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Research projects
BELGIUM
ANTWERPEN
EDEGEM (ANTWERPEN)
101 Genomes Marfans Project (P101GM)
University Hospital Antwerp - UZA
Aortakliniek - UZA
BELGIUM
OOST-VLAANDEREN
GENT
Characterisation of genes and molecular mechanisms involved in hereditary connective tissue diseases by studying transgenic animal models and human tissues
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Centrum Medische Genetica Gent / Centre for Medical Genetics Ghent
BELGIUM
OOST-VLAANDEREN
GENT
Designing an integrated platform for the development of more precise medicine in Heritable Thoracic Aortic Disease
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Centrum Medische Genetica Gent / Centre for Medical Genetics Ghent
BELGIUM
OOST-VLAANDEREN
GENT
Genome-wide Epistasis for cardiovascular severity in Marfan Study (GEMS)
Centrum Medische Genetica Gent - Universitair Ziekenhuis Gent
Centrum Medische Genetica Gent / Centre for Medical Genetics Ghent
BELGIUM
OOST-VLAANDEREN
GENT
101 Genomes Marfans Project (P101GM)
Ghent University Hospital - UZ Gent
Aorta Team Ghent
CANADA
Colombie-Britannique
VANCOUVER
Cellular Mechanisms underlying vascular dysfunction & aortic aneurysm in Marfan syndrome
University of British Columbia
CFRI - Child and Family Research Institute
NORWAY
Řstlandet
NESODDTANGEN
Norsk studie om Marfans syndrom, del 2: Ny undersřkelse etter 10 ĺr av voksne med antatt Marfans syndrom
Sunnaas Rehabilitation Hospital
TRS kompetansesenter for sjeldne diagnoser
NORWAY
Řstlandet
NESODDTANGEN
Levels of activity and independence: a study of the interface of current health policy discourse and subjective realities
Sunnaas Rehabilitation Hospital
TRS kompetansesenter for sjeldne diagnoser
NORWAY
Řstlandet
OSLO
Marfans syndrom og sřvnapné
Lovisenberg Diakonale Sykehus AS
TAKO-senteret Nasjonalt kompetansesenter for oral helse ved sjeldne diagnoser
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
Marfan aortic embryologic origin influences mir-29b regulators and targets
Institution: Information not provided - US
FRANCE
AUVERGNE-RHONE-ALPES
ADDRESS: NOT PROVIDED - FR
Involvement of CXCL12 and CXCL14 chemokines in connective tissue-mediated limb muscle morphogenesis.
Institution: Information not provided - FR
FRANCE
ILE-DE-FRANCE
PARIS
Dynamique structurale des complexes NMD : détecteur et effecteur
Institut Pasteur
AUSTRIA
OBERÖSTERREICH
LINZ
EuRR-Bone: European Registry for Rare Bone and Mineral Conditions - AT
Kepler Universitätsklinikum - Med Campus IV.
Universitätsklinik für Kinder- und Jugendheilkunde
CANADA
Colombie-Britannique
VICTORIA
Silent Genomes: Reducing health care disparities and improving diagnostic success for children with genetic diseases from Indigenous populations
University of Victoria
Community Genetics Research Program/Island Medical Program
CANADA
Ontario
OTTAWA, ONTARIO
Detection and simulation of femoroacetabular impingement
University of Ottawa
School of Electrical Engineering and Computer Science (EECS)
CANADA
Ontario
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
SPAIN
Madrid
MADRID
Identification of new genes causing rare diseases in pediatric patients, searching of genetic pharmacological targets, and drugs discovery, the steps for a personalized medicine
Instituto de Investigación Hospital 12 de Octubre
Grupo de investigación en enfermedades raras, mitocondriales y neuromusculares
UNITED STATES
Washington
ADDRESS: NOT PROVIDED - US
A powerful web-based discovery platform for rare disease genetics
Institution: Information not provided - US
GERMANY
Sachsen-Anhalt
MAGDEBURG
EUROlinkCAT: Establishing a linked European Cohort of Children with Congenital Anomalies (partner DE)
Universitätsklinikum Magdeburg A.ö.R
MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
UNITED KINGDOM
Tyne & Wear
NEWCASTLE UPON TYNE
Human Developmental Biology Resource (HDBR): an embryonic and fetal tissue bank for functional genetics and cell-based research
Newcastle University
Institute of Genetic Medicine
Multicentric Research projects
- AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
- Thérapie cellulaire en pathologie cardiovasculaire
- Fondazione IRCCS Policlinico San Matteo
- Laboratorio di Diagnostica Molecolare, Patologia Cardiovascolare e dei Trapianti
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
FRANCE
ILE-DE-FRANCE
PARIS
MITRAL
ITALY
LOMBARDIA
PAVIA
GIMS: Interdisciplinary Team for Marfan Syndrome
GERMANY
Sachsen-Anhalt
MAGDEBURG