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 · 546 citations

Life Sciences, Genetics, Molecular Genetics +13

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

Frédéric Sacher, Vincent Probst, Philippe Maury et al. · Circulation · 2013 · 446 citations · Full text

Medicine, Cardiology, Clinical Cardiology +11

Replacement Myocardial Fibrosis in Patients With Mitral Valve Prolapse

Anne-Laure Constant Dit Beaufils, Olivier Huttin, Antoine Jobbé‐Duval et al. · Circulation · 2021 · 152 citations

Medicine, Cardiology, Radiology +17

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 · 141 citations · Full text

Life Sciences, Cardiology, Genetics +15

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

Life Sciences, Genetics, Molecular Genetics +14