Julien Barc

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

KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron

Hélène Louis-Dit-Picard, Julien Barc, Daniel Trujillano et al. · Nature Genetics · 2012 · 330 citations · Full text

Ion Transport, Hypertonicity, Urology +9

SCN5A Mutations and the Role of Genetic Background in the Pathophysiology of Brugada Syndrome

Vincent Probst, Arthur A.M. Wilde, Julien Barc et al. · Circulation Cardiovascular Genetics · 2009 · 315 citations · Full text

HCN4 Mutations in Multiple Families With Bradycardia and Left Ventricular Noncompaction Cardiomyopathy

Annalisa Milano, Alexa M.C. Vermeer, Elisabeth M. Lodder et al. · Journal of the American College of Cardiology · 2014 · 195 citations

Cardiac Muscle, Cardiomyopathy, Heart Failure +8

A Mutation in CALM1 Encoding Calmodulin in Familial Idiopathic Ventricular Fibrillation in Childhood and Adolescence

Roos F. Marsman, Julien Barc, Leander Beekman et al. · Journal of the American College of Cardiology · 2013 · 178 citations · Full text

Cardiomyopathy, Heart Failure, Genetics +7