부산대학교 도서관

Racine C; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon, Dijon, France.; Callier P; UMR1231 GAD, Inserm-Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique Des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Touraine R; Service de Biochimie et Génétique Moléculaire, CHU Clermont-Ferrand, Laboratoire AURAGEN (Plan France Médecine Génomique 2025), Clermont-Ferrand, France.; Vitobello A; UMR1231 GAD, Inserm-Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique Des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Hanna N; Laboratory for Vascular Translational Science, INSERM U1148, Université Paris Cité, Hôpital Bichat, APHP, Paris, France.; Département de Génétique, Centre de référence Syndrome de Marfan et Pathologies apparentés, APHP, Hôpital Bichat, Paris, France.; Arnaud P; Laboratory for Vascular Translational Science, INSERM U1148, Université Paris Cité, Hôpital Bichat, APHP, Paris, France.; Département de Génétique, Centre de référence Syndrome de Marfan et Pathologies apparentés, APHP, Hôpital Bichat, Paris, France.; Jondeau G; Laboratory for Vascular Translational Science, INSERM U1148, Université Paris Cité, Hôpital Bichat, APHP, Paris, France.; Département de Génétique, Centre de référence Syndrome de Marfan et Pathologies apparentés, APHP, Hôpital Bichat, Paris, France.; Boileau C; Laboratory for Vascular Translational Science, INSERM U1148, Université Paris Cité, Hôpital Bichat, APHP, Paris, France.; Département de Génétique, Centre de référence Syndrome de Marfan et Pathologies apparentés, APHP, Hôpital Bichat, Paris, France.; Thauvin-Robinet C; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon, Dijon, France.; UMR1231 GAD, Inserm-Université Bourgogne-Franche Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique Des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.; Creveaux I; Service de Biochimie et Génétique Moléculaire, CHU Clermont-Ferrand, Laboratoire AURAGEN (Plan France Médecine Génomique 2025), Clermont-Ferrand, France.; Gatinois V; Plateforme ChromoStem, Unité de génétique Chromosomique, Département de génétique moléculaire et cytogénomique, CHU de Montpellier, Université de Montpellier, Montpellier, France.; Willems M; Département de Génétique Médicale, Maladies Rares et Médecine Personnalisée, CHU Montpellier, Montpellier, France.; Faivre L; Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon, Dijon, France.; UMR1231 GAD, Inserm-Université Bourgogne-Franche Comté, Dijon, France.

Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

Eliahou L; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France. Ludivine.eliahou@aphp.fr.; Milleron O; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Haviari S; Université Sorbonne Paris Nord, IAME, INSERM, Paris, 75018, France.; Département Epidémiologie Biostatistiques et Recherche Clinique, AP-HP, Hôpital Bichat, Paris, 75018, France.; Université Paris Cité, Paris, France.; Arnoult F; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Hanna N; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Département de génétique AP-HP, Hopital Bichat, Paris, France.; INSERM U1148, LVTS, Hopital Bichat, Paris, France.; Arnaud P; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Université Paris Cité, Paris, France.; Département de génétique AP-HP, Hopital Bichat, Paris, France.; INSERM U1148, LVTS, Hopital Bichat, Paris, France.; Toure F; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Jadoui S; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Mirmiran A; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Boileau C; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Université Paris Cité, Paris, France.; Département de génétique AP-HP, Hopital Bichat, Paris, France.; INSERM U1148, LVTS, Hopital Bichat, Paris, France.; Jondeau G; Centre National de Référence pour le syndrome de Marfan et apparentés, maladies aortiques rares, VASCERN HCP, Service de Cardiologie, Hôpital Bichat, 46 rue Henri Huchard, Paris, 75018, France.; Université Paris Cité, Paris, France.; INSERM U1148, LVTS, Hopital Bichat, Paris, France.

Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE

Tchitchinadze M; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Milleron O; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Eliahou L; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Jadoui S; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Ouali NO; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Hanna N; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Département de génétique, AP-HP, Hôpital Bichat, Paris, France.; INSERM U1148, LVTS, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Arnaud P; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Département de génétique, AP-HP, Hôpital Bichat, Paris, France.; INSERM U1148, LVTS, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Université Paris Cité, 45 rue des Saint Pères, Paris 75006, France.; Ropers J; Unité De Recherche Clinique, AP-HP, Pitié Salpêtrière-Charles Foix, Paris, France.; Boileau C; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Département de génétique, AP-HP, Hôpital Bichat, Paris, France.; INSERM U1148, LVTS, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Université Paris Cité, 45 rue des Saint Pères, Paris 75006, France.; Gouya L; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Université Paris Cité, 45 rue des Saint Pères, Paris 75006, France.; Jondeau G; Centre National de Reference Pour le Syndrome de Marfan et Apparentés, VASCERN HCP, Service de Cardiologie, AP-HP, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; INSERM U1148, LVTS, Hôpital Bichat, 46 rue Henri Huchard, Paris 75018, France.; Université Paris Cité, 45 rue des Saint Pères, Paris 75006, France.

