Belbachir, Nadjet; Portero, Vincent; Al Sayed, Zeina R.; Gourraud, Jean-Baptiste; Dilasser, Florian; Jesel, Laurence; Guo, Hongchao; Wu, Haodi; Gaborit, Nathalie; Guilluy, Christophe; Girardeau, Aurore; Bonnaud, Stephanie; Simonet, Floriane; Karakachoff, Matilde; Pattier, Sabine; Scott, Carol; Burel, Sophie; Marionneau, Celine; Chariau, Caroline; Gaignerie, Anne; David, Laurent; Genin, Emmanuelle; Deleuze, Jean-Francois; Dina, Christian; Sauzeau, Vincent; Loirand, Gervaise; Baro, Isabelle; Schott, Jean-Jacques; Probst, Vincent; Wu, Joseph C.; Redon, Richard; Charpentier, Flavien; Le Scouarnec, Solena

KV4.3 Expression Modulates NaV1.5 Sodium Current

FRONTIERS IN PHYSIOLOGY

IF3.4

2018-03-1227

OAAI

Anti-arrhythmic potential of the late sodium current inhibitor GS-458967 in murine Scn5a-1798insD+/- and human SCN5A-1795insD+/- iPSC-derived cardiomyocytes

CARDIOVASCULAR RESEARCH

IF13.3

2017-04-1843

OAAI

Dysfunction of the Voltage-Gated K+ Channel β2 Subunit in a Familial Case of Brugada Syndrome

JOURNAL OF THE AMERICAN HEART ASSOCIATION

IF5.3

2016-06-1321

OAAI

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death (vol 45, pg 1044, 2013)

NATURE GENETICS

IF31.8

2013-10-295

OAAI

Bezzina, Connie R.; Barc, Julien; Mizusawa, Yuka; Remme, Carol Ann; Gourraud, Jean-Baptiste; Simonet, Floriane; Verkerk, Arie O.; Schwartz, Peter J.; Crotti, Lia; Dagradi, Federica; Guicheney, Pascale; Fressart, Veronique; Leenhardt, Antoine; Antzelevitch, Charles; Bartkowiak, Susan; Schulze-Bahr, Eric; Zumhagen, Sven; Behr, Elijah R.; Bastiaenen, Rachel; Tfelt-Hansen, Jacob; Olesen, Morten Salling; Kaeaeb, Stefan; Beckmann, Britt M.; Weeke, Peter; Watanabe, Hiroshi; Endo, Naoto; Minamino, Tohru; Horie, Minoru; Ohno, Seiko; Hasegawa, Kanae; Makita, Naomasa; Nogami, Akihiko; Shimizu, Wataru; Aiba, Takeshi; Froguel, Philippe; Balkau, Beverley; Lantieri, Olivier; Torchio, Margherita; Wiese, Cornelia; Weber, David; Wolswinkel, Rianne; Coronel, Ruben; Boukens, Bas J.; Bezieau, Stephane; Charpentier, Eric; Chatel, Stephanie; Despres, Aurore; Gros, Francoise; Kyndt, Florence; Lecointe, Simon; Lindenbaum, Pierre; Portero, Vincent; Violleau, Jade; Gessler, Manfred; Tan, Hanno L.; Roden, Dan M.; Christoffels, Vincent M.; Le Marec, Herve; Wilde, Arthur A.; Probst, Vincent; Schott, Jean-Jacques; Dina, Christian; Redon, Richard; Borggrefe, Martin; Schimpf, Rainer

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

NATURE GENETICS

IF31.8

2013-07-21409

Vincent Portero

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