| 2018 ESC guidelines for the management of cardiovascular diseases during pregnancy: the task force for the management of cardiovascular diseases during pregnancy of the … V Regitz-Zagrosek, JW Roos-Hesselink, J Bauersachs, ... European heart journal 39 (34), 3165-3241, 2018 | 3862 | 2018 |
| The revised Ghent nosology for the Marfan syndrome BL Loeys, HC Dietz, AC Braverman, BL Callewaert, J De Backer, ... Journal of medical genetics 47 (7), 476-485, 2010 | 2396 | 2010 |
| A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 BL Loeys, J Chen, ER Neptune, DP Judge, M Podowski, T Holm, ... Nature genetics 37 (3), 275-281, 2005 | 1967 | 2005 |
| Aneurysm syndromes caused by mutations in the TGF-β receptor BL Loeys, U Schwarze, T Holm, BL Callewaert, GH Thomas, H Pannu, ... New England Journal of Medicine 355 (8), 788-798, 2006 | 1854 | 2006 |
| The 2017 international classification of the Ehlers–Danlos syndromes F Malfait, C Francomano, P Byers, J Belmont, B Berglund, J Black, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2017 | 1606 | 2017 |
| 2020 ESC Guidelines for the management of adult congenital heart disease: the Task Force for the management of adult congenital heart disease of the European Society of … H Baumgartner, J De Backer, SV Babu-Narayan, W Budts, M Chessa, ... European heart journal 42 (6), 563-645, 2021 | 1555 | 2021 |
| Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study L Faivre, G Collod-Beroud, BL Loeys, A Child, C Binquet, E Gautier, ... The American Journal of Human Genetics 81 (3), 454-466, 2007 | 601 | 2007 |
| Atenolol versus losartan in children and young adults with Marfan's syndrome RV Lacro, HC Dietz, LA Sleeper, AT Yetman, TJ Bradley, SD Colan, ... New England Journal of Medicine 371 (22), 2061-2071, 2014 | 547 | 2014 |
| Outcome of pregnancy in patients with structural or ischaemic heart disease: results of a registry of the European Society of Cardiology JW Roos-Hesselink, TPE Ruys, JI Stein, U Thilen, GD Webb, K Niwa, ... European heart journal 34 (9), 657-665, 2013 | 519 | 2013 |
| Mutations in the facilitative glucose transporter GLUT10 alter angiogenesis and cause arterial tortuosity syndrome PJ Coucke, A Willaert, MW Wessels, B Callewaert, N Zoppi, J De Backer, ... Nature genetics 38 (4), 452-457, 2006 | 433 | 2006 |
| Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial KT Ong, J Perdu, J De Backer, E Bozec, P Collignon, J Emmerich, ... The Lancet 376 (9751), 1476-1484, 2010 | 385 | 2010 |
| Circulating transforming growth factor-β in Marfan syndrome P Matt, F Schoenhoff, J Habashi, T Holm, C Van Erp, D Loch, OD Carlson, ... Circulation 120 (6), 526-532, 2009 | 339 | 2009 |
| FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders LY Sakai, DR Keene, M Renard, J De Backer Gene 591 (1), 279-291, 2016 | 321 | 2016 |
| Early surgical experience with Loeys-Dietz: a new syndrome of aggressive thoracic aortic aneurysm disease JA Williams, BL Loeys, LU Nwakanma, HC Dietz, PJ Spevak, ND Patel, ... The Annals of thoracic surgery 83 (2), S757-S763, 2007 | 313 | 2007 |
| Diagnosis, natural history, and management in vascular Ehlers–Danlos syndrome PH Byers, J Belmont, J Black, J De Backer, M Frank, X Jeunemaitre, ... American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2017 | 306 | 2017 |
| Comprehensive molecular screening of the FBN1 gene favors locus homogeneity of classical Marfan syndrome B Loeys, J De Backer, P Van Acker, K Wettinck, G Pals, L Nuytinck, ... Human mutation 24 (2), 140-146, 2004 | 302 | 2004 |
| Pregnancy outcomes in women with cardiovascular disease: evolving trends over 10 years in the ESC Registry Of Pregnancy And Cardiac disease (ROPAC) J Roos-Hesselink, L Baris, M Johnson, J De Backer, C Otto, A Marelli, ... European Heart Journal 40 (47), 3848-3855, 2019 | 299 | 2019 |
| Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome IMBH van de Laar, D van der Linde, EHG Oei, PK Bos, JH Bessems, ... Journal of medical genetics 49 (1), 47-57, 2012 | 277 | 2012 |
| Heart failure in pregnant women with cardiac disease: data from the ROPAC TPE Ruys, JW Roos-Hesselink, R Hall, MT Subirana-Domènech, ... Heart 100 (3), 231-238, 2014 | 258 | 2014 |
| Clinical validity of genes for heritable thoracic aortic aneurysm and dissection M Renard, C Francis, R Ghosh, AF Scott, PD Witmer, LC Adès, ... Journal of the American College of Cardiology 72 (6), 605-615, 2018 | 232 | 2018 |
