Work

A phenome-wide association study identifies effects of copy-number variation of VNTRs and multicopy genes on multiple human traits

Year: 2022

Type: article

Study design: Observational Study

Source: The American Journal of Human Genetics

DOI: 10.1016/j.ajhg.2022.04.016

Authors: Paras Garg, Bharati Jadhav, William Lee, Oscar L. Rodriguez, Alejandro Martin-Trujillo, Andrew J. Sharp

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: bronze

Funders: Icahn School of Medicine at Mount Sinai, National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of Neurological Disorders and Stroke

Awards: G1316828812, Identification of novel pathogenic tandem repeat expansions using long read sequencing, Transforming Genomics with 5 PB Big Omics Data Engine Cray CS300-AC Supercomputer, Big Omics Data Engine 2 Supercomputer, G5407203003, Identification of novel pathogenic tandem repeat expansions using long read sequencing, Development and application of a pipeline to identify tandem repeat expansions as a cause of Parkinson's disease in the AMP PD cohort, COVID and Translational Science supercomputer (CATS), G861748693

OpenAlex ID: W4281291847

FWCI: 3.321

Cites: 46

Cited by: 23

Related to: 10