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Research projects
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
BRETAGNE
RENNES
Identification of genes involved in syndromic disorders of sex development
CHU de Rennes - Hôpital Pontchaillou
Service de Cytogénétique et Biologie Cellulaire
GERMANY
Berlin
BERLIN
DSD-Life: Clinical European study on the outcome of surgical and hormonal therapy and psychological intervention in disorders of sex development (DSD) - DE
Charité - Universitätsmedizin Berlin (CVK)
BCSE - Berliner Centrum für Seltene Erkrankungen (ZSE)
GERMANY
Schleswig-Holstein
LÜBECK
DSDCare: Standardized healthcare-center-centered care of DSD over the life span
Universitätsklinikum Schleswig-Holstein - Campus Lübeck
Hormonzentrum für Kinder und Jugendliche - Lübeck
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
SWEDEN
Region Stockholm
STOCKHOLM
Inborn errors of endocrinology and metabolism
Karolinska Institutet - Solna
Department of Molecular Medicine and Surgery (MMK)
SWITZERLAND
Suisse Romande
FRIBOURG
Understanding human sex development and its defects: novel approaches
Université de Fribourg
Département d'endocrinologie, métabolisme et systčme cardiovasculaire (EMC)
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
- Universitätsklinikum Schleswig-Holstein - Campus Lübeck
- Hormonzentrum für Kinder und Jugendliche - Lübeck
- Charité - Universitätsmedizin Berlin (CVK)
- BCSE - Berliner Centrum für Seltene Erkrankungen (ZSE)
- UCL Institute for Women's Health
- UCLH Women's Health Division
- Universitätsklinikum Magdeburg A.ö.R
- MONZ - Fehlbildungsmonitoring Sachsen-Anhalt
GERMANY
Schleswig-Holstein
LÜBECK
EURODSD : Erforschung der molekularen Pathogenese und Pathophysiologie von Störungen der Geschlechtsentwicklung (DSD) - beenedet
GERMANY
Berlin
BERLIN
DSD-Life: Clinical European study on the outcome of surgical and hormonal therapy and psychological intervention in disorders of sex development (DSD)
UNITED KINGDOM
Greater London
LONDON
EuroPSI - European Network for Psychosocial Studies in Intersex / Diverse Sex Development
GERMANY
Sachsen-Anhalt
MAGDEBURG