Floriane Simonet

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

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

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

Christian Dina, Nabila Bouatia‐Naji, Nathan R. Tucker et al. · Nature Genetics · 2015 · 135 citations · Full text

Medicine, Cardiology, Genetics +13

<i>RRAD</i> mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndrome

Nadjet Belbachir, Vincent Portero, Zeina R. Al Sayed et al. · European Heart Journal · 2019 · 52 citations · Full text

Life Sciences, Cardiology, Genetics +15

Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm

Romain Bourcier, Solena Le Scouarnec, Stéphanie Bonnaud et al. · The American Journal of Human Genetics · 2018 · 49 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11