Stéphanie Chatel
Stéphanie Chatel
l'institut du thorax, INSERM, CNRS, Univ Nantes, CHU Nantes, Nantes, France
Verified email at univ-nantes.fr
Title
Cited by
Cited by
Year
Executive summary: heart disease and stroke statistics—2013 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, WB Borden, ...
circulation 127 (1), 143-152, 2013
21729*2013
Executive summary: heart disease and stroke statistics—2015 update: a report from the American Heart Association
D Mozaffarian, EJ Benjamin, AS Go, DK Arnett, MJ Blaha, M Cushman, ...
circulation 131 (4), 434-441, 2015
139112015
American heart association statistics committee and stroke statistics subcommittee
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
Heart disease and stroke statistics-2017 update: a report from the American …, 2017
2157*2017
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
CR Bezzina, J Barc, Y Mizusawa, CA Remme, JB Gourraud, F Simonet, ...
Nature genetics 45 (9), 1044-1049, 2013
3442013
Ventricular Fibrillation with Prominent Early Repolarization Associated with a Rare Variant of KCNJ8/KATP Channel
M Haïssaguerre, S Chatel, F Sacher, R Weerasooriya, V Probst, ...
Journal of cardiovascular electrophysiology 20 (1), 93-98, 2009
3152009
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization
DE Arking, SL Pulit, L Crotti, P Van Der Harst, PB Munroe, TT Koopmann, ...
Nature genetics 46 (8), 826-836, 2014
1942014
Experimental and numerical analyses of textile reinforcement forming of a tetrahedral shape
S Allaoui, P Boisse, S Chatel, N Hamila, G Hivet, D Soulat, E Vidal-Salle
Composites Part A: Applied Science and Manufacturing 42 (6), 612-622, 2011
1552011
Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel
H Liu, S Chatel, C Simard, N Syam, L Salle, V Probst, J Morel, G Millat, ...
PloS one 8 (1), 2013
1042013
Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome
S Le Scouarnec, M Karakachoff, JB Gourraud, P Lindenbaum, S Bonnaud, ...
Human molecular genetics 24 (10), 2757-2763, 2015
972015
First steps towards an advanced simulation of composites manufacturing by automated tape placement
F Chinesta, A Leygue, B Bognet, C Ghnatios, F Poulhaon, F Bordeu, ...
International journal of material forming 7 (1), 81-92, 2014
952014
Prevalence and prognostic role of various conduction disturbances in patients with the Brugada syndrome
P Maury, A Rollin, F Sacher, JB Gourraud, F Raczka, JL Pasquié, ...
The American journal of cardiology 112 (9), 1384-1389, 2013
812013
Identification of large families in early repolarization syndrome
JB Gourraud, S Le Scouarnec, F Sacher, S Chatel, N Derval, V Portero, ...
Journal of the American College of Cardiology 61 (2), 164-172, 2013
812013
Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndrome
P Maury, F Sacher, JB Gourraud, JL Pasquié, F Raczka, V Bongard, ...
Heart Rhythm 12 (12), 2469-2476, 2015
722015
Prevalence, characteristics, and prognosis role of type 1 ST elevation in the peripheral ECG leads in patients with Brugada syndrome
A Rollin, F Sacher, JB Gourraud, JL Pasquié, F Raczka, A Duparc, ...
Heart Rhythm 10 (7), 1012-1018, 2013
512013
Biallelic variants in UBA5 reveal that disruption of the UFM1 cascade can result in early-onset encephalopathy
E Colin, J Daniel, A Ziegler, J Wakim, A Scrivo, TB Haack, S Khiati, ...
The American Journal of Human Genetics 99 (3), 695-703, 2016
402016
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block
AE Baruteau, A Behaghel, S Fouchard, P Mabo, JJ Schott, C Dina, ...
Circulation 126 (12), 1469-1477, 2012
342012
Experimental device for the preforming step of the RTM process
D Soulat, S Allaoui, S Chatel
International Journal of Material Forming 2 (1), 181, 2009
272009
Rare RNF213 variants in the C-terminal region encompassing the RING-finger domain are associated with moyamoya angiopathy in Caucasians
S Guey, M Kraemer, D Hervé, T Ludwig, M Kossorotoff, F Bergametti, ...
European Journal of Human Genetics 25 (8), 995-1003, 2017
222017
Composites preforms simulations for helicopters parts
F Dumont, C Weimer, D Soulat, J Launay, S Chatel, S Maison-Le-Poec
International journal of material forming 1 (1), 847-850, 2008
212008
Variants of transient receptor potential melastatin member 4 in childhood atrioventricular block
N Syam, S Chatel, LC Ozhathil, V Sottas, JS Rougier, A Baruteau, ...
Journal of the American Heart Association 5 (5), e001625, 2016
202016
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