Verstraeten, Aline; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Perik, Melanie H A M; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Baranowska, Anna A; Department of Cardiovascular Sciences and National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.A.B., T.W., A.A.-H., N.J.S., D.A
Meester, Josephina A N; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Van Den Heuvel, Lotte; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Bastianen, Jarl; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Kempers, Marlies; Department of Human Genetics (M.K., B.L.), Radboud University Nijmegen Medical Center, The Netherlands
Krapels, Ingrid P C; Department of Clinical Genetics (I.P.C.K.), Maastricht University Medical Centre, The Netherlands
Maas, Angela; Department of Cardiology (A.M.), Radboud University Nijmegen Medical Center, The Netherlands
Rideout, Andrea; Maritime Medical Genetics Service, Izaak Walton Killam (IWK) Health Centre, Halifax, Canada (A.R., A. Vandersteen
Vandersteen, Anthony; Maritime Medical Genetics Service, Izaak Walton Killam (IWK) Health Centre, Halifax, Canada (A.R., A. Vandersteen ; Division of Medical Genetics, Department of Pediatrics, Dalhousie University, Halifax, Canada (A. Vandersteen
Sobey, Glenda; Ehlers Danlos Syndrome National Diagnostic Service, Sheffield Clinical Genetics Department, Northern General Hospital, United Kingdom (G.S., D.J
Johnson, Diana; Ehlers Danlos Syndrome National Diagnostic Service, Sheffield Clinical Genetics Department, Northern General Hospital, United Kingdom (G.S., D.J
Fransen, Erik; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L ; StatUa Center for Statistics, University of Antwerp, Belgium (E.F
Ghali, Neeti; Ehlers-Danlos Syndrome, National Diagnostic Service, Northwick Park and St. Mark's Hospitals, Harrow, United Kingdom (N.G., F.S.V.D
Webb, Tom; Department of Cardiovascular Sciences and National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.A.B., T.W., A.A.-H., N.J.S., D.A
Al-Hussaini, Abtehale; Department of Cardiovascular Sciences and National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.A.B., T.W., A.A.-H., N.J.S., D.A
de Leeuw, Peter; Department of Medicine (P.D.L.), Maastricht University Medical Centre, The Netherlands
Delmotte, Philippe; Division of Cardiology, Centre Hospitalier Universitaire Ambroise Paré, Mons, Belgium (P.D
Lopez-Sublet, Marilucy; Department of Internal Medicine, European Society of Hypertension Excellence Centre, Centre Hospitalier Universitaire (CHU) Avicenne, assistance publique hôpitaux de paris (AP-HP), Bobigny, France (M.L.-S
Pappaccogli, Marco; Pole of Cardiovascular Research, Institut de Recherche Expérimentale et Clinique, Division of Cardiology, Cliniques Universitaires Saint-Luc (M.P., A.P.), Université Catholique de Louvain, Brussels, Belgium ; Division of Internal Medicine and Hypertension Unit, Department of Medical Sciences, University of Turin, Italy (M.P
Sprynger, Muriel ; Université de Liège - ULiège > Département des sciences cliniques
Toubiana, Laurent; Sorbonne Université, Université Paris 13, Sorbonne Paris Cité, Institut national de la santé et de la recherche médicale (INSERM), UMR_S 1142, Laboratoire d'Informatique Médicale et d'Ingénieurie des Connaissances en e-Santé (LIMICS), Institut de recherche pour la valorisation des données de santé (IRSAN), France (L.T
European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)
Van Laer, Lut; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L
Van Dijk, Fleur S; Ehlers-Danlos Syndrome, National Diagnostic Service, Northwick Park and St. Mark's Hospitals, Harrow, United Kingdom (N.G., F.S.V.D
Vikkula, Miikka; Human Molecular Genetics, de Duve Institute (M.V.), Université Catholique de Louvain, Brussels, Belgium
Samani, Nilesh J; Department of Cardiovascular Sciences and National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.A.B., T.W., A.A.-H., N.J.S., D.A
Persu, Alexandre; Pole of Cardiovascular Research, Institut de Recherche Expérimentale et Clinique, Division of Cardiology, Cliniques Universitaires Saint-Luc (M.P., A.P.), Université Catholique de Louvain, Brussels, Belgium
Adlam, David; Department of Cardiovascular Sciences and National Institute for Health Research Leicester Biomedical Research Centre, Glenfield Hospital, United Kingdom (A.A.B., T.W., A.A.-H., N.J.S., D.A
Loeys, Bart; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Belgium (A. Verstraeten, M.H.A.M.P., J.A.N.M., L.V.D.H., J.B., E.F., L.V.L., B.L ; Department of Human Genetics (M.K., B.L.), Radboud University Nijmegen Medical Center, The Netherlands
Collaborators of the European/International Fibromuscular Dysplasia Registry and Initiative (FEIRI)
Hayes SN, Kim ESH, Saw J, Adlam D, Arslanian-Engoren C, Economy KE, Ganesh SK, Gulati R, Lindsay ME, Mieres JH,. Spontaneous coronary artery dissection: current state of the science: a scientific statement from the American Heart Association. Circulation 2018 137 e523-e557. doi: 10.1161/CIR.0000000000000564
Maas AHEM, Bouatia-Naji N, Persu A, Adlam D,. Spontaneous coronary artery dissections and fibromuscular dysplasia: current insights on pathophysiology, sex and gender. Int J Cardiol 2019 286 220-225. doi: 10.1016/j.ijcard.2018.11.023
Poloskey SL, Kim ESH, Sanghani R, Al-Quthami AH, Arscott P, Moran R, Rigelsky CM, Gornik HL,. Low yield of genetic testing for known vascular connective tissue disorders in patients with fibromuscular dysplasia. Vasc Med 2012 17 371-378. doi: 10.1177/1358863X12459650
Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G,. Candidate gene resequencing in a large bicuspid aortic valve-associated thoracic aortic aneurysm cohort: SMAD6 as an important contributor. Front Physiol 2017 8 400. doi: 10.3389/fphys.2017.00400
Bertoli-Avella AM, Gillis E, Morisaki H, Verhagen JMA, de Graaf BM, van de Beek G, Gallo E, Kruithof BPT, Venselaar H, Myers LA,. Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections. J Am Coll Cardiol 2015 65 1324-1336. doi: 10.1016/j.jacc.2015.01.040
