Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R. Bezzina, F Gros, Lia Crotti et al.|Nature Genetics|2013Cited by 550
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Héctor Barajas-Martínez, Rafik Tadros et al.|Nature Genetics|2022Cited by 144
Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R. Bezzina, Simon Lecointe, Julien Barc et al.|Nature Genetics|2013Cited by 20
Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibilityJulien Barc, Héctor Barajas-Martínez, Leslie Placide et al.|Nature Genetics|2022Cited by 3