Cesar S, Coll M, Fiol V, Fernandez-Falgueras A, Cruzalegui J, Iglesias A, Moll I, Perez-Serra A, Martínez-Barrios E, Ferrer-Costa C, Del Olmo B, Puigmulè M, Alcalde M, Lopez L, Pico F, Berrueco R, Brugada J, Zschaeck I, Nater "LMNA-related muscular dystrophy: Identification of variants in alternative genes and personalized clinical translation." Frontiers In Genetics 14 (2023): -. Cesar S, Campuzano O, Cruzalegui J, Fiol V, Moll I, Martínez-Barrios E, Zschaeck I, Natera-de Benito D, Ortez C, Carrera L, Expósito J, Berrueco R, Bautista-Rodriguez C, Dabaj I, Gómez García-de-la-Banda M, Quijano-Roy S, Bru "Characterization of cardiac involvement in children with LMNA-related muscular dystrophy." Frontiers in Cell and Developmental Biology 11 (2023): -. Martinez-Barrios E, Sarquella-Brugada G, Perez-Serra A, Fernandez-Falgueras A, Cesar S, Alcalde M, Coll M, Puigmulé M, Iglesias A, Ferrer-Costa C, Del Olmo B, Picó F, Lopez L, Fiol V, Cruzalegui J, Hernandez C, Arbelo E, Díez "Reevaluation of ambiguous genetic variants in sudden unexplained deaths of a young cohort." International Journal of Legal Medicine 13 (2023): 347-351. Vallverdú-Prats, M.; Carreras, D.; Pérez, G.J.; Campuzano, O.; Brugada, R.; Alcalde, M. "Alterations in calcium handling are a common feature in an arrhythmogenic cardiomyopathy cell model triggered by desmosome genes loss." International Journal of Molecular Sciences 24 (2023): 2109-. Monica Coll, Anna Fernandez-Falgueras, Anna Iglesias, Bernat del Olmo, Laia Nogue-Navarro, Adria Simon, Alexandra Perez Serra, Marta Puigmule, Laura Lopez, Ferran Pico, Monica Corona, Marta Vallverdu-Prats, Coloma Tiron, Osca "Unpredicted Aberrant Splicing Products Identified in Postmortem Sudden Cardiac Death Samples." International Journal of Molecular Sciences 23 (2022): 12640-. de Frutos F, Ochoa JP, Navarro-Peñalver M, Baas A, Bjerre JV, Zorio E, Méndez I, Lorca R, Verdonschot JAJ, García-Granja PE, Bilinska Z, Fatkin D, Fuentes-Cañamero ME, García-Pinilla JM, García-Álvarez MI, Girolami F, Barrial "Natural History of MYH7-Related Dilated Cardiomyopathy." Journal of the American College of Cardiology (2022): -. Grassi S, Campuzano O, Coll M, Cazzato F, Iglesias A, Ausania F, Scarnicci F, Sarquella-Brugada G, Brugada J, Arena V, Oliva A, Brugada R "Eosinophilic Infiltration of the Sino-Atrial Node in Sudden Cardiac Death Caused by Long QT Syndrome." International Journal of Molecular Sciences 23 (2022): 11666-. Mangas A, Pérez-Serra A, Bonet F, Muñiz O, Fuentes F, Gonzalez-Estrada A, Campuzano O, Rodriguez Roca JS, Alonso-Villa E, Toro R. "A microRNA Signature for the Diagnosis of Statins Intolerance." International Journal of Molecular Sciences 23 (2022): 8146-. Coll M, Fernàndez-Falgueras A, Tiron C, Iglesias A, Buxó M, Simón A, Nogué-Navarro L, Moral S, Pérez-Serra A, Puigmulé M, Del Olmo B, Campuzano O, Castellà J, Picó F, Lopez L, Neto N, Corona M, Alcalde M, Brugada R. "Post-mortem toxicology analysis in a young sudden cardiac death cohort." Forensic Science International:Genetics 59 (2022): -. Tiron C; Campuzano OM Fernández-Falgueras A; Alcalde M; Loma-Osorio P; Zamora E; Caballero A; Sarquella-Brugada G; Cesar S; Garcia-Cuenllas L; García-Álvarez A; Jordà P; Arbelo E; Tomás-Querol C; Pineda V; Martínez D; Brugada "Prevalence of Pathogenic Variants in Cardiomyopathy-Associated Genes in Myocarditis." Circulation-Genomic And Precision Medicine (2022): -. Alcalde M, Nogué-Navarro L, Tiron C, Fernandez-Falgueras A, Iglesias A, Simon A, Buxó M, Pérez-Serra A, Puigmulé M, López L, Picó F, Del Olmo B, Corona M, Campuzano O, Moral S, Castella J, Coll M, Brugada R. "Rare variants in genes encoding structural myocyte contribute to a thickened ventricular septum in sudden death population without ventricular alterations." Forensic Science International:Genetics 58 (2022): -. Cruzalegui J, Cesar S, Campuzano O, Fiol V, Brugada J, Sarquella-Brugada G "Pediatric Left Posteroseptal Accessory Pathway Ablation from Giant Coronary Sinus with Persistent Left Superior Cava." Journal Of Cardiovascular Development And Disease 9 (2022): 109-. Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Pa "Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.." Nature Genetics (2022): -. Jordà P, Martínez D, Farrero M, Marcos MÁ, Sandoval E, Castel MÁ, Pereda D, Quintana E, Arbelo E, Sánchez A, Campuzano Ò, Tirón de Llano C, Brugada R, Brugada J, Castellá M, Pérez-Villa F, García-Álvarez A. "BAG3 Genetic Cardiomyopathy May Overlap Fulminant Myocarditis Clinical Findings.." Circulation-Heart Failure (2022): -. Martínez-Barrios E, Sarquella-Brugada G, Pérez-Serra A, Fernández-Falgueras A, Cesar S, Coll M, Puigmulé M, Iglesias A, Alcalde M, Vallverdú-Prats M, Ferrer-Costa C, Del Olmo B, Picó F, López L, Fiol V, Cruzalegui J, Hernánde "Discerning the Ambiguous Role of Missense TTN Variants in Inherited Arrhythmogenic Syndromes." Journal Of Personalized Medicine 12 (2022): 241-. Toro R, Pérez-Serra A, Mangas A, Campuzano O, Sarquella-Brugada G, Quezada-Feijoo M, Ramos M, Alcalá M, Carrera E, García-Padilla C, Franco D, Bonet F. "miR-16-5p Suppression Protects Human Cardiomyocytes against Endoplasmic Reticulum and Oxidative Stress-Induced Injury." International Journal of Molecular Sciences 23 (2022): 1036-. Tiron C, Ramos R, Iglesies J, Fernandez-Falgueras A, Campuzano O, Loma-Osorio P, Brugada R. "The Peguero-Lo Presti ECG criteria improve diagnostic accuracy of left ventricular