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Wülfers, Eike M; Moss, Robin; Lehrmann, Heiko; Arentz, Thomas; Westermann, Dirk; Seemann, Gunnar; Odening, Katja E; Steinfurt, Johannes (2024). Whole-heart computational modelling provides further mechanistic insights into ST-elevation in Brugada syndrome. International Journal of Cardiology. Heart & Vasculature, 51(101373) Elsevier 10.1016/j.ijcha.2024.101373
Steinfurt, Johannes; Nazer, Babak; Aguilar, Martin; Moss, Joshua; Higuchi, Satoshi; Zarse, Markus; Trolese, Luca; Gressler, Alexander; Faber, Thomas S.; Odening, Katja E; Zehender, Manfred; Bode, Christoph; Scheinman, Melvin M.; Tedrow, Usha B.; Bogossian, Harilaos (2022). Catheter ablation of short-coupled variant of torsade de pointes. Clinical research in cardiology, 111(5), pp. 502-510. Springer-Verlag 10.1007/s00392-021-01840-z
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
Steinfurt, Johannes; Bezzina, Connie R; Biermann, Jürgen; Staudacher, Dawid; Marschall, Christoph; Trolese, Luca; Faber, Thomas S; Duerschmied, Daniel; Zehender, Manfred; Bode, Christoph; Wilde, Arthur A M; Odening, Katja E; Lodder, Elisabeth M (2021). Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing. EP Europace, 23(5), pp. 775-780. Oxford University Press 10.1093/europace/euaa357
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
