CV Stephanie CHATEL

Vincent L'Allinec, Stéphanie Chatel, Matilde Karakachoff, Emmanuelle Bourcereau, Zeineb Es-Salah-Lamoureux, et al.. Prediction of Unruptured Intracranial Aneurysm Evolution: The UCAN Project. Neurosurgery, Lippincott, Williams & Wilkins, 2020. ⟨hal-02889889⟩

Romain Bourcier, Solena Le Scouarnec, Stephanie Bonnaud, Matilde Karakachoff, Emmanuelle Bourcereau, et al.. Rare Coding Variants in ANGPTL6 Are Associated with Familial Forms of Intracranial Aneurysm. American Journal of Human Genetics, Elsevier (Cell Press), 2018, 102 (1), pp.133 - 141. ⟨10.1016/j.ajhg.2017.12.006⟩. ⟨hal-01808225⟩

Romain Bourcier, Stéphanie Chatel, Emmanuelle Bourcereau, Solène Jouan, Hervé Le Marec, et al.. Understanding the Pathophysiology of Intracranial Aneurysm: The ICAN Project. Neurosurgery, Lippincott, Williams & Wilkins, 2017, 80 (4), pp.621-626. ⟨10.1093/neuros/nyw135⟩. ⟨hal-01768333⟩

Vincent Portero, Solena Le Scouarnec, Zeineb Es-Salah-Lamoureux, Sophie Burel, Jean-Baptiste Gourraud, et al.. Dysfunction of the Voltage-Gated K+ Channel beta 2 Subunit in a Familial Case of Brugada Syndrome. Journal of the American Heart Association, Wiley-Blackwell, 2016, 5 (6), pp.e003122. ⟨10.1161/JAHA.115.003122⟩. ⟨hal-01414464⟩

Nobue Yagihara, Hiroshi Watanabe, Phil Barnett, Laetitia Duboscq-Bidot, Atack C. Thomas, et al.. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes. Journal of the American Heart Association, Wiley-Blackwell, 2016, 5 (9), ⟨10.1161/JAHA.116.003644⟩. ⟨hal-01831755⟩

Solena Le Scouarnec, Matilde Karakachoff, Jean-Baptiste Gourraud, Pierre Lindenbaum, Stéphanie Bonnaud, et al.. Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome. Human Molecular Genetics, Oxford University Press (OUP), 2015, 24 (10), pp.2757--2763. ⟨10.1093/hmg/ddv036⟩. ⟨hal-01201946⟩

Philippe Maury, Frédéric Sacher, Jean-Baptiste Gourraud, Jean Luc Pasquié, Franck Raczka, et al.. Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndrome. Heart Rhythm, Elsevier, 2015, 12 (12), pp.2469 - 2476. ⟨10.1016/j.hrthm.2015.07.029⟩. ⟨hal-01773236⟩

Jean-Baptiste Gourraud, Solena Le Scouarnec, Frederic Sacher, Stéphanie Chatel, Nicolas Derval, et al.. Identification of Large Families in Early Repolarization Syndrome.. Journal of the American College of Cardiology, Elsevier, 2013, 61 (2), pp.164-72. ⟨10.1016/j.jacc.2012.09.040⟩. ⟨hal-00879642⟩

Jean-Baptiste Gourraud, Florence Kyndt, Swanny Fouchard, Eric Rendu, Philippe Jaafar, et al.. Identification of a strong genetic background for progressive cardiac conduction defect by epidemiological approach. Heart, BMJ Publishing Group, 2012, 98 (17), pp.1305 - 1310. ⟨10.1136/heartjnl-2012-301872⟩. ⟨inserm-01667205⟩

Alban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, Philippe Mabo, Jean-Jacques Schott, et al.. Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block.. Circulation, American Heart Association, 2012, 126 (12), pp.1469-77. ⟨10.1161/CIRCULATIONAHA.111.069161⟩. ⟨hal-00880957⟩