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 · 134 citations · Full text

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

Cardiac Muscle, Genetics, Molecular Genetics +23

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

Pasquale Parisi, Antonio Oliva, Monica Coll Vidal et al. · Epilepsy Research · 2013 · 103 citations

Mendelian Disorder, Genetic Disorder, Genetics +10

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 · 100 citations · Full text

Increased levels of proinflammatory cytokines in the aged rat brain attenuate injury‐induced cytokine response after excitotoxic damage

Óscar Campuzano, Maria del Mar Castillo-Ruiz, Laia Acarín et al. · Journal of Neuroscience Research · 2009 · 92 citations