Ligne de temps
Nathalie Lemiere
Technicien(ne)
13 juin 2022
project
Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “C07/C16”)
Lire plus07 août 2020
publication
A chimeric mouse model to study human iPSC-derived neurons: the case of a truncating SHANK3 mutation.
Lire plus11 juin 2020
21 janv. 2019
publication
Both rare and common genetic variants contribute to autism in the Faroe Islands.
Lire plus27 févr. 2018
14 nov. 2016
22 févr. 2016
01 déc. 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Lire plus16 juil. 2015
01 déc. 2014
01 sept. 2014
publication
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.
Lire plus03 mars 2014
publication
Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders
Lire plus09 juil. 2012
publication
Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway
Lire plus09 févr. 2012
publication
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Lire plus01 nov. 2011
publication
Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.
Lire plus04 mars 2011
publication
Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.
Lire plus15 juil. 2010
publication