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Publications

  • Grassi S, Campuzano O, Ferri E, Leone G, Rossi R, Ortega-Sánchez M, Barberia E, Landin I, Arena V, Sarquella-Brugada G, Brugada R and Oliva A.

    Forensic pathological and genetic landmarks in sudden cardiac death in the young: An update.

    FORENSIC SCIENCE INTERNATIONAL-GENETICS . 80: 103334-103334.

    [doi:10.1016/j.fsigen.2025.103334]

  • Miyake CY, Kallas D, Stephens SB, Moore OM, Wehrens XHT, Fischbach PS, LaPage MJ, Landstrom AP, Law IH, Hill AC, Kannankeril PJ, Fish FA, Howard TS, Valdes SO, Pham TD, Kim JJ, Dhillon S, Johnsrude CL, Krause U, Sarquella-Brugada G, Kubus P, Tavacova T, Kwok SY, Etheridge SP, Tisma-Dupanovic S, Kean AC, Krahn AD, Ebrahim M, Atallah J, Fournier A, Batra AS, Young ML, Perry J, Kovach JR, Kamp AN, Clark BC, Jimenez E, Charafeddine F, Hamilton RM, Balaji S and Sanatani S.

    Intellectual and Neurodevelopmental Delays in Pediatric Catecholaminergic Polymorphic Ventricular Tachycardia: Distinct Characteristics and a More Malignant Neurocardiac Phenotype.

    CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY . 18(10): .

    [doi:10.1161/CIRCEP.124.013437]

  • Campuzano O, Grassi S, Martínez-Barrios E, Greco A, Arena V, Sarquella-Brugada G and Oliva A.

    Brugada syndrome in the forensic field: what do we know to date?

    frontiers in cardiovascular medicine . 12: 1618762-1618762.

    [doi:10.3389/fcvm.2025.1618762]

  • Norrish G, Hall K, Field E, Cervi E, Boleti O, Ziólkowska L, Olivotto I, Passantino S, Khraiche D, Limongelli G, Weintraub RG, Anastasakis A, Biagini E, Ragni L, Sarquella-Brugada G, César-Díaz S, Prendiville T, McLeod K, Ilina M, Baban A, Ojala TH, Spentzou G, Bhole V, Gran F, Brown E, Delle Donne G, Khodaghalian B, Fernandez A, Daubeney PEF, Linter K, Kubus P, Uzun O, Bökenkamp R, Raimondi F, Marrone C, Medrano C, Gonzalez-Lopez E, Siles A, Luczak-Wozniak K, Bharucha T, Adwani S, Klaassen S, Castro FJ, Guereta L, Yamazawa H, Sinagra G, Popoiu A, Perin F, Chana B, De Wilde H, Rasmussen TB, Mogensen J, Mathur S, Centeno F, Reinhardt Z, Barriales-Villa R, Kubo T, Felice T, Radulescu C, Schouvey S, Chaker M and Kaski JP.

    Sex Differences in Children and Adolescents With Hypertrophic Cardiomyopathy

    JACC-ADVANCES . 4(8): 101907-101907.

    [doi:10.1016/j.jacadv.2025.101907]

  • Monda E, Biagini E, Blom N, Drago F, Krapels I, Krebsová A, Koubsky K, Khraiche D, Martins E, Merlo M, Michels M, Mizia-Stec K, Mörner S, Peña Peña ML, Planinc I, Robyns T, Rydberg A, Saenen J, Rodríguez Palomares JF, Rutger H, Sarquella-Brugada G, Scheirlynck E, Schulze-Bahr E, Tfelt-Hansen J, Wolf CM, Hofman N, Amin AS, Wilde A, Charron P and Limongelli G.

    Current management of transition and multidisciplinary care of patients with inherited and rare cardiomyopathies in Europe: results of the European Reference Network for rare and low prevalence complex diseases of the heart

    EUROPEAN HEART JOURNAL-QUALITY OF CARE AND CLINICAL OUTCOMES . : .

    [doi:10.1093/ehjqcco/qcaf055]

  • Zanchi, B, Monachino, G, Faraci, FD, Metaldi, M, Brugada, P, Sarquella-Brugada G, Behr, ER, Brugada-Terradellas J, Crotti, L, Belhassen, B and Conte, G.

    Synthetic electrocardiograms for Brugada syndrome: from data generation to expert cardiologists evaluation.

    european heart journal - digital health . 6(4): 683-687.

    [doi:10.1093/ehjdh/ztaf039]

  • Martínez-Barrios E, Greco A, César-Díaz S, Díez-López C, Cruzalegui JC, Nuria Díez Escuté, Patricia Cerralbo Martín, Chipa F, Zschaeck-Luzardo I, Grassi S, Oliva A, Balderrábano N, Toro R, Sarquella-Brugada G and Campuzano O.

    Appropriate time interval to update ambiguous genetic diagnosis in inherited arrhythmogenic syndromes

    iScience . 28(5): 112300-112300. Number of citations: 1

    [doi:10.1016/j.isci.2025.112300]

  • Behr ER, Winkel BG, Ensam B, Alfie A, Arbelo E, Berry C, Cerrone M, Conte G, Crotti L, Corcia CMG, Kaski JC, Nademanee K, Postema PD, Priori S, Probst V, Sarquella-Brugada G, Schulze-Bahr E, Tadros R, Wilde A and Tfelt-Hansen J.

    The diagnostic role of pharmacological provocation testing in cardiac electrophysiology: a clinical consensus statement of the European Heart Rhythm Association and the European Association of Percutaneous Cardiovascular Interventions (EAPCI) of the ESC, the ESC Working Group on Cardiovascular Pharmacotherapy, the Association of European Paediatric and Congenital Cardiology (AEPC), the Paediatric & Congenital Electrophysiology Society (PACES), the Heart Rhythm Society (HRS), the Asia Pacific Heart Rhythm Society (APHRS), and the Latin American Heart Rhythm Society (LAHRS).

    Europace . 27(4): . Number of citations: 7

    [doi:10.1093/europace/euaf067]

  • Greco A, Martínez-Barrios E, Cruzalegui JC, César-Díaz S, Chipa, F, Nuria Díez Escuté, Patricia Cerralbo Martín, Zschaeck-Luzardo I, Loredo, P, Sarquella-Brugada G and Campuzano, O.

    Brugada Syndrome and GPD1L: Definite Genotype-Phenotype Association?

    cardiogenetics . 15(1): .

    [doi:10.3390/cardiogenetics15010009]

  • Conte G, Bergonti M, Probst V, Morita H, Tfelt-Hansen J, Behr ER, Kengo K, Arbelo E, Crotti L, Sarquella-Brugada G, Wilde AAM, Calò L, Sarkozy A, de Asmundis C, Mellor G, Migliore F, Letsas K, Vicentini A, Levinstein M, Berne P, Chen SA, Veltmann C, Biernacka EK, Carvalho P, Kabawata M, Sojema K, Gonzalez MC, Tse G, Thollet A, Svane J, Caputo ML, Scrocco C, Kamakura T, Pardo LF, Lee S, Juárez CK, Martino A, Lo LW, Monaco C, Reyes-Quintero ÁE, Martini N, Oezkartal T, Klersy C, Brugada-Terradellas J, Schwartz PJ, Brugada P, Belhassen B and Auricchio A.

    aTrial arrhythmias in inhEriTed aRrhythmIa Syndromes: results from the TETRIS study

    Europace . 26(12): . Number of citations: 2

    [doi:10.1093/europace/euae288]