European ancestry cohort
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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)
- An overview of DNA methylation-derived trait score methods and applications. (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)
- Machine learning for genetics-based classification and treatment response prediction in cancer of unknown primary. (2023)
- Genetic nurture effects for alcohol use disorder. (2023)
- Multiomic prioritisation of risk genes for anorexia nervosa. (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)
- Economic Burden of Health Conditions Associated With Adverse Childhood Experiences Among US Adults. (2023)
- Polygenic scoring accuracy varies across the genetic ancestry continuum. (2023)
- Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
- Multi-ancestry study of the genetics of problematic alcohol use in over 1 million individuals. (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)
- Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
- DNA methylation and general psychopathology in childhood: an epigenome-wide meta-analysis from the PACE consortium. (2023)
- Multi-trait genome-wide association study of opioid addiction: OPRM1 and beyond. (2022)
- Genetic architecture of 11 major psychiatric disorders at biobehavioral, functional genomic and molecular genetic levels of analysis. (2022)
- The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
- Meta-analysis of epigenome-wide association studies in newborns and children show widespread sex differences in blood DNA methylation. (2022)
- Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
- Item-Level Genome-Wide Association Study of the Alcohol Use Disorders Identification Test in Three Population-Based Cohorts. (2022)
- A saturated map of common genetic variants associated with human height. (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)
- Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
- Expansion of Schizophrenia Gene Network Knowledge Using Machine Learning Selected Signals From Dorsolateral Prefrontal Cortex and Amygdala RNA-seq Data. (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)
- Genetic variants associated with longitudinal changes in brain structure across the lifespan. (2022)
- Cross-sectional and prospective associations of drinking characteristics with scores from the Self-Report of the Effects of Alcohol questionnaire and findings from alcohol challenges. (2021)
- Multi-environment gene interactions linked to the interplay between polysubstance dependence and suicidality. (2021)
- Factors associated with phosphatidylethanol (PEth) sensitivity for detecting unhealthy alcohol use: An individual patient data meta-analysis. (2021)
- A latent class analysis of alcohol and posttraumatic stress symptoms among offspring of parents with and without alcohol use disorder. (2021)
- Epigenome-wide change and variation in DNA methylation in childhood: trajectories from birth to late adolescence. (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)
- Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (2021)
- Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
- Frequent LPA KIV-2 Variants Lower Lipoprotein(a) Concentrations and Protect Against Coronary Artery Disease. (2021)
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. (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)
- 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)
- Genetics of substance use disorders in the era of big data. (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)
- 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)
- Polygenic risk scores: from research tools to clinical instruments. (2020)
- Structural variation in the sequencing era. (2020)
- Klotho gene polymorphism, brain structure and cognition in early-life development. (2020)
- Pan-cancer analysis of whole genomes. (2020)
- Sibling comparisons elucidate the associations between educational attainment polygenic scores and alcohol, nicotine and cannabis. (2020)
- Association between DNA methylation and ADHD symptoms from birth to school age: a prospective meta-analysis. (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)
- ENIGMA and global neuroscience: A decade of large-scale studies of the brain in health and disease across more than 40 countries. (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)
- Sex differences in the genetic architecture of obsessive-compulsive disorder. (2019)
- Neurodevelopmental effects of ante-partum and post-partum antiretroviral exposure in HIV-exposed and uninfected children versus HIV-unexposed and uninfected children in Uganda and Malawi: a prospective cohort study. (2019)
- Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. (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)
- Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. (2019)
- Ethanol activates immune response in lymphoblastoid cells. (2019)
- Identification of common genetic risk variants for autism spectrum disorder. (2019)
- Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance. (2019)
- Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. (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)
- Longitudinally Mapping Childhood Socioeconomic Status Associations with Cortical and Subcortical Morphology. (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)
- The Early Developmental Outcomes of Prenatal Alcohol Exposure: A Review. (2018)
- Integrative transcriptome analyses of the aging brain implicate altered splicing in Alzheimer's disease susceptibility. (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)
