{
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        [
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        ],
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                "Brugada Syndrome",
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            [
                [
                    "Thomas Rosseel, Wouter L'Hoyes, Martijn Rogiers, Peter Haemers, Christophe Garweg, Rik Willems, Joris Ector, Tomas Robyns, Bert Vandenberk (2024). Ajmaline infusion for unmasking short-coupled Purkinje ectopy: Need for speed? Heart rhythm. https://doi.org/10.1016/j.hrthm.2024.08.056 PMID: 39216716",
                    "39216716"
                ],
                [
                    "Miguel Fogaça-da-Mata, Estefanía Martínez-Barrios, Lorenzo Jiménez-Montañés, José Cruzalegui, Fredy Chipa-Ccasani, Andrea Greco, Sergi Cesar, Núria Díez-Escuté, Patricia Cerralbo, Irene Zschaeck, Marcos Clavero Adell, Ariadna Ayerza-Casas, Daniel Palanca-Arias, Marta López, Oscar Campuzano, Josep Brugada, Georgia Sarquella-Brugada (2024). Brugada Syndrome and Pulmonary Atresia with Intact Interventricular Septum: Fortuitous Finding or New Genetic Connection? Genes. https://doi.org/10.3390/genes15050638 PMID: 38790267",
                    "38790267"
                ],
                [
                    "Avi Sabbag, Gisella Amoroso, Orr Tomer, Giulio Conte, Roy Beinart, Eyal Nof, Tardu Özkartal, Pierre Ollitrault, Mikael Laredo, Oholi Tovia-Brodie, Estelle Gandjbakhch, Michele de Benedictis, Rachel M A Ter Bekke, Anat Milman (2024). Clinical differences between drug-induced type 1 Brugada pattern and syndrome. Journal of arrhythmia, 982-990. https://doi.org/10.1002/joa3.13053 PMID: 39139869",
                    "39139869"
                ],
                [
                    "Saverio Iacopino, Emmanuel Fabiano, Paolo Sorrenti, Andrea Petretta, Jacopo Colella, Alessandro Di Vilio, Giovanni Statuto, Pasquale Filannino, Paolo Artale, Daniele Giacopelli, Gianluca Peluso, Gennaro Fabiano, Giuseppe Campagna, Federico Cecchini (2024). Predicting ventricular arrhythmia inducibility in ajmaline-induced Brugada type I pattern: Validation of the dST-Tiso interval. Journal of cardiovascular electrophysiology, 1747-1753. https://doi.org/10.1111/jce.16348 PMID: 38923783",
                    "38923783"
                ],
                [
                    "Sara Latrofa, Valentina Hartwig, Lorenzo Bachi, Pasquale Notarstefano, Silvia Garibaldi, Luca Panchetti, Martina Nesti, Paolo Seghetti, Umberto Startari, Gianluca Mirizzi, Maria Sole Morelli, Martina Modena, Andrea Mazzanti, Michele Emdin, Alberto Giannoni, Andrea Rossi (2024). Endocardial repolarization dispersion in BrS: A novel automatic algorithm for mapping activation recovery interval. Journal of cardiovascular electrophysiology, 965-974. https://doi.org/10.1111/jce.16244 PMID: 38477371",
                    "38477371"
                ],
                [
                    "Paul-Adrian Călburean, Luigi Pannone, Cinzia Monaco, Domenico Della Rocca, Antonio Sorgente, Alexandre Almorad, Gezim Bala, Filippo Aglietti, Robbert Ramak, Ingrid Overeinder, Erwin Ströker, Gudrun Pappaert, Marius Măru'teri, Marius Harpa, Mark La Meir, Pedro Brugada, Juan Sieira, Andrea Sarkozy, Gian-Battista Chierchia, Carlo de Asmundis (2024). Predicting and Recognizing Drug-Induced Type I Brugada Pattern Using ECG-Based Deep Learning. Journal of the American Heart Association, e033148. https://doi.org/10.1161/JAHA.123.033148 PMID: 38726893",
                    "38726893"