Publisher: Oxford University Press Country of Publication: England NLM ID: 8006263 Publication Model: Print Cited Medium: Internet ISSN: 1522-9645 (Electronic) Linking ISSN: 0195668X NLM ISO Abbreviation: Eur Heart J Subsets: MEDLINE; In Process

Kopel H; Moderna, Inc., Cambridge, MA 02139, USA.; Nguyen VH; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Bogdanov A; Veradigm, Chicago, IL 60654, USA.; Winer I; Veradigm, Chicago, IL 60654, USA.; Boileau C; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Ducruet T; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Zeng N; Veradigm, Chicago, IL 60654, USA.; Winer-Jones JP; Veradigm, Chicago, IL 60654, USA.; Esposito DB; Moderna, Inc., Cambridge, MA 02139, USA.; Bausch-Jurken M; Moderna, Inc., Cambridge, MA 02139, USA.; Beck E; Moderna, Inc., Cambridge, MA 02139, USA.; Bonafede M; Veradigm, Chicago, IL 60654, USA.; Mansi JA; Moderna, Inc., Cambridge, MA 02139, USA.

Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101629355 Publication Model: Electronic Cited Medium: Print ISSN: 2076-393X (Print) Linking ISSN: 2076393X NLM ISO Abbreviation: Vaccines (Basel) Subsets: PubMed not MEDLINE

Juge PA; Université de Paris Cité, INSERM UMR 1152, Paris, France.; Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Sparks JA; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.; Gazal S; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.; Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.; Ebstein E; Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Borie R; Université de Paris Cité, INSERM UMR 1152, Paris, France.; Service de Pneumologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Debray MP; Service de Radiologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Kannengiesser C; Université de Paris Cité, INSERM UMR 1152, Paris, France.; Service de Génétique, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; McDermott GC; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.; Cui J; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.; Hayashi K; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.; Doyle TJ; Harvard Medical School, Boston, MA, USA.; Division of Pulmonary and Critical Care, Brigham and Women's Hospital, Boston, MA, USA.; van Moorsel CHM; Interstitial Lung Disease Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.; Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.; van der Vis JJ; Interstitial Lung Disease Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.; Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.; Grutters JC; Interstitial Lung Disease Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.; Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.; Knevel R; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.; Translational & Clinical Research Institute, Newcastle University, UK.; Heckert SL; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.; Vasarmidi E; Laboratory of Molecular and Cellular Pneumonology, Department of Respiratory Medicine, School of Medicine, University of Crete, Heraklion, Greece.; Antoniou KM; Laboratory of Molecular and Cellular Pneumonology, Department of Respiratory Medicine, School of Medicine, University of Crete, Heraklion, Greece.; van der Helm van Mil AHM; Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.; Department of Rheumatology, Erasmus MC, Rotterdam, The Netherlands.; Boileau C; Service de Génétique, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Crestani B; Université de Paris Cité, INSERM UMR 1152, Paris, France.; Service de Pneumologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.; Dieudé P; Université de Paris Cité, INSERM UMR 1152, Paris, France.; Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.

Publisher: Oxford University Press Country of Publication: England NLM ID: 101736676 Publication Model: eCollection Cited Medium: Internet ISSN: 2514-1775 (Electronic) Linking ISSN: 25141775 NLM ISO Abbreviation: Rheumatol Adv Pract Subsets: PubMed not MEDLINE

