dbGaP cohort

Aliases

Database of Genotypes and Phenotypes, NCBI database of Genotypes and Phenotypes, database of Genotypes and Phenotypes, dbGaP repository, phs000417.v2.p1

Related entities (6)

Mentioned in (28)

Papers in which this entity is mentioned.

• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• Mutations in the bone morphogenetic protein signaling pathway sensitize zebrafish and humans to ethanol-induced jaw malformations. (2025)
• The Collaborative Study on the Genetics of Alcoholism: Overview. (2023)
• Mapping clustered mutations in cancer reveals APOBEC3 mutagenesis of ecDNA. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• The Data Use Ontology to streamline responsible access to human biomedical datasets. (2021)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• Rapid and reversible suppression of ALT by DAXX in osteosarcoma cells. (2019)
• Integrating predicted transcriptome from multiple tissues improves association detection. (2019)
• VCF2CNA: A tool for efficiently detecting copy-number alterations in VCF genotype data and tumor purity. (2019)
• Attention and corpus callosum volumes in individuals with mucopolysaccharidosis type I. (2019)
• Comprehensive analysis of structural variants in breast cancer genomes using single molecule sequencing (2019)
• Pan-cancer genome and transcriptome analyses of 1,699 paediatric leukaemias and solid tumours. (2018)
• Genome-wide somatic variant calling using localized colored de Bruijn graphs. (2018)
• An open access pilot freely sharing cancer genomic data from participants in Texas. (2016)
• KAT2B polymorphism identified for drug abuse in African Americans with regulatory links to drug abuse pathways in human prefrontal cortex. (2016)
• A gene-based association method for mapping traits using reference transcriptome data. (2015)
• Rise and fall of subclones from diagnosis to relapse in pediatric B-acute lymphoblastic leukaemia. (2015)
• Unraveling the clonal hierarchy of somatic genomic aberrations. (2014)
• Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine. (2014)
• Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
• An APOBEC cytidine deaminase mutagenesis pattern is widespread in human cancers. (2013)
• The Genotype-Tissue Expression (GTEx) project. (2013)
• Novel mutations target distinct subgroups of medulloblastoma. (2012)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• Genomic regions identified by overlapping clusters of nominally-positive SNPs from genome-wide studies of alcohol and illegal substance dependence. (2011)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)

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