population cohort

Aliases

combined cohort, different populations, human chromosomes, multiple population groups, overall population, population, population cohort, population cohorts, population-based study, present study population, subpopulation, total population, worldwide human population

Related entities (13)

Mentioned in (151)

Papers in which this entity is mentioned.

• Integrated in vivo combinatorial functional genomics and spatial transcriptomics of tumours to decode genotype-to-phenotype relationships. (2026)
• Robust and accurate Bayesian inference of genome-wide genealogies for hundreds of genomes. (2025)
• Genome-wide association testing beyond SNPs. (2025)
• Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition. (2025)
• Principles and methods for transferring polygenic risk scores across global populations. (2024)
• Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
• A harmonized public resource of deeply sequenced diverse human genomes. (2024)
• Pitfalls of predicting age-related traits by polygenic risk scores. (2023)
• Pervasive Downward Bias in Estimates of Liability-Scale Heritability in Genome-wide Association Study Meta-analysis: A Simple Solution. (2023)
• Polygenic prediction across populations is influenced by ancestry, genetic architecture, and methodology. (2023)
• Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
• A methodological pipeline to generate an epigenetic marker of prenatal exposure to air pollution indicators. (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)
• Principal Component Analyses (PCA)-based findings in population genetic studies are highly biased and must be reevaluated. (2022)
• Closing the life-cycle of normative modeling using federated hierarchical Bayesian regression. (2022)
• Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
• A practical guide to cancer subclonal reconstruction from DNA sequencing. (2021)
• Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood. (2021)
• Data structures based on -mers for querying large collections of sequencing data sets. (2021)
• Genotypes of informative loci from 1000 Genomes data allude evolution and mixing of human populations. (2021)
• Gestational age and birth growth parameters as early predictors of fetal alcohol spectrum disorders. (2021)
• Polygenic risk scores: from research tools to clinical instruments. (2020)
• Newborn amygdalar volumes are associated with maternal prenatal psychological distress in a sex-dependent way. (2020)
• Tutorial: a guide to performing polygenic risk score analyses. (2020)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• Comprehensive analysis of structural variants in breast cancer genomes using single-molecule sequencing. (2020)
• Developmental topography of cortical thickness during infancy. (2019)
• Highly Efficient CRISPR-Cas9-Based Methods for Generating Deletion Mutations and F0 Embryos that Lack Gene Function in Zebrafish. (2019)
• A review on neuroimaging studies of genetic and environmental influences on early brain development. (2019)
• Effects of nicotine exposure on murine mandibular development. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Comparison of the 4-Digit Code, Canadian 2015, Australian 2016 and Hoyme 2016 fetal alcohol spectrum disorder diagnostic guidelines. (2019)
• The GenomeAsia 100K Project enables genetic discoveries across Asia. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Risk and protective factors for child development: An observational South African birth cohort. (2019)
• Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. (2019)
• Perinatal depression among mothers in a South African birth cohort study: Trajectories from pregnancy to 18 months postpartum. (2019)
• Collider scope: when selection bias can substantially influence observed associations. (2018)
• mSignatureDB: a database for deciphering mutational signatures in human cancers. (2018)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• Structural brain development: A review of methodological approaches and best practices. (2018)
• Epigenetic mechanisms in alcohol- and adversity-induced developmental origins of neurobehavioral functioning. (2018)
• Drakenstein Child Health Study (DCHS): investigating determinants of early child development and cognition. (2018)
• Immune diversity sheds light on missing variation in worldwide genetic diversity panels. (2018)
• Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. (2018)
• Picky comprehensively detects high-resolution structural variants in nanopore long reads. (2018)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• Cortical gyrification is abnormal in children with prenatal alcohol exposure. (2017)
