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Sieliwonczyk, Ewa; Alaerts, Maaike; Robyns, Tomas; Schepers, Dorien; Claes, Charlotte; Corveleyn, Anniek; Willems, Rik; Van Craenenbroeck, Emeline M; Simons, Eline; Nijak, Aleksandra; Vandendriessche, Bert; Mortier, Geert; Vrints, Christiaan; Koopman, Pieter; Heidbuchel, Hein; Van Laer, Lut; Saenen, Johan; Loeys, Bart

Clinical characterization of the first Belgian SCN5A founder mutation cohort

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Oxford University Press (OUP), 2021

Published in: EP Europace
Lieve, Krystien V.V.; Dusi, Veronica; van der Werf, Christian; Bos, J. Martijn; Lane, Conor M.; Stokke, Mathis Korseberg; Roston, Thomas M.; Djupsjöbacka, Aurora; Wada, Yuko; Denjoy, Isabelle; Bundgaard, Henning; Noguer, Ferran Roses I.; Semsarian, Christopher; Robyns, Tomas; Hofman, Nynke; Tanck, Michael W.; van den Berg, Maarten P.; Kammeraad, Janneke A.E.; Krahn, Andrew D.; Clur, Sally-Ann B.; Sacher, Frederic; Till, Jan; Skinner, Jonathan R.; Tfelt-Hansen, Jacob; [...]

Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

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Ovid Technologies (Wolters Kluwer Health), 2020

Published in: Circulation: Arrhythmia and Electrophysiology
van der Werf, Christian; Lieve, Krystien V; Bos, J Martijn; Lane, Conor M; Denjoy, Isabelle; Roses-Noguer, Ferran; Aiba, Takeshi; Wada, Yuko; Ingles, Jodie; Leren, Ida S; Rudic, Boris; Schwartz, Peter J; Maltret, Alice; Sacher, Frederic; Skinner, Jonathan R; Krahn, Andrew D; Roston, Thomas M; Tfelt-Hansen, Jacob; Swan, Heikki; Robyns, Tomas; Ohno, Seiko; Roberts, Jason D; van den Berg, Maarten P; Kammeraad, Janneke A; [...]

Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest

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Oxford University Press (OUP), 2019

Published in: European Heart Journal
Bergeman, Auke T.; Lieve, Krystien V.V.; Kallas, Dania; Bos, J. Martijn; Rosés i Noguer, Ferran; Denjoy, Isabelle; Zorio, Esther; Kammeraad, Janneke A.E.; Peltenburg, Puck J.; Tobert, Katie; Aiba, Takeshi; Atallah, Joseph; Drago, Fabrizio; Batra, Anjan S.; Brugada, Ramon; Borggrefe, Martin; Clur, Sally-Ann B.; Cox, Moniek G.P.J.; Davis, Andrew; Dhillon, Santokh; Etheridge, Susan P.; Fischbach, Peter; Franciosi, Sonia; Haugaa, Kristina; [...]

Flecainide Is Associated With a Lower Incidence of Arrhythmic Events in a Large Cohort of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

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Ovid Technologies (Wolters Kluwer Health), 2023

Published in: Circulation
Peltenburg, Puck J.; Kallas, Dania; Bos, Johan M.; Lieve, Krystien V.V.; Franciosi, Sonia; Roston, Thomas M.; Denjoy, Isabelle; Sorensen, Katrina B.; Ohno, Seiko; Roses-Noguer, Ferran; Aiba, Takeshi; Maltret, Alice; LaPage, Martin J.; Atallah, Joseph; Giudicessi, John R.; Clur, Sally-Ann B.; Blom, Nico A.; Tanck, Michael; Extramiana, Fabrice; Kato, Koichi; Barc, Julien; Borggrefe, Martin; Behr, Elijah R.; Sarquella-Brugada, Georgia; [...]

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

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Ovid Technologies (Wolters Kluwer Health), 2022

Published in: Circulation
Ng, Kevin; Titus, Erron W.; Lieve, Krystien V.; Roston, Thomas M.; Mazzanti, Andrea; Deiter, Frederick H.; Denjoy, Isabelle; Ingles, Jodie; Till, Jan; Robyns, Tomas; Connors, Sean P.; Steinberg, Christian; Abrams, Dominic J.; Pang, Benjamin; Scheinman, Melvin M.; Bos, J. Martijn; Duffett, Stephen A.; van der Werf, Christian; Maltret, Alice; Green, Martin S.; Rutberg, Julie; Balaji, Seshadri; Cadrin-Tourigny, Julia; Orland, Kate M.; [...]

An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms ofCASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia

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Ovid Technologies (Wolters Kluwer Health), 2020

Published in: Circulation
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; Campuzano, Oscar; Castelletti, Silvia; Celen, Candan; Clauss, Sebastian; [...]

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

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Elsevier BV, 2021

Published in: Genetics in Medicine
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; Christiansen, Michael; Winbo, Annika; Jabbari, Reza; Lubitz, Steven A.; [...]

Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

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Ovid Technologies (Wolters Kluwer Health), 2020

Published in: Circulation
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.; Muir, Alison; Papadakis, Michael; Castelletti, Silvia; Torchio, Margherita; [...]

Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

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Springer Science and Business Media LLC, 2022

Published in: Nature Genetics
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.; Muir, Alison; Papadakis, Michael; Castelletti, Silvia; Torchio, Margherita; [...]

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

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Springer Science and Business Media LLC, 2022

Published in: Nature Genetics

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