                ],
                [
                    "Eraldo Occhetta, Federica De Vecchi, Lorella Barbonaglia, Chiara Devecchi, Mario Matta, Maurizio Malacrida, Giuseppe Patti, Francesco Rametta (2023). Can specific ECG markers identify a pharmacologically induced type 1 Brugada pattern? Insights from a large, single-center cohort. Journal of electrocardiology, 123-131. https://doi.org/10.1016/j.jelectrocard.2023.08.017 PMID: 37688842",
                    "37688842"
                ],
                [
                    "Angelo Auricchio, Andrea Demarchi, Tardu Özkartal, Daniela Campanale, Maria Luce Caputo, Marcello di Valentino, Andrea Menafoglio, Francois Regoli, Marco Facchini, Alessandro Del Bufalo, Pietro Foglia, Nicola Ferrari, Fulvio Bomio, Argelia Medeiros-Domingo, Tiziano Moccetti, Giovanni B Pedrazzini, Catherine Klersy, Giulio Conte (2023). Role of genetic testing in young patients with idiopathic atrioventricular conduction disease. Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology, 643-650. https://doi.org/10.1093/europace/euac196 PMID: 36352534",
                    "36352534"
                ],
                [
                    "Antonio Bisignani, Luigi Pannone, Alvise Del Monte, Ivan Eltsov, Ida Anna Cappello, Juan Sieira, Cinzia Monaco, Gezim Bala, Sahar Mouram, Domenico Giovanni Della Rocca, Erwin Ströker, Ingrid Overeinder, Alexandre Almorad, Gudrun Pappaert, Anaïs Gauthey, Thomy de Ravel, Sonia Van Dooren, Antonio Sorgente, Mark La Meir, Andrea Sarkozy, Pedro Brugada, Gian-Battista Chierchia, Carlo de Asmundis (2023). Atrial Abnormalities in Brugada Syndrome: Evaluation With ECG Imaging. JACC. Clinical electrophysiology, 2096-2105. https://doi.org/10.1016/j.jacep.2023.06.011 PMID: 37565952",
                    "37565952"
                ],
                [
                    "Hans Ebbinghaus, Laura Ueberham, Daniela Husser-Bollmann, Andreas Bollmann, Ulrich Laufs, Borislav Dinov (2023). Case Report: Four cases of cardiac sarcoidosis in patients with inherited cardiomyopathy-a phenotypic overlap, co-existence of two rare cardiomyopathies or a second-hit disease. Frontiers in cardiovascular medicine, 1328802. https://doi.org/10.3389/fcvm.2023.1328802 PMID: 38173816",
                    "38173816"
                ]
            ]
        ],
        [
            [
                "Brugada Syndrome",
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            14.056824,
            [
                [
                    "Hei-To Leung, Sit-Yee Kwok, Fong-Ying Shih, Kin-Shing Lun, Tak-Cheung Yung, Sabrina Tsao (2025). A Tale of Two Conditions: Pediatric Brugada Syndrome Unveiled-Navigating the Challenges of Coexisting Arrhythmia and Fever-Induced ECG Pattern. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc, e70009. https://doi.org/10.1111/anec.70009 PMID: 39726150",
                    "39726150"
                ],
                [
                    "Jack Jnani, Dorota Gruber, Tafadzwa Mtisi, Moussa Saleh, Bani M Azari (2024). Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family. Cureus, e64883. https://doi.org/10.7759/cureus.64883 PMID: 39156269",
                    "39156269"
                ],
                [
                    "Leonie Verkerk, Arie O Verkerk, Ronald Wilders (2024). Zebrafish as a Model System for Brugada Syndrome. Reviews in cardiovascular medicine, 313. https://doi.org/10.31083/j.rcm2509313 PMID: 39355588",
                    "39355588"
                ],
                [