Bouhatous YM; Clinical Genetics, University Hospital Centre Dijon Bourgogne, Dijon, France laurence.faivre@chu-dijon.fr bouhatousyordi@gmail.com.; Arnaud P; Département de Génétique, Assistance Publique - Hopitaux de Paris, Paris, France.; LVTS, INSERM U1148, Paris, France.; Jondeau G; LVTS, INSERM U1148, Paris, France.; Centre de Référence Maladies Rares Syndrome de Marfan et apparentés, Hôpital Bichat, Assistance Publique - Hopitaux de Paris, Paris, Île-de-France, France.; Bonneau D; Service de génétique, Centre Hospitalier Universitaire d'Angers, Angers, Pays de la Loire, France.; Rouleau F; Service médicochirurgical des valvulopathies, Centre Hospitalier Universitaire, Angers, France.; Plessis G; Service de Génétique, CHU Clémenceau, Caen, France.; Vincent A; Service de génétique, Centre Hospitalier Universitaire, Caen, France.; Labombarda F; Service de Cardiologie, CHU Caen, Caen, France.; Maragnes P; Cardiologie pédiatrique, Service de pédiatrie, CHU Caen, Caen, Basse-Normandie, France.; Delanne J; Clinicl genetics, University Hospital Centre Dijon Bourgogne, Dijon, France.; Muller M; Unité de cardiologie congénitale et pédiatrique, Hôpital d'Enfants, Dijon, France.; Coubes C; Genetic Services, A. de Villeneuve Hospital, Montpellier, France.; Bredy C; Service de cardiologie, Centre Hospitalier Universitaire, Montpellier, France.; Gouya L; Centre de Référence Maladies Rares Syndrome de Marfan et apparentés, Hôpital Bichat, AP-HP, Paris, Île-de-France, France.; Odent S; Service de Génétique Clinique, CLAD Ouest, CHU Rennes, RENNES, France.; Basquin A; Cardiology Office, Rennes, Bretagne, France.; Dupuis-Girod S; HHT Reference center and genetics department, Hospices Civils de Lyon, BRON, France.; Barthelet M; Service des explorations fonctionnelles cardiovasculaires, Hôpital cardiologique Louis Pradel, Bron, France.; Ginglinger E; Génétique médicale, GHRMSA, Mulhouse, France.; Delobel B; Genetics, GHICL, Lille, France.; Vaksmann G; Cabinet Vendôme de cardiologie adulte et pédiatrique, Intercard, Lille, France.; Alessandri JL; service de pédiatrie, CHU Félix Guyon, Saint-Denis, La Réunion, Réunion.; Arsac LA; Service de cardiologie, Centre Hospitalier Universitaire de La Réunion, Saint-Denis, La Réunion, Réunion.; Thomas E; Reference Center for Marfan syndrome and related diseases, CHU Toulouse, Toulouse, France.; INSERM U1301, Paul Sabatier University, RESTORE, Toulouse, France.; Julia S; Reference Center for Marfan syndrome and related diseases, CHU Toulouse, Toulouse, France.; INSERM U1301, Paul Sabatier University, RESTORE, Toulouse, France.; Chesneau B; Reference Center for Marfan syndrome and related diseases, CHU Toulouse, Toulouse, France.; INSERM U1301, Paul Sabatier University, RESTORE, Toulouse, France.; Dulac Y; Reference Center for Marfan syndrome and related diseases, CHU Toulouse, Toulouse, France.; INSERM U1301, Paul Sabatier University, RESTORE, Toulouse, France.; Callewaert B; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Loeys B; Antwerp University Hospital, Antwerp, Belgium.; Vaerle M; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Menke LA; Department of Pediatrics, Amsterdam UMC location University of Amsterdam, Amsterdam, The Netherlands.; Neuroscience - Cellular and Molecular Mechanisms, Amsterdam Neuroscience, Amsterdam, North Holland, The Netherlands.; Groenink M; Cardiologie Centra Nederland, Cardiologie Centra Nederland, Amsterdam, The Netherlands.; Ades L; Department of Clinical Genetics, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.; Marfan Research Group, The Children's Hospital at Westmead, Westmead, New South Wales, Australia.; Ballesta-Martinez MJ; Unit of Medical Genetics. Pediatric Service, University Hospital Virgen de la Arrixaca, MURCIA, Murcia, Spain.; Shanske AL; Center for Craniofacial Disorders, Children's Hospital at Montefiore Medical Center, Bronx, New York, USA.; Tinschert S; Zentrum Medizinische Genetik, Medizinische Universität Innsbruck, Innsbruck, Tirol, Austria.; Gehle P; Charité Universitätsmedizin Berlin Medizinische Klinik mit Schwerpunkt Kardiologie, Berlin, BE, Germany.; Thauvin-Robinet C; Centre de Génétique, Hôpital d'Enfants, CHU Dijon, Dijon, France.; INSERM UMR1231, Équipe Génétique des Anomalies du Développement, Université de Bourgogne, Dijon, France.; Eicher JC; Service de cardiologie 2 : Rythmologie et Insuffisance Cardiaque, University Hospital Centre Dijon Bourgogne, Dijon, France.; Falcon-Eicher S; Unité de cardiologie congénitale et pédiatrique, Hôpital d'Enfants, Dijon, France.; Boileau C; Département de Génétique, Assistance Publique - Hopitaux de Paris, Paris, France.; LVTS, INSERM U1148, Paris, France.; Binquet C; CIC-EC, Dijon, France.; Hanna N; Département de Génétique, Assistance Publique - Hopitaux de Paris, Paris, France.; LVTS, INSERM U1148, Paris, France.; Faivre L; Centre de Génétique, Hôpital d'Enfants, Dijon, France laurence.faivre@chu-dijon.fr bouhatousyordi@gmail.com.

Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Bouleti C; University of Poitiers, Clinical Investigation Center (INSERM 1402), FACT and Poitiers Hospital, Cardiology Department, Poitiers, France. Electronic address: claire.bouleti@gmail.com.; Tence N; Private Hospital Jacques Cartier, Cardiology Department, Massy, France.; Thuillier R; Inserm Unit Ischémie Reperfusion, Métabolisme et Inflammation Stérile en Transplantation (IRMETIST), UMR U1313, Poitiers, France; Faculty of Medicine and Pharmacy, University of Poitiers, Poitiers, France; Biochemistry Department, CHU Poitiers, Poitiers, France.; Nicot F; Hospital of Versailles, Cardiology Department, Le Chesnay, France.; Pasi N; Private Hospital Paul Degine, Radiology Department, Champigny-sur-Marne, France.; Alos B; University of Poitiers, Clinical Investigation Center (INSERM 1402), FACT and Poitiers Hospital, Cardiology Department, Poitiers, France.; Suc G; Bichat University Hospital, AP-HP, Cardiology Department, Paris, France.; Milleron O; Bichat University Hospital, AP-HP, Reference Center for Marfan Disease, Cardiology Department, U1148 LVTS, INSERM, Université Paris Cité, Paris, France.; Arnoult F; Bichat University Hospital, AP-HP, Reference Center for Marfan Disease, Cardiology Department, U1148 LVTS, INSERM, Université Paris Cité, Paris, France.; Tchitchinadze M; Bichat University Hospital, AP-HP, Reference Center for Marfan Disease, Cardiology Department, U1148 LVTS, INSERM, Université Paris Cité, Paris, France.; Langeois M; University Hospital of Toulouse, Genetic Department, Toulouse, France.; Boileau C; Bichat University Hospital, AP-HP, Reference Center for Marfan Disease, Genetic Department, Université Paris Cité, Paris, France.; Gouya L; Bichat University Hospital, AP-HP, Genetic Department, U1148 LVTS, INSERM, Université Paris Cité, Paris, France.; Ou P; Bichat University Hospital, AP-HP, Radiology Department, Paris, France.; Jondeau G; Bichat University Hospital, AP-HP, Cardiology Department, Paris, France.

