Emmanuel Somm, PhD
Centre Hospitalier Universitaire Vaudois (CHUV)
Our group of research focuses on genetic cause of congenital hypogonadotropic hypogonadism (CHH), a severe form of gonadotropin-releasing hormone (GnRH) deficiency. Presently, we try to study the role of FGF21 signalling pathway as a probable important link between metabolism and reproduction.
Click HERE to see his publications in Researchgate.net