Genetic basis of atrial fibrillation

od Campuzano, Oscar, Perez-Serra, Alexandra, Iglesias, Anna, Brugada, Ramon
izdano v Genes Dis (2016)

Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies

od Campuzano, Oscar, Allegue, Catarina, Fernandez, Anna, Iglesias, Anna, Brugada, Ramon
izdano v Sci Rep (2015)

Familial Dilated Cardiomyopathy Caused by a Novel Frameshift in the BAG3 Gene

od Toro, Rocio, Pérez-Serra, Alexandra, Campuzano, Oscar, Moncayo-Arlandi, Javier, Allegue, Catarina, Iglesias, Anna, Mangas, Alipio, Brugada, Ramon
izdano v PLoS One (2016)

Short QT and atrial fibrillation: A KCNQ1 mutation–specific disease. Late follow-up in three unrelated children

od Sarquella-Brugada, Georgia, Campuzano, Oscar, Iglesias, Anna, Grueso, Josefina, Bradley, David J., Kerst, Gunter, Shmorhun, Daniel, Brugada, Josep, Brugada, Ramon
izdano v HeartRhythm Case Rep (2015)

Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings

od Grassi, Simone, Vidal, Mònica Coll, Campuzano, Oscar, Arena, Vincenzo, Alfonsetti, Alessandro, Rossi, Sabina Strano, Scarnicci, Francesca, Iglesias, Anna, Brugada, Ramon, Oliva, Antonio
izdano v Diagnostics (Basel) (2021)

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome

od Allegue, Catarina, Coll, Mònica, Mates, Jesus, Campuzano, Oscar, Iglesias, Anna, Sobrino, Beatriz, Brion, Maria, Amigo, Jorge, Carracedo, Angel, Brugada, Pedro, Brugada, Josep, Brugada, Ramon
izdano v PLoS One (2015)

Stop-Gain Mutations in PKP2 Are Associated with a Later Age of Onset of Arrhythmogenic Right Ventricular Cardiomyopathy

od Alcalde, Mireia, Campuzano, Oscar, Berne, Paola, García-Pavía, Pablo, Doltra, Ada, Arbelo, Elena, Sarquella-Brugada, Georgia, Iglesias, Anna, Alonso-Pulpon, Luis, Brugada, Josep, Brugada, Ramon
Izdano 2014

Identification of Genetic Alterations, as Causative Genetic Defects in Long QT Syndrome, Using Next Generation Sequencing Technology

od Campuzano, Oscar, Sarquella-Brugada, Georgia, Mademont-Soler, Irene, Allegue, Catarina, Cesar, Sergi, Ferrer-Costa, Carles, Coll, Monica, Mates, Jesus, Iglesias, Anna, Brugada, Josep, Brugada, Ramon
izdano v PLoS One (2014)

Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death

od Campuzano, Oscar, Sanchez-Molero, Olallo, Mademont-Soler, Irene, Riuró, Helena, Allegue, Catarina, Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, Picó, Ferran, Iglesias, Anna, Brugada, Ramon
izdano v Int J Mol Sci (2015)

Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death

od Coll, Monica, Pérez-Serra, Alexandra, Mates, Jesus, del Olmo, Bernat, Puigmulé, Marta, Fernandez-Falgueras, Anna, Iglesias, Anna, Picó, Ferran, Lopez, Laura, Brugada, Ramon, Campuzano, Oscar
izdano v Biology (Basel) (2017)

Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP

od Coll, Monica, Striano, Pasquale, Ferrer-Costa, Carles, Campuzano, Oscar, Matés, Jesús, del Olmo, Bernat, Iglesias, Anna, Pérez-Serra, Alexandra, Mademont, Irene, Picó, Ferran, Oliva, Antonio, Brugada, Ramon
izdano v PLoS One (2017)

Electrocardiographic Assessment and Genetic Analysis in Neonates: A Current Topic of Discussion

od Sarquella-Brugada, Georgia, Cesar, Sergi, Zambrano, Maria Dolores, Fernandez-Falgueras, Anna, Fiol, Victoria, Iglesias, Anna, Torres, Francesc, Garcia-Algar, Oscar, Arbelo, Elena, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar
izdano v Curr Cardiol Rev (2019)

