Asian cohort

Aliases

Asia, Asian, Asian American population, Asian cohort, Asian ethnicity, Asian individuals, Asian locales, Asian participants, Asian population, Asian populations, Asians, Chinese, Indian, Malaysian, majority Asian, other Asians

Related entities (46)

Mentioned in (151)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Child Ability and Parental Attributions: Development and Validation of the Reasons for Children's Behavior Scale. (2026)
• Cardiovascular and Metabolic Outcomes in Adults with Fetal Alcohol Spectrum Disorders: A Retrospective Cohort Study. (2026)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Cognitive Processes Influencing Written Sentence Construction in School-Aged Children With Prenatal Alcohol Exposure. (2025)
• BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability. (2024)
• Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank. (2024)
• Childhood trauma is associated with developmental trajectories of EEG coherence, alcohol-related outcomes, and PTSD symptoms. (2024)
• Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseases. (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)
• Predicting Fetal Alcohol Spectrum Disorders Using Machine Learning Techniques: Multisite Retrospective Cohort Study. (2023)
• Hospitalizations for COVID-19 Among American Indian and Alaska Native Adults (≥ 18 Years Old) - New Mexico, March-September 2020. (2023)
• Racial/Ethnic Disparity in Association Between Fetal Alcohol Syndrome and Alcohol Intake During Pregnancy: Multisite Retrospective Cohort Study. (2023)
• Genetic Influences on the Developing Young Brain and Risk for Neuropsychiatric Disorders. (2023)
• Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. (2022)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Long-term follow-up of a randomized controlled trial of choline for neurodevelopment in fetal alcohol spectrum disorder: corpus callosum white matter microstructure and neurocognitive outcomes. (2022)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• The clinical course of antisocial behaviors in men and women of three racial groups. (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)
• Factors associated with phosphatidylethanol (PEth) sensitivity for detecting unhealthy alcohol use: An individual patient data meta-analysis. (2021)
• Genetics of substance use disorders in the era of big data. (2021)
• Newborn amygdalar volumes are associated with maternal prenatal psychological distress in a sex-dependent way. (2020)
• Longitudinal development of hippocampal subregions from early- to mid-childhood. (2020)
• Longitudinal white matter and cognitive development in pediatric carriers of the apolipoprotein ε4 allele. (2020)
• Cancer PRSweb: An Online Repository with Polygenic Risk Scores for Major Cancer Traits and Their Evaluation in Two Independent Biobanks. (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)
• CHASMplus Reveals the Scope of Somatic Missense Mutations Driving Human Cancers. (2019)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• Polygenic risk for neuropsychiatric disease and vulnerability to abnormal deep grey matter development. (2019)
• Ethanol activates immune response in lymphoblastoid cells. (2019)
• Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. (2019)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• The Immune Landscape of Cancer. (2018)
• Diagnosis and Pharmacotherapy of Alcohol Use Disorder: A Review. (2018)
• Human Genetics of Addiction: New Insights and Future Directions. (2018)
• Two-year cortical trajectories are abnormal in children and adolescents with prenatal alcohol exposure. (2018)
• FKBP5 Moderates the Association between Antenatal Maternal Depressive Symptoms and Neonatal Brain Morphology. (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)
• Cortical gyrification is abnormal in children with prenatal alcohol exposure. (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)
• Review: Prevalence and co-occurrence of addictions in US ethnic/racial groups: Implications for genetic research. (2017)
• Machine learning shows association between genetic variability in and cerebral connectivity in preterm infants. (2017)
• Comparison of DSM-IV and DSM-5 criteria for alcohol use disorders in VA primary care patients with frequent heavy drinking enrolled in a trial. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• Structural brain anomalies in healthy adolescents in the NCANDA cohort: relation to neuropsychological test performance, sex, and ethnicity. (2017)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• Novel genetic loci underlying human intracranial volume identified through genome-wide association. (2016)
• Fetal alcohol spectrum disorders: Clinical phenotype among a high-risk group of children and adolescents in Korea. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Possible relationship between common genetic variation and white matter development in a pilot study of preterm infants. (2016)
• Epidemiology, Etiology, and Treatment of Isolated Cleft Palate. (2016)
• The role of romantic relationship status in pathways of risk for emerging adult alcohol use. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Alcohol Dependence Genetics: Lessons Learned From Genome-Wide Association Studies (GWAS) and Post-GWAS Analyses. (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)
• Epidemiology of DSM-5 Alcohol Use Disorder: Results From the National Epidemiologic Survey on Alcohol and Related Conditions III. (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)
• Candidate gene-environment interaction research: reflections and recommendations. (2015)
• Vitamin D deficiency in early pregnancy. (2015)
• A global reference for human genetic variation. (2015)
• Prevalence of Marijuana Use Disorders in the United States Between 2001-2002 and 2012-2013. (2015)
• Evaluation of the influence of alcohol dehydrogenase polymorphisms on alcohol elimination rates in African Americans. (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)
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
• Pharmacogenetics of OPRM1. (2014)
• Protective effects of the alcohol dehydrogenase-ADH1B*3 allele on attention and behavior problems in adolescents exposed to alcohol during pregnancy. (2014)
• Brain region- and sex-specific alterations in DAMGO-stimulated [(35) S]GTPγS binding in mice with Oprm1 A112G. (2014)
• Expression of ZNF804A in human brain and alterations in schizophrenia, bipolar disorder, and major depressive disorder: a novel transcript fetally regulated by the psychosis risk variant rs1344706. (2014)