- 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)
- Glucocorticoid Receptor (NR3C1) Gene Polymorphism Moderate Intervention Effects on the Developmental Trajectory of African-American Adolescent Alcohol Abuse. (2018)
- Incorporating Functional Genomic Information to Enhance Polygenic Signal and Identify Variants Involved in Gene-by-Environment Interaction for Young Adult Alcohol Problems. (2018)
- Annotation-free quantification of RNA splicing using LeafCutter. (2018)
- Activity-dependent Signaling and Epigenetic Abnormalities in Mice Exposed to Postnatal Ethanol. (2018)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Effects of Antenatal Maternal Depressive Symptoms and Socio-Economic Status on Neonatal Brain Development are Modulated by Genetic Risk. (2017)
- Review: Pharmacogenetics of alcoholism treatment: Implications of ethnic diversity. (2017)
- Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure. (2017)
- Genetic contributors to variation in alcohol consumption vary by race/ethnicity in a large multi-ethnic genome-wide association study. (2017)
- Post-traumatic stress disorder associated with natural and human-made disasters in the World Mental Health Surveys. (2017)
- Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
- Associations between cortical thickness and neurocognitive skills during childhood vary by family socioeconomic factors. (2017)
- Genetic correlates of the development of theta event related oscillations in adolescents and young adults. (2017)
- Genome-wide association analysis identifies common variants influencing infant brain volumes. (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)
- Genome-Wide Association Studies of a Broad Spectrum of Antisocial Behavior. (2017)
- Usual Choline Intakes Are Associated with Egg and Protein Food Consumption in the United States. (2017)
- The impact of structural variation on human gene expression. (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)
- G = E: What GWAS Can Tell Us about the Environment. (2016)
- 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)
- Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
- Parental divorce and initiation of alcohol use in early adolescence. (2016)
- Gray matter maturation and cognition in children with different APOE ε genotypes. (2016)
- KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
- Changes in Cannabis Potency Over the Last 2 Decades (1995-2014): Analysis of Current Data in the United States. (2016)
- Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
- The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. (2016)
- Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
- The continuum of fetal alcohol spectrum disorders in a community in South Africa: Prevalence and characteristics in a fifth sample. (2016)
- The continuum of fetal alcohol spectrum disorders in four rural communities in South Africa: Prevalence and characteristics. (2016)
- Epidemiology, Etiology, and Treatment of Isolated Cleft Palate. (2016)
- Presence of an epigenetic signature of prenatal cigarette smoke exposure in childhood. (2016)
- Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
- Glymphatic distribution of CSF-derived apoE into brain is isoform specific and suppressed during sleep deprivation. (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)
- Family income, parental education and brain structure in children and adolescents. (2015)
- mHealthApps: A Repository and Database of Mobile Health Apps. (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)
- Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans. (2015)
- Genome-Wide Meta-Analysis of Longitudinal Alcohol Consumption Across Youth and Early Adulthood. (2015)
- A South African mixed race lip/philtrum guide for diagnosis of fetal alcohol spectrum disorders. (2015)
- A global reference for human genetic variation. (2015)
- ERBB4 polymorphism and family history of psychiatric disorders on age-related cortical changes in healthy children. (2015)
- Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis. (2015)
- A global reference for human genetic variation. (2015)
- Describing and predicting developmental profiles of externalizing problems from childhood to adulthood. (2015)
- Passive smoking in the etiology of non-syndromic orofacial clefts: a systematic review and meta-analysis. (2015)
- Genome-wide association study of nicotine dependence in American populations: identification of novel risk loci in both African-Americans and European-Americans. (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)
- Parental separation, parental alcoholism, and timing of first sexual intercourse. (2015)
- The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
- Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
- Comorbidity of severe psychotic disorders with measures of substance use. (2014)
- Intended and unintended pregnancies worldwide in 2012 and recent trends. (2014)
- Is vitamin D deficiency a major global public health problem? (2014)
- Linking Childhood Maltreatment with Girls' Internalizing Symptoms: Early Puberty as a Tipping Point. (2014)
- Genome-wide association study of cocaine dependence and related traits: FAM53B identified as a risk gene. (2014)
- Pharmacogenetics of OPRM1. (2014)
- Neurodevelopmental benefits of antiretroviral therapy in Ugandan children aged 0-6 years with HIV. (2014)
- Distinct pharmacology and metabolism of K2 synthetic cannabinoids compared to Δ(9)-THC: mechanism underlying greater toxicity? (2014)
