case-control sample cohort

Aliases

case-control design, case-control sample, case-control studies, case-control study, case-control study design

Related entities (19)

Mentioned in (43)

Papers in which this entity is mentioned.

• High-Parameter Spatial Multi-Omics through Histology-Anchored Integration (2025)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Association between Maternal Choline, Fetal Brain Development, and Child Neurocognition: Systematic Review and Meta-Analysis of Human Studies. (2022)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data. (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)
• ASEP: Gene-based detection of allele-specific expression across individuals in a population by RNA sequencing. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• Alcohol Use in Pregnancy and Miscarriage: A Systematic Review and Meta-Analysis. (2019)
• Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis. (2019)
• Collider scope: when selection bias can substantially influence observed associations. (2018)
• Case-control meta-analysis of blood DNA methylation and autism spectrum disorder. (2018)
• De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
• Social cognition as an RDoC domain. (2016)
• Association between alcohol consumption during pregnancy and risks of congenital heart defects in offspring: meta-analysis of epidemiological observational studies. (2016)
• Genetic and environmental contributions to the relationships between brain structure and average lifetime cigarette use. (2015)
• Prenatal Alcohol Exposure and Congenital Heart Defects: A Meta-Analysis. (2015)
• Is vitamin D deficiency a major global public health problem? (2014)
• The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. (2014)
• Dietary intake, nutrition, and fetal alcohol spectrum disorders in the Western Cape Province of South Africa. (2014)
• Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
• Prevalence of DSM-IV and DSM-5 alcohol, cocaine, opioid, and cannabis use disorders in a largely substance dependent sample. (2013)
• Dosage transmission disequilibrium test (dTDT) for linkage and association detection. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits. (2012)
• Pharmacogenetics of smoking cessation: role of nicotine target and metabolism genes. (2012)
• The AVPR1A gene and substance use disorders: association, replication, and functional evidence. (2011)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Discovering genetic ancestry using spectral graph theory. (2010)
• Maternal folate-related gene environment interactions and congenital heart defects. (2010)
• A review of estrogen receptor alpha gene (ESR1) polymorphisms, mood, and cognition. (2010)
• Gene--environment-wide association studies: emerging approaches. (2010)
• Meta-analysis in genome-wide association studies. (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)
• Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk. (2009)
• A haplotype containing quantitative trait loci for SLC1A1 gene expression and its association with obsessive-compulsive disorder. (2009)
• Mapping white matter integrity and neurobehavioral correlates in children with fetal alcohol spectrum disorders. (2008)
• Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
• A hybrid design for studying genetic influences on risk of diseases with onset early in life. (2005)
• Macrophage-derived tumor necrosis factor alpha, an early developmental signal for motoneuron death. (2004)

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