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 (104)

Mentioned in (195)

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)
• Choline-An Underappreciated Component of a Mother-to-Be's Diet. (2024)
• Combination of genomic instability score and TP53 status for prognosis prediction in lung adenocarcinoma. (2023)
• Effect of schizophrenia common variants on infant brain volumes: cross-sectional study in 207 term neonates in developing Human Connectome Project. (2023)
• Pruning and thresholding approach for methylation risk scores in multi-ancestry populations. (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)
• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
• Associations Between Cannabis Use, Polygenic Liability for Schizophrenia, and Cannabis-related Experiences in a Sample of Cannabis Users. (2023)
• Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
• DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. (2023)
• Brain charts for the human lifespan. (2022)
• 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)
• 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)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. (2022)
• Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. (2021)
• 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)
• 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)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Genetics of substance use disorders in the era of big data. (2021)
• Gestational age and birth growth parameters as early predictors of fetal alcohol spectrum disorders. (2021)
• Interpretation of risk loci from genome-wide association studies of Alzheimer's disease. (2020)
• Genome-wide association analysis of opioid use disorder: A novel approach using clinical data. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis. (2020)
• Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson's disease. (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)
• Defining the Genetic, Genomic, Cellular, and Diagnostic Architectures of Psychiatric Disorders. (2019)
• Exploring the relationship between polygenic risk for cannabis use, peer cannabis use and the longitudinal course of cannabis involvement. (2019)
• Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
• Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Epigenetics and depression
. (2019)
• Identification of common genetic risk variants for autism spectrum disorder. (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)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (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)
• Human Genetics of Addiction: New Insights and Future Directions. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. (2018)
• The Impact of Peer Substance Use and Polygenic Risk on Trajectories of Heavy Episodic Drinking Across Adolescence and Emerging Adulthood. (2017)
• An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues. (2017)
• Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
• Review: Pharmacogenetics of alcoholism treatment: Implications of ethnic diversity. (2017)
• Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. (2017)
• Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (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)
• Phenotypic and familial associations between childhood maltreatment and cannabis initiation and problems in young adult European-American and African-American women. (2017)
• Ancient DNA and the rewriting of human history: be sparing with Occam's razor. (2016)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
• Genome-wide association study identifies 74 loci associated with educational attainment. (2016)
• Structural brain development between childhood and adulthood: Convergence across four longitudinal samples. (2016)
• Next-generation genotype imputation service and methods. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• 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)
• Tools and best practices for data processing in allelic expression analysis. (2015)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (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)
• Genomic influences on alcohol problems in a population-based sample of young adults. (2015)
• Can Genetics Predict Response to Complex Behavioral Interventions? Evidence from a Genetic Analysis of the Fast Track Randomized Control Trial. (2015)
• HLAreporter: a tool for HLA typing from next generation sequencing data. (2015)
• Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis. (2015)
• Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank. (2015)
• The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
• 708 Common and 2010 rare DISC1 locus variants identified in 1542 subjects: analysis for association with psychiatric disorder and cognitive traits. (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)
• Pharmacogenetics of OPRM1. (2014)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• Distinct pharmacology and metabolism of K2 synthetic cannabinoids compared to Δ(9)-THC: mechanism underlying greater toxicity? (2014)
• DNA methylation signatures link prenatal famine exposure to growth and metabolism. (2014)
• Heritability and genomics of gene expression in peripheral blood. (2014)
• Genome-wide association discoveries of alcohol dependence. (2014)
• Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
• EWS-FLI1 utilizes divergent chromatin remodeling mechanisms to directly activate or repress enhancer elements in Ewing sarcoma. (2014)
• Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
• Differential sensitivity to prevention programming: a dopaminergic polymorphism-enhanced prevention effect on protective parenting and adolescent substance use. (2014)
• A general approach for haplotype phasing across the full spectrum of relatedness. (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 mega-analysis of genome-wide association studies for major depressive disorder. (2013)
• 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)
• The CRHR1 gene, trauma exposure, and alcoholism risk: a test of G × E effects. (2013)
• A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
• Maternal alcohol consumption producing fetal alcohol spectrum disorders (FASD): quantity, frequency, and timing of drinking. (2013)
• Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
• DNA methylation contributes to natural human variation. (2013)
• Preliminary evidence for a gene-environment interaction in predicting alcohol use disorders in adolescents. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Nicotinic acetylcholine receptor variation and response to smoking cessation therapies. (2013)
• The Genomic Revolution and Beliefs about Essential Racial Differences: A Backdoor to Eugenics? (2013)
• High prevalence of vitamin D deficiency in pregnant women: a national cross-sectional survey. (2012)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
• Population-specificity of human DNA methylation. (2012)
• Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome. (2012)
• Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. (2012)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• The genetic basis of addictive disorders. (2012)
• Evolution and functional impact of rare coding variation from deep sequencing of human exomes. (2012)
• Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
• The genetics of the opioid system and specific drug addictions. (2012)
• HLA typing from RNA-Seq sequence reads. (2012)
• Assessing the impact of nicotine dependence genes on the risk of facial clefts: An example of the use of national registry and biobank data. (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)
• Meta-analysis and genome-wide interpretation of genetic susceptibility to drug addiction. (2011)
• 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)
• Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence. (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 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)
• Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
• Incorporating age at onset of smoking into genetic models for nicotine dependence: evidence for interaction with multiple genes. (2010)
• New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. (2010)
• Obesity, smoking, and frontal brain dysfunction. (2010)
• Convergence of genetic findings for nicotine dependence and smoking related diseases with chromosome 15q24-25. (2010)
• Genetic and epigenetic insights into fetal alcohol spectrum disorders. (2010)
• Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. (2010)
• Association study of 182 candidate genes in anorexia nervosa. (2010)
• ADH1B*3 and response to alcohol in African-Americans. (2010)
• Discovering genetic ancestry using spectral graph theory. (2010)
• Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. (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)
• Fine mapping of calcineurin (PPP3CA) gene reveals novel alternative splicing patterns, association of 5'UTR trinucleotide repeat with addiction vulnerability, and differential isoform expression in Alzheimer's disease. (2010)
• Genome-wide association studies in diverse populations. (2010)
• A review of estrogen receptor alpha gene (ESR1) polymorphisms, mood, and cognition. (2010)
• Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)
• Genetic structure of Europeans: a view from the North-East. (2009)
• Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• Nicotine withdrawal sensitivity, linkage to chr6q26, and association of OPRM1 SNPs in the SMOking in FAMilies (SMOFAM) sample. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• Finding the missing heritability of complex diseases. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Dense genomewide linkage scan for alcohol dependence in African Americans: significant linkage on chromosome 10. (2009)
• Genetic utility of broadly defined bipolar schizoaffective disorder as a diagnostic concept. (2009)
• Association of psychiatric and substance use disorder comorbidity with cocaine dependence severity and treatment utilization in cocaine-dependent individuals. (2009)
• Genome-wide association study of alcohol dependence. (2009)
• Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
• Alcohol consumption indices of genetic risk for alcohol dependence. (2009)
• Common and rare variants in multifactorial susceptibility to common diseases. (2008)
• Toward a global view of alcohol, tobacco, cannabis, and cocaine use: findings from the WHO World Mental Health Surveys. (2008)
• Analysis and application of European genetic substructure using 300 K SNP information. (2008)
• Short scales to assess cannabis-related problems: a review of psychometric properties. (2008)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)

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