Publisher: Elsevier Inc Country of Publication: United States NLM ID: 9918419284106676 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2772-963X (Electronic) Linking ISSN: 2772963X NLM ISO Abbreviation: JACC Adv Subsets: PubMed not MEDLINE

Calderon-Martinez E; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Velasco WV; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Guo D; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Hostetler EH; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Xun Z; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Stephens S; Division of Cardiology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.; Shalhub S; Division of Vascular and Endovascular Surgery, Department of Surgery, Oregon Health Science University, Portland, Oregon, USA.; De Backer J; Department of Cardiology and Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Ouzounian M; Division of Cardiovascular Surgery, Department of Surgery, University of Toronto, Toronto General Hospital, Toronto, Ontario, Canada.; LeMaire SA; Division of Cardiothoracic Surgery, Michael E. DeBakey Department of Surgery, Baylor College of Medicine, Houston, Texas, USA; Texas Heart Institute, Houston, Texas, USA.; Milleron O; Centre National de Reference pour le Syndrome de Marfan et les Syndromes Apparentés, VASCERN HTAD European Reference Centre, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France; Université de Paris, LVTS, INSERM U1148, Hôpital Bichat-Claude-Bernard, Paris, France; Service de Cardiologie, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Hanna N; Centre National de Reference pour le Syndrome de Marfan et les Syndromes Apparentés, VASCERN HTAD European Reference Centre, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France; Université de Paris, LVTS, INSERM U1148, Hôpital Bichat-Claude-Bernard, Paris, France; Département de Génétique, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Arnaud P; Centre National de Reference pour le Syndrome de Marfan et les Syndromes Apparentés, VASCERN HTAD European Reference Centre, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France; Université de Paris, LVTS, INSERM U1148, Hôpital Bichat-Claude-Bernard, Paris, France; Département de Génétique, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Tchitchinadze M; Centre National de Reference pour le Syndrome de Marfan et les Syndromes Apparentés, VASCERN HTAD European Reference Centre, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Prakash SK; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Lindsay M; Cardiovascular Genetics Program, Massachusetts General Hospital, Boston, Massachusetts, USA; Cardiovascular Research Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.; Marcadier J; Department of Medical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada.; Jeremy R; Central Clinical School, Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia; Marfan and Aortic Disease Service, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.; Morris SA; Division of Cardiology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.; Yetman AT; Division of Pediatric Cardiology, Children's Hospital & Medical Center, University of Nebraska Medical Center, Omaha, Nebraska, USA.; Boileau C; Département de Génétique, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Braverman AC; Cardiovascular Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.; Jondeau G; Centre National de Reference pour le Syndrome de Marfan et les Syndromes Apparentés, VASCERN HTAD European Reference Centre, AP-HP, Hôpital Bichat-Claude-Bernard, Paris, France.; Milewicz DM; Division of Medical Genetics, Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA. Electronic address: Dianna.M.Milewicz@uth.tmc.edu.

Publisher: Elsevier Biomedical Country of Publication: United States NLM ID: 8301365 Publication Model: Print Cited Medium: Internet ISSN: 1558-3597 (Electronic) Linking ISSN: 07351097 NLM ISO Abbreviation: J Am Coll Cardiol Subsets: MEDLINE

Boccara F; Department of Cardiology, Saint-Antoine Research Center, Institut National de la Santé et de la Recherche Médicale (INSERM) UMR S938, Saint-Antoine Hospital, Hôpitaux de l'Est Parisien, Assistance Publique-Hôpitaux de Paris (AP-HP), Sorbonne University, Paris, France - franck.boccara@aphp.fr.; Sabouret P; Service of Cardiology, Institute of Cardiology, Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France.; Boileau C; Department of Genetics, LVTS - Institut National de la Santé et de la Recherche Médicale (INSERM) U1148, Bichat-Claude Bernard Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Université Paris Cité, Paris, France.; Georges JL; Service of Cardiology, Center Hospitalier de Versailles, Le Chesnay, France.; Annales de Cardiologie et Angéiologie, Elsevier Masson SAS, Issy les Moulineaux, France.; Leclercq C; Service of Cardiology, Rennes University Hospital, University of Rennes, Rennes, France.; Lesnik P; Institut National de la Santé et de la Recherche Médicale (INSERM) UMR_S 1166, Pitié-Salpêtrière University Hospital, Sorbonne University, Paris, France.; Bruckert E; Health Center, Paris, France.

Publisher: Panminerva Medica Country of Publication: Italy NLM ID: 0421110 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1827-1898 (Electronic) Linking ISSN: 00310808 NLM ISO Abbreviation: Panminerva Med Subsets: MEDLINE

Huguet Herrero J; Arnaud P; Bibimbou A; Seifert DE; Mougin Z; Benarroch L; Michot C; Capri Y; Ruaud L; Dupuis-Girod S; Guilhem A; Beyer C; Bajolle F; Milleron O; Jondeau G; Hanna N; Reinhardt DP; Guo DC; Milewicz D; Boileau C; Aubart M; Mead TJ; Le Goff C

Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE

Kopel H; Moderna, Inc., Cambridge, MA 02139, USA.; Nguyen VH; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Boileau C; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Bogdanov A; Veradigm, Chicago, IL 60654, USA.; Winer I; Veradigm, Chicago, IL 60654, USA.; Ducruet T; VHN Consulting Inc., Montreal, QC H2V 3L8, Canada.; Zeng N; Veradigm, Chicago, IL 60654, USA.; Bonafede M; Veradigm, Chicago, IL 60654, USA.; Esposito DB; Moderna, Inc., Cambridge, MA 02139, USA.; Martin D; Moderna, Inc., Cambridge, MA 02139, USA.; Rosen A; Moderna, Inc., Cambridge, MA 02139, USA.; Van de Velde N; Moderna, Inc., Cambridge, MA 02139, USA.; Vermund SH; Yale School of Public Health, Yale University, New Haven, CT 06510, USA.; Gravenstein S; Alpert Medical School and School of Public Health, Brown University, Providence, RI 02903, USA.; Mansi JA; Moderna, Inc., Cambridge, MA 02139, USA.

