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Archives of Cardiovascular Diseases|July 30, 2026
Intercentre heterogeneity and determinants of implantable cardioverter-defibrillator technology selection in FranceFawzi Kerkouri, Marc Badoz, Rodrigue Garcia, et al.
European Journal of Human Genetics : EJHG|September 4, 2014
Fine-scale human genetic structure in Western FranceMatilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet, et al.
Heart Rhythm|November 24, 2015
Benign vs. malignant inferolateral early repolarization: Focus on the T waveLaurent Roten, Nicolas Derval, Philippe Maury, et al.
Heart Rhythm|July 26, 2015
Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndromePhilippe Maury, Frederic Sacher, Jean-Baptiste Gourraud, et al.
Plos One|February 23, 2010
Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse modelAnne-Laure Leoni, Bruno Gavillet, Jean-Sébastien Rougier, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|February 13, 2024
Insights into adherence to medication and lifestyle recommendations in an international cohort of patients with catecholaminergic polymorphic ventricular tachycardiaPuck J Peltenburg, Lieke M van den Heuvel, Dania Kallas, et al.
Human Mutation|July 12, 2022
Burden of rare variants in arrhythmogenic cardiomyopathy with right dominant form-associated genes provides new insights for molecular diagnosis and clinical managementAdeline Goudal, Matilde Karakachoff, Pierre Lindenbaum, et al.
International Journal of Cardiology|January 29, 2016
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Mohamed-Yassine Amarouch, Pierre Lindenbaum, et al.
Basic Research in Cardiology|October 25, 2014
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutationsDelphine M Béziau, Julien Barc, Thomas O'Hara, et al.
Human Molecular Genetics|March 17, 2012
Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in humanNathalie Roux-Buisson, Marine Cacheux, Anne Fourest-Lieuvin, et al.
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