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Circulation|December 7, 2021
An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular TachycardiaPuck J Peltenburg, Dania Kallas, Johan M Bos, et al.European Heart Journal|July 31, 2018
SCN5A mutations in 442 neonates and children: genotype-phenotype correlation and identification of higher-risk subgroupsAlban-Elouen Baruteau, Florence Kyndt, Elijah R Behr, et al.Circulation|July 23, 2020
An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular TachycardiaKevin Ng, Erron W Titus, Krystien V Lieve, et al.European Heart Journal|January 9, 2024
Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and EuropeRichard T Carrick, Corrado De Marco, Alessio Gasperetti, et al.Circulation|January 17, 2020
An International Multicenter Evaluation of Type 5 Long QT Syndrome: A Low Penetrant Primary Arrhythmic ConditionJason D Roberts, S Yukiko Asaki, Andrea Mazzanti, et al.European Heart Journal|December 19, 2025
Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratificationKrystien V Lieve, Christian van der Werf, Dania Kallas, et al.The Journal of Clinical Investigation|July 3, 2019
Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapyJason D Roberts, Nathaniel P Murphy, Robert M Hamilton, et al.Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.Pageof 43