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Identification of novel and rare variants associated with handgrip strength using whole genome seque...

Identification of novel and rare variants associated with handgrip strength using whole genome seque...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2547897962

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

Handgrip strength is a widely used measure of muscle strength and a predictor of a range of morbidities including cardiovascular diseases and all-cause mortality. Previous genome-wide association studies of handgrip strength have focused on common variants primarily in persons of European descent. We aimed to identify rare and ancestry-specific gen...

Alternative Titles

Full title

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_2547897962

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2547897962

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0253611

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