cases cohort

Aliases

343 cases, SCZ cases, alcohol-dependent cases, case, case group, case subjects, cases, diseased individuals, individuals with chronic psychotic disorders, individuals with severe psychotic disorder, individuals with severe psychotic illness, lung cancer cases, study cases

Related entities (51)

Mentioned in (103)

Papers in which this entity is mentioned.

• Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
• Three-dimensional genome landscape of primary human cancers. (2025)
• Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders. (2024)
• An overview of DNA methylation-derived trait score methods and applications. (2023)
• Biobank-scale methods and projections for sparse polygenic prediction from machine learning. (2023)
• Pitfalls of predicting age-related traits by polygenic risk scores. (2023)
• Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses. (2023)
• The Genetic Architecture of Obsessive-Compulsive Disorder: Contribution of Liability to OCD From Alleles Across the Frequency Spectrum. (2022)
• Brain charts for the human lifespan. (2022)
• Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA. (2022)
• Prenatal alcohol exposure can be determined from baby teeth: Proof of concept. (2022)
• Virtual Ontogeny of Cortical Growth Preceding Mental Illness. (2022)
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia. (2022)
• Med-BERT: pretrained contextualized embeddings on large-scale structured electronic health records for disease prediction. (2021)
• Bi-ancestral depression GWAS in the Million Veteran Program and meta-analysis in >1.2 million individuals highlight new therapeutic directions. (2021)
• Whole-genome analysis reveals the contribution of non-coding de novo transposon insertions to autism spectrum disorder. (2021)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data. (2021)
• Rapid genotype imputation from sequence with reference panels. (2021)
• Gene Expression in Patient-Derived Neural Progenitors Implicates WNT5A Signaling in the Etiology of Schizophrenia. (2020)
• Tutorial: a guide to performing polygenic risk score analyses. (2020)
• DNA methylation and brain structure and function across the life course: A systematic review. (2020)
• Detecting cell-type-specific allelic expression imbalance by integrative analysis of bulk and single-cell RNA sequencing data (2020)
• De Novo Damaging DNA Coding Mutations Are Associated With Obsessive-Compulsive Disorder and Overlap With Tourette's Disorder and Autism. (2020)
• Impact of Proliferator-Activated Receptor γ Gene Polymorphisms on Risk of Schizophrenia: A Case-Control Study and Computational Analyses. (2020)
• 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)
• Identification of common genetic risk variants for autism spectrum disorder. (2019)
• Cannabis Teratology Explains Current Patterns of Coloradan Congenital Defects: The Contribution of Increased Cannabinoid Exposure to Rising Teratological Trends. (2019)
• Psychiatric Genomics: An Update and an Agenda. (2018)
• Genome doubling shapes the evolution and prognosis of advanced cancers. (2018)
• Elevated polygenic burden for autism is associated with differential DNA methylation at birth. (2018)
• Neonatal Cytokine Profiles Associated With Autism Spectrum Disorder. (2017)
• Human Brain Abnormalities Associated With Prenatal Alcohol Exposure and Fetal Alcohol Spectrum Disorder. (2017)
• De Novo Coding Variants Are Strongly Associated with Tourette Disorder. (2017)
• SonoNet: Real-Time Detection and Localisation of Fetal Standard Scan Planes in Freehand Ultrasound. (2017)
• The National Birth Defects Prevention Study: A review of the methods. (2015)
• Integrative clinical genomics of advanced prostate cancer. (2015)
• The human gene damage index as a gene-level approach to prioritizing exome variants. (2015)
• Maternal periconceptional alcohol consumption and congenital heart defects. (2015)
• The discovery of integrated gene networks for autism and related disorders. (2015)
• The association of cord serum cytokines with neurodevelopmental outcomes. (2015)
• Passive smoking in the etiology of non-syndromic orofacial clefts: a systematic review and meta-analysis. (2015)
• The dopamine receptor D2 (DRD2) SNP rs1076560 is associated with opioid addiction. (2014)
• Comorbidity of severe psychotic disorders with measures of substance use. (2014)
• Guidelines for investigating causality of sequence variants in human disease. (2014)
• Common DNA methylation alterations in multiple brain regions in autism. (2014)
• Maternal periconceptional alcohol consumption and congenital limb deficiencies. (2014)