hypertrophy in hypertrophic cardiomyopathy patients.." Journal Of Cardiovascular Medicine (2021): -. Georgia Sarquella‑Brugada, Anna Fernandez‑Falgueras, Sergi Cesar, Elena Arbelo, Mónica Coll, Alexandra Perez‑Serra, Marta Puigmulé, Anna Iglesias, Mireia Alcalde, Marta Vallverdú‑Prats, Victoria Fiol, "Clinical impact of rare variants associated with inherited channelopathies: a 5-year update." Human Genetics undef (2021): undef-. Costa MC, Calderon-Dominguez M, Mangas A, Campuzano O, Sarquella-Brugada G, Ramos M, Quezada-Feijoo M, Pinilla JMG, Robles-Mezcua A, Del Aguila Pacheco-Cruz G, Belmonte T, Enguita FJ, Toro R. "Circulating circRNA as biomarkers for dilated cardiomyopathy etiology." Journal of Molecular Medicine-JMM 99 (2021): 1711-1725. Lanza GA, Coll M, Grassi S, Arena V, Campuzano O, Calò L, De Ruvo E, Brugada R, Oliva A. "An enigmatic case of cardiac death in an 18-years old girl.." European Review For Medical And Pharmacological Sciences 25 (2021): 4999-5005. Sarquella-Brugada G, García-Algar O, Zambrano MD, Fernández-Falgueres A, Sailer S, Cesar S, Sebastiani G, Martí-Almor J, Aurensanz E, Cruzalegui JC, Merchan EF, Coll M, Pérez-Serra A, Del Olmo B, Fiol V, Iglesias A, Ferrer-Co "Early Identification of Prolonged QT Interval for Prevention of Sudden Infant Death.." Frontiers In Pediatrics 9 (2021): -. Diz OM, Toro R, Cesar S, Gomez O, Sarquella-Brugada G, Campuzano O. "Personalized Genetic Diagnosis of Congenital Heart Defects in Newborns." Journal Of Personalized Medicine 11 (2021): 562-. Rodríguez-Mañero M, Jordá P, Hernandez J, Muñoz C, Grima EZ, García-Fernández A, Cañadas-Godoy MV, Jiménez-Ramos V, Oloriz T, Basterra N, Calvo D, Pérez-Álvarez L, Arias MA, Expósito V, Alemán A, Díaz-Infante E, Guerra-Ramos "Long-term prognosis of women with Brugada syndrome and electrophysiological study." Heart Rhythm 18 (2021): 664-671. Grassi S, Vidal MC, Campuzano O, Arena V, Alfonsetti A, Rossi SS, Scarnicci F, Iglesias A, Brugada R, Oliva A. "Sudden Death without a Clear Cause after Comprehensive Investigation: An Example of Forensic Approach to Atypical/Uncertain Findings.." Diagnostics 11 (2021): 886-. Calderon-Dominguez M, Belmonte T, Quezada-Feijoo M, Ramos M, Calderon-Dominguez J, Campuzano O, Mangas A, Toro R. "Plasma microrna expression profile for reduced ejection fraction in dilated cardiomyopathy.." Scientific Reports 11 (2021): -. Marta Vallverdú-Prats, Mireia Alcalde, Georgia Sarquella-Brugada, Sergi Cesar, Elena Arbelo, Anna Fernandez-Falgueras, Mónica Coll, Alexandra Pérez-Serra, Marta Puigmulé, Anna Iglesias, Victoria Fiol, Carles Ferrer-Costa, Ber "Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later." Journal Of Personalized Medicine 11 (2021): 162-. Banfi P, Coll M, Oliva A, Alcalde M, Striano P, Mauri M, Princiotta L, Campuzano O, Versino M, Brugada R "Lamotrigine induced Brugada-pattern in a patient with genetic epilepsy associated with a novel variant in SCN9A." Gene (2020): -. Lahrouchi N, Tadros R, Crotti L, Mizusawa Y, Postema PG, Beekman L, Walsh R, Hasegawa K, Barc J, Ernsting M, Turkowski KL, Mazzanti A, Beckmann BM, Shimamoto K, Diamant UB, Wijeyeratne YD, Kucho Y, Robyns T, Ishikawa T, Arbel "Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome." Circulation 142 (2020): 324-338. Lopez-Sainz A, Dominguez F, Lopes LR, Ochoa JP, Barriales-Villa R, Climent V, Linschoten M, Tiron C, Chiriatti C, Marques N, Rasmussen TB, Espinosa MÁ, Beinart R, Quarta G, Cesar S, Field E, Garcia-Pinilla JM, Bilinska Z, Mui "Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis." Journal of the American College of Cardiology (2020): -. Grassi S, Campuzano O, Coll M, Brión M, Arena V, Iglesias A, Carracedo Á, Brugada R, Oliva A "Genetic variants of uncertain significance: How to match scientific rigour and standard of proof in sudden cardiac death?." Legal Medicine 45 (2020): -. Campuzano O, Sarquella-Brugada G, Arbelo E, Cesar S, Jordà P, Pérez-Serra A, Toro R, Brugada J, Brugada R. "Genetic Variants as Sudden-Death Risk Markers in Inherited Arrhythmogenic Syndromes: Personalized Genetic Interpretation." Journal of Clinical Medicine 9 (2020): 1866-. Salazar-Mendiguchía J, Díez-López C, Claver E, Cesar S, Campuzano O, Sarquella-Brugada G, Monserrat L. "Familial evaluation reveals a distinct genetic cause in a large Spanish family with neurofibromatosis 1 and hypertrophic cardiomyopathy.." Gene (2020): -. Belmonte T, Mangas A, Calderon-Dominguez M, Quezada-Feijoo M, Ramos M, Campuzano O, Gomez S, Peña ML, Cubillos-Arango AM, Dominguez F, Llorente-Cortés V, de Gonzalo-Calvo D, Toro R "Peripheral microRNA panels to guide the diagnosis of familial cardiomyopathy.." Translational Research (2020): -. Mazzanti A, Guz D, Trancuccio A, Pagan E, Kukavica D, Chargeishvili T, Olivetti N, Biernacka EK, Sacilotto L, Sarquella-Brugada G, Campuzano O, Nof E, Anastasakis A, Sansone VA, Jimenez-Jaimez J, Cruz F, Sánchez-Quiñones J, H "Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1." Journal of the American College of Cardiology (2020): -. Sarquella-Brugada G, Campuzano O, Brugada J "Paediatric arrhythmology: The challenge of the 21st century." Anales de Pediatría 92 (2020): -. Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škorić-Milosavljević D, Krijger C, Arbelo E, Babuty D, Barajas-Martinez H, Beckmann BM, Béziea "Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls." Genetics in Medicine 23 (2020): 47-58. Hernandez-Ojeda J, Arbelo E, Jorda P, Borras R, Campuzano O, Sarquella-Brugada G, Iglesias A, Mont L, Brugada R, Brugada J. "The role of clinical assessment and electrophysiology study in Brugada syndrome patients with syncope." American Heart Journal (2019): -. Herranz Barbero A, Cesar S, Martinez-Osorio J, Margarit A, Moreno J, Campuzano O, Iglesias-Platas I, Brugada J, Sarquella-Brugada G. "Long-term outcome of neonates and infants with permanent junctional reciprocating tachycardia. When cardiac ablation changes natural history." Journal of Electrocardiology 56 (2019): 85-89. Campuzano O, Sarquella-Brugada G, Cesar S, Garcia-Algar O, Brugada J, Brugada R. "Electrocardiogram in Newborns: Beneficial or Not?." Pediatric Cardiology (2019): -. Campuzano O, Fernandez-Falgueras A, Lemus X, Sarquella-Brugada G, Cesar S, Coll M, Mates J, Arbelo E, Jordà P, Perez-Serra A, Del Olmo B, Ferrer-Costa C, Iglesias A, Fiol V, Puigmulé M, Lopez L, Pico F, Brugada J, Brugada R. "Short QT Syndrome: A Comprehensive Genetic Interpretation and Clinical Translation of Rare Variants." Journal of Clinical Medicine 8 (2019): 1035-. Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Coll M, Mates J, Arbelo E, Perez-Serra A, Del Olmo B, Jordá P, Fiol V, Iglesias A, Puigmulé M, Lopez L, Pico F, Brugada J, Brugada R. "Genetic interpretation and clinical translation of minor genes related to Brugada syndrome.." Human Mutation (2019): -. Campuzano O, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Coll M, Fiol V, Iglesias A, Perez-Serra A, Mates J, Del Olmo B, Ferrer C, Alcalde M, Puigmulé M, Mademont-Soler I, Pico F, "Personalized Interpretation and Clinical Translation of Genetic Variants Associated With Cardiomyopathies.." Frontiers In Genetics 10 (2019): -. Pieroni M, Notarstefano P, Oliva A, Campuzano O, Santangeli P, Coll M, Nesti M, Carnevali A, Fraticelli A, Iglesias A, Grassi S, Brugada R, Bolognese L. "Electroanatomic and Pathologic Right Ventricular Outflow Tract Abnormalities in Patients With Brugada Syndrome.." Journal of the American College of Cardiology (2018): -. Campuzano O, Beltramo P, Fernandez A, Iglesias A, García L, Allegue C, Sarquella-Brugada G, Coll M, Perez-Serra A, Mademont-Soler I, Mates J, Del Olmo B, Rodríguez Á, Maciel N, Puigmulé M, Pico F, Cesar S, Brugada J, Cuesta A "Molecular autopsy in a cohort of infants died suddenly at rest." Forensic Science International:Genetics 37 (2018): 54-63. Scumaci D, Oliva A, Concolino A, Curcio A, Fiumara CV, Tammè L, Campuzano O, Pascali VL, Coll M, Iglesias A, Berne P, Casu G, Olivo E, Ausania F, Ricci P, Indolfi C, Brugada J, Brugada R, Cuda G. "Integration of 'Omics' Strategies for Biomarkers Discovery and for the Elucidation of Molecular Mechanisms Underlying Brugada Syndrome." Proteomics. Clinical applications 12 (2018): 1800065-. Espinosa Á, Ripollés-Melchor J, Brugada R, Campuzano Ó, Sarquella-Brugada G, Abad-Motos A, Zaballos-García M, Abad-Torrent A, Prieto-Gundin A, Brugada J. "Brugada Syndrome: anaesthetic considerations and management algorithm.." Minerva Anestesiologica (2018): -. Bonilla JC, Parra-Medina R, Chaves JJ, Campuzano O, Sarquella-Brugada G, Brugada R, Brugada J. "La autopsia molecular en la muerte súbita cardiaca = Molecular autopsy in sudden cardiac death." Archivos de Cardiología de México 88 (2018): 306-312. Brugada J, Campuzano O, Arbelo E, Sarquella-Brugada G, Brugada R. "Present Status of Brugada Syndrome: JACC State-of-the-Art Review." Journal of the American College of Cardiology 72 (2018): 1046-1059. López-Sainz Á, Salazar-Mendiguchía J, García-Álvarez A, Campuzano Larrea O, López-Garrido MÁ, García-Guereta L, Fuentes Cañamero ME, Climent Payá V, Peña-Peña ML, Zorio-Grima E, Jordá-Burgos P, Díez-López C, Brugada R, García "Clinical Findings and Prognosis of Danon Disease. An Analysis of the Spanish Multicenter Danon Registry.." Revista Española de Cardiologia (2018): -. Toro R, Blasco-Turrión S, Morales-Ponce FJ, Gonzalez P, Martínez-Camblor P, López-Granados A, Brugada R, Campuzano O, Pérez-Serra A, Rosa Longobardo F, Mangas A, Llorente-Cortes V, de Gonzalo-Calvo D. "Plasma microRNAs as biomarkers for Lamin A/C-related dilated cardiomyopathy." Journal of Molecular Medicine-JMM 96 (2018): 845-856. Coll M, Ferrer-Costa C, Pich S, Allegue C, Rodrigo E, Fernández-Fresnedo G, Barreda P, Mates J, Martinez de Francisco AL, Ortega I, Iglesias A, Campuzano O, Salas E, Arias M, Brugada R. "Role of genetic and electrolyte abnormalities in prolonged QTc interval and sudden cardiac death in end-stage renal disease patients." PLoS One 13 (2018): e0200756-. Wangüemert Pérez F; Hernández Afonso JS; Groba Marco MDV; Caballero Dorta E; Álvarez Acosta L; Campuzano Larrea O; Pérez G; Brugada Terradellas J; Brugada Terradellas R. "Flecainide Reduces Ventricular Arrhythmias in Patients With Genotype RyR2-positive Catecholaminergic Polymorphic Ventricular Tachycardia.." Revista Española de Cardiologia (2018): -. Mates, J; Mademont-Soler, I; del Olmo, B; Ferrer-Costa, C; Coll, M; Pérez-Serra, A; Picó, F; Allegue, C; Fernandez-Falgueras, A; Álvarez, P; Yotti, R; Espinosa, MA; Sarquella-Brugada, G; Cesar, S; Carro, E; Brugada, J; Arbelo "Role of Copy Number Variants in sudden cardiac death and related diseases: genetic analysis and translation into clinical practice." European Journal of Human Genetics 26 (2018): 1014-1025. Coll, Mònica; Pérez-Serra, Alexandra; Del