Publisher: MDPI AG Country of Publication: Switzerland NLM ID: 101629355 Publication Model: Electronic Cited Medium: Print ISSN: 2076-393X (Print) Linking ISSN: 2076393X NLM ISO Abbreviation: Vaccines (Basel) Subsets: PubMed not MEDLINE

Boileau C; Aix-Marseille Univ. INSERM, Marseille, France.; Deforges S; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Peret A; Aix-Marseille Univ. INSERM, Marseille, France.; Scavarda D; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Pediatric Neurosurgery, Marseille, France.; Bartolomei F; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Giles A; REGENXBIO, Rockville, MD, USA.; Partouche N; Aix-Marseille Univ. INSERM, Marseille, France.; Corlieve Therapeutics SAS, uniQure NV, Paris, France.; Gautron J; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Corlieve Therapeutics SAS, uniQure NV, Paris, France.; Viotti J; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Janowitz H; REGENXBIO, Rockville, MD, USA.; Penchet G; Pellegrin Hospital, Neurosurgery Department, Bordeaux, France.; Marchal C; Pellegrin Hospital, Neurosurgery Department, Bordeaux, France.; Lagarde S; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Trebuchon A; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Villeneuve N; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Rumi J; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Marissal T; Aix-Marseille Univ. INSERM, Marseille, France.; Khazipov R; Aix-Marseille Univ. INSERM, Marseille, France.; Khalilov I; Aix-Marseille Univ. INSERM, Marseille, France.; Martineau F; Aix-Marseille Univ. INSERM, Marseille, France.; Maréchal M; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Lepine A; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Milh M; APHM, INSERM, Aix Marseille Univ, INS, Timone Hospital, Epileptology Department, Marseille, France.; Figarella-Branger D; APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service d'Anatomie Pathologique et de Neuropathologie, Aix-Marseille Univ, Marseille, France.; Dougy E; APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service d'Anatomie Pathologique et de Neuropathologie, Aix-Marseille Univ, Marseille, France.; Tong S; APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service d'Anatomie Pathologique et de Neuropathologie, Aix-Marseille Univ, Marseille, France.; Appay R; APHM, CNRS, INP, Inst Neurophysiopathol, CHU Timone, Service d'Anatomie Pathologique et de Neuropathologie, Aix-Marseille Univ, Marseille, France.; Baudouin S; Corlieve Therapeutics SAS, uniQure NV, Paris, France.; Mercer A; REGENXBIO, Rockville, MD, USA.; Smith JB; REGENXBIO, Rockville, MD, USA.; Danos O; REGENXBIO, Rockville, MD, USA.; Porter R; Corlieve Therapeutics SAS, uniQure NV, Paris, France.; Mulle C; Univ. Bordeaux, CNRS, Interdisciplinary Institute for Neuroscience IINS, UMR 5297, Bordeaux, France.; Crépel V; Aix-Marseille Univ. INSERM, Marseille, France.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1531-8249 (Electronic) Linking ISSN: 03645134 NLM ISO Abbreviation: Ann Neurol Subsets: MEDLINE

Tesi B; Department of Molecular Medicine and Surgery and Centre of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.; Center for Hematology and Regenerative Medicine, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.; Boileau C; Département de Génétique, APHP, Hôpital Bichat-Claude Bernard, Université Paris Cité, Paris, France.; Boycott KM; Children's Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, Ontario, Canada.; Canaud G; INSERM U1151, Unité de médecine translationnelle et thérapies ciblées, Hôpital Necker-Enfants Malades, Université Paris Cité, AP-HP, Paris, France.; Caulfield M; William Harvey Research Institute, Queen Mary University of London, London, UK.; Choukair D; Division of Pediatric Endocrinology and Diabetes, Center for Pediatrics and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany and Center for Rare Diseases, University Hospital Heidelberg, Heidelberg, Germany.; Hill S; Chief Scientific Officer, NHS England, London, UK.; Spielmann M; Institute of Human Genetics, University Hospitals Schleswig-Holstein, University of Lübeck and Kiel University, Lübeck, Kiel, Germany.; Wedell A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.; Centre for Inherited Metabolic Diseases, Karolinska University Hospital, Stockholm, Sweden.; Wirta V; Science for Life Laboratory, Department of Microbiology, Tumour and Cell Biology, Karolinska Institutet, Stockholm, Sweden.; Science for Life Laboratory, School of Engineering Sciences in Chemistry, Biotechnology and Health, KTH Royal Institutet of Technology, Stockholm, Sweden.; Nordgren A; Department of Molecular Medicine and Surgery and Centre of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.; Department of Laboratory Medicine, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden.; Department of Clinical Genetics and Genomics, Sahlgrenska University Hospital, Gothenburg, Sweden.; Lindstrand A; Department of Molecular Medicine and Surgery and Centre of Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.; Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.

Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 8904841 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2796 (Electronic) Linking ISSN: 09546820 NLM ISO Abbreviation: J Intern Med Subsets: MEDLINE

Arnaud P; Département de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.; Université Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.; Cadenet M; Département de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.; Mougin Z; Université Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.; Le Goff C; Université Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.; Perbet S; Pôle de Médecine Péri-Opératoire, CHU Clermont-Ferrand, F-63000 Clermont-Ferrand, France.; Francois M; Service de Génétique, Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, F-69500 Bron, France.; Dupuis-Girod S; Service de Génétique, Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, F-69500 Bron, France.; Boileau C; Département de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.; Université Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.; Hanna N; Département de Génétique, AP-HP, Hôpital Bichat, F-75018 Paris, France.; Université Paris Cité, Inserm, LVTS U1148, F-75018 Paris, France.

Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: eCollection Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE

Lim MS; Cardiovascular Division, Department of Medicine, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Guo DC; Department of Internal Medicine, The University of Texas Health Science Center at Houston John P and Katherine G McGovern Medical School, Houston, Texas, USA.; Velasco Torrez W; Department of Internal Medicine, The University of Texas Health Science Center at Houston John P and Katherine G McGovern Medical School, Houston, Texas, USA.; Lai A; Cardiovascular Division, Department of Medicine, Washington University in St Louis School of Medicine, St Louis, Missouri, USA.; Schweber J; The Hospital for Sick Children, Toronto, Ontario, Canada.; Garg N; Department of Paediatrics, Southern Illinois University School of Medicine, Springfield, Illinois, USA.; Fleischer J; Department of Paediatrics, Southern Illinois University School of Medicine, Springfield, Illinois, USA.; Boileau C; Département de Génétique, Universite Paris Cite, Paris, France.; De Backer J; Division of Cardiology and Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Evangelista A; Servei de Cardiologia, Hospital Universitari Vall d'Hebron, Barcelona, Spain.; Jondeau G; CRMR Marfan et apparentés, APHP, Hopital Bichat, Université Paris Cité, Paris, France.; Le Goff C; Laboratory of Vascular Translational Science, Bichat Hospital, Université Paris Cité and Université Sorbonne Paris Nord, Paris, France.; Milleron O; Centre de Référence Maladies Rares Syndrome de Marfan et apparentés, Hôpital Bichat, Paris, France.; Muiño-Mosquera L; Department of Paediatrics, Division of Paediatric Cardiology and Center for Medical Genetics, Universitair Ziekenhuis Gent, Ghent, Belgium.; Morris S; Division of Cardiology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, Texas, USA.; Ouzounian M; Cardiothoracic Surgery, University of Toronto, Toronto, Ontario, Canada.; Cervi E; 14Great Ormond Street Hospital for Children, NHS Foundation Trust, London, UK.; Marcadier J; Department of Medical Genetics, Alberta Children's Hospital, Calgary, Alberta, Canada.; Caffarelli A; Department of Cardiac Surgery, Hoag Memorial Presbyterian Hospital, Newport Beach, California, USA.; Shalhub S; Division of Vascular Surgery, University of Oregon Health Sciences, Portland, Oregon, USA.; Pyeritz R; University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.; Yetman A; Department of Paediatrics, Division of Cardiology, University of Nebraska, Children's Hospital, Omaha, Nebraska, USA.; Milewicz D; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.; Braverman AC; Cardiovascular Division, Department of Medicine, Washington University in St Louis School of Medicine, St Louis, Missouri, USA abraverm@wustl.edu.

Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

Delaye M; Department of Medical Oncology, Gastrointestinal Oncology, Institut Curie, Université Versailles Saint-Quentin-Université Paris-Saclay, Saint-Cloud, France; Association pour l'étude des Cancers et Affections des voies Biliaires (ACABi), France; GERCOR, Paris, France. Electronic address: matthieu.delaye@curie.fr.; Boilève A; Department of Medical Oncology, Gustave Roussy Hospital, Villejuif, France; Paris-Saclay University, Orsay, France.; Henriques J; Franche-Comté University, EFS, INSERM, UMR RIGHT, Besançon, France; Oncology Methodology and Quality of Life Unit, CHU Besançon, Jean Minjoz Hospital, Besançon, France.; Rouault A; Department of Hepatobiliary Surgery and Liver Transplantation, CHU Claude Huriez, Lille, France.; Paccard JR; E. Herriot and Croix-Rousse Hospital, Hospices Civils de Lyon, Medical Oncology and Hepatogastroenterology Department, 69000 Lyon, France.; Fares N; Department of Digestive Oncology, CHU de Toulouse (IUCT Rangueil Larrey), France.; Assenat E; Department of Medical Oncology, CHU Saint Eloi, Montpellier, France.; Lecomte T; Department of Gastroenterology and Digestive Oncology, CHU de Tours, Tours, France.; Hautefeuille V; Department of Gastroenterology, CHU d'Amiens, Amiens, France.; Tougeron D; Department of Hepato-gastro-enterology, CHU de Poitiers, Poitiers, France.; Edeline J; Department of Medical Oncology, INSERM, Univ Rennes, CLCC Eugène Marquis, COSS [(Chemistry Oncogenesis Stress Signaling)] - UMR_S 1242, Rennes, France.; Boileau C; AstraZeneca France, Courbevoie, France.; Ducroux A; AstraZeneca France, Courbevoie, France.; Hollebecque A; Department of Medical Oncology, Gustave Roussy Hospital, Villejuif, France; Paris-Saclay University, Orsay, France; Department of Therapeutic Innovation and Early Trials, Gustave Roussy Villejuif, France.; Vernerey D; Franche-Comté University, EFS, INSERM, UMR RIGHT, Besançon, France; Oncology Methodology and Quality of Life Unit, CHU Besançon, Jean Minjoz Hospital, Besançon, France.; Turpin A; Univ. Lille, CNRS, INSERM, CHU Lille, Institut Pasteur de Lille, UMR9020-U1277 - CANTHER - Cancer Heterogeneity Plasticity and Resistance to Therapies, Lille, France; Department of Medical Oncology, Lille University Hospital, Lille, France.; Neuzillet C; Department of Medical Oncology, Gastrointestinal Oncology, Institut Curie, Université Versailles Saint-Quentin-Université Paris-Saclay, Saint-Cloud, France; Association pour l'étude des Cancers et Affections des voies Biliaires (ACABi), France; GERCOR, Paris, France.

