| A randomized comparison of high clopidogrel loading doses in patients with non–ST-segment elevation acute coronary syndromes: the ALBION (Assessment of the Best Loading Dose of … G Montalescot, G Sideris, C Meuleman, C Bal-dit-Sollier, N Lellouche, ... Journal of the American College of Cardiology 48 (5), 931-938, 2006 | 723 | 2006 |
| Benefits of obstructive sleep apnoea treatment in coronary artery disease: a long-term follow-up study O Milleron, R Pillière, A Foucher, F de Roquefeuil, P Aegerter, G Jondeau, ... European heart journal 25 (9), 728-734, 2004 | 577 | 2004 |
| Marfan Sartan: a randomized, double-blind, placebo-controlled trial O Milleron, F Arnoult, J Ropers, P Aegerter, D Detaint, G Delorme, D Attias, ... European heart journal 36 (32), 2160-2166, 2015 | 229 | 2015 |
| Aortic event rate in the Marfan population: a cohort study G Jondeau, D Detaint, F Tubach, F Arnoult, O Milleron, F Raoux, ... Circulation 125 (2), 226-232, 2012 | 229 | 2012 |
| Nomograms for aortic root diameters in children using two-dimensional echocardiography M Gautier, D Detaint, C Fermanian, P Aegerter, G Delorme, F Arnoult, ... The American journal of cardiology 105 (6), 888-894, 2010 | 205 | 2010 |
| International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium) G Jondeau, J Ropers, E Regalado, A Braverman, A Evangelista, ... Circulation: Cardiovascular Genetics 9 (6), 548-558, 2016 | 180 | 2016 |
| MFAP5 loss-of-function mutations underscore the involvement of matrix alteration in the pathogenesis of familial thoracic aortic aneurysms and dissections M Barbier, MS Gross, M Aubart, N Hanna, K Kessler, DC Guo, L Tosolini, ... The American Journal of Human Genetics 95 (6), 736-743, 2014 | 141 | 2014 |
| Aortic stenosis and transthyretin cardiac amyloidosis: the chicken or the egg? A Galat, A Guellich, D Bodez, M Slama, M Dijos, DM Zeitoun, O Milleron, ... European heart journal 37 (47), 3525-3531, 2016 | 136 | 2016 |
| Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosis F Boccara, M Mary-Krause, E Teiger, S Lang, P Lim, K Wahbi, F Beygui, ... European heart journal 32 (1), 41-50, 2011 | 135 | 2011 |
| Dissection in Marfan syndrome: the importance of the descending aorta L Mimoun, D Detaint, D Hamroun, F Arnoult, G Delorme, M Gautier, ... European heart journal 32 (4), 443-449, 2011 | 96 | 2011 |
| Clinical relevance of genotype–phenotype correlations beyond vascular events in a cohort study of 1500 Marfan syndrome patients with FBN1 pathogenic variants P Arnaud, O Milleron, N Hanna, J Ropers, NO Ouali, A Affoune, ... Genetics in Medicine 23 (7), 1296-1304, 2021 | 91 | 2021 |
| Incidence, diagnostic methods, and evolution of left ventricular thrombus in patients with anterior myocardial infarction and low left ventricular ejection fraction: a … P Meurin, VB Carreira, R Dumaine, A Shqueir, O Milleron, B Safar, ... American heart journal 170 (2), 256-262, 2015 | 90 | 2015 |
| Association of modifiers and other genetic factors explain Marfan syndrome clinical variability M Aubart, S Gazal, P Arnaud, L Benarroch, MS Gross, J Buratti, A Boland, ... European Journal of Human Genetics 26 (12), 1759-1772, 2018 | 83 | 2018 |
| False lumen embolization in chronic aortic dissection promotes thoracic aortic remodeling at midterm follow-up Q Pellenc, A Roussel, R De Blic, A Girault, P Cerceau, IB Abdallah, ... Journal of Vascular Surgery 70 (3), 710-717, 2019 | 55 | 2019 |
| Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD) P Arnaud, N Hanna, L Benarroch, M Aubart, L Bal, P Bouvagnet, T Busa, ... Genetics in Medicine 21 (9), 2015-2024, 2019 | 54 | 2019 |
| Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials A Pitcher, E Spata, J Emberson, K Davies, H Halls, L Holland, K Wilson, ... The Lancet 400 (10355), 822-831, 2022 | 47 | 2022 |
| Pathogenic FBN1 Genetic Variation and Aortic Dissection in Patients With Marfan Syndrome O Milleron, F Arnoult, G Delorme, D Detaint, Q Pellenc, R Raffoul, ... Journal of the American College of Cardiology 75 (8), 843-853, 2020 | 46 | 2020 |
| Optimising aortic endovascular repair in patients with Marfan syndrome Q Pellenc, A Girault, A Roussel, R De Blic, P Cerceau, R Raffoul, ... European Journal of Vascular and Endovascular Surgery 59 (4), 577-585, 2020 | 43 | 2020 |
| Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome P Arnaud, N Hanna, M Aubart, B Leheup, S Dupuis-Girod, S Naudion, ... Journal of Medical Genetics 54 (2), 100-103, 2017 | 39 | 2017 |
| Pathogenic variants in THSD4, encoding the ADAMTS-like 6 protein, predispose to inherited thoracic aortic aneurysm S Elbitar, M Renard, P Arnaud, N Hanna, MP Jacob, DC Guo, K Tsutsui, ... Genetics in Medicine 23 (1), 111-122, 2021 | 38 | 2021 |
