| Heart disease and stroke statistics—2016 update: a report from the American Heart Association D Mozaffarian, EJ Benjamin, AS Go, DK Arnett, MJ Blaha, M Cushman, ... circulation 133 (4), e38-e360, 2016 | 72631* | 2016 |
| 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 | 538 | 2013 |
| 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 | 374 | 2009 |
| 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 | 319 | 2014 |
| 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 | 216 | 2011 |
| 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), e54131, 2013 | 167 | 2013 |
| 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 | 142 | 2015 |
| 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, 81-92, 2014 | 139 | 2014 |
| 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 | 116 | 2013 |
| 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 | 103 | 2013 |
| 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 | 99 | 2015 |
| 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 | 95 | 2016 |
| 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 | 91 | 2017 |
| Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility J Barc, R Tadros, C Glinge, DY Chiang, M Jouni, F Simonet, SJ Jurgens, ... Nature genetics 54 (3), 232-239, 2022 | 64 | 2022 |
| 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 | 60 | 2013 |
| Rare coding variants in ANGPTL6 are associated with familial forms of intracranial aneurysm R Bourcier, S Le Scouarnec, S Bonnaud, M Karakachoff, E Bourcereau, ... The American Journal of Human Genetics 102 (1), 133-141, 2018 | 55 | 2018 |
| Integrated clinical and omics approach to rare diseases: novel genes and oligogenic inheritance in holoprosencephaly A Kim, C Savary, C Dubourg, W Carré, C Mouden, H Hamdi-Roze, ... Brain 142 (1), 35-49, 2019 | 47 | 2019 |
| 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 | 45 | 2016 |
| 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 | 41 | 2012 |
| Understanding the pathophysiology of intracranial aneurysm: the ICAN project R Bourcier, S Chatel, E Bourcereau, S Jouan, H Le Marec, ... Neurosurgery 80 (4), 621-626, 2017 | 36 | 2017 |
Alban-Elouen BaruteauL'institut du thorax, INSERM, CNRS, UNIV Nantes, CHU Nantes, Nantes, FranceVerified email at chu-nantes.fr
