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Delinière, Antoine; Haddad, Christelle; Herrera-Siklody, Claudia; Hermida, Alexis; Pruvot, Etienne; Bressieux-Degueldre, Sabrina; Millat, Gilles; Janin, Alexandre; Hermida, Jean-Sylvain; Asatryan, Babken; Chevalier, Philippe (2023). Phenotypic Characterization of Timothy Syndrome Caused by the CACNA1C p.Gly402Ser Variant. Circulation. Genomic and precision medicine, 16(3), pp. 280-282. American Heart Association 10.1161/CIRCGEN.122.004010
Chevalier, Philippe; Moreau, Adrien; Bessière, Francis; Richard, Sylvain; Chahine, Mohamed; Millat, Gilles; Morel, Elodie; Paganelli, Franck; Lesavre, Nathalie; Placide, Leslie; Montestruc, François; Ankou, Bénédicte; Puertas, Rosa Doñate; Asatryan, Babken; Delinière, Antoine (2023). Identification of Cx43 variants predisposing to ventricular fibrillation in the acute phase of ST-elevation myocardial infarction. Europace, 25(1), pp. 101-111. Oxford University Press 10.1093/europace/euac128
Doñate Puertas, Rosa; Arora, Rishi; Rome, Sophie; Asatryan, Babken; Roderick, H Llewelyn; Chevalier, Philippe (2021). Epigenetics in atrial fibrillation: A reappraisal. Heart rhythm, 18(5), pp. 824-832. Elsevier 10.1016/j.hrthm.2021.01.007
Asatryan, Babken; Yee, Lauren; Ben-Haim, Yael; Dobner, Stephan; Servatius, Helge; Roten, Laurent; Tanner, Hildegard; Crotti, Lia; Skinner, Jonathan R.; Remme, Carol Ann; Chevalier, Philippe; Medeiros-Domingo, Argelia; Behr, Elijah R.; Reichlin, Tobias; Odening, Katja E.; Andrew D., Krahn (2021). Sex-Related Differences in Cardiac Channelopathies: Implications for Clinical Practice. Circulation, 143(7), pp. 739-752. American Heart Association 10.1161/CIRCULATIONAHA.120.048250
Fressart, Veronique; Duthoit, Guillaume; Donal, Erwan; Probst, Vincent; Deharo, Jean-Claude; Chevalier, Philippe; Klug, Didier; Dubourg, Olivier; Delacretaz, Etienne; Cosnay, Pierre; Scanu, Patrice; Extramiana, Fabrice; Keller, Dagmar; Hidden-Lucet, Françoise; Simon, Françoise; Bessirard, Vanessa; Roux-Buisson, Nathalie; Hebert, Jean-Louis; Azarine, Arshid; Casset-Senon, Daniele; ... (2010). Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice. Europace, 12(6), pp. 861-8. Oxford: Oxford University Press 10.1093/europace/euq104