                    "Majid Haghjoo, Amir Askarinejad, Shabnam Madadi, Amirfarjam Fazelifar, Farzad Kamali, Abolfath Alizadeh-Diz, Zahra Emkanjoo (2024). Brugada syndrome in Iran: Insights from a 12-year longitudinal study. Journal of cardiovascular electrophysiology, 708-714. https://doi.org/10.1111/jce.16206 PMID: 38348526",
                    "38348526"
                ],
                [
                    "Katharina Koepsel, Tobias C Dreher, Christian Blockhaus, Michael Gotzmann, Norbert Klein, Thomas Kuntz, Dong-In Shin, Hendrik Lapp, Fabian Schiedat, Mohammad Abumayyaleh, Thomas Beiert, Christian Weth, Boldizsar Kovacs, Stephanie Rosenkaimer, Jacqueline Kowitz, Ardan Muammer Saguner, Julia W Erath, Firat Duru, Andreas Mügge, Ibrahim Akin, Assem Aweimer, Nazha Hamdani, Ibrahim El-Battrawy (2024). No beneficial use of the wearable cardioverter defibrillator among patients suffering from inherited and congenital heart disease: data from a European multicenter registry. Frontiers in cardiovascular medicine, 1384736. https://doi.org/10.3389/fcvm.2024.1384736 PMID: 39049954",
                    "39049954"
                ],
                [
                    "Athanasios Saplaouras, Ourania Kariki, Panagiotis Mililis, Andromahi Zygouri, Aggeliki Gkouziouta, George Poulos, Stamatis Adamopoulos, Michael Efremidis, Evangelia Nyktari, Konstantinos P Letsas (2023). Diagnostic and therapeutic dilemmas in a patient with myocarditis, Brugada syndrome and arrhythmic syncope. Journal of electrocardiology, 45-50. https://doi.org/10.1016/j.jelectrocard.2023.04.006 PMID: 37187131",
                    "37187131"
                ],
                [
                    "Zahid Khan (2023). A Case of Young Brugada Syndrome Patient With Implantable Cardioverter Defibrillator Complication Requiring Device Extraction and Reimplantation. Cureus, e43576. https://doi.org/10.7759/cureus.43576 PMID: 37719594",
                    "37719594"
                ],
                [
                    "Vincenzo Russo, Alfredo Caturano, Federico Guerra, Federico Migliore, Giuseppe Mascia, Andrea Rossi, Martina Nesti, Vincenzo Ezio Santobuono, Emilio Attena, Gianfranco Tola, Luigi Sciarra, Giulio Conte, Alessandro Paoletti Perini, Pietro Francia, Gregory Dendramis, Zefferino Palamà, Stefano Albani, Andrea Ottonelli Ghidini, Leonardo Calò, Antonio D'Onofrio, Enrico Baldi,   (2023). Subcutaneous versus transvenous implantable cardioverter-defibrillator among drug-induced type-1 ECG pattern Brugada syndrome: a propensity score matching analysis from IBRYD study. Heart and vessels, 680-688. https://doi.org/10.1007/s00380-022-02204-x PMID: 36418560",
                    "36418560"
                ],
                [
                    "Maria d'Apolito, Francesco Santoro, Rosa Santacroce, Giorgia Cordisco, Ilaria Ragnatela, Girolamo D'Arienzo, Pier Luigi Pellegrino, Natale Daniele Brunetti, Maurizio Margaglione (2023). A Novel DLG1 Variant in a Family with Brugada Syndrome: Clinical Characteristics and In Silico Analysis. Genes. https://doi.org/10.3390/genes14020427 PMID: 36833354",
                    "36833354"
                ],
                [
                    "Ivan Eltsov, Cinzia Monaco, Gian-Battista Chierchia, Mark La Meir, Carlo de Asmundis (2022). Hybrid Surgical Ablation of Recurrent Ventricular Tachycardia in a Patient With High-Risk Brugada Syndrome. JACC. Case reports, 214-220. https://doi.org/10.1016/j.jaccas.2021.11.018 PMID: 35199019",
                    "35199019"
                ]
            ]
        ],
        [