• One-Carbon Metabolism in Health and Disease. (2017)
• A method to reduce ancestry related germline false positives in tumor only somatic variant calling. (2017)
• Ancient DNA and the rewriting of human history: be sparing with Occam's razor. (2016)
• Perinatal maternal alcohol consumption and methylation of the dopamine receptor in the offspring: the Triple B study. (2016)
• G = E: What GWAS Can Tell Us about the Environment. (2016)
• Eigenanalysis of SNP data with an identity by descent interpretation. (2016)
• The Essential Role of Growth Deficiency in the Diagnosis of Fetal Alcohol Spectrum Disorder. (2016)
• Alcohol-Induced Developmental Origins of Adult-Onset Diseases. (2016)
• Detecting Genomic Signatures of Natural Selection with Principal Component Analysis: Application to the 1000 Genomes Data. (2016)
• Quantifying Clonal and Subclonal Passenger Mutations in Cancer Evolution. (2016)
• Trace elements as paradigms of developmental neurotoxicants: Lead, methylmercury and arsenic. (2015)
• Prevalence and characteristics of fetal alcohol syndrome and partial fetal alcohol syndrome in a Rocky Mountain Region City. (2015)
• Tools and best practices for data processing in allelic expression analysis. (2015)
• Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
• Genome-wide association study in obsessive-compulsive disorder: results from the OCGAS. (2015)
• Dissecting ancestry genomic background in substance dependence genome-wide association studies. (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)
• Vitamin D deficiency in early pregnancy. (2015)
• Evaluating historical candidate genes for schizophrenia. (2015)
• DNA methylation and healthy human aging. (2015)
• DR-BUDDI (Diffeomorphic Registration for Blip-Up blip-Down Diffusion Imaging) method for correcting echo planar imaging distortions. (2015)
• A global reference for human genetic variation. (2015)
• HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data. (2015)
• Inappropriate feeding behaviors and dietary intakes in children with fetal alcohol spectrum disorder or probable prenatal alcohol exposure. (2014)
• The Effects of Arsenic Exposure on Neurological and Cognitive Dysfunction in Human and Rodent Studies: A Review. (2014)
• 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)
• Screening tests: a review with examples. (2014)
• Face shape differs in phylogenetically related populations. (2014)
• The prevalence of confirmed maltreatment among US children, 2004 to 2011. (2014)
• The validity of phosphatidylethanol in dried blood spots of newborns for the identification of prenatal alcohol exposure. (2014)
• The teratogenic effects of prenatal ethanol exposure are exacerbated by Sonic Hedgehog or GLI2 haploinsufficiency in the mouse. (2014)
• Physical exercise-induced adult neurogenesis: a good strategy to prevent cognitive decline in neurodegenerative diseases? (2014)
• THetA: inferring intra-tumor heterogeneity from high-throughput DNA sequencing data. (2013)
• Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
• Maternal alcohol consumption producing fetal alcohol spectrum disorders (FASD): quantity, frequency, and timing of drinking. (2013)
• DNA methylation contributes to natural human variation. (2013)
• Combined analysis of circulating β-endorphin with gene polymorphisms in OPRM1, CACNAD2 and ABCB1 reveals correlation with pain, opioid sensitivity and opioid-related side effects. (2013)
• Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
• Structure and function of complex brain networks. (2013)
• Bridging animal and human models of exercise-induced brain plasticity. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
• Fine tuning of craniofacial morphology by distant-acting enhancers. (2013)
• Common liability to addiction and "gateway hypothesis": theoretical, empirical and evolutionary perspective. (2012)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• Opposing actions of ethanol and nicotine on microRNAs are mediated by nicotinic acetylcholine receptors in fetal cerebral cortical-derived neural progenitor cells. (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)
• Improving bioinformatic pipelines for exome variant calling. (2012)
• Real-time motion and B0 correction for localized adiabatic selective refocusing (LASER) MRSI using echo planar imaging volumetric navigators. (2012)
• An integrated map of genetic variation from 1,092 human genomes. (2012)
• Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)
• CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
