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 (24)

Mentioned in (47)

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)
• A saturated map of common genetic variants associated with human height. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Feasibility of whole genome and transcriptome profiling in pediatric and young adult cancers. (2022)
• Opportunities for increased reproducibility and replicability of developmental neuroimaging. (2021)
• Polygenic risk scores for alcohol involvement relate to brain structure in substance-naïve children: Results from the ABCD study. (2021)
• 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)
• The Gene Encoding Protocadherin 9 (PCDH9), a Novel Risk Factor for Major Depressive Disorder. (2018)
• Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics. (2018)
• 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)
• Genetic effects on gene expression across human tissues. (2017)
• Genetic loci associated with chronic obstructive pulmonary disease overlap with loci for lung function and pulmonary fibrosis. (2017)
• 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)
• The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository. (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)
• PolymiRTS Database 3.0: linking polymorphisms in microRNAs and their target sites with human diseases and biological pathways. (2014)
• Sensitive detection of somatic point mutations in impure and heterogeneous cancer samples. (2013)
• 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)
• Managing incidental findings and research results in genomic research involving biobanks and archived data sets. (2012)
• Novel mutations target distinct subgroups of medulloblastoma. (2012)
• 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)
• Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. (2011)
• The PhenX Toolkit: get the most from your measures. (2011)
• The FaceBase Consortium: a comprehensive program to facilitate craniofacial research. (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)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• The psychiatric GWAS consortium: big science comes to psychiatry. (2010)
• Recurring mutations found by sequencing an acute myeloid leukemia genome. (2009)
• Genome-wide association for major depressive disorder: a possible role for the presynaptic protein piccolo. (2009)

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