            [
                "Brugada Syndrome",
                "SCN10A"
            ],
            10.310587,
            [
                [
                    "Lu-Chen Weng, Shaan Khurshid, Amelia Weber Hall, Victor Nauffal, Valerie N Morrill, Yan V Sun, Joel T Rämö, Dominik Beer, Simon Lee, Girish Nadkarni, Renee Johnson, Laura Andreasen, Anne Clayton, Clive R Pullinger, Zachary T Yoneda, Daniel J Friedman, Matthew C Hyman, Renae L Judy, Allan C Skanes, Kate M Orland, Paloma Jordà, Timothy M Treu, Matthew T Oetjens, Rajesh Subbiah, Jacob P Hartmann, Heidi T May, John P Kane, Tariq Z Issa, Navid A Nafissi, Peter Leong-Sit, Marie-Pierre Dubé, Carolina Roselli, Seung Hoan Choi,  , Jean-Claude Tardif, Habib R Khan, Stacey Knight, Jesper H Svendsen, Bruce Walker, Richard Karlsson Linnér, J Michael Gaziano, Rafik Tadros, Diane Fatkin, Daniel J Rader, Svati H Shah, Dan M Roden, Gregory M Marcus, Ruth J F Loos, Scott M Damrauer, Christopher M Haggerty, Kelly Cho, Aarno Palotie, Morten S Olesen, Lee L Eckhardt, Jason D Roberts, Michael J Cutler, M Benjamin Shoemaker, Peter W F Wilson, Patrick T Ellinor, Steven A Lubitz (2024). Meta-Analysis of Genome-Wide Association Studies Reveals Genetic Mechanisms of Supraventricular Arrhythmias. Circulation. Genomic and precision medicine, e004320. https://doi.org/10.1161/CIRCGEN.123.004320 PMID: 38804128",
                    "38804128"
                ],
                [
                    "Aaron Isaacs, Andrei Barysenka, Rachel M A Ter Bekke, Apollonia T J M Helderman-van den Enden, Arthur van den Wijngaard, Paul G A Volders, Monika Stoll (2023). Standing genetic variation affects phenotypic heterogeneity in an SCN5A-mutation founder population with excess sudden cardiac death. Heart rhythm, 720-727. https://doi.org/10.1016/j.hrthm.2023.02.004 PMID: 36764349",
                    "36764349"
                ],
                [
                    "Nico Hartmann, Maria Knierim, Wiebke Maurer, Nataliya Dybkova, Gerd Hasenfuß, Samuel Sossalla, Katrin Streckfuss-Bömeke (2023). Molecular and Functional Relevance of NaV1.8-Induced Atrial Arrhythmogenic Triggers in a Human SCN10A Knock-Out Stem Cell Model. International journal of molecular sciences. https://doi.org/10.3390/ijms241210189 PMID: 37373335",
                    "37373335"
                ],
                [
                    "Zhenxing Liao, Yingrui Li, Xuehui Fan, Zhen Yang, Ibrahim El-Battrawy, Xiaobo Zhou, Ibrahim Akin (2022). Lipopolysaccharide Modifies Sodium Current Kinetics through ROS and PKC Signalling in Induced Pluripotent Stem-Derived Cardiomyocytes from Brugada Syndrome Patient. Journal of cardiovascular development and disease. https://doi.org/10.3390/jcdd9040119 PMID: 35448095",
                    "35448095"
                ],
                [
                    "Yan Huang, Xiao-Meng Chen, Hector Barajas-Martinez, Hong Jiang, Charles Antzelevitch, Dan Hu (2021). Common variants in SCN10A gene associated with Brugada syndrome. Human molecular genetics, 157-165. https://doi.org/10.1093/hmg/ddab217 PMID: 34312669",
                    "34312669"
                ],
                [
                    "Richa Tambi, Reem Abdel Hameid, Asma Bankapur, Nasna Nassir, Ghausia Begum, Alawi Alsheikh-Ali, Mohammed Uddin, Bakhrom K Berdiev (2021). Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome. American journal of physiology. Heart and circulatory physiology, H1935-H1948. https://doi.org/10.1152/ajpheart.00061.2021 PMID: 33797273",
                    "33797273"
                ],
