Genetic Research Centres
- More that 20 genes have been associated with GnRH deficiency, yet these genes only identify genetics causes of GnRH deficiency in about 50% of cases.
- Several research centres across Europe are working actively to discover new genes associated with GnRH deficiency (including Kallmann syndrome).
- The leading centres in our COST network are listed below.
- This research is enabled by the active participation of patients.
- Patients interested in research studies should visit Join a Research Study.
Country | Center | Investigator | Services |
| Finland | University of Helsinki | Taneli Raivio | Sanger, Exome, Targeted High-Throughput Sequencing |
| France | Genetic Centre Robert Debré, Paris | Nicolas de Roux | Sanger, Exome, Targeted High-Throughput Sequencing, Linkage |
| France | Hôpital Cochin, Paris | Catherine Dode | Sanger, Exome, Targeted High-Throughput Sequencing |
| France | Paris sud Bicetre | Anne Mantel | Sanger, Exome, Targeted High-Throughput Sequencing |
| Italy | University of Milan, Instituto Auxologico | Luca Persani | Sanger, Exome, Targeted High-Throughput Sequencing |
| Switzerland | Centre Hospitalier Vaudois Universitaire, Lausanne | Nelly Pitteloud | Sanger, Exome, Targeted High-Throughput Sequencing |
| United Kingdom | William Harvey Research Institute, London | Leo Dunkel | Sanger, Exome, Targeted High-Throughput Sequencing |
GNRH Network
COST European Cooperation in Science and Technology
ACTION BM1105
CH - 1011 Lausanne, Vaud, Suisse
COST European Cooperation in Science and Technology
ACTION BM1105
CH - 1011 Lausanne, Vaud, Suisse
GNRH Network
COST European Cooperation in Science and Technology
ACTION BM1105
CH - 1011 Lausanne, Vaud, Suisse
COST European Cooperation in Science and Technology
ACTION BM1105
CH - 1011 Lausanne, Vaud, Suisse