Simon Lecointe

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

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

New insights into mitral valve dystrophy: a Filamin-A genotype–phenotype and outcome study

Thierry Le Tourneau, Solena Le Scouarnec, Caroline Cueff et al. · European Heart Journal · 2017 · 73 citations · Full text

Medicine, Cardiology, Genetics +17

Fine-scale human genetic structure in Western France

Matilde Karakachoff, Nicolas Duforet-Frebourg, Floriane Simonet et al. · European Journal of Human Genetics · 2014 · 36 citations · Full text

Life Sciences, Biology, Genetics +14

Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations

Delphine Béziau, Julien Barc, Tom O’Hara et al. · Basic Research in Cardiology · 2014 · 25 citations

Life Sciences, Genetics, Molecular Genetics +6