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

    
FinlandUniversity of HelsinkiTaneli RaivioSanger, Exome, Targeted High-Throughput Sequencing
FranceGenetic Centre Robert Debré, ParisNicolas de RouxSanger, Exome, Targeted High-Throughput Sequencing, Linkage
FranceHôpital Cochin, ParisCatherine DodeSanger, Exome, Targeted High-Throughput Sequencing
FranceParis sud BicetreAnne MantelSanger, Exome, Targeted High-Throughput Sequencing
ItalyUniversity of Milan, Instituto AuxologicoLuca PersaniSanger, Exome, Targeted High-Throughput Sequencing
SwitzerlandCentre Hospitalier Vaudois Universitaire, LausanneNelly PitteloudSanger, Exome, Targeted High-Throughput Sequencing
United KingdomWilliam Harvey Research Institute, LondonLeo DunkelSanger, Exome, Targeted High-Throughput Sequencing
 Last updated on 17/06/2018 at 12:56