Olmo, Bernat; Puigmulé, Marta; Fernandez-Falgueras, Anna; Iglesias, Anna; Picó, Ferran, Lopez, Laura; Brugada, Ramon; Campuzano, Oscar "Incomplete Penetrance and Variable Expressivity: Hallmarks in Channelopathies Associated with Sudden Cardiac Death." Biology 7 (2017): 3-. Coll M, Striano P, Ferrer-Costa C, Campuzano O, Matés J, Del Olmo B, Iglesias A, Pérez-Serra A, Mademont I, Picó F, Oliva A, Brugada R. "Targeted next-generation sequencing provides novel clues for associated epilepsy and cardiac conduction disorder/SUDEP." PLoS One 12 (2017): e0189618-. Hernandez-Ojeda J;Arbelo E;Borras R;Berne P;Tolosana JM;Gomez-Juanatey A;Berruezo A;Campuzano O;Sarquella-Brugada G;Mont L;Brugada R;Brugada J "Patients With Brugada Syndrome and Implanted Cardioverter-Defibrillators: Long-Term Follow-Up." Journal of the American College of Cardiology 70 (2017): 1991-2002. Campuzano O;Sanchez-Molero O;Fernandez A;Mademont-Soler I;Coll M;Perez-Serra A;Mates J;Del Olmo B;Pico F;Nogue-Navarro L;Sarquella-Brugada G;Iglesias A;Cesar S;Carro E;Borondo JC;Brugada J;Castellà J; Medallo J;Brugada R. "Sudden Arrhythmic Death During Exercise: A Post-Mortem Genetic Analysis." Sports Medicine 47 (2017): 2101-2115. Mademont Soler, Irene ; Matés Ramírez, Jesús ; Yotti, Raquel ; Espinosa, Maria Angeles ; Pérez Serra, Alexandra ; Fernandez Avila, Ana Isabel ; Coll, Monica ; Méndez, Irene ; Iglesias, Anna ; Olmo, Bernat del ; Riuró Cáceres, "Additional value of screening for minor genes and copy number variants in hypertrophic cardiomyopathy." PLoS One 12 (2017): e0181465-. van der Steld LP;Campuzano O;Pérez-Serra A;Moura de Barros Zamorano M;Sousa Matos S;Brugada R "Wolff-Parkinson-White Syndrome with Ventricular Hypertrophy in a Brazilian Family." American Journal of case Reports 18 (2017): 766-776. Villalba-Orero M;Sánchez-Elexpuru G;López-Olañeta M;Campuzano O;Bello-Arroyo E;García-Pavía P;Serratosa JM;Brugada R;Sánchez MP;Lara-Pezzi E "Lafora Disease Is an Inherited Metabolic Cardiomyopathy." Journal of the American College of Cardiology 69 (2017): 3006-3013. D'Ovidio C;Carnevale A;Grassi VM;Rosato E;Del Olmo B;Coll M;Campuzano O;Iglesias A;Brugada R;Oliva A "Sudden death due to catecholaminergic polymorphic ventricular tachycardia following negative stress-test outcome: genetics and clinical implications." Forensic Science Medicine And Pathology (2017): -. Pereira R; Campuzano O; Sarquella-Brugada G; Cesar S; Iglesias A; Brugada J; Cruz Filho FES; Brugada R "Short QT syndrome in pediatrics." Clinical Research In Cardiology 106 (2017): 393-400. Gigli L;Bertero G;Vidal MC;Iglesias A;Campuzano O;Striano P;Oliva A;Brugada R. "Juvenile myoclonic epilepsy and Brugada type 1 ECG pattern associated with (a novel) plakophillin 2 mutation." Journal of Neurology (2017): -. Oscar Campuzano; Olallo Sanchez-Molero; Irene Mademont-Soler; Monica Coll; Catarina Allegue; Carles Ferrer-Costa; Jesus Mates; Alexandra Perez-Serra; Bernat del Olmo; Anna Iglesias; Georgia Sarquella-Brugada; Josep Brugada; J "Genetic analysis in post-mortem samples with micro-ischemic alterations." Forensic Science International 271 (2017): 120-125. Alejandra Restrepo-Cordoba M;Campuzano O;Ripoll-Vera T;Cobo-Marcos M;Mademont-Soler I;Gámez JM;Dominguez F;Gonzalez-Lopez E;Padron-Barthe L;Lara-Pezzi E;Alonso-Pulpon L;Brugada R;Garcia-Pavia P "Usefulness of Genetic Testing in Hypertrophic Cardiomyopathy: an Analysis Using Real-World Data." Journal Of Cardiovascular Translational Research (2017): -. Fernández-Falgueras, A; Sarquella-Brugada, G.; Brugada, J.; Brugada R.C.; Campuzano, O "Cardiac Channelopathies and Sudden Death: Recent Clinical and Genetic Advances." Biology 6 (2017): art. 7-. Bosch C;Campuzano O;Sarquella-Brugada G;Cesar S;Perez-Serra A;Coll M;Mademont I;Mates J;Del Olmo B;Iglesias A;Brugada J;Petersen V;Brugada R "A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia." Forensic Science International 270 (2017): 173-177. Sánchez, Olallo ; Campuzano Larrea, Oscar ; Fernández-Falgueras, Anna ; Sarquella-Brugada, Georgia ; Cesar, Sergi ; Mademont-Soler, Irene ; Matés Ramírez, Jesús ; Pérez Serra, Alexandra ; Coll, Monica ; Picó, Ferran ; Iglesia "Natural and Undetermined Sudden Death: Value of Post-Mortem Genetic Investigation." PLoS One 11 (2016): e0167358-. Pérez-Serra A, Toro R, Sarquella-Brugada G, de Gonzalo-Calvo D, Cesar S, Carro E, Llorente-Cortes V, Iglesias A, Brugada J, Brugada R, Campuzano O. "Genetic basis of dilated cardiomyopathy." International Journal of Cardiology 224 (2016): 461-472. Izquierdo I; Rosa I; Bravo SB; Guitián E; Pérez-Serra A; Campuzano O; Brugada R; Mangas A,; García Á; Toro R "Proteomic identification of putative biomarkers for early detection of sudden cardiac death in a family with a LMNA gene mutation causing dilated cardiomyopathy." Journal of Proteomics 148 (2016): 75-84. Mademont-Soler, Irene ; Pinsach-Abuin, Mel·lina ; Riuró Cáceres, Helena ; Matés Ramírez, Jesús ; Pérez Serra, Alexandra ; Coll, Monica ; Porres, José M. ; Olmo, Bernat del ; Iglesias, Anna ; Selga Coma, Elisabet ; Picó, Ferra "Large Genomic Imbalances in Brugada Syndrome." PLoS One 11 (2016): e0163514-. Javier Moncayo-Arlandi; Eduard Guasch; Maria Sanz, Marta Casado; Nahuel Aquiles Garcia; Lluis Mont; Marta Sitges; Ralph Knoll; Byambajav Buyandelger; Oscar Campuzano; Antonio Diez-Juan; Ramon Brugada "Molecular disturbance underlies to arrhythmogenic cardiomyopathy induced by transgene content, age and exercise in a truncated PKP2 mouse model." Human Molecular Genetics 