• Cannabis controversies: how genetics can inform the study of comorbidity. (2014)
• Genome-wide association discoveries of alcohol dependence. (2014)
• Fetal alcohol spectrum disorders and their transmission through genetic and epigenetic mechanisms. (2014)
• Identification of CHRNA5 rare variants in African-American heavy smokers. (2014)
• The influence of puberty on subcortical brain development. (2014)
• DNA-Mutation Inventory to Refine and Enhance Cancer Treatment (DIRECT): a catalog of clinically relevant cancer mutations to enable genome-directed anticancer therapy. (2013)
• Prevalence of amblyopia or strabismus in asian and non-Hispanic white preschool children: multi-ethnic pediatric eye disease study. (2013)
• Comorbidity of posttraumatic stress disorder with alcohol dependence among US adults: results from National Epidemiological Survey on Alcohol and Related Conditions. (2013)
• A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. (2013)
• Vital signs: current cigarette smoking among adults aged ≥18 years with mental illness - United States, 2009-2011. (2013)
• Large-scale genotyping identifies 41 new loci associated with breast cancer risk. (2013)
• DNA methylation contributes to natural human variation. (2013)
• Preconceptional motivational interviewing interventions to reduce alcohol-exposed pregnancy risk. (2013)
• Effortful control in "hot" and "cool" tasks differentially predicts children's behavior problems and academic performance. (2013)
• ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. (2013)
• A developmental study of the feedback-related negativity from 10-17 years: age and sex effects for reward versus non-reward. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• The Genomic Revolution and Beliefs about Essential Racial Differences: A Backdoor to Eugenics? (2013)
• The "Reading the Mind in the Eyes" test: systematic review of psychometric properties and a validation study in Italy. (2013)
• Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
• Large-scale objective phenotyping of 3D facial morphology. (2012)
• Delta and kappa opioid receptor polymorphisms influence the effects of naltrexone on subjective responses to alcohol. (2012)
• Microsatellites with macro-influence in ewing sarcoma. (2012)
• Annotation of functional variation in personal genomes using RegulomeDB. (2012)
• A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. (2012)
• The genetic basis of alcoholism: multiple phenotypes, many genes, complex networks. (2012)
• Implication of European-derived adiposity loci in African Americans. (2012)
• A longitudinal study of the long-term consequences of drinking during pregnancy: heavy in utero alcohol exposure disrupts the normal processes of brain development. (2012)
• The lifetime impact of attention deficit hyperactivity disorder: results from the National Epidemiologic Survey on Alcohol and Related Conditions (NESARC). (2012)
• Pharmacogenetics of smoking cessation: role of nicotine target and metabolism genes. (2012)
• The genetics of the opioid system and specific drug addictions. (2012)
• A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (2011)
• The investigation into CYP2E1 in relation to the level of response to alcohol through a combination of linkage and association analysis. (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)
• Evidence for gene-environment interaction in a genome wide study of nonsyndromic cleft palate. (2011)
• Does lack of multinutrient supplementation during early pregnancy increase vulnerability to alcohol-related preterm or small-for-gestational-age births? (2011)
• The serotonin transporter gene and startle response during nicotine deprivation. (2011)
• Maternal salivary cortisol differs by fetal sex during the second half of pregnancy. (2011)
• Prenatal methamphetamine exposure and neonatal neurobehavioral outcome in the USA and New Zealand. (2011)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Genome-wide scan for self-rating of the effects of alcohol in American Indians. (2010)
• Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
• Parent-child communication and substance use among adolescents: do father and mother communication play a different role for sons and daughters? (2010)
• Fetal alcohol spectrum disorders: Extending the range of structural defects. (2010)
• Longitudinal characterization of white matter maturation during adolescence. (2010)
• ADH1B*3 and response to alcohol in African-Americans. (2010)
• Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (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)
• SNPinfo: integrating GWAS and candidate gene information into functional SNP selection for genetic association studies. (2009)
• Interaction between the serotonin transporter gene (5-HTTLPR), stressful life events, and risk of depression: a meta-analysis. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Lack of association between the A118G polymorphism of the mu opioid receptor gene (OPRM1) and opioid dependence: A meta-analysis. (2009)
• Social information processing skills in children with histories of heavy prenatal alcohol exposure. (2009)
• Discrimination and racial disparities in health: evidence and needed research. (2009)
• New insights into the genetics of addiction. (2009)
• Genome-wide and candidate gene association study of cigarette smoking behaviors. (2009)
• Alcohol consumption indices of genetic risk for alcohol dependence. (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)
• Childhood or adolescent parental divorce/separation, parental history of alcohol problems, and offspring lifetime alcohol dependence. (2008)
• Association of a single nucleotide polymorphism in neuronal acetylcholine receptor subunit alpha 5 (CHRNA5) with smoking status and with 'pleasurable buzz' during early experimentation with smoking. (2008)
• Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development. (2007)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
• ALDH2, ADH1B, and ADH1C genotypes in Asians: a literature review. (2007)
• The genetics of alcohol metabolism: role of alcohol dehydrogenase and aldehyde dehydrogenase variants. (2007)
• Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome. (2006)
• The nutrient intakes of mothers of low birth weight babies - a comparison of ethnic groups in East London, UK. (2005)
• Estimating the prevalence of fetal alcohol syndrome. A summary. (2001)

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