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23 Result(s)
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Research projects
FRANCE
HAUTS-DE-FRANCE
LILLE
Research of genes and mutations involved in ventricle disorders with sudden death risk
CHRU de Lille - Hôpital Albert Calmette
Service de cardiologie
FRANCE
ILE-DE-FRANCE
PARIS
Research of genes and mutations involved in ventricle disorders with sudden death risk
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie
FRANCE
ILE-DE-FRANCE
PARIS
Clinical, electrophysiological and genetic aspects of Brugada syndrome
CHU Paris Nord-Val de Seine - Hôpital Xavier Bichat-Claude Bernard
Service de cardiologie - Rythmologie
FRANCE
ILE-DE-FRANCE
PARIS
Research of genes and mutations involved in ventricle disorders with sudden death risk
Hôpital Necker-Enfants Malades
Cardiologie pédiatrique : Unité médico-chirurgicale de cardiologie congénitale et pédiatrique
FRANCE
PAYS DE LA LOIRE
NANTES
Clinical research on Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
FRANCE
PAYS DE LA LOIRE
NANTES
Phenotype profile of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
FRANCE
PAYS DE LA LOIRE
NANTES
Genetics of the Brugada syndrome
Faculté de médecine de Nantes
Physiopathologie et pharmacologie cellulaire et moléculaire
SPAIN
Cataluña
BARCELONA
Characterization and risk stratification in Brugada syndrome through the development and validation of novel artificial intelligence model-based approaches for precision medicine
Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS)
Grupo de investigación en arritmias, resincronización e imágenes cardíacas
SWITZERLAND
Suisse Alémanique
BERN
Co-regulation of cardiac ion channels: focus on the sodium channel Nav1.5
Universität Bern
Institute of Biochemistry and Molecular Medicine (IBMM)
GERMANY
Bayern
MÜNCHEN
Characterization of the arrhythmia substrates in hereditary in comparison to non-hereditary arrhythmogenic cardiomyopathy by cardiac magnetic resonance imaging
Helios Klinikum München West
Klinik für Kardiologie und Internistische Intensivmedizin
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
TORONTO
Beyond the Genome: Transcriptome Based Diagnostics for Rare Diseases and Cancer
Hospital for Sick Children, Research Institute
FRANCE
PROVENCE-ALPES-COTE D'AZUR
MARSEILLE
Modelisation and Therapeutic Approaches for Rare Diseases
Université de médecine Aix-Marseille Université
Centre de Génétique de Marseille (Marseille Medical Genetics - MMG)
SPAIN
Andalucía
SEVILLA
Development of bioinformatic tools for the automatic handling of secondary findings and their use in genetic and pharmacogenetic counseling
Fundación Progreso y Salud
Área de bioinformática clínica
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Centro de Regulación Genómica
Archivo europeo de genomas y fenomas del CRG
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Clínic de Barcelona
Servicio de Inmunologia
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari Vall d'Hebron
Laboratorio de Genética
SPAIN
Cataluña
BARCELONA
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital de la Santa Creu i Sant Pau
Servicio de Genética
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Federated network for functional genomics of undiagnosed and rare diseases, RareFunction
Fundació Sant Joan de Déu - Institut de Recerca Sant Joan de Déu
Grupo de investigación en Neurogenética y Medicina Molecular
SPAIN
Cataluña
ESPLUGUES DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Sant Joan de Déu Barcelona
Servicio de Laboratorio
SPAIN
Cataluña
L'HOSPITALET DE LLOBREGAT
Catalan Interhospital Network of Genetic Variants to improve genetic diagnosis in rare diseases
Hospital Universitari de Bellvitge
Unidad de Genética Molecular
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
Multicentric Research projects
- AP-HP. Centre - Université de Paris - HEGP Hôpital Européen Georges Pompidou
- Thérapie cellulaire en pathologie cardiovasculaire
FRANCE
ILE-DE-FRANCE
PARIS