- Genetic influences on alcohol use across stages of development: GABRA2 and longitudinal trajectories of drunkenness from adolescence to young adulthood. (2014)
- The CXCL12/CXCR4 chemokine ligand/receptor axis in cardiovascular disease. (2014)
- Neuronal substrates and functional consequences of prenatal cannabis exposure. (2014)
- Imbalances in the knowledge about infant mental health in rich and poor countries: too little progress in bridging the gap. (2014)
- Face shape differs in phylogenetically related populations. (2014)
- Genetic variability in the regulation of gene expression in ten regions of the human brain. (2014)
- Risks for early substance involvement associated with parental alcoholism and parental separation in an adolescent female cohort. (2014)
- In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014)
- Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
- Gene × environment interaction studies have not properly controlled for potential confounders: the problem and the (simple) solution. (2014)
- Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
- Using genetic information from candidate gene and genome-wide association studies in risk prediction for alcohol dependence. (2014)
- Maternal factors predicting cognitive and behavioral characteristics of children with fetal alcohol spectrum disorders. (2013)
- Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
- Genome-wide variation of cytosine modifications between European and African populations and the implications for complex traits. (2013)
- Nominal association with CHRNA4 variants and nicotine dependence. (2013)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- A mega-analysis of genome-wide association studies for major depressive disorder. (2013)
- COMT Val158Met modulates subjective responses to intravenous nicotine and cognitive performance in abstinent smokers. (2013)
- A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
- The feasibility and cost of neonatal screening for prenatal alcohol exposure by measuring phosphatidylethanol in dried blood spots. (2013)
- Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
- Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD. (2013)
- Effects of alcohol on the endocrine system. (2013)
- ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. (2013)
- Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
- Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Approaching the prevalence of the full spectrum of fetal alcohol spectrum disorders in a South African population-based study. (2013)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
- Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
- The aggregate effect of dopamine genes on dependence symptoms among cocaine users: cross-validation of a candidate system scoring approach. (2012)
- Multi-Method Assessment of ADHD Characteristics in Preschool Children: Relations between Measures. (2012)
- Delta and kappa opioid receptor polymorphisms influence the effects of naltrexone on subjective responses to alcohol. (2012)
- Neuronal calcium sensor-1 and cocaine addiction: a genetic association study in African-Americans and European Americans. (2012)
- Population-specificity of human DNA methylation. (2012)
- Racial Differences in Exposure and Reactivity to Daily Family Stressors. (2012)
- The genetics of alcohol dependence: advancing towards systems-based approaches. (2012)
- Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (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)
- Deletion of the gabra2 gene results in hypersensitivity to the acute effects of ethanol but does not alter ethanol self administration. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (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 meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. (2012)
- Genome-wide search for replicable risk gene regions in alcohol and nicotine co-dependence. (2012)
- Pharmacogenetics of smoking cessation: role of nicotine target and metabolism genes. (2012)
- The genetics of the opioid system and specific drug addictions. (2012)
- Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
- Prevalence of children with severe fetal alcohol spectrum disorders in communities near Rome, Italy: new estimated rates are higher than previous estimates. (2011)
- A survey of Italian and Spanish neonatologists and paediatricians regarding awareness of the diagnosis of FAS and FASD and maternal ethanol use during pregnancy. (2011)
- The AVPR1A gene and substance use disorders: association, replication, and functional evidence. (2011)
- Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. (2011)
- Human aggression across the lifespan: genetic propensities and environmental moderators. (2011)
- Cleft lip and palate: understanding genetic and environmental influences. (2011)
- Haplotype block structure of the genomic region of the mu opioid receptor gene. (2011)
- Nonreplication of an association of SGIP1 SNPs with alcohol dependence and resting theta EEG power. (2011)
- Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. (2011)
- Expanding the range of ZNF804A variants conferring risk of psychosis. (2011)
- Maternal risk factors predicting child physical characteristics and dysmorphology in fetal alcohol syndrome and partial fetal alcohol syndrome. (2011)
- Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
- The neuronal transporter gene SLC6A15 confers risk to major depression. (2011)
- The prevalence and clinical presentation of antenatal depression in rural South Africa. (2011)
- Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
