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Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 13, 2020
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditionsXiaolei Zhang, Roddy Walsh, Nicola Whiffin, et al.
Nature Medicine|September 24, 2021
Valsartan in early-stage hypertrophic cardiomyopathy: a randomized phase 2 trialCarolyn Y Ho, Sharlene M Day, Anna Axelsson, et al.
Nature Genetics|April 8, 2025
Common-variant and rare-variant genetic architecture of heart failure across the allele-frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Common- and rare-variant genetic architecture of heart failure across the allele frequency spectrumDavid S M Lee, Kathleen M Cardone, David Y Zhang, et al.
JAMA Cardiology|September 6, 2023
Cardiac Remodeling in Subclinical Hypertrophic Cardiomyopathy: The VANISH Randomized Clinical TrialChristoffer Rasmus Vissing, Anna Axelsson Raja, Sharlene M Day, et al.
Circulation. Heart Failure|December 10, 2019
Baseline Characteristics of the VANISH CohortAnna Axelsson Raja, Ling Shi, Sharlene M Day, et al.
Nature Communications|November 14, 2022
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failureMichael G Levin, Noah L Tsao, Pankhuri Singhal, et al.
JAMA Cardiology|May 17, 2023
Vigorous Exercise in Patients With Hypertrophic CardiomyopathyRachel Lampert, Michael J Ackerman, Bradley S Marino, et al.
Circulation. Genomic and Precision Medicine|July 8, 2026
Variant Site-Specific Natural History of Titin-Induced Cardiomyopathy: An International Multicenter RegistryMaria Perotto, Cinzia Radesich, Alessia Paldino, et al.
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