Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Richard Redon, Julien Barc et al.|Human Molecular Genetics|2015Cited by 136
Targeted resequencing identifies TRPM4 as a major gene predisposing to progressive familial heart block type IXavier Daumy, Jean‐Jacques Schott, Mohamed‐Yassine Amarouch et al.|International Journal of Cardiology|2016Cited by 62
Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial AneurysmRomain Bourcier, Alain Bonafé, Solena Le Scouarnec et al.|The American Journal of Human Genetics|2018Cited by 50
Progressive Atrial Conduction Defects Associated With Bone Malformation Caused by a Connexin-45 MutationAkiko Seki, Naomasa Makita, Taisuke Ishikawa et al.|Journal of the American College of Cardiology|2017Cited by 39
Dysfunction of the Voltage‐Gated K <sup>+</sup> Channel β2 Subunit in a Familial Case of Brugada SyndromeVincent Portero, Richard Redon, Solena Le Scouarnec et al.|Journal of the American Heart Association|2016Cited by 27