                [
                    "Joyce C K Man, Fernanda M Bosada, Koen T Scholman, Joost A Offerhaus, Roddy Walsh, Karel van Duijvenboden, Vincent W W van Eif, Connie R Bezzina, Arie O Verkerk, Bastiaan J Boukens, Phil Barnett, Vincent M Christoffels (2021). Variant Intronic Enhancer Controls SCN10A-short Expression and Heart Conduction. Circulation, 229-242. https://doi.org/10.1161/CIRCULATIONAHA.121.054083 PMID: 33910361",
                    "33910361"
                ],
                [
                    "Adrian Pérez-Agustín, Mel Lina Pinsach-Abuin, Sara Pagans (2020). Role of Non-Coding Variants in Brugada Syndrome. International journal of molecular sciences. https://doi.org/10.3390/ijms21228556 PMID: 33202810",
                    "33202810"
                ],
                [
                    "Liang Hong, Meihong Zhang, Arvind Sridhar, Dawood Darbar (2020). Pathogenic mutations perturb calmodulin regulation of Nav1.8 channel. Biochemical and biophysical research communications, 168-174. https://doi.org/10.1016/j.bbrc.2020.08.010 PMID: 32948286",
                    "32948286"
                ],
                [
                    "Pattarapong Makarawate, Charlotte Glinge, Apichai Khongphatthanayothin, Roddy Walsh, John Mauleekoonphairoj, Montawatt Amnueypol, Somchai Prechawat, Wanwarang Wongcharoen, Rungroj Krittayaphong, Alisara Anannab, Peter Lichtner, Thomas Meitinger, Fleur V Y Tjong, Krystien V V Lieve, Ahmad S Amin, Dujdao Sahasatas, Tachapong Ngarmukos, Duangdao Wichadakul, Sunchai Payungporn, Boosamas Sutjaporn, Pharawee Wandee, Yong Poovorawan, Jacob Tfelt-Hansen, Michael W T Tanck, Rafik Tadros, Arthur A M Wilde, Connie R Bezzina, Gumpanart Veerakul, Koonlawee Nademanee (2020). Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand. Heart rhythm, 2145-2153. https://doi.org/10.1016/j.hrthm.2020.06.027 PMID: 32619740",
                    "32619740"
                ]
            ]
        ],
        [
            [
                "Brugada Syndrome",
                "CACNA1C"
            ],
            10.31055,
            [
                [
                    "Lorenzo Cipriano, Raffaele Piscopo, Chiara Aiello, Antonio Novelli, Achille Iolascon, Carmelo Piscopo (2024). Expanding the Phenotype of the CACNA1C-Associated Neurological Disorders in Children: Systematic Literature Review and Description of a Novel Mutation. Children (Basel, Switzerland). https://doi.org/10.3390/children11050541 PMID: 38790536",
                    "38790536"
                ],
                [
                    "Asami Kashiwa, Takeru Makiyama, Hirohiko Kohjitani, Thomas L Maurissen, Taisuke Ishikawa, Yuta Yamamoto, Yimin Wuriyanghai, Jingshan Gao, Hai Huang, Tomohiko Imamura, Takanori Aizawa, Misato Nishikawa, Kazuhisa Chonabayashi, Hiroyuki Mishima, Seiko Ohno, Futoshi Toyoda, Seiichi Sato, Koh-Ichiro Yoshiura, Kazuhiro Takahashi, Yoshinori Yoshida, Knut Woltjen, Minoru Horie, Naomasa Makita, Takeshi Kimura (2023). Disrupted CaV1.2 selectivity causes overlapping long QT and Brugada syndrome phenotypes in the CACNA1C-E1115K iPS cell model. Heart rhythm, 89-99. https://doi.org/10.1016/j.hrthm.2022.08.021 PMID: 36007726",
                    "36007726"
                ],
                [
                    "Bin Zeng, Xiang Zhang, Rainer Schimpf, Andrew Powers, Michael Glikson, Charles Antzelevitch, Dan Hu, Hector Barajas-Martinez (2023). Functional identification of hot-spot mutations in cardiac calcium channel genes associated with the J wave syndromes. Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 20220286. https://doi.org/10.1098/rstb.2022.0286 PMID: 37122210",
