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Medrxiv : the Preprint Server for Health Sciences|April 17, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.Genome Medicine|October 23, 2023
Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditionsKatherine S Josephs, Angharad M Roberts, Pantazis Theotokis, et al.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.Hepatology International|May 19, 2023
An international multidisciplinary consensus statement on MAFLD and the risk of CVDXiao-Dong Zhou, Giovanni Targher, Christopher D Byrne, et al.Pageof 12