- LocusZoom: regional visualization of genome-wide association scan results. (2010)
- Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
- Modeling the interplay of multilevel risk factors for future academic and behavior problems: a person-centered approach. (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)
- Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. (2010)
- LocusZoom: regional visualization of genome-wide association scan results. (2010)
- Large copy-number variations are enriched in cases with moderate to extreme obesity. (2010)
- 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)
- 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)
- From child maltreatment to adolescent cannabis abuse and dependence: a developmental cascade model. (2010)
- Genome-wide association studies in diverse populations. (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)
- Genome-wide association study of bipolar disorder in European American and African American individuals. (2009)
- SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (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)
- Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. (2009)
- Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
- Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
- The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation. (2009)
- Developmental origins of health and disease: environmental exposures. (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)
- Can we identify genes for alcohol consumption in samples ascertained for heterogeneous purposes? (2009)
- Marker selection for genetic case-control association studies. (2009)
- New insights into the genetics of addiction. (2009)
- Interaction between two independent CNR1 variants increases risk for cocaine dependence in European Americans: a replication study in family-based sample and population-based sample. (2009)
- Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
- Nicotinic acetylcholine receptor beta2 subunit gene implicated in a systems-based candidate gene study of smoking cessation. (2008)
- Toward a global view of alcohol, tobacco, cannabis, and cocaine use: findings from the WHO World Mental Health Surveys. (2008)
- Geographic patterns of genome admixture in Latin American Mestizos. (2008)
- Analysis and application of European genetic substructure using 300 K SNP information. (2008)
- The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
- Population structure and eigenanalysis. (2006)
- Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN
Merged raw entities (65)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| european ancestry | cohort | 140 | 274 |
| european american | cohort | 58 | 163 |
| european americans | cohort | 56 | 172 |
| europe | cohort | 51 | 80 |
| european ancestry | phenotype | 50 | 67 |
| european | cohort | 47 | 87 |
| european ancestry cohort | cohort | 24 | 31 |
| european american cohort | cohort | 17 | 20 |
| european cohort | cohort | 13 | 22 |
| european american sample | cohort | 12 | 13 |
| european american | phenotype | 8 | 9 |
| european american participants | cohort | 7 | 9 |
| european ancestry individuals | cohort | 7 | 7 |
| eur ancestry | cohort | 6 | 13 |
| european american subjects | cohort | 5 | 5 |
| european | phenotype | 4 | 5 |
| european ancestries | cohort | 4 | 5 |
| european ancestry cohorts | cohort | 4 | 4 |
| european american (ea) | cohort | 3 | 3 |
| european american (ea) cohort | cohort | 3 | 3 |
| european american families | cohort | 3 | 5 |
| european ancestry (ea) | cohort | 3 | 3 |
| european (eur) | cohort | 3 | 3 |
| european group | cohort | 3 | 3 |
| eur sample | cohort | 3 | 3 |
| eur cohort | cohort | 2 | 3 |
| european american adolescents | cohort | 2 | 6 |
| european american adults | cohort | 2 | 2 |
| european american samples | cohort | 2 | 2 |
| european ancestry adults | cohort | 2 | 2 |
| ea adolescents | cohort | 1 | 1 |
| ea adults | cohort | 1 | 2 |
| ea analytic sample | cohort | 1 | 1 |
| ea coga | cohort | 1 | 1 |
| ea cohort | cohort | 1 | 1 |
| eur cohorts | cohort | 1 | 1 |
| european american women | cohort | 1 | 2 |
| european ancestry group | cohort | 1 | 1 |
| non-hispanic ea | cohort | 1 | 4 |
| non-hispanic european americans | cohort | 1 | 1 |
| nycpea | cohort | 1 | 2 |
| 12 population-based samples of european ancestry | cohort | — | — |
| 6,845 eas | cohort | — | — |
| 93 adult individuals of european ancestry | cohort | — | — |
| ea ethnicity | cohort | — | — |
| european american ancestry cohort | cohort | — | — |
| european american (ea) adolescents | cohort | — | — |
| european-ancestry cluster | cohort | — | — |
| european ancestry ld reference panel | cohort | — | — |
| european ancestry proportion | cohort | — | — |
| european genetic structure | cohort | — | — |
| european origin | cohort | — | — |
| european-origin individuals | cohort | — | — |
| genetic ea | cohort | — | — |
| grandparental european country of origin | cohort | — | — |
| individuals of european ancestries | cohort | — | — |
| individuals of european ancestry | cohort | — | — |
| individuals of european descent | cohort | — | — |
| participants primarily of european ancestry | cohort | — | — |
| persons with self-identified european ancestry | cohort | — | — |
| population-based cohort of european ancestry | cohort | — | — |
| populations of european ancestry | cohort | — | — |
| recent european ancestry | cohort | — | — |
| self-reported european american | cohort | — | — |
| self-reported european ancestry | cohort | — | — |