People / Staff

Georgia Sarquella Brugada

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Publications

  • Gomez, CI, Sequeros, OG, Sarquella-Brugada G, del Rey, MLP and Martinez, DS.

    Usefulness of SCT in detecting clinical reasoning deficits among pediatric professionals

    Progress in Pediatric Cardiology . 61: . Number of citations: 1

    [doi:10.1016/j.ppedcard.2020.101340]

  • 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 JM, Fernández-Armenta J, Arce-Leon Á, Sanchez-Gómez JM, Sousa P, García-Bolao I, Baluja A, Campuzano O, Sarquella-Brugada G, Martinez-Sande JL, González-Juanatey JR, Gimeno JR, Brugada-Terradellas J and Arbelo E.

    Long-term prognosis of women with Brugada syndrome and electrophysiological study

    Heart Rhythm . 18(5): 664-671. Number of citations: 9

    [doi:10.1016/j.hrthm.2020.12.020]

  • Grassi S, Campuzano O, Coll M, Cazzato F, Sarquella-Brugada G, Rossi R, Arena V, Brugada-Terradellas J, Brugada R and Oliva A.

    Update on the Diagnostic Pitfalls of Autopsy and Post-Mortem Genetic Testing in Cardiomyopathies

    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES . 22(8): 4124. Number of citations: 15

    [doi:10.3390/ijms22084124]

  • Vallverdú-Prats M, Alcalde M, Sarquella-Brugada G, César-Díaz S, Arbelo E, Fernandez-Falgueras A, Coll M, Pérez-Serra A, Puigmulé M, Iglesias A, Fiol JV, Ferrer-Costa C, Olmo BD, Picó F, Lopez L, Jordà P, García-Álvarez A, Llano CT, Toro R, Grassi S, Oliva A, Brugada-Terradellas J, Brugada R and Campuzano O.

    Rare Variants Associated with Arrhythmogenic Cardiomyopathy: Reclassification Five Years Later

    Journal of Personalized Medicine . 11(3): 162. Number of citations: 13

    [doi:10.3390/jpm11030162]

  • Sarquella-Brugada G, Fernandez-Falgueras A, César-Díaz S, Arbelo E, Jordà P, García-Álvarez A, Cruzalegui JC, Merchan EF, Fiol JV, Brugada-Terradellas J, Brugada R and Campuzano O.

    Pediatric Malignant Arrhythmias Caused by Rare Homozygous Genetic Variants in TRDN: A Comprehensive Interpretation

    Frontiers in pediatrics . 8: 601708-601708. Number of citations: 3

    [doi:10.3389/fped.2020.601708]

  • 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, César-Díaz S, Tiron C, Iglesias A, Brugada J, Brugada R and Campuzano O.

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

    Journal of Personalized Medicine . 11(2): 130. Number of citations: 4

    [doi:10.3390/jpm11020130]

  • Walsh R, Lahrouchi N, Tadros R, Kyndt F, Glinge C, Postema PG, Amin AS, Nannenberg EA, Ware JS, Whiffin N, Mazzarotto F, Škoric-Milosavljevic D, Krijger C, Arbelo E, Babuty D, Barajas-Martinez H, Beckmann BM, Bézieau S, Bos JM, Breckpot J, Campuzano O, Castelletti S, Celen C, Clauss S, Corveleyn A, Crotti L, Dagradi F, de Asmundis C, Denjoy I, Dittmann S, Ellinor PT, Ortuño CG, Giustetto C, Gourraud JB, Hazeki D, Horie M, Ishikawa T, Itoh H, Kaneko Y, Kanters JK, Kimoto H, Kotta MC, Krapels IPC, Kurabayashi M, Lazarte J, Leenhardt A, Loeys BL, Lundin C, Makiyama T, Mansourati J, Martins RP, Mazzanti A, Mörner S, Napolitano C, Ohkubo K, Papadakis M, Rudic B, Molina MS, Sacher F, Sahin H, Sarquella-Brugada G, Sebastiano R, Sharma S, Sheppard MN, Shimamoto K, Shoemaker MB, Stallmeyer B, Steinfurt J, Tanaka Y, Tester DJ, Usuda K, van der Zwaag PA, Van Dooren S, Van Laer L, Winbo A, Winkel BG, Yamagata K, Zumhagen S, Volders PGA, Lubitz SA, Antzelevitch C, Platonov PG, Odening KE, Roden DM, Roberts JD, Skinner JR, Tfelt-Hansen J, van den Berg MP, Olesen MS, Lambiase PD, Borggrefe M, Hayashi K, Rydberg A, Nakajima T, Yoshinaga M, Saenen JB, Kääb S, Brugada P, Robyns T, Giachino DF, Ackerman MJ, Brugada R, Brugada-Terradellas J, Gimeno JR, Hasdemir C, Guicheney P, Priori SG, Schulze-Bahr E, Makita N, Schwartz PJ, Shimizu W, Aiba T, Schott JJ, Redon R, Ohno S, Probst V, Behr ER, Barc J, Bezzina CR and Nantes Referral Center for inherited cardiac arrhythmia.

    Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls

    GENETICS IN MEDICINE . 23(1): 47-58. Number of citations: 44

    [doi:10.1038/s41436-020-00946-5]

  • Clark BC, Sanchez deToledo J, Bautista Rodríguez C, Choueiter N, Lara D, Kang H, Mohsin S, Fraisse A, César-Díaz S, Sattar Shaikh A, Escobar-Diaz MC, Hsu DT, Randanne PC, Aslam N, Kleinmahon J, Lamour JM, Johnson JN, Sarquella-Brugada G and Chowdhury D.

    Cardiac Abnormalities Seen in Pediatric Patients During the SARS-CoV2 Pandemic: An International Experience

    JOURNAL OF THE AMERICAN HEART ASSOCIATION . 9(21): . Number of citations: 35

    [doi:10.1161/JAHA.120.018007]

  • 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 2020.

    CARDIOLOGY IN THE YOUNG . 30(11): 1572-1587.

    [doi:10.1017/S1047951120003455]

  • 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 Syndrome

    JACC-CLINICAL ELECTROPHYSIOLOGY . 6(12): 1561-1570. Number of citations: 21

    [doi:10.1016/j.jacep.2020.06.001]