You are here: » People » Research Groups » France » Hamel, Christian ✝

Genetics and therapy of retinal blindness

Twenty researchers and technicians working on inherited retinal dystrophies and hereditary optic neuropathies. Genetics, physiopathological studies and strategy for therapies are studied. The research group is working in close collaboration with the clinical group.


  • Molecular genetics, SNPs microarrays
  • Cell biology, gene expression and regulation
  • Protein-protein interactions

Scientific Cooperations

  • Cooperation 1:
    Bernd Wissinger, Tübingen, Germany
  • Cooperation 2:
    Shomi Bhattacharya, London, UK
  • Cooperation 3:
    Josseline Kaplan, Paris, France
  • Cooperation 4:
    Pascal Reynier, Angers, France
  • Cooperation 5:
    Gabriel Travis, Philadelphia, USA

Group Leader

Prof. Christian Hamel ✝
[more information]



Institute of Neurosciences of Montpellier, Hôpital Saint Eloi

BP 74103
80, avenue Augustin Fliche
34091 Montpellier cedex 5

Phone: (33) 499 636 010
Fax: (33) 499 636 020



Current Research Projects

  • Project 1:
    Genetics of retinitis pigmentosa and allied diseases : identification of new genes / loci, genotype/phenotype correlations
  • Project 2:
    Dominant optic atrophy : pathophysiological studies and therapeutic strategies
  • Project 3:
    Visual cycle : regulation and dysregulation in retinal dystrophies
  • Project 4:
    Gene therapy in retinal dystrophies

Research Groups


Related Research Groups

Oops, an error occurred! Code: 202103090130001addebad
gene microarray
Oops, an error occurred! Code: 20210309013000ad881d7d
gene transfer/gene therapy
Oops, an error occurred! Code: 20210309013000c2b89c7c
Oops, an error occurred! Code: 202103090130007179a48a
retinal degenerations: hereditary
Oops, an error occurred! Code: 2021030901300096f74899
retinal pigment epithelium
Oops, an error occurred! Code: 20210309013000bf204051
retinitis pigmentosa
Oops, an error occurred! Code: 20210309013000ee21d6a9
Retinal dystrophy
Oops, an error occurred! Code: 2021030901300062761be4
Dominant optic atrophy
Oops, an error occurred! Code: 2021030901300029b44b8c