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Medrxiv : the Preprint Server for Health Sciences|August 8, 2025
The contribution of RBM20 truncating variants to human cardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.JAMA Cardiology|April 8, 2026
RBM20 Truncating Variants and Human CardiomyopathyBrendan J Floyd, Joyce N Njoroge, Vikki A Krysov, et al.European Journal of Heart Failure|May 29, 2021
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathyMaria A Restrepo-Cordoba, Karim Wahbi, Anca R Florian, et al.Journal of the American College of Cardiology|August 25, 2022
Natural History of MYH7-Related Dilated CardiomyopathyFernando de Frutos, Juan Pablo Ochoa, Marina Navarro-Peñalver, et al.European Heart Journal|September 10, 2025
Fulminant myocarditis: outcome predictors in an international cohort studyNicolas Majunke, Franz Haertel, Leonhard Binzenhöfer, et al.European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.European Heart Journal|August 29, 2014
Atlas of the clinical genetics of human dilated cardiomyopathyJan Haas, Karen S Frese, Barbara Peil, et al.Research Square|February 6, 2026
Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathiesDaria Kramarenko, Poeya Haydarlou, George Powell, et al.Nature Genetics|November 21, 2024
Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilienceSean J Jurgens, Joel T Rämö, Daria R Kramarenko, et al.European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.Pageof 27