• Mosaic epigenetic dysregulation of ectodermal cells in autism spectrum disorder. (2014)
• Genome-wide SNP and CNV analysis identifies common and low-frequency variants associated with severe early-onset obesity. (2013)
• The CRHR1 gene, trauma exposure, and alcoholism risk: a test of G × E effects. (2013)
• ANKK1, TTC12, and NCAM1 polymorphisms and heroin dependence: importance of considering drug exposure. (2013)
• A Practical Testing Battery to Measure Neurobehavioral Ability among Children with FASD. (2013)
• The Growing Importance of CNVs: New Insights for Detection and Clinical Interpretation. (2013)
• Genome-wide association study identifies new susceptibility loci for posttraumatic stress disorder. (2013)
• Quantification of multiple-sclerosis-related brain atrophy in two heterogeneous MRI datasets using mixed-effects modeling. (2013)
• Approaching the prevalence of the full spectrum of fetal alcohol spectrum disorders in a South African population-based study. (2013)
• Associations between maternal genotypes and metabolites implicated in congenital heart defects. (2012)
• Copy number variations in 6q14.1 and 5q13.2 are associated with alcohol dependence. (2012)
• Genome-wide association study of primary open angle glaucoma risk and quantitative traits. (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)
• High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011)
• Association of CHRNA4 polymorphisms with smoking behavior in two populations. (2011)
• A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. (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)
• Genetic polymorphisms in 15q25 and 19q13 loci, cotinine levels, and risk of lung cancer in EPIC. (2011)
• MicroRNA expression aberration as potential peripheral blood biomarkers for schizophrenia. (2011)
• Significant differences in global genomic DNA methylation by gender and race/ethnicity in peripheral blood. (2011)
• Haplotype block structure of the genomic region of the mu opioid receptor gene. (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)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Genome wide association for addiction: replicated results and comparisons of two analytic approaches. (2010)
• Genetics of psychiatric disorders methods: molecular approaches. (2010)
• Incorporating age at onset of smoking into genetic models for nicotine dependence: evidence for interaction with multiple genes. (2010)
• Statistical analysis strategies for association studies involving rare variants. (2010)
• Replication of association between schizophrenia and ZNF804A in the Irish Case-Control Study of Schizophrenia sample. (2010)
• Association study of 182 candidate genes in anorexia nervosa. (2010)
• Genome-wide association study identifies genes that may contribute to risk for developing heroin addiction. (2010)
• A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. (2010)
• Using public control genotype data to increase power and decrease cost of case-control genetic association studies. (2010)
• A new statistic to evaluate imputation reliability. (2010)
• Population differences in dysmorphic features among children with fetal alcohol spectrum disorders. (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• Maternal folate-related gene environment interactions and congenital heart defects. (2010)
• Gene--environment-wide association studies: emerging approaches. (2010)
• Tackling the widespread and critical impact of batch effects in high-throughput data. (2010)
• Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. (2009)
• Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America. (2009)
• A hybrid design: case-parent triads supplemented by control-mother dyads. (2009)
• Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)
• Magnetic resonance spectroscopy outcomes from a comprehensive magnetic resonance study of children with fetal alcohol spectrum disorders. (2009)
• Genome-wide association studies in ADHD. (2009)
• Marker selection for genetic case-control 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)
• Potential role for plasma placental growth factor in predicting coronary heart disease risk in women. (2009)
• Association study of Wnt signaling pathway genes in bipolar disorder. (2008)
• Analysis and application of European genetic substructure using 300 K SNP information. (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)
• Genetic and environmental factors in complex neurodevelopmental disorders. (2007)
• Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. (2007)
• Population structure and eigenanalysis. (2006)

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