A Novel Missense Mutation, I890T, in the Pore Region of Cardiac Sodium Channel Causes Brugada Syndrome

od Tarradas, Anna, Selga, Elisabet, Beltran-Alvarez, Pedro, Pérez-Serra, Alexandra, Riuró, Helena, Picó, Ferran, Iglesias, Anna, Campuzano, Oscar, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Pérez, Guillermo J., Scornik, Fabiana S., Brugada, Ramon
Izdano 2013

Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients

od Coll, Monica, Ferrer-Costa, Carles, Pich, Sara, Allegue, Catarina, Rodrigo, Emilio, Fernández-Fresnedo, Gema, Barreda, Paloma, Mates, Jesus, Martinez de Francisco, Angel Luis, Ortega, Israel, Iglesias, Anna, Campuzano, Oscar, Salas, Eduardo, Arias, Manuel, Brugada, Ramon
izdano v PLoS One (2018)

Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes

od Campuzano, Oscar, Sarquella-Brugada, Georgia, Fernandez-Falgueras, Anna, Coll, Mónica, Iglesias, Anna, Ferrer-Costa, Carles, Cesar, Sergi, Arbelo, Elena, García-Álvarez, Ana, Jordà, Paloma, Toro, Rocío, Tiron de Llano, Coloma, Grassi, Simone, Oliva, Antonio, Brugada, Josep, Brugada, Ramon
izdano v EBioMedicine (2020)

Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach

od Jordà, Paloma, Toro, Rocío, Diez, Carles, Salazar-Mendiguchía, Joel, Fernandez-Falgueras, Anna, Perez-Serra, Alexandra, Coll, Monica, Puigmulé, Marta, Arbelo, Elena, García-Álvarez, Ana, Sarquella-Brugada, Georgia, Cesar, Sergi, Tiron, Coloma, Iglesias, Anna, Brugada, Josep, Brugada, Ramon, Campuzano, Oscar
izdano v J Pers Med (2021)

Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants

od Campuzano, Oscar, Fernandez-Falgueras, Anna, Lemus, Ximena, Sarquella-Brugada, Georgia, Cesar, Sergi, Coll, Monica, Mates, Jesus, Arbelo, Elena, Jordà, Paloma, Perez-Serra, Alexandra, del Olmo, Bernat, Ferrer-Costa, Carles, Iglesias, Anna, Fiol, Victoria, Puigmulé, Marta, Lopez, Laura, Pico, Ferran, Brugada, Josep, Brugada, Ramon
izdano v J Clin Med (2019)

Analysis of Brugada syndrome loci reveals that fine-mapping clustered GWAS hits enhances the annotation of disease-relevant variants

od Pinsach-Abuin, Mel·lina, del Olmo, Bernat, Pérez-Agustin, Adrian, Mates, Jesus, Allegue, Catarina, Iglesias, Anna, Ma, Qi, Merkurjev, Daria, Konovalov, Sergiy, Zhang, Jing, Sheikh, Farah, Telenti, Amalio, Brugada, Josep, Brugada, Ramon, Gymrek, Melissa, di Iulio, Julia, Garcia-Bassets, Ivan, Pagans, Sara
izdano v Cell Rep Med (2021)

Genetic analysis, in silico prediction, and family segregation in long QT syndrome

od Riuró, Helena, Campuzano, Oscar, Berne, Paola, Arbelo, Elena, Iglesias, Anna, Pérez-Serra, Alexandra, Coll-Vidal, Mònica, Partemi, Sara, Mademont-Soler, Irene, Picó, Ferran, Allegue, Catarina, Oliva, Antonio, Gerstenfeld, Edward, Sarquella-Brugada, Georgia, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Mont, Lluís, Brugada, Josep, Scornik, Fabiana S, Brugada, Ramon
izdano v Eur J Hum Genet (2015)

Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort

od Selga, Elisabet, Campuzano, Oscar, Pinsach-Abuin, Mel·lina, Pérez-Serra, Alexandra, Mademont-Soler, Irene, Riuró, Helena, Picó, Ferran, Coll, Mònica, Iglesias, Anna, Pagans, Sara, Sarquella-Brugada, Georgia, Berne, Paola, Benito, Begoña, Brugada, Josep, Porres, José M., López Zea, Matilde, Castro-Urda, Víctor, Fernández-Lozano, Ignacio, Brugada, Ramon
izdano v PLoS One (2015)