Jean‐Baptiste Gourraud

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

Connie R. Bezzina, Julien Barc, Yuka Mizusawa et al. · Nature Genetics · 2013 · 540 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +9

Outcome After Implantation of a Cardioverter-Defibrillator in Patients With Brugada Syndrome

Frédéric Sacher, Vincent Probst, Philippe Maury et al. · Circulation · 2013 · 444 citations · Full text

Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse

Anne-Laure Constant Dit Beaufils, Olivier Huttin, Antoine Jobbé‐Duval et al. · Circulation · 2021 · 146 citations

Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome

Solena Le Scouarnec, Matilde Karakachoff, Jean‐Baptiste Gourraud et al. · Human Molecular Genetics · 2015 · 135 citations · Full text

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Najim Lahrouchi, Rafik Tadros, Lia Crotti et al. · Circulation · 2020 · 134 citations · Full text