- Role of Olig1 and Olig2 in Down syndrome.
- TUBA1A mutations cause wide spectrum lissencephaly.
- Cell cloning-based transcriptome analysis in Rett patients.
Our laboratory is located in "La Timone" Medical School in Marseilles, in a research unit of the French Institute for Health and Medical Research (INSERM) and of Aix-Marseille University.
Our research unit is called "Medical Genetics & Functional Genomics".
It is composed of 5 independent teams headed by :
INSERM
Aix-Marseille University (Université de la Méditerranée)
National Research Agency (Agence Nationale de la Recherche, ANR)
French Rett Syndrome Association (Association Française du Syndrome de Rett, AFSR)
Jérôme Lejeune Foundation
City of Marseille
ERA-Net for research programmes on rare diseases (E-RARE)
Marie Curie Initial Training Networks (ITN)
French Foundation for Research on Epilepsy (FFRE)
Clinical Research Program Funds (PHRC)
Provence-Alps-Côte d'Azur Regional Council