Véronique Fressart

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Jamie D. Kapplinger, David J. Tester, Mariëlle Alders et al. · Heart Rhythm · 2009 · 753 citations · Full text

Channelopathies, Cardiomyopathy, Genetic Disorder +7

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

Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice

Véronique Fressart, Guillaume Duthoit, Erwan Donal et al. · EP Europace · 2010 · 236 citations · Full text

The genetics underlying acquired long QT syndrome: impact for genetic screening

Hideki Itoh, Lia Crotti, Takeshi Aiba et al. · European Heart Journal · 2015 · 209 citations · Full text

Brugada syndrome and fever: Genetic and molecular characterization of patients carrying mutations

Dagmar I. Keller, Jean‐Sébastien Rougier, Jan Kučera et al. · Cardiovascular Research · 2005 · 192 citations · Full text