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Journal of the American College of Cardiology|July 9, 2016
Genotype and Phenotype of Transthyretin Cardiac Amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey)Mathew S Maurer, Mazen Hanna, Martha Grogan, et al.
Genome Medicine|January 31, 2019
Quantitative approaches to variant classification increase the yield and precision of genetic testing in Mendelian diseases: the case of hypertrophic cardiomyopathyRoddy Walsh, Francesco Mazzarotto, Nicola Whiffin, et al.
Lancet (London, England)|September 2, 2020
Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trialIacopo Olivotto, Artur Oreziak, Roberto Barriales-Villa, et al.
Circulation|January 28, 2020
Myosin Sequestration Regulates Sarcomere Function, Cardiomyocyte Energetics, and Metabolism, Informing the Pathogenesis of Hypertrophic CardiomyopathyChristopher N Toepfer, Amanda C Garfinkel, Gabriela Venturini, et al.
Circulation|April 20, 2021
Genetic and Phenotypic Landscape of Peripartum CardiomyopathyRahul Goli, Jian Li, Jeff Brandimarto, et al.
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.
JACC. Clinical Electrophysiology|July 4, 2021
Predictors of Major Atrial Fibrillation Endpoints in the National Heart, Lung, and Blood Institute HCMRChristopher M Kramer, John P DiMarco, Paul Kolm, et al.
ESC Heart Failure|October 18, 2022
Impact of SARS-Cov-2 infection in patients with hypertrophic cardiomyopathy: results of an international multicentre registryJuan R Gimeno, Iacopo Olivotto, Ana Isabel Rodríguez, et al.
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