alcohol spectrum disorders in communities near Rome, Italy: new estimated rates are higher than previous estimates. (2011)
• The AVPR1A gene and substance use disorders: association, replication, and functional evidence. (2011)
• A framework for variation discovery and genotyping using next-generation DNA sequencing data. (2011)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Obesity, smoking, and frontal brain dysfunction. (2010)
• Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)

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