• Ethanol-induced face-brain dysmorphology patterns are correlative and exposure-stage dependent. (2012)
• Ethanol exposure during pregnancy persistently attenuates cranially directed blood flow in the developing fetus: evidence from ultrasound imaging in a murine second trimester equivalent model. (2012)
• Quantitative tract-based white matter development from birth to age 2years. (2012)
• An integrated encyclopedia of DNA elements in the human genome. (2012)
• The Pediatric Cancer Genome Project. (2012)
• A prospective cohort study of the prevalence of growth, facial, and central nervous system abnormalities in children with heavy prenatal alcohol exposure. (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)
• Bayesian inference of ancient human demography from individual genome sequences. (2011)
• Early childhood exposure to anesthesia and risk of developmental and behavioral disorders in a sibling birth cohort. (2011)
• Automatic Skull-stripping of Rat MRI/DTI Scans and Atlas Building. (2011)
• Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples. (2011)
• Infant brain atlases from neonates to 1- and 2-year-olds. (2011)
• Imaging the impact of prenatal alcohol exposure on the structure of the developing human brain. (2011)
• Maternal risk factors predicting child physical characteristics and dysmorphology in fetal alcohol syndrome and partial fetal alcohol syndrome. (2011)
• The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. (2011)
• Risks of overweight and abdominal obesity at age 16 years associated with prenatal exposures to maternal prepregnancy overweight and gestational diabetes mellitus. (2010)
• A tract-specific framework for white matter morphometry combining macroscopic and microscopic tract features. (2010)
• Statistical analysis strategies for association studies involving rare variants. (2010)
• Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
• Multiple cholinergic nicotinic receptor genes affect nicotine dependence risk in African and European Americans. (2010)
• Neuroimaging study designs, computational analyses and data provenance using the LONI pipeline. (2010)
• Genome-wide association studies in diverse populations. (2010)
• Genetics and beyond--the transcriptome of human monocytes and disease susceptibility. (2010)
• The plausibility of maternal nutritional status being a contributing factor to the risk for fetal alcohol spectrum disorders: the potential influence of zinc status as an example. (2010)
• Functional CRH variation increases stress-induced alcohol consumption in primates. (2009)
• A hybrid design: case-parent triads supplemented by control-mother dyads. (2009)
• The CHRNA5-CHRNA3-CHRNB4 nicotinic receptor subunit gene cluster affects risk for nicotine dependence in African-Americans and in European-Americans. (2009)
• Group analysis of DTI fiber tract statistics with application to neurodevelopment. (2009)
• Choline: an essential nutrient for public health. (2009)
• Magnetic resonance spectroscopy outcomes from a comprehensive magnetic resonance study of children with fetal alcohol spectrum disorders. (2009)
• Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009)
• Marker selection for genetic case-control association studies. (2009)
• Discrimination and racial disparities in health: evidence and needed research. (2009)
• Why IQ is not a covariate in cognitive studies of neurodevelopmental disorders. (2009)
• The enrichment study of the Minnesota twin family study: increasing the yield of twin families at high risk for externalizing psychopathology. (2009)
• Accuracy and usefulness of BMI measures based on self-reported weight and height: findings from the NHANES & NHIS 2001-2006. (2009)
• Differences in acute alcohol-induced behavioral responses among zebrafish populations. (2008)
• In Vivo 3D Digital Atlas Database of the Adult C57BL/6J Mouse Brain by Magnetic Resonance Microscopy. (2008)
• Analysis and application of European genetic substructure using 300 K SNP information. (2008)
• The changing impact of genes and environment on brain development during childhood and adolescence: initial findings from a neuroimaging study of pediatric twins. (2008)
• Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
• Choline: critical role during fetal development and dietary requirements in adults. (2006)
• Accurate and reliable high-throughput detection of copy number variation in the human genome. (2006)
• Using whole-genome sequencing to evaluate copy number variants of the LPA Kringle-IV type 2 domain with DRAGEN

Merged raw entities (18)

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.