                    "37122210"
                ],
                [
                    "Gang Yu, Susmita Chakrabarti, Miroslava Tischenko, Ai-Lan Chen, Zhijie Wang, Hyosuk Cho, Brent A French, Sathyamangla V Naga Prasad, Qiuyun Chen, Qing K Wang (2022). Gene therapy targeting protein trafficking regulator MOG1 in mouse models of Brugada syndrome, arrhythmias, and mild cardiomyopathy. Science translational medicine, eabf3136. https://doi.org/10.1126/scitranslmed.abf3136 PMID: 35675436",
                    "35675436"
                ],
                [
                    "Valeria Novelli, Mirella Memmi, Alberto Malovini, Andrea Mazzanti, Nian Liu, Ruan Yanfei, Rossana Bongianino, Marco Denegri, Nicola Monteforte, Raffaella Bloise, Massimo Morini, Carlo Napolitano (2022). Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing. Heart rhythm, 798-806. https://doi.org/10.1016/j.hrthm.2021.12.032 PMID: 34999275",
                    "34999275"
                ],
                [
                    "Michelle M Monasky, Carola Rutigliani, Emanuele Micaglio, Carlo Pappone (2021). Commentary: Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome. Frontiers in physiology, 682567. https://doi.org/10.3389/fphys.2021.682567 PMID: 34177625",
                    "34177625"
                ],
                [
                    "Vittoria Di Mauro, Paola Ceriotti, Francesco Lodola, Nicolò Salvarani, Jessica Modica, Marie-Louise Bang, Andrea Mazzanti, Carlo Napolitano, Silvia G Priori, Daniele Catalucci (2020). Peptide-Based Targeting of the L-Type Calcium Channel Corrects the Loss-of-Function Phenotype of Two Novel Mutations of the CACNA1 Gene Associated With Brugada Syndrome. Frontiers in physiology, 616819. https://doi.org/10.3389/fphys.2020.616819 PMID: 33488405",
                    "33488405"
                ],
                [
                    "Catia Mio, Nadia Passon, Federica Baldan, Elisa Bregant, Elisabetta Monaco, Loretta Mancini, Eliana Demori, Giuseppe Damante (2020). CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers. European journal of medical genetics, 103843. https://doi.org/10.1016/j.ejmg.2020.103843 PMID: 31953239",
                    "31953239"
                ],
                [
                    "P E Maltese, E Aldanova, N Kriuchkova, A Averianov, E Manara, S Paolacci, A Bruson, R Miotto, M Sartori, G Guerri, M Zuntini, G Marceddu, S Tezzele, K Tadtaeva, A Chernova, N Aksyutina, S Nikulina, S Nodari, M Bertelli (2019). Putative role of Brugada syndrome genes in familial atrial fibrillation. European review for medical and pharmacological sciences, 7582-7598. https://doi.org/10.26355/eurrev_201909_18880 PMID: 31539150",
                    "31539150"
                ],
                [
                    "Xiuhua Bozarth, Jennifer N Dines, Qian Cong, Ghayda M Mirzaa, Kimberly Foss, J Lawrence Merritt, Jenny Thies, Heather C Mefford, Edward Novotny (2018). Expanding clinical phenotype in CACNA1C related disorders: From neonatal onset severe epileptic encephalopathy to late-onset epilepsy. American journal of medical genetics. Part A, 2733-2739. https://doi.org/10.1002/ajmg.a.40657 PMID: 30513141",
                    "30513141"
                ]
            ]
        ],
        [
            [
                "Brugada Syndrome",
                "SCN5A"
            ],
            18.973053,
            [
                [
