Óscar Campuzano

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 · 141 citations · Full text

Life Sciences, Cardiology, Genetics +15

A Missense Mutation in the Sodium Channel β2 Subunit Reveals<i>SCN2B</i>as a New Candidate Gene for Brugada Syndrome

Helena Riuró, Pedro Beltrán-Álvarez, Anna Tarradas et al. · Human Mutation · 2013 · 109 citations · Full text

Life Sciences, Cardiology, Genetics +17

Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation

Pasquale Parisi, Antonio Oliva, Monica Coll Vidal et al. · Epilepsy Research · 2013 · 106 citations

Medicine, Genetics, Neurology +12

Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

Roddy Walsh, Najim Lahrouchi, Florence Kyndt et al. · Genetics in Medicine · 2020 · 105 citations · Full text

Life Sciences, Cardiology, Genetics +17

Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

Ángela López‐Sainz, Fernándo Domínguez, Luís R. Lopes et al. · Journal of the American College of Cardiology · 2020 · 100 citations · Full text

Medicine, Cardiology, Genetics +9