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Haïssaguerre, Michel; Sellal, Jean-Marc; Benali, Karim; de Becker, Benjamin; Defaye, Pascal; Pascale, Patrizio; Martins, Raphael; Mabo, Philippe; Xhaet, Olivier; Extramiana, Fabrice; Surget, Elodie; Lavergne, Thomas; Marijon, Eloi; Adragao, Pedro; Carvalho, Maria Salomé; Milliez, Paul-Ursmar; Laredo, Mickael; Gandjbakhch, Estelle; Giustetto, Carla; Gaita, Fiorenzo; ... (2024). Distinct Substrates of Idiopathic Ventricular Fibrillation Revealed by Arrhythmia Characteristics on Implantable Cardioverter-Defibrillator. JACC Clinical electrophysiology, 10(9), pp. 1982-1994. Elsevier 10.1016/j.jacep.2024.04.028
Belhassen, Bernard; Conte, Giulio; Steinberg, Christian; Whitaker, John; Khan, Habib R; Laredo, Mikael; Doldi, Florian; Ho, Reginald; Tadros, Rafik; Dinov, Boris; Chorin, Ehud; Hansom, Simon; Waintraub, Xavier; Eckardt, Lars; Jankelson, Lior; Peichl, Petr; Mellor, Greg; Sy, Raymond W; Rattanawong, Pattara; Stojkovic, Stefan; ... (2024). Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation: A THESIS Substudy. JACC Clinical electrophysiology, 10(8), pp. 1794-1809. Elsevier 10.1016/j.jacep.2024.03.036
Josephs, Katherine S; Roberts, Angharad M; Theotokis, Pantazis; Walsh, Roddy; Ostrowski, Philip J; Edwards, Matthew; Fleming, Andrew; Thaxton, Courtney; Roberts, Jason D; Care, Melanie; Zareba, Wojciech; Adler, Arnon; Sturm, Amy C; Tadros, Rafik; Novelli, Valeria; Owens, Emma; Bronicki, Lucas; Jarinova, Olga; Callewaert, Bert; Peters, Stacey; ... (2023). Beyond gene-disease validity: capturing structured data on inheritance, allelic requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac conditions. Genome medicine, 15(1), p. 86. BioMed Central 10.1186/s13073-023-01246-8
Barc, Julien; Tadros, Rafik; Glinge, Charlotte; Chiang, David Y.; Jouni, Mariam; Simonet, Floriane; Jurgens, Sean J.; Baudic, Manon; Nicastro, Michele; Potet, Franck; Offerhaus, Joost A.; Walsh, Roddy; Choi, Seung Hoan; Verkerk, Arie O.; Mizusawa, Yuka; Anys, Soraya; Minois, Damien; Arnaud, Marine; Duchateau, Josselin; Wijeyeratne, Yanushi D.; ... (2022). Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. Nature genetics, 54(3), pp. 232-239. Springer Nature 10.1038/s41588-021-01007-6
Walsh, Roddy; Lahrouchi, Najim; Tadros, Rafik; Kyndt, Florence; Glinge, Charlotte; Postema, Pieter G; Amin, Ahmad S; Nannenberg, Eline A; Ware, James S; Whiffin, Nicola; Mazzarotto, Francesco; Škorić-Milosavljević, Doris; Krijger, Christian; Arbelo, Elena; Babuty, Dominique; Barajas-Martinez, Hector; Beckmann, Britt M; Bézieau, Stéphane; Bos, J Martijn; Breckpot, Jeroen; ... (2021). Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls. Genetics in medicine, 23(1), pp. 47-58. Springer Nature 10.1038/s41436-020-00946-5
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L; Mazzanti, Andrea; Beckmann, Britt M; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D; Kucho, Yu; Robyns, Tomas; Ishikawa, Taisuke; Arbelo, Elena; ... (2020). Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Circulation, 142(4), pp. 324-338. American Heart Association 10.1161/CIRCULATIONAHA.120.045956
