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Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.
Verstraeten, Aline; Perik, Melanie H A M; Baranowska, Anna A; Meester, Josephina A N; Van Den Heuvel, Lotte; Bastianen, Jarl; Kempers, Marlies; Krapels, Ingrid P C; Maas, Angela; Rideout, Andrea; Vandersteen, Anthony; Sobey, Glenda; Johnson, Diana; Fransen, Erik; Ghali, Neeti; Webb, Tom; Al-Hussaini, Abtehale; de Leeuw, Peter; Delmotte, Philippe; Lopez-Sublet, Marilucy; Pappaccogli, Marco; Sprynger, Muriel; Toubiana, Laurent; Van Laer, Lut; Van Dijk, Fleur S; Vikkula, Miikka; Samani, Nilesh J; Persu, Alexandre; Adlam, David; Loeys, Bart.
Afiliação
  • Verstraeten A; 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 MHAM; 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 AA; 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 JAN; 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 L; 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 J; 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 M; Department of Human Genetics (M.K., B.L.), Radboud University Nijmegen Medical Center, The Netherlands.
  • Krapels IPC; Department of Clinical Genetics (I.P.C.K.), Maastricht University Medical Centre, The Netherlands.
  • Maas A; Department of Cardiology (A.M.), Radboud University Nijmegen Medical Center, The Netherlands.
  • Rideout A; Maritime Medical Genetics Service, Izaak Walton Killam (IWK) Health Centre, Halifax, Canada (A.R., A. Vandersteen).
  • Vandersteen A; Maritime Medical Genetics Service, Izaak Walton Killam (IWK) Health Centre, Halifax, Canada (A.R., A. Vandersteen).
  • Sobey G; Division of Medical Genetics, Department of Pediatrics, Dalhousie University, Halifax, Canada (A. Vandersteen).
  • Johnson D; Ehlers Danlos Syndrome National Diagnostic Service, Sheffield Clinical Genetics Department, Northern General Hospital, United Kingdom (G.S., D.J.).
  • Fransen E; Ehlers Danlos Syndrome National Diagnostic Service, Sheffield Clinical Genetics Department, Northern General Hospital, United Kingdom (G.S., D.J.).
  • Ghali 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.).
  • Webb T; StatUa Center for Statistics, University of Antwerp, Belgium (E.F.).
  • Al-Hussaini A; Ehlers-Danlos Syndrome, National Diagnostic Service, Northwick Park and St. Mark's Hospitals, Harrow, United Kingdom (N.G., F.S.V.D.).
  • de Leeuw P; 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.).
  • Delmotte P; 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.).
  • Lopez-Sublet M; Department of Medicine (P.D.L.), Maastricht University Medical Centre, The Netherlands.
  • Pappaccogli M; Division of Cardiology, Centre Hospitalier Universitaire Ambroise Paré, Mons, Belgium (P.D.).
  • Sprynger M; 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.).
  • Toubiana L; 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.
  • Van Laer L; Cardiology Department, University of Liège Hospital, Belgium (M.S.).
  • Van Dijk FS; 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 (
  • Samani NJ; 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.).
  • Persu A; Ehlers-Danlos Syndrome, National Diagnostic Service, Northwick Park and St. Mark's Hospitals, Harrow, United Kingdom (N.G., F.S.V.D.).
  • Adlam D; Human Molecular Genetics, de Duve Institute (M.V.), Université Catholique de Louvain, Brussels, Belgium.
  • Loeys B; 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.).
Circulation ; 142(10): 1021-1024, 2020 09 08.
Article em En | MEDLINE | ID: mdl-32897753
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Anomalias dos Vasos Coronários / Síndrome de Loeys-Dietz / Displasia Fibromuscular / Mutação Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Anomalias dos Vasos Coronários / Síndrome de Loeys-Dietz / Displasia Fibromuscular / Mutação Tipo de estudo: Clinical_trials Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Circulation Ano de publicação: 2020 Tipo de documento: Article