25 (2016): 3676-3688. Rocio Toro; Alexandra Pérez-Serra; Oscar Campuzano; Javier Moncayo-Arlandi; Catarina Allegue; Anna Iglesias; Alipio Mangas; Ramon Brugada "Familial dilated cardiomyopathy caused by a novel frameshift in the BAG3 gene." PLoS One (2016): -. Campuzano, O; Fernández-Falgueras, A; Iglesias, A, Brugada, R. "Brugada Syndrome and PKP2: Evidences and uncertainties." International Journal of Cardiology 214 (2016): 403-405. Oliva A, Grassi VM, Campuzano O, Brion M, Arena V, Partemi S, Coll M, Pascali VL, Brugada J, Carracedo A, Brugada R. "Medico-legal perspectives on sudden cardiac death in young athletes." International Journal of Legal Medicine 131 (2016): 393-409. Sarquella-Brugada, G; Campuzano, O; Cesar, S; Iglesias, A; Fernandez, A; Brugada, J; Brugada, R. "Sudden infant death syndrome caused by cardiac arrhythmias: only a matter of genes encoding ion channels?." International Journal of Legal Medicine 130 (2016): 415-420. Coll, M; Allegue, C; Partemi, S; Mates, J; Del Olmo, B; Campuzano, O; Pascali, V; Iglesias, A; Striano, P; Oliva, A; Brugada, R "Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing." International Journal of Legal Medicine (2016): 331-339. Campuzano O; Fernández-Falgueras A; Sarquella-Brugada G; Sanchez O; Cesar S; Mademont I; Allegue C; Mates J; Pérez-Serra A; Coll M; Alcalde M; Iglesias A; Tiron C; Gallego MÁ; Ferrer-Costa C; Hospital A; Escribano C; Dasí C; "A Genetically Vulnerable Myocardium May Predispose to Myocarditis." Journal of the American College of Cardiology 66 (2015): 2913-2914. Campuzano O; Brugada R "Age, Genetics, and Fibrosis in the Brugada Syndrome." Journal of the American College of Cardiology 66 (2015): 1987-1989. Campuzano, O; Sanchez-Molero, O; Mademont-Soler, I; Riuró, H; Allegue, C; Coll, M; Pérez-Serra, A; Mates, J; Picó, F; Iglesias, A; Brugada, R. "Rare Titin (TTN) Variants in Diseases Associated with Sudden Cardiac Death." International Journal of Molecular Sciences 16 (2015): 25773-25787. Campuzano, O; Sarquella-Brugada, G; Brugada, R; Brugada, J "Genetics of channelopathies associated with sudden cardiac death." Global Cardiology Science and Practice 2015 (2015): 39-. Allegue, C; Coll, M; Mates, J; Campuzano, O; Iglesias, A; Sobrino, B; Brion, M; Amigo, J; Carracedo, A; Brugada, P; Brugada, J; Brugada, R. "Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome." PLoS One 10 (2015): e0133037-. Selga Coma, Elisabet; Campuzano Larrea, Oscar; Pinsach-Abuin, Mel·lina; Pérez Serra, Alexandra; Mademont-Soler, Irene; Riuró Cáceres, Helena; Picó, Ferran; Coll, Monica; Iglesias, Anna; Pagans i Lista, Sara; Sarquella-Brugada "Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort." PLoS One 10 (2015): e0132888-. Wangüemert, F; Bosch Calero, C; Pérez, C; Campuzano, O; Beltran-Alvarez, P; Scornik, FS; Iglesias, A; Berne, P; Allegue, C; Ruiz Hernandez, P; Brugada, J; Pérez, GJ; Brugada, R "Clinical and molecular characterization of a cardiac ryanodine receptor founder mutation causing catecholaminergic polymorphic ventricular tachycardia." Heart Rhythm 12 (2015): 1636-1643. Blancafort, A; Giro-Perafita, A; Oliveras, G; Palomeras, S; Turrado, C; Campuzano, O; Carrion-Salip, D; Massaguer, A; Brugada, R; Palafox, M; Gomez-Miragaya, J; Gonzalez-Suarez, E; Puig, T "Dual Fatty Acid Synthase and HER2 Signaling Blockade Shows Marked Antitumor Activity against Breast Cancer Models Resistant to Anti-HER2 Drugs." PLoS One 10 (2015): e0131241-. Sarquella-Brugada, G; Campuzano, O; Arbelo, E; Brugada, J; Brugada, R "Brugada syndrome: clinical and genetic findings." Genetics in Medicine 18 (2015): 3-12. Campuzano O; Allegue C; Fernandez A; Iglesias A; Brugada R. "Determining the Pathogenicity of Genetic Variants Associated with Cardiac Channelopathies." Scientific Reports (2015): Art.núm:7953-. Alcalde, M; Campuzano, O; Sarquella-Brugada, G; Arbelo, E; Allegue, C; Partemi, S; Iglesias, A; Oliva, A; Brugada, J; Brugada, R. "Clinical interpretation of genetic variants in arrhythmogenic right ventricular cardiomyopathy." Clinical Research In Cardiology 104 (2015): 288-303. Riuró, H; Campuzano, O; Berne, P; Arbelo, E; Iglesias, A; Pérez-Serra, A; Coll-Vidal, M; Partemi, S; Mademont-Soler, I; Picó, F; Allegue, C; Oliva, A; Gerstenfeld, E; Sarquella-Brugada, G; Castro-Urda, V; Fernández-Lozano, I; "Genetic analysis, in silico prediction and family segregation in Long QT Syndrome." European Journal of Human Genetics 23 (2015): 79-85. Coloma Tiron de Llano; Oscar Campuzano; Alexandra Pérez-Serra; Irene Mademont; Monica Coll; Catarina Allegue; Anna Iglesias; Sara Partemi; Pasquale Striano; Antonio Oliva; Ramon Brugada "Further evidence of the association between LQT syndrome and epilepsy in a family with KCNQ1 pathogenic variant." Seizure-European Journal of Epilepsy 25 (2015): 65-67. Cittadini, Francesca; Giovanni, Nadia De; Alcalde, Mireia; Partemi, Sara; Campuzano, Oscar; Brugada, Ramon; Oliva, Antonio "Genetic and toxicologic investigation of Sudden Cardiac Death in a patient with Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) under cocaine and alcohol effects." International Journal of Legal Medicine 129 (2014): 89-96. Campuzano O; Sarquella-Brugada G; Mademont-Soler I; Allegue C; Cesar S; Ferrer-Costa C; Coll M; Mates J; Iglesias A; Brugada J; Brugada R "Identification of genetic alterations, as causative genetic defects in long qt syndrome, using next generation sequencing technology.." PLoS One 9 (2014): e114894-. Lenises de Paula van der Steld, Oscar Campuzano, Ramon Brugada, Mario de Seixas Rocha "A novel mutation in the PRKAG2 gene, associated with cardiac arrest, congestive heart failure and multiple accessory pathways." Revista Latino-Americana de Marcapasso e Arritmias (2014): -. Cristina Bosch, Oscar Campuzano, Georgia Sarquella-Brugada, Elena Arbelo, Catarina Allegue, Anna Iglesias, Pablo M. Ruiz-Hernández, Fernando Wanguemert, Josep Brugada, Ramon Brugada "Genetics of Catecholaminergic Polymorphic Ventricular Tachycardia.." Journal of Gene Therapy for Genetic Disorders (2014): -. Campuzano O; Sanchez-Molero O; Allegue C; Coll M; Mademont-Soler I; Selga E; Ferrer-Costa C; Mates J; Iglesias A; Sarquella-Brugada G; Cesar S; Brugada J; Castellà J; Medallo J; Brugada R "Post-mortem genetic analysis in juvenile cases of sudden cardiac death.." Forensic Science International 245 (2014): 30-37. Campuzano O; Allegue C; Sarquella-Brugada G; Coll M; Mates J; Alcalde M; Ferrer-Costa C; Iglesias A; Brugada J; Brugada R "The Role of clinical, genetic and segregation evaluation in sudden infant death." Forensic Science International 242 (2014): 9-15. Riuró, H; Campuzano, O; Arbelo, E; Iglesias, A; Batlle, M; Pérez-Villa, F; Brugada, J; Pérez, GJ; Scornik, FS; Brugada, R. "A missense mutation in the sodium channel β1b subunit reveals SCN1B as a susceptibly gene underlying LQT Syndrome." Heart Rhythm 11 (2014): 1202-1209. Pérez-Serra, A; Toro, R; Campuzano, O; Sarquella-Brugada, G; Berne, P; Iglesias, A; Mangas, A; Brugada, J; Brugada, R. "A novel mutation in Lamin A/C causing familial dilated cardiomyopathy associated with sudden cardiac death." Journal of Cardiac Failure 21 (2014): 217-225. Alcalde M, Campuzano O, Allegue C, Torres M, Arbelo E, Partemi S, Iglesias A, Brugada J, Oliva A, Carracedo A, Brugada R "Sequenom MassARRAY approach in the arrhythmogenic right ventricular cardiomyopathy post-mortem setting: clinical and forensic implications." International Journal of Legal Medicine 129 (2014): 1-10. Partemi S; Vidal MC; Striano P; Campuzano O; Allegue C; Pezzella M; Elia M; Parisi P; Belcastro V; Casellato S; Giordano L; Mastrangelo M; Pietrafusa N; Striano S; Zara F; Bianchi A; Buti D; La Neve A; Tassinari CA; Oliva A; "Genetic and forensic implications in epilepsy and cardiac arrhythmias: a case series." International Journal of Legal Medicine 129 (2014): 495-504. Brugada R, Campuzano O, Sarquella-Brugada G, Brugada J, Brugada P "Brugada syndrome." Methodist DeBakey Cardiovascular Journal 10 (2014): 25-28. Campuzano, O; Allegue, C; Partemi, S; Iglesias, A; Oliva, A; Brugada R. "Negative autopsy and sudden cardiac death." International Journal of Legal Medicine 128 (2014): 599-606. Campuzano, O; Berne, P; Selga, E; Allegue, C; Iglesias, A; Brugada, J; Brugada, R. "Brugada syndrome and p.E61X_RANGRF." Cardiology Journal 21 (2014): 121-127. Fernando Wangüemert-Pérez MD, PhD, Pablo M. Ruiz-Hernández MD, Oscar Campuzano PhD, Eduardo Caballero-Dorta, PhD, Cristina Bosch MSc, Josep Brugada MD, PhD, Ramon Brugada MD, PhD "Flecainide in patient with aggressive catecholaminergic polymorphic ventricular tachycardia due to novel RYR2 mutation." Minerva Cardioangiologica 62 (2014): 363-366. 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 "Stop-gain mutations in PKP2 are associated with a later age of onset of arrhythmogenic right ventricular cardiomyopathy." PLoS One 9 (2014): e100560-. Campuzano O, Alcalde M, Berne P, Zorio E, Iglesias A, Navarro-Manchon J, Brugada J, Brugada R "Role of novel DSP_p.Q986X genetic variation in arrhythmogenic right ventricular cardiomyopathy." European Journal of Medical Genetics (Títol anterior: Annales de Génétique) 56 (2013): 541-545. Riuró, H; Beltran-Alvarez, P; Tarradas, A; Selga, E; Campuzano, O; Vergés, M; Pagans, S; Iglesias, A; Brugada, J; Brugada, P; Vázquez, FM; Pérez, GJ; Scornik, FS; Brugada R. "A missense mutation in the sodium channel β2 subunit reveals SCN2B as a new candidate gene for Brugada Syndrome." Human Mutation 34 (2013): 961-966. Campuzano, O; Alcalde, M; Allegue, C; Iglesias, A; García-Pavía, P; Partemi, S; Oliva, A; Pascali, VL; Berne, P; Sarquella-Brugada, G; Brugada, J; Brugada, P; Brugada, R. "Genetics of arrhythmogenic right ventricular cardiomyopathy." Journal of Medical Genetics 50 (2013): 280-289. Noris, M; Carrillo, A; Campuzano, O; Santaella, A; Brugada, R; García-Niebla, J; Fiol, M. "Syncope and polymorphic ventricular tachycardia in the setting of a febrile illness." Journal of Electrocardiology 46 (2013): 666-669. Anna Tarradas; Elisabet Selga; Pedro Beltran-Alvarez, Alexandra Pérez-Serra; Helena Riuró; Ferran Picó; Anna Iglesias; Oscar Campuzano; Victor Castro-Urda; Ignasio Fernández-Lozano; Guillermo J. Pérez; Fabiana S. Scornik FS; "A Novel missense mutation, I890T, in the pore region of cardiac sodium channel causes Brugada Syndrome." PLoS One 8 (2013): Epub-. Parisi; P; Oliva, A; Coll, M; Partemi, S; Campuzano, O; Iglesias, A; Pisani, D; Pascali, V; Villa, M; Paolino, M; Zara, F; Tassinari, C; Striano, P; Brugada, R. "Coexistence of epilepsy and Brugada syndrome in a family with SCN5A mutation." Epilepsy Research 105 (2013): 415-418. Partemi, S; Cestele, S; Pezzella, M; Campuzano, O; Paravidino, R; Pascali, V; Zara, F; Tassinari, CA; Striano, S; Oliva, A; Brugada, R; Mantegazza, M; Striano, P. "Loss of function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.." Epilepsia 54 (2013): e112-e116. S. Partemi, M. Coll Vidal, O. Campuzano, M. Pezzella, R. Paravidino, V.L. Pascali, C.A. Tassinari, S. Striano, F. Zara, R. Brugada, P. Striano, A. Oliva "Importance of post-mortem genetic testing in SUDEP patients." Forensic Science International:Genetics (2013): -. Allegue C, Campuzano O, Castillo S, Coll M, Iglesias A, Brugada R "New diagnostic tools in genetics of sudden cardiac death." Revista Española de Cardiologia (2012): -. Campuzano O; Alcalde M; Iglesias A; Barahona-Dussault C; Sarquella-Brugada G; Benito B; Arzamendi D; Flores J; Leung TK; Talajic M; Oliva A; Brugada R. "Arrhythmogenic right ventricular cardiomyopathy: severe structural alterations are associated with inflammation.." Journal of Clinical Pathology (2012): -. Cho T, Aguettaz P, Campuzano O, Charriaut-Marlangue C, Riou A, Berthezène Y, Nighoghossian N, Ovize M, Wiart M, Chauveau F "Pre- and post-treatment with cyclosporine A in a rat model of transient focal cerebral ischaemia with multimodal MRI screening." International Journal of Stroke (2012): -. Brion M, Allegue C, Santori M, Gil R, Haas C, Bartsch C, Poster S, Madea B, Campuzano O, Brugada R, Carracedo A "Sarcomeric gene mutations in sudden infant death syndrome (SIDS)." Forensic Science International (2012): -. Campuzano O; Alcalde M; Berne P; Castro V; Guzzo G; Iglesias A; Alonso-Pulpon L; Garcia-Pavia P, Brugada J; Brugada R "Genetic Testing of Candidate Genes in Arrhythmogenic Right Ventricular Cardiomyopathy/ Dysplasia." European Journal of Medical Genetics (Títol anterior: Annales de Génétique) 55 (2012): -. Campuzano O, Castillo-Ruiz MM, Acarin L, Castellano B and Gonzalez B "Decreased myeloperoxidase expressing cells in the aged rat brain after excitotoxic damage." Experimental Gerontology (2011): -. Oliva A, Flores J, Merigioli S, Leduc L, Benito B, Partemi S, Arzamendi D, Campuzano O, Leung TL, Iglesias A, Talajic M, Pascali VL, Brugada R. "Autopsy investigation and Bayesian approach to coronary artery disease in victims of motor-vehicle accidents.." Atherosclerosis (2011): -. Arzamendi D, Benito B, Tizon-Marcos H, Flores J, Tanguay JF, Ly H, Doucet S, Leduc L, Leung TK, Campuzano O, Iglesias A, Talajic M, Brugada R "Increase in sudden death from coronary artery disease in young adults.." American Heart Journal (2011): -. Barahona-Dussault C, Benito B, Campuzano O, Iglesias A, Li Leung T, Robb L, Talajic M, Brugada R. "Role of genetic testing in arrhythmogenic right ventricular cardiomyopathy/dysplasia.." Clinical Genetics (2010): -. Oliveras G; Blancafort A; Urruticoechea A; Campuzano O; Gómez-Cabello D; Brugada R; López-Rodríguez ML; Colomer R; Puig T "Novel Anti-FASN (Fatty Acid Synthase) Compounds with Anti-Cancer Activity in HER2+ Breast Cancer." Annals of the New York Academy of Sciences 1210 (2010): 86-92. Campuzano O, Castillo-Ruiz MM, Acarin L, Castellano B and Gonzalez B "Increased levels of proinflammatory cytokines in the aged cortex and striatum, but moderate induction after excitotoxic damage.." Journal of Neuroscience Research (2009): -. Sànchez J, Campuzano O, Iglesias A, Brugada R. "Genetics and sport." Apunts Medicina de l'Esport (2009): -. Campuzano O, Castillo-Ruiz MM, Acarin L, Castellano B and Gonzalez B "Distinct patterns of microglial response, cyclooxygenase-2 (COX2) and inducible nitric oxide synthase (iNOS) expression after excitotoxic damage to the aged rat brain." Journal of Neuroscience Research (2008): -. Castillo-Ruiz MM, Campuzano O, Acarin L, Castellano B and Gonzalez B "Delayed neurodegeneration and early astrogliosis after excitotoxicity to the aged brain.." Experimental Gerontology (2007): -.
Alcalde M, Toro R, Bonet F, Córdoba-Caballero J, Martínez-Barrios E, Ranea JA, Vallverdú-Prats M, Brugada R, Meraviglia V, Bellin M, Sarquella-Brugada G, Campuzano O "Role of MicroRNAs in Arrhythmogenic Cardiomyopathy: translation as biomarkers into clinical practice." Translational Research 259 (2023): 72-82. Grassi S, Campuzano O, Cazzato F, Coll M, Puggioni A, Zedda M, Arena V, Iglesias A, Sarquella-Brugada G, Pinchi V, Brugada R, Oliva A. "Postmortem diagnosis of Takotsubo syndrome on autoptic findings: is it reliable? A systematic review." Cardiovascular Pathology 65 (2023): -. Díez-Escuté N, Arbelo E, Martínez-Barrios E, Cerralbo P, Cesar S, Cruzalegui J, Chipa F, Fiol V, Zschaeck I, Hernández C, Campuzano O, Sarquella-Brugada G "Sex differences in Long QT Syndrome." Frontiers In Cardiovascular Medicine 10 (2023): -. Martínez-Barrios E, Grassi S, Brión M, Toro R, Cesar S, Cruzalegui J, Coll M, Alcalde M, Brugada R, Greco A, Ortega-Sánchez ML, Barberia E, Oliva A, Sarquella-Brugada G, Campuzano O "Molecular autopsy: Twenty years of post-mortem diagnosis in sudden cardiac death." Frontiers In Medicine 10 (2023): -. Sarquella-Brugada, G., Martínez-Barrios, E., Cesar, S., Arbelo, E., Diez, C., Campuzano, O "Deporte y síndromes arritmogénicos hereditarios (Sport and inherited arrhythmogenic syndromes)." Retos: nuevas tendencias en educación física, deporte y recreación 51 (2023): 719-725. Alonso-Villa E, Bonet F, Hernandez-Torres F, Campuzano Ó, Sarquella-Brugada G, Quezada-Feijoo M, Ramos M, Mangas A, Toro R. "The Role of MicroRNAs in Dilated Cardiomyopathy: New Insights for an Old Entity." International Journal of Molecular Sciences 23 (2022): 13573-. Antonio Oliva; Simone Grassi; Vilma Pinchi; Francesca Cazzato; Mónica Coll; Mireia Alcalde; Marta Vallverdú-Prats; Alexandra