European ancestry cohort

Aliases

12 population-based samples of European ancestry, 6,845 EAs, 93 adult individuals of European ancestry, CEU, EA, EA COGA, EA adolescents, EA adults, EA analytic sample, EA cohort, EA ethnicity, EA families, EA individuals, EA participants, EA sample, EA samples, EA subjects, EAs, EUR, EUR ancestry, EUR cohort, EUR cohorts, European, European American, European American (EA) adolescents, European American (EA) cohort, European American ancestry cohort, European American participants, European American sample, European American women, European Americans, European ancestry, European ancestry LD reference panel, European ancestry cohort, European ancestry group, European ancestry individuals, European ancestry proportion, European ancestry sample, European descent, European genetic structure, European group, European individuals, European origin, European population, European samples, European studies, European-American, European-ancestry cluster, European-origin individuals, Europeans, NYCPEA, genetic EA, grandparental European country of origin, individuals of European ancestries, individuals of European ancestry, individuals of European descent, non-Hispanic EA, non-Hispanic European Americans, participants primarily of European ancestry, persons with self-identified European ancestry, population-based cohort of European ancestry, populations of European ancestry, recent European ancestry, self-reported European American, self-reported European ancestry, white

Related entities (91)

Mentioned in (118)

Papers in which this entity is mentioned.

• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Advancing regulatory variant effect prediction with AlphaGenome. (2026)
• The Impact of Polygenic Risk, Parental Separation, and Parental Relationship Discord on Heavy Episodic Drinking Across Adolescence and Young Adulthood in a High-Risk Sample. (2025)
• Meta-analysis reveals differences in somatic alterations by genetic ancestry across common cancers. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• OXSeg: Multidimensional Attention UNet-Based Lip Segmentation Using Semi-Supervised Lip Contours. (2025)
• Mutations in the bone morphogenetic protein signaling pathway sensitize zebrafish and humans to ethanol-induced jaw malformations. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• Machine learning approaches to the identification of children affected by prenatal alcohol exposure: A narrative review. (2024)
• BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
• MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups. (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Alcohol Use Disorder Polygenic Score Compared With Family History and ADH1B. (2024)
• Reduction of APOE accounts for neurobehavioral deficits in fetal alcohol spectrum disorders. (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)
• Clinical, genomic, and neurophysiological correlates of lifetime suicide attempts among individuals with alcohol dependence. (2024)
• The Polygenic Score Catalog: new functionality and tools to enable FAIR research. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (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)
• A harmonized public resource of deeply sequenced diverse human genomes. (2024)
• A New Era of Data-Driven Cancer Research and Care: Opportunities and Challenges. (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)
• Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary. (2023)
• Genetic nurture effects for alcohol use disorder. (2023)
• Unsupervised discovery of ancestry-informative markers and genetic admixture proportions in biobank-scale datasets. (2023)
• Predicting Alcohol-Related Memory Problems in Older Adults: A Machine Learning Study with Multi-Domain Features. (2023)
• Alcohol use polygenic risk score, social support, and alcohol use among European American and African American adults. (2023)
• Comprehensive analysis of mutational signatures reveals distinct patterns and molecular processes across 27 pediatric cancers. (2023)
• Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
• Associations Between Cannabis Use, Polygenic Liability for Schizophrenia, and Cannabis-related Experiences in a Sample of Cannabis Users. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. (2022)
• Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
• Parsing genetically influenced risk pathways: genetic loci impact problematic alcohol use via externalizing and specific risk. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• AFA: Ancestry-specific allele frequency estimation in admixed populations: The Hispanic Community Health Study/Study of Latinos. (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)
• The clinical course of antisocial behaviors in men and women of three racial groups. (2022)
• Gene-based polygenic risk scores analysis of alcohol use disorder in African Americans. (2022)
• A latent class analysis of alcohol and posttraumatic stress symptoms among offspring of parents with and without alcohol use disorder. (2021)
• 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)
• Using a developmental perspective to examine the moderating effects of marriage on heavy episodic drinking in a young adult sample enriched for risk. (2021)
• Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
• Multivariate analysis of 1.5 million people identifies genetic associations with traits related to self-regulation and addiction. (2021)
• Genetic association study of childhood aggression across raters, instruments, and age. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences. (2021)
• Predicting risk for Alcohol Use Disorder using longitudinal data with multimodal biomarkers and family history: a machine learning study. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Structural variation in the sequencing era. (2020)
• Pan-cancer analysis of whole genomes. (2020)
• Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Genome-wide meta-analysis of problematic alcohol use in 435,563 individuals yields insights into biology and relationships with other traits. (2020)
• Transcriptomic signatures across human tissues identify functional rare genetic variation. (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)
• CYP2A6 is associated with obesity: studies in human samples and a high fat diet mouse model. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• A Pilot Follow-Up Study of Older Alcohol-Dependent COGA Adults. (2019)
• Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. (2019)
• Ethanol activates immune response in lymphoblastoid cells. (2019)
• Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. (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)
• The Early Developmental Outcomes of Prenatal Alcohol Exposure: A Review. (2018)
• Evidence-based design and evaluation of a whole genome sequencing clinical report for the reference microbiology laboratory. (2018)
• Genome-wide association study identifies a novel locus for cannabis dependence. (2018)
• Influence of Parental Alcohol Dependence Symptoms and Parenting on Adolescent Risky Drinking and Conduct Problems: A Family Systems Perspective. (2018)
• Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity. (2018)
• Annotation-free quantification of RNA splicing using LeafCutter. (2018)
• Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure. (2017)
• Genetic correlates of the development of theta event related oscillations in adolescents and young adults. (2017)
• Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• The impact of structural variation on human gene expression. (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)
• Genome-wide Association Study of Cannabis Dependence Severity, Novel Risk Variants, and Shared Genetic Risks. (2016)
• KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (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)
• Genomewide Association Study for Maximum Number of Alcoholic Drinks in European Americans and African Americans. (2015)
• Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans. (2015)
• A global reference for human genetic variation. (2015)
• Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (2015)
• Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
• Comorbidity of severe psychotic disorders with measures of substance use. (2014)
• Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
• Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
• Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
• Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
• A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
• Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD. (2013)
• Effects of alcohol on the endocrine system. (2013)
• Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
• Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
• Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
• The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (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)
• Nonreplication of an association of SGIP1 SNPs with alcohol dependence and resting theta EEG power. (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)
• A new statistic to evaluate imputation reliability. (2010)
• Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts. (2010)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

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