Servane Alirol
Université de Tours(FR)Inserm(FR)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Genomics and Chromatin Dynamics, CRISPR and Genetic Engineering, Ubiquitin and proteasome pathways
Most-Cited Works
- → ZC4H2 Mutations Are Associated with Arthrogryposis Multiplex Congenita and Intellectual Disability through Impairment of Central and Peripheral Synaptic Plasticity(2013)90 cited
- → GABA/Glutamate synaptic pathways targeted by integrative genomic and electrophysiological explorations distinguish autism from intellectual disability(2015)36 cited
- → A novel mutation in the transmembrane 6 domain of GABBR2 leads to a Rett‐like phenotype(2018)27 cited
- Mutation of the PTCHD1 gene, which encodes a transmembrane protein expressed in postsynaptic dendritic spines, is associated with non syndromic intellectual disability and autism(2013)
- Etude génétique du complexe synaptique lié au récepteur NMDA et caractérisation de modèles à complexité variable dans l'autisme(2015)
- Genetic study of the NMDA receptor associated multi-protein complex in autism : characterization of variable complexity genetic models(2015)