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Iscience|April 25, 2025
Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromesEstefanía Martínez-Barrios, Andrea Greco, Sergi Cesar, et al.Forensic Science International|December 3, 2014
Post-mortem genetic analysis in juvenile cases of sudden cardiac deathOscar Campuzano, Olallo Sanchez-Molero, Catarina Allegue, et al.Translational Research : the Journal of Laboratory and Clinical Medicine|September 11, 2019
Emerging role of microRNAs in dilated cardiomyopathy: evidence regarding etiologyMaria Calderon-Dominguez, Thalía Belmonte, Maribel Quezada-Feijoo, et al.Pediatric Neurology|December 17, 2020
The Phenotype and Genotype of Congenital Myopathies Based on a Large Pediatric CohortDaniel Natera-de Benito, Carlos Ortez, Cristina Jou, et al.Ebiomedicine|April 9, 2020
Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromesOscar Campuzano, Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, et al.Biomedicines|November 27, 2024
Actionable Variants of Unknown Significance in Inherited Arrhythmogenic Syndromes: A Further Step Forward in Genetic DiagnosisEstefanía Martínez-Barrios, Andrea Greco, José Cruzalegui, et al.Human Mutation|March 2, 2019
Genetic interpretation and clinical translation of minor genes related to Brugada syndromeOscar Campuzano, Georgia Sarquella-Brugada, Anna Fernandez-Falgueras, et al.Journal of Personalized Medicine|March 6, 2021
Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized ApproachPaloma Jordà, Rocío Toro, Carles Diez, et al.Genes|November 27, 2025
The Role of Molecular Autopsy in Concealed CardiomyopathiesOscar Campuzano, Coloma Tirón, Estefanía Martínez-Barrios, et al.Journal of Clinical Medicine|July 19, 2019
Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare VariantsOscar Campuzano, Anna Fernandez-Falgueras, Ximena Lemus, et al.Pageof 7