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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
Blancard, Malorie; Debbiche, Amal; Kato, Koichi; Cardin, Christelle; Guichard, Sabrina Lucienne Anny; Gandjbakhch, Estelle; Probst, Vincent; Haissaguerre, Michel; Extramiana, Fabrice; Hocini, Mélèze; Olivier, Geoffroy; Leenhardt, Antoine; Guicheney, Pascale; Rougier, Jean-Sébastien (2018). An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation. Scientific Reports, 8(1), p. 14619. Nature Publishing Group 10.1038/s41598-018-32867-4
Roten, Laurent; Derval, Nicolas; Maury, Philippe; Mahida, Saagar; Pascale, Patrizio; Leenhardt, Antoine; Jesel, Laurence; Deisenhofer, Isabel; Kautzner, Josef; Probst, Vincent; Rollin, Anne; Ruidavets, Jean-Bernard; Ferrières, Jean; Sacher, Frédéric; Heg, Dik; Scherr, Daniel; Komatsu, Yuki; Daly, Matthew; Denis, Arnaud; Shah, Ashok; ... (2016). Benign vs malignant inferolateral early repolarization: Focus on the T wave. Heart rhythm, 13(4), pp. 894-902. Elsevier 10.1016/j.hrthm.2015.11.020
Mahida, Saagar; Derval, Nicolas; Sacher, Frederic; Leenhardt, Antoine; Deisenhofer, Isabel; Babuty, Dominique; Schläpfer, Jürg; de Roy, Luc; Frank, Robert; Yli-Mayry, Sinikka; Mabo, Philippe; Rostock, Thomas; Nogami, Akihiko; Pasquié, Jean-Luc; de Chillou, Christian; Kautzner, Josef; Jesel, Laurence; Maury, Philippe; Berte, Benjamin; Yamashita, Seigo; ... (2015). Role of electrophysiological studies in predicting risk of ventricular arrhythmia in early repolarization syndrome. Journal of the American College of Cardiology, 65(2), pp. 151-159. Elsevier 10.1016/j.jacc.2014.10.043
