Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndromeSolena Le Scouarnec, Richard Redon, Floriane Simonet et al.|Human Molecular Genetics|2015Cited by 136
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
Human genetic structure in Northwest France provides new insights into West European historical demographyIsabel Alves, Jean‐François Deleuze, Joanna Giemza et al.|Nature Communications|2024Cited by 8
GAIN-OF-FUNCTION MUTATION IN THE VOLTAGE-GATED K+ CHANNEL BETA-2 SUBUNIT IS ASSOCIATED WITH BRUGADA SYNDROMEVincent Portero, Richard Redon, Solena Le Scouarnec et al.|Heart Rhythm|2014Cited by 1