Publisher: Elsevier Country of Publication: Netherlands NLM ID: 100958385 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-3562 (Electronic) Linking ISSN: 15908658 NLM ISO Abbreviation: Dig Liver Dis Subsets: MEDLINE

Drackley A; Department of Pathology & Laboratory Medicine, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, USA.; Somerville C; Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Arnaud P; Genetics Department, Hôpital Bichat, Université Paris Cité, Paris, France.; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Baudhuin LM; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Hanna N; Genetics Department, Hôpital Bichat, Université Paris Cité, Paris, France.; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Kluge ML; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Kotzer K; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.; Boileau C; Genetics Department, Hôpital Bichat, Université Paris Cité, Paris, France.; Bronicki L; Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, ON, Canada.; Callewaert B; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.; Cecchi A; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.; Dietz H; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.; Guo D; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.; Harris S; Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.; Jarinova O; Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, ON, Canada.; Lindsay M; Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA, USA.; Little L; Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Loeys B; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Centre of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.; MacCarrick G; McKusick-Nathans Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.; Meester J; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Centre of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.; Milewicz D; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.; Morisaki T; IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Minato-Ku, Tokyo, Japan.; Morisaki H; IMSUT Hospital, The Institute of Medical Science, The University of Tokyo, Minato-Ku, Tokyo, Japan.; Department of Medical Genetics, Sakakibara Heart Institute, Fuchu, Tokyo, Japan.; Murdock D; Department of Internal Medicine, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.; Renard M; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Richer J; Department of Medical Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.; Robert L; Department of Cardiology, Guy's and St Thomas' Foundation Trust, London, UK.; Ouzounian M; Division of Cardiac Surgery, University of Toronto, Toronto, ON, Canada.; Van Laer L; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Centre of Medical Genetics, Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.; De Backer J; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France.; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of Cardiology, Ghent University Hospital, Ghent, Belgium.; Department of Internal Medicine and Paediatrics, Ghent University, Ghent, Belgium.; Muiño-Mosquera L; European Reference Network for Rare Multisystemic Vascular Disease (VASCERN), HTAD and MSA Rare Disease, Working Group, Paris, France. Laura.muinomosquera@uzgent.be.; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium. Laura.muinomosquera@uzgent.be.; Department of Internal Medicine and Paediatrics, Ghent University, Ghent, Belgium. Laura.muinomosquera@uzgent.be.; Division of Paediatric Cardiology, Department of Paediatrics, Ghent University Hospital, Ghent, Belgium. Laura.muinomosquera@uzgent.be.

Publisher: BioMed Central Country of Publication: England NLM ID: 101475844 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-994X (Electronic) Linking ISSN: 1756994X NLM ISO Abbreviation: Genome Med Subsets: MEDLINE

