CONTEXT
Alexandra Durr and Sandrine Humbert’s team focus on neurogenetic diseases, spinocerebellar degenerations (spastic paraplegias and cerebellar ataxias) and Huntington disease. These rare conditions share clinical, genetic and functional characteristics but are extremely heterogeneous both in molecular and clinical aspects. The genetic group is interested in understanding causes and genetic factors of this variability thanks to a large cohort of 2000 families. The functional group explores the link between the genetic variants and the cellular consequences.
POSITION
Under the supervision of the manager, the post-Doc will be in charge of :
- Identifying genetic causes of spinocerebellar degeneration using bioinformatic and statistical analysis.
- Analysing RNA sequencing studies from several species, including human postmortem samples
- Searching for genetic modifiers to explain clinical variability
For those missions, the entire team is composed by researchers in the field of neurosciences and clinical experts as well as dedicated platforms at the Institute.
Profil recherché