Genome-wide association for heart failure: from discovery to clinical use

Eur Heart J. 2021 May 21;42(20):2012-2014. doi: 10.1093/eurheartj/ehab172.

Authors

Dominic E Fullenkamp^{1

2}, Megan J Puckelwartz^{1

3}, Elizabeth M McNally^{1

2}

Affiliations

¹ Center for Genetic Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
² Bluhm Cardiovascular Institute, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
³ Department of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

PMID: 33851998
DOI: 10.1093/eurheartj/ehab172

No abstract available

Publication types

Editorial
Comment

MeSH terms

Cardiomyopathy, Dilated* / genetics
Chromosomes
Genome-Wide Association Study
Heart Failure, Systolic*
Humans
Polymorphism, Single Nucleotide

Grants and funding

F32 HL154712/HL/NHLBI NIH HHS/United States