Perez-Serra; Estefanía Martínez-Barrios; Sergi Cesar; Anna Iglesias; José Cruzalegui; Clara Hernánde "Structural Heart Alterations in Brugada Syndrome: Is it Really a Channelopathy? A Systematic Review." Journal of Clinical Medicine 11 (2022): 4406-. Martínez-Barrios E, Arbelo E, Cesar S, Cruzalegui J, Fiol V, Díez-Escuté N, Hernández C, Brugada R, Brugada J, Campuzano O, Sarquella-Brugada G. "Brugada Syndrome in Women: What Do We Know After 30 Years?." Frontiers In Cardiovascular Medicine 9 (2022): -. Martínez-Barrios E, Cesar S, Cruzalegui J, Hernandez C, Arbelo E, Fiol V, Brugada J, Brugada R, Campuzano O, Sarquella-Brugada G. "Clinical Genetics of Inherited Arrhythmogenic Disease in the Pediatric Population." Biomedicines 10 (2022): 106-. Meraviglia V, Alcalde M, Campuzano O, Bellin M. "Inflammation in the Pathogenesis of Arrhythmogenic Cardiomyopathy: Secondary Event or Active Driver?." Frontiers In Cardiovascular Medicine (2021): -. Grassi S, Campuzano O, Coll M, Cazzato F, Sarquella-Brugada G, Rossi R, Arena V, Brugada J, Brugada R, Oliva A. "Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies." International Journal of Molecular Sciences 22 (2021): 4124-. Sarquella-Brugada G, Fernandez-Falgueras A, Cesar S, Arbelo E, Jordà P, García-Álvarez A, Cruzalegui JC, Merchan EF, Fiol V, Brugada J, Brugada R, Campuzano O. "Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation.." Frontiers In Pediatrics 8 (2021): -. Jordà P, Toro R, Diez C, Salazar-Mendiguchía J, Fernandez-Falgueras A, Perez-Serra A, Coll M, Puigmulé M, Arbelo E, García-Álvarez A, Sarquella-Brugada G, Cesar S, Tiron C, Iglesias A, Brugada J, Brugada R, Campuzano O. "Malignant Arrhythmogenic Role Associated with RBM20: A Comprehensive Interpretation Focused on a Personalized Approach." Journal Of Personalized Medicine 11 (2021): 130-. Campuzano O, Sarquella-Brugada G, Cesar S, Arbelo E, Brugada J, Brugada R "Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?." International Journal of Molecular Sciences 21 (2020): 7155-. Campuzano O, Sarquella-Brugada G, Fernandez-Falgueras A, Coll M, Iglesias A, Ferrer-Costa C, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Tiron de Llano C, Grassi S, Oliva A, Brugada J, Brugada R "Reanalysis and reclassification of rare genetic variants associated with inherited arrhythmogenic syndromes." Ebiomedicine 54 (2020): -. Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, Cesar S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol V, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C "Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?." Forensic Science International:Genetics (2020): -. Coll M, Oliva A, Grassi S, Brugada R, Campuzano O. "Update on the Genetic Basis of Sudden Unexpected Death in Epilepsy." International Journal of Molecular Sciences 20 (2019): 8-. Campuzano O, Sarquella-Brugada G, Cesar S, Arbelo E, Brugada J, Brugada R. "Recent Advances in Short QT Syndrome." Frontiers In Cardiovascular Medicine 5 (2018): 149-. Sarquella-Brugada G, Cesar S, Zambrano MD, Fernandez-Falgueras A, Fiol V, Iglesias A, Torres F, Garcia-Algar O, Arbelo E, Brugada J, Brugada R, Campuzano O. "Electrocardiographic Assessment and Genetic Analysis in Neonates: a Current Topic of Discussion.." Current Cardiology Reviews (2018): -. Oscar Campuzano;Olallo Sanchez-Molero;Anna Fernandez;Anna Iglesias;Ramón Brugada "Muerte súbita cardiaca de origen arrítmico: valor del análisis genético post mortem." Revista Española de Medicina Legal (2017): -. Pérez-Serra A;Campuzano O;Brugada R. "Update about atrial fibrillation genetics." Current Opinion in Cardiology (2017): -. de Gonzalo-Calvo D;Quezada M;Campuzano O;Perez-Serra A;Broncano J;Ayala R;Ramos M;Llorente-Cortes V;Blasco-Turrión S;Morales FJ;Gonzalez P;Brugada R;Mangas A;Toro R "Familial dilated cardiomyopathy: A multidisciplinary entity, from basic screening to novel circulating biomarkers." International Journal of Cardiology 228 (2016): 870-880. Campuzano, O; Sarquella-Brugada, G; Cesar, S; Iglesias, A; Arbelo, E; Brugada, J; Brugada, R. "Genetics of inherited arrhythmias in pediatrics." Current Opinion in Pediatrics 27 (2015): 665-674. Campuzano O, Riuro H, Allegue C, Mademont I, Iglesias A, Brugada R "Genetics of Long QT Syndrome." Experimental & Clinical Cardiology (2014): -. Campuzano O, Allegue C, Brugada R "Genética de la Muerte Súbita Cardíaca." Medicina Clinica (2013): -. Campuzano O, Allegue C, Iglesias A, Brugada R "Genetic basis of Brugada syndrome." Journal of Genetic Syndromes and Gene Therapy (2013): -. Sarquella-Brugada G, Campuzano O, Iglesias A, Sánchez J, Brugada R "Genetics of sudden death in children and young during exercise.." Cardiology in the Young (2012): -. Sarquella-Brugada G, Campuzano O, Brugada R "Trastornos del ritmo cardíaco más frecuentes en pediatría: Síndrome de QT largo." pediatria inetgral (2012): -. Campuzano O; Beltrán-Alvarez P; Iglesias A; Scornik F; Pérez G; Brugada R "Genetics and cardiac channelopathies." Genetics in Medicine 12 (2010): 260-267. Campuzano O, Brugada R, Iglesias A. "Genetics of Brugada Syndrome." Current Opinion in Cardiology (2010): -. Campuzano O, Brugada R. "Genetics of familial atrial fibrillation." EP-Europace (2009): -. Campuzano O, Sarquella-Brugada G, Brugada R, Brugada P, Brugada J. "Cardiovascular translational medicine: genetic basis of malignant arrhythmias and cardiomyopathies.." Revista Española de Cardiologia (2009): -.