Multimodal fusion learning for long QT syndrome pathogenic genotypes in a racially diverse population-Reference-Cited by-同舟云学术

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Multimodal fusion learning for long QT syndrome pathogenic genotypes in a racially diverse population

Published:2024-08-24 Issue:1 Volume:7 Page:
ISSN:2398-6352
Container-title:npj Digital Medicine
language:en
Short-container-title:npj Digit. Med.

Author:

Jiang Joy^ORCID,Thi Vy Ha My,Charney Alexander^ORCID,Kovatch Patricia^ORCID,Reddy Vivek,Jayaraman Pushkala^ORCID,Do Ron^ORCID,Khera Rohan^ORCID,Chugh Sumeet,Bhatt Deepak L.^ORCID,Vaid Akhil^ORCID,Lampert Joshua^ORCID,Nadkarni Girish Nitin^ORCID

Funder

American Heart Association

U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute

U.S. Department of Health & Human Services | NIH | National Center for Advancing Translational Sciences

U.S. Department of Health & Human Services | NIH | National Institute of General Medical Sciences

Publisher

Springer Science and Business Media LLC

Link

https://www.nature.com/articles/s41746-024-01218-1.pdf

Reference38 articles.

1. Schwartz, P. J. & Ackerman, M. J. The long QT syndrome: a transatlantic clinical approach to diagnosis and therapy. Eur. Heart J. 34, 3109–3116 (2013).

2. Nakano, Y. & Shimizu, W. Genetics of long-QT syndrome. J. Hum. Genet. 61, 51–55 (2016).

3. Krahn, A. D. et al. Congenital long QT syndrome. Clin. Electrophysiol. 8, 687–706 (2022).

4. Katsanis, S. H. & Katsanis, N. Molecular genetic testing and the future of clinical genomics. Nat. Rev. Genet. 14, 415–426 (2013).

5. Veltmann, C. & Borggrefe, M. A’Schwartz score’for short QT syndrome. Nat. Rev. Cardiol. 8, 251–252 (2011).

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