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Circulation. Arrhythmia and Electrophysiology|July 13, 2012
Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relativesChristian van der Werf, Ineke Nederend, Nynke Hofman, et al.
Circulation|March 30, 2012
Mutations in cytoplasmic loops of the KCNQ1 channel and the risk of life-threatening events: implications for mutation-specific response to β-blocker therapy in type 1 long-QT syndromeAlon Barsheshet, Ilan Goldenberg, Jin O-Uchi, et al.
Circulation. Cardiovascular Genetics|March 5, 2015
Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2Iris C R M Kolder, Michael W T Tanck, Pieter G Postema, et al.
Circulation|August 28, 2016
Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter StudyArthur A M Wilde, Arthur J Moss, Elizabeth S Kaufman, et al.
European Heart Journal. Quality of Care & Clinical Outcomes|July 11, 2025
Current Management of Transition and Multidisciplinary Care of Patients with Inherited and Rare Cardiomyopathies in Europe: Results of the European Reference Network for Rare and Low Prevalence Complex Diseases of the Heart (ERN GUARD-HEART)Emanuele Monda, Elena Biagini, Nico Blom, et al.
Circulation. Arrhythmia and Electrophysiology|February 18, 2020
Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular TachycardiaKrystien V V Lieve, Veronica Dusi, Christian van der Werf, 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.
Nature Genetics|June 23, 2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarizationDan E Arking, Sara L Pulit, Lia Crotti, et al.
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