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    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUSSELS
    • CARDIOGENET: definizione di un network della patologia congenita cardiaca
    • European Commission
    • DG Research - Directorate General for Research
    • More details
    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Unravelling the molecular-genetic basis of hereditary disorders of elastin.
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics Ghent
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • Familial forms of congenital heart diseases in Estonia: identification of the responsible genes and development of molecular diagnostics
    • University of Tartu
    • Laboratory of Molecular Pathology
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Mechanical properties of the arterial wall in elastinopathies
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Unité Médico-Chirurgicale de Cardiologie Congénitale et Pédiatrique
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Non-invasive arterial physiology in child
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Unité Médico-Chirurgicale de Cardiologie Congénitale et Pédiatrique
    • More details
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Identification of new genes responsible for congenital heart defects
    • CHU de Lyon-GH Est - Hospices Civils de Lyon
    • Laboratoire cardiogénétique - Malformations cardiaques congénitales
    • More details
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Molecular basis of laterality defects including congenital heart and vessel malformations
    • Universitätsklinikum Freiburg
    • Arbeitsgruppe Professor Dr. med. Heymut Omran
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular Aspects of Congenital Heart Defects
    • Charité / Max-Delbrück-Centrum für Molekulare Medizin
    • KardioGenetisches Labor/Arbeitsgruppe Özcelik
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • CardioGeNet - Subprojekt: Analysis of T-box transcription networks in congenital heart disease (WP 4)
    • Charité / Max-Delbrück-Centrum für Molekulare Medizin
    • Experimental and Clinical Research Center - Kardiovaskuläre Genetik
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Molecular basis of congenital heart defects showing an oligogenic background
    • Charité / Max-Delbrück-Centrum für Molekulare Medizin
    • Experimental and Clinical Research Center - Kardiovaskuläre Genetik
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Competence Network for Congenital Heart Defects : Prevalence of congenital heart defects in newborns in Germany (PAN study)
    • Kompetenznetz Angeborene Herzfehler
    • Kompetenznetz Angeborene Herzfehler - Netzwerkzentrale
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Competence Network for Congenital Heart Defects: Quality of life and social situation of adults with congenital heart defects (LESSIE study)
    • Kompetenznetz Angeborene Herzfehler
    • Kompetenznetz Angeborene Herzfehler - Netzwerkzentrale
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Competence Network for Congenital Heart Defects: Information-related behaviour and information needs of patients with congenital heart defects
    • Kompetenznetz Angeborene Herzfehler
    • Kompetenznetz Angeborene Herzfehler - Netzwerkzentrale
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • CHD PLATFORM: Establishment of a European parent- and patient-oriented information and communication platform on Congenital Heart Defects (coordination)
    • Kompetenznetz Angeborene Herzfehler
    • Nationales Register für angeborene Herzfehler e. V.
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Competence Network for Congenital Heart Defects: Family-based studies for the identification of genetic causes for congenital heart disease
    • Max-Delbrück-Centrum für Molekulare Medizin
    • Kardiovaskuläre Molekulargenetik
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • BAD OEYNHAUSEN
    • Competence Network for Congenital Heart Defects: Objective exercise tolerance of patients with congenital heart defects
    • Ruhr-Universität Bochum
    • Klinik für Angeborene Herzfehler / Kinderkardiologie
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Competence Network for Congenital Heart Defects: Coherence and quality of life in adolescents with congenital Heart defects (CoalaH Study)
    • Universitätsklinikum Münster
    • Institut für Epidemiologie und Sozialmedizin
    • More details
    • GERMANY
    • Nordrhein-Westfalen
    • MÜNSTER
    • Competence Network for Congenital Heart Defects : Prevalence of congenital heart defects in newborns in Germany (PAN study)
    • Universitätsklinikum Münster
    • Institut für Epidemiologie und Sozialmedizin
    • More details
    • GERMANY
    • Saarland
    • HOMBURG
    • Competence Network for Congenital Heart Defects : Prevalence of congenital heart defects in newborns in Germany (PAN study)
    • Universitätsklinikum des Saarlandes
    • Klinik für Pädiatrische Kardiologie
    • More details
    • ITALY
    • CAMPANIA
    • NAPOLI
    • CARDIOGENET: definizione di un network della patologia congenita cardiaca
    • TIGEM - Telethon Institute of Genetics and Medicine
    • Laboratorio di Ricerca
    • More details
    • ITALY
    • VENETO
    • PADOVA
    • Regulation of tgf-beta signaling by emilins and other proteins of elastic fiber. role in mouse models of monogenic forms of hypertension, marfan syndrome and supra-valvular aortic stenosis
    • Università degli Studi di Padova
    • Dipartimento di Istologia, Microbiologia e Tecnologie Mediche
    • More details
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • CHEARTED: gene-environment interactions in heart development (coordination)
    • AMC - Academisch Medisch Centrum
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • County Antrim
    • NEWTOWNABBEY
    • Epidemiological studies on congenital anomaly prevalence, risk factors, prevention and prenatal screening
    • University of Ulster
    • EUROCAT Central Registry
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details