Elisa Mastantuono

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

Novel Calmodulin Mutations Associated With Congenital Arrhythmia Susceptibility

Naomasa Makita, Nobue Yagihara, Lia Crotti et al. · Circulation Cardiovascular Genetics · 2014 · 184 citations · Full text

Identification of Cadherin 2 ( <i>CDH2</i> ) Mutations in Arrhythmogenic Right Ventricular Cardiomyopathy

Bongani M. Mayosi, Maryam Fish, Gasnat Shaboodien et al. · Circulation Cardiovascular Genetics · 2017 · 145 citations · Full text

Congenital heart disease risk loci identified by genome-wide association study in European patients

Harald Lahm, Meiwen Jia, Martina Dreßen et al. · Journal of Clinical Investigation · 2020 · 107 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +19

Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies

René G. Feichtinger, Monika Oláhová, Yoshihito Kishita et al. · The American Journal of Human Genetics · 2017 · 85 citations · Full text