Vincent Portero

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 · 540 citations · Full text

Cardiomyopathy, Genetic Disorder, Genetics +9

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

Identification of Large Families in Early Repolarization Syndrome

Jean‐Baptiste Gourraud, Solena Le Scouarnec, Frédéric Sacher et al. · Journal of the American College of Cardiology · 2013 · 90 citations

Early Repolarization Syndrome, Pediatrics, Developmental Anomaly

Chronically elevated branched chain amino acid levels are pro-arrhythmic

Vincent Portero, T. NICOL, Svitlana Podliesna et al. · Cardiovascular Research · 2021 · 69 citations · Full text

<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 · 51 citations · Full text