Nathalie Roux-Buisson

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human

Nathalie Roux-Buisson, Marine Cacheux, Anne Fourest‐Lieuvin et al. · Human Molecular Genetics · 2012 · 258 citations · Full text

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

Véronique Fressart, Guillaume Duthoit, Erwan Donal et al. · EP Europace · 2010 · 236 citations · Full text

The role of stress test for predicting genetic mutations and future cardiac events in asymptomatic relatives of catecholaminergic polymorphic ventricular tachycardia probands

Miyuki Hayashi, Isabelle Denjoy, Meiso Hayashi et al. · EP Europace · 2012 · 78 citations · Full text

Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: Results of a systematic screening

Nathalie Roux-Buisson, Estelle Gandjbakhch, Erwan Donal et al. · Heart Rhythm · 2014 · 66 citations

Cardiomyopathy, Heart Failure, Cardiovascular Disease +7

New Family With Catecholaminergic Polymorphic Ventricular Tachycardia Linked to the Triadin Gene

Caroline Rooryck, Florence Kyndt, Dominique Bozon et al. · Journal of Cardiovascular Electrophysiology · 2015 · 54 citations

Cardiac Muscle, Heart Failure, Genetics +17