Publications
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                        Heying R, Albert DC, Voges I, Sendzikaite S, Sarquella-Brugada G, Pluchinotta F, Brzezinska-Rajszys G, Stein JI and Milanesi O. Association for European Paediatric and Congenital Cardiology recommendations for basic training in paediatric and congenital cardiology 2020CARDIOLOGY IN THE YOUNG . 30(11): 1572-1587. Number of citations: 15 
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                        Moore JP, Gallotti RG, Shannon KM, Bos JM, Sadeghi E, Strasburger JF, Wakai RT, Horigome H, Clur SA, Hill AC, Shah MJ, Behere S, Sarquella-Brugada G, Czosek R, Etheridge SP, Fischbach P, Kannankeril PJ, Motonaga K, Landstrom AP, Williams M, Patel A, Dagradi F, Tan RB, Stephenson E, Krishna MR, Miyake CY, Lee ME, Sanatani S, Balaji S, Young ML, Siddiqui S, Schwartz PJ, Shivkumar K and Ackerman MJ. Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT SyndromeJACC-CLINICAL ELECTROPHYSIOLOGY . 6(12): 1561-1570. Number of citations: 30 
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                        Campuzano O, Sarquella-Brugada G, César-Díaz S, Arbelo E, Brugada-Terradellas J and Brugada R. Update on Genetic Basis of Brugada Syndrome: Monogenic, Polygenic or Oligogenic?INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 21(19): . Number of citations: 36 
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                        París-Coderch, L, Soriano, A, Jiménez, C, Erazo, T, Muñoz-Guardiola, P, Masanas, M, Antonelli, R, Boloix, A, Alfón, J, Pérez-Montoyo, H, Yeste-Velasco, M, Domènech, C, Roma, J, Sanchez deToledo J, Moreno, L, Lizcano, JM, Gallego, S and Segura, MF. The antitumour drug ABTL0812 impairs neuroblastoma growth through endoplasmic reticulum stress-mediated autophagy and apoptosisCELL DEATH & DISEASE . 11(9): . Number of citations: 10 
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                        Abulí M, Grazioli G, Sanz de la Garza M, Montserrat S, Vidal B, Doltra A, Sarquella-Brugada G, Bellver M, Pi R, Brotons D, Oxborough D and Sitges M. Aortic root remodelling in competitive athletesEUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY . 27(14): 1518-1526. Number of citations: 15 
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                        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, Arbelo E, Christiansen M, Winbo A, Jabbari R, Lubitz SA, Steinfurt J, Rudic B, Loeys B, Shoemaker MB, Weeke PE, Pfeiffer R, Davies B, Andorin A, Hofman N, Dagradi F, Pedrazzini M, Tester DJ, Bos JM, Sarquella-Brugada G, Campuzano Ó, Platonov PG, Stallmeyer B, Zumhagen S, Nannenberg EA, Veldink JH, van den Berg LH, Al-Chalabi A, Shaw CE, Shaw PJ, Morrison KE, Andersen PM, Müller-Nurasyid M, Cusi D, Barlassina C, Galan P, Lathrop M, Munter M, Werge T, Ribasés M, Aung T, Khor CC, Ozaki M, Lichtner P, Meitinger T, van Tintelen JP, Hoedemaekers Y, Denjoy I, Leenhardt A, Napolitano C, Shimizu W, Schott JJ, Gourraud JB, Makiyama T, Ohno S, Itoh H, Krahn AD, Antzelevitch C, Roden DM, Saenen J, Borggrefe M, Odening KE, Ellinor PT, Tfelt-Hansen J, Skinner JR, van den Berg MP, Olesen MS, Brugada-Terradellas J, Brugada R, Makita N, Breckpot J, Yoshinaga M, Behr ER, Rydberg A, Aiba T, Kääb S, Priori SG, Guicheney P, Tan HL, Newton-Cheh C, Ackerman MJ, Schwartz PJ, Schulze-Bahr E, Probst V, Horie M, Wilde AA, Tanck MWT and Bezzina CR. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeCirculation . 142(4): 324-338. Number of citations: 102 
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                        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, César-Díaz S, Field E, Garcia-Pinilla JM, Bilinska Z, Muir AR, Roberts AM, Santas E, Zorio E, Peña-Peña ML, Navarro-Aguirre M, Fernandez A, Palomino-Doza J, Azevedo O, Lorenzini M, García-Álvarez MI, Bento D, Jensen MK, Méndez I, Pezzoli L, Sarquella-Brugada G, Campuzano O, Gonzalez-Lopez E, Mogensen J, Kaski JP, Arad M, Brugada-Terradellas J, Asselbergs FW, Monserrat L, Olivotto I, Elliott PM, Garcia-Pavia P and European Genetic Cardiomyopathies Initiative Investigators. Clinical Features and Natural History of PRKAG2 Variant Cardiac GlycogenosisJOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY . 76(2): 186-197. Number of citations: 60 
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                        Antonelli, R, Jiménez, C, Riley, M, Servidei, T, Riccardi, R, Soriano, A, Roma, J, Martínez-Saez, E, Martini, M, Ruggiero, A, Moreno, L, Sanchez deToledo J, Gallego, S, Bové, J, Hooker, JM and Segura, MF. CN133, a Novel Brain-Penetrating Histone Deacetylase Inhibitor, Hampers Tumor Growth in Patient-Derived Pediatric Posterior Fossa Ependymoma ModelsCancers . 12(7): . Number of citations: 9 
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                        Walter CC, Bartrons J, Gómez O, Caffarena-Calvar JM and Carretero JM. Idiopathic dilatation of the right atrium: a not so benign entityCARDIOLOGY IN THE YOUNG . 30(7): 919-922. Number of citations: 5 
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                        Mates J, Mademont-Soler I, Fernandez-Falgueras A, Sarquella-Brugada G, César-Díaz S, Arbelo E, García-Álvarez A, Jordà P, Toro R, Coll M, Fiol JV, Iglesias A, Perez-Serra A, Olmo BD, Alcalde M, Puigmulé M, Pico F, Lopez L, Ferrer C, Tiron C, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O. Sudden Cardiac Death and Copy Number Variants: What Do We Know after 10 Years of Genetic Analysis?FORENSIC SCIENCE INTERNATIONAL-GENETICS . 47: 102281-102281. Number of citations: 32 