                    "Roddy Walsh, John Mauleekoonphairoj, Isabella Mengarelli, Fernanda M Bosada, Arie O Verkerk, Karel van Duijvenboden, Yong Poovorawan, Wanwarang Wongcharoen, Boosamas Sutjaporn, Pharawee Wandee, Nitinan Chimparlee, Ronpichai Chokesuwattanaskul, Kornkiat Vongpaisarnsin, Piyawan Dangkao, Cheng-I Wu, Rafik Tadros, Ahmad S Amin, Krystien V V Lieve, Pieter G Postema, Maarten Kooyman, Leander Beekman, Dujdao Sahasatas, Montawatt Amnueypol, Rungroj Krittayaphong, Somchai Prechawat, Alisara Anannab, Pattarapong Makarawate, Tachapong Ngarmukos, Keerapa Phusanti, Gumpanart Veerakul, Zoya Kingsbury, Taksina Newington, Uma Maheswari, Mark T Ross, Andrew Grace, Pier D Lambiase, Elijah R Behr, Jean-Jacques Schott, Richard Redon, Julien Barc, Vincent M Christoffels, Arthur A M Wilde, Koonlawee Nademanee, Connie R Bezzina, Apichai Khongphatthanayothin (2025). A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand. Circulation, 31-44. https://doi.org/10.1161/CIRCULATIONAHA.124.069041 PMID: 39391988",
                    "39391988"
                ],
                [
                    "Ioannis Doundoulakis, Luigi Pannone, Pedro Brugada, Carlo de Asmundis (2025). Reply to the Editor- Revisiting the prognostic role of SCN5A in Brugada syndrome. Heart rhythm, 281. https://doi.org/10.1016/j.hrthm.2024.06.023 PMID: 38906516",
                    "38906516"
                ],
                [
                    "Deni Kukavica, Alessandro Trancuccio, Andrea Mazzanti, Carlo Napolitano, Massimo Morini, Gianluca Pili, Mirella Memmi, Patrick Gambelli, Raffaella Bloise, Jannì Nastoli, Barbara Colombi, Alessio Guarracino, Maira Marino, Carlo Ceriotti, Paola Galimberti, Luca Ottaviano, Massimo Mantica, Silvia G Priori (2024). Nonmodifiable Risk Factors Predict Outcomes in Brugada Syndrome. Journal of the American College of Cardiology, 2087-2098. https://doi.org/10.1016/j.jacc.2024.07.037 PMID: 39387761",
                    "39387761"
                ],
                [
                    "Michael Litt, Rajat Deo (2024). Brugada Syndrome Risk Stratification: Selecting the Population of Interest. Journal of the American College of Cardiology, 2099-2101. https://doi.org/10.1016/j.jacc.2024.08.076 PMID: 39387765",
                    "39387765"
                ],
                [
                    "Mohammad Iqbal, Michael Aditya Lesmana, Iwan Cahyo Santosa Putra, Giky Karwiky, Chaerul Achmad, Hanna Goenawan, Mohammad Rizki Akbar, Arief Sjamsulaksan Kartasasmita (2024). Implications of Associated Atrial Fibrillation in Brugada Syndrome for Sudden Cardiac Death ‒ A Case Series Analysis. The American journal of case reports, e945005. https://doi.org/10.12659/AJCR.945005 PMID: 39449185",
                    "39449185"
                ],
                [
                    "Jack Jnani, Dorota Gruber, Tafadzwa Mtisi, Moussa Saleh, Bani M Azari (2024). Identification of a SCN5A Genetic Variant Associated With Type 1 Brugada Syndrome (BrS) in a Family. Cureus, e64883. https://doi.org/10.7759/cureus.64883 PMID: 39156269",
                    "39156269"
                ],
                [
                    "Hangping Fan, Jun Su, Xiaochen Wang, Hao Wang, Xianzhen Chen, Yaxun Sun, Chenyang Jiang, Ping Liang (2024). Generation of an induced pluripotent stem cell line from a Brugada syndrome patient carrying SCN5A/c.3118G>C mutation. Stem cell research, 103529. https://doi.org/10.1016/j.scr.2024.103529 PMID: 39121653",
                    "39121653"
                ],
                [
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}