Federica Dagradi

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

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

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Lia Crotti, Cherisse A. Marcou, David J. Tester et al. · Journal of the American College of Cardiology · 2012 · 199 citations · Full text

Genetic Disorder, Medicine, Genetics +10

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

Lia Crotti, Carla Spazzolini, David J. Tester et al. · European Heart Journal · 2019 · 177 citations · Full text

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

Najim Lahrouchi, Rafik Tadros, Lia Crotti et al. · Circulation · 2020 · 134 citations · Full text