Azar Y; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France; Saint-Joseph University of Beirut, Faculty of Pharmacy, Laboratory of Biochemistry and Molecular Therapeutics (LBTM), Beirut, 1004 2020, Lebanon.; Ludwig TE; CHRU and Brest University, Inserm, EFS, INSERM UMR 1078, GGB, F-29200, Brest, France.; Le Bon H; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France.; Strøm TB; Oslo University Hospital, Department of Medical Genetics, 0450, Oslo, Norway.; Bluteau O; Sorbonne University, Faculty of Medicine Pitié-Salpêtrière, INSERM UMRS 1166, F-75005, Paris, France.; Di-Filippo M; Lyon-1 University, INSERM U1060, CarMeN Laboratory, Oullins, F-69600, France; Hospices Civil de Lyon, Department of Biochemistry and Molecular Biology, Bron, F-69002, France.; Carrié A; Sorbonne University, Faculty of Medicine Pitié-Salpêtrière, INSERM UMRS 1166, F-75005, Paris, France.; Chtioui H; Aix-Marseille University, La Conception Hospital, Nutrition Department, AP-HM, INSERM, INRAE, C2VN, Marseille, F-13001, France.; Béliard S; Aix-Marseille University, La Conception Hospital, Nutrition Department, AP-HM, INSERM, INRAE, C2VN, Marseille, F-13001, France.; Marmontel O; Lyon-1 University, INSERM U1060, CarMeN Laboratory, Oullins, F-69600, France; Hospices Civil de Lyon, Department of Biochemistry and Molecular Biology, Bron, F-69002, France.; Fonteille A; Centre Hospitalier d'Annecy Genevois, Médecine Interne, Epagny Metz-Tessy, F-74370, France.; Gebhart M; CHU Jean Minjoz, F-25000, Besançon, France.; Peretti N; Lyon-1 University, INSERM U1060, CarMeN Laboratory, Oullins, F-69600, France; Hospices Civil de Lyon, Department of Pediatric Gastroenterology-Hepatology and Nutrition, Bron, F-69002, France.; Moulin P; Lyon-1 University, INSERM U1060, CarMeN Laboratory, Oullins, F-69600, France; Hospices Civil de Lyon, Department of Endocrinology and Nutrition, Bron, F-69002, France.; Ferrières J; Toulouse Rangueil University Hospital, Department of Cardiology, INSERM, UMR 1295, F-31400, Toulouse, France.; Pradignac A; CHU of Strasbourg, Department of Internal Medicine, Endocrinology and Nutrition, Strasbourg, F-67000, France.; Farnier M; University of Bourgogne Franche-Comté, PEC2 Team, Dijon, Cedex, F-25000, France.; Gallo A; Sorbonne University, Faculty of Medicine Pitié-Salpêtrière, INSERM UMRS 1166, F-75005, Paris, France.; Yelnik C; CHUR of Lille, Department of Internal Medicine and Immunology, Lille, France; INSERM, UMR 1167 RID-AGE, Lille, F-59000, France.; Blom D; University of Cape Town, Division of Lipidology and Cape Heart Institute, Cape Town, 7925, South Africa.; Génin E; CHRU and Brest University, Inserm, EFS, INSERM UMR 1078, GGB, F-29200, Brest, France.; Bogsrud MP; Oslo University Hospital, Department of Medical Genetics, 0450, Oslo, Norway.; Leren TP; Oslo University Hospital, Department of Medical Genetics, 0450, Oslo, Norway.; Boileau C; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France; Bichat-Claude Bernard Hospital, Genetic Department, AP-HP, F-75018, Paris, France.; Abifadel M; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France; Saint-Joseph University of Beirut, Faculty of Pharmacy, Laboratory of Biochemistry and Molecular Therapeutics (LBTM), Beirut, 1004 2020, Lebanon.; Rabès JP; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France; Paris-Saclay University and Versailles-Saint-Quentin-en-Yvelines University, Ambroise Paré University Hospital, Biochemistry and Molecular Genetics Department, AP-HP, F-92104, Boulogne-Billancourt, France.; Varret M; Paris Cité University and Sorbonne Paris Nord University, INSERM UMRS 1148, Laboratory for Vascular Translational Science (LVTS), F-75018, Paris, France. Electronic address: mathilde.varret@inserm.fr.

Publisher: Elsevier Country of Publication: Ireland NLM ID: 0242543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-1484 (Electronic) Linking ISSN: 00219150 NLM ISO Abbreviation: Atherosclerosis Subsets: MEDLINE

Abifadel M; UMR1148, Inserm, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, F-75018 Paris, France.; Laboratory of Biochemistry and Molecular Therapeutics (LBTM), Faculty of Pharmacy, Pôle Technologie-Santé, Saint Joseph University of Beirut, Beirut, Lebanon.; Boileau C; UMR1148, Inserm, Hôpital Bichat-Claude Bernard, 46 rue Henri Huchard, F-75018 Paris, France.; Département de Génétique, AP-HP, Hôpital Bichat-Claude Bernard, Paris, France.

Publisher: Blackwell Scientific Publications Country of Publication: England NLM ID: 8904841 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2796 (Electronic) Linking ISSN: 09546820 NLM ISO Abbreviation: J Intern Med Subsets: MEDLINE

Baudouin SJ; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.; Giles AR; REGENXBIO Inc., Rockville, MD 20850, USA.; Pearson N; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.; Deforges S; Institute for Neuroscience, 33000 Bordeaux, France.; He C; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.; Boileau C; INSERM, INMED, Aix-Marseille University, 13009 Marseille, France.; Partouche N; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.; Borta A; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.; Gautron J; Institute for Neuroscience, 33000 Bordeaux, France.; Wartel M; uniQure biopharma B.V., 1105BP Amsterdam, the Netherlands.; Bočkaj I; uniQure biopharma B.V., 1105BP Amsterdam, the Netherlands.; Scavarda D; APHM, INSERM, Aix-Marseille University, Timone Hospital, Pediatric Neurosurgery, 13005 Marseille, France.; Bartolomei F; APHM, INSERM, Aix-Marseille University, INS, Timone Hospital, Epileptology Department, 13005 Marseille, France.; Penchet G; Pellegrin Hospital, Neurosurgery Department, CHU, 33000 Bordeaux, France.; Aupy J; Pellegrin Hospital, Neurosurgery Department, CHU, 33000 Bordeaux, France.; Sims J; Integrated Biologix GmbH, 4051 Basel, Switzerland.; Smith J; REGENXBIO Inc., Rockville, MD 20850, USA.; Mercer A; REGENXBIO Inc., Rockville, MD 20850, USA.; Danos O; REGENXBIO Inc., Rockville, MD 20850, USA.; Mulle C; Institute for Neuroscience, 33000 Bordeaux, France.; Crépel V; INSERM, INMED, Aix-Marseille University, 13009 Marseille, France.; Porter R; uniQure (Corlieve Therapeutics AG), 4052 Basel, Switzerland.

Publisher: Cell Press Country of Publication: United States NLM ID: 101624857 Publication Model: eCollection Cited Medium: Print ISSN: 2329-0501 (Print) Linking ISSN: 23290501 NLM ISO Abbreviation: Mol Ther Methods Clin Dev Subsets: PubMed not MEDLINE