Ligne de temps

Nathalie Lemiere
Technicien(ne)
07 Aug 2020
publication

A chimeric mouse model to study human iPSC-derived neurons: the case of a truncating SHANK3 mutation.

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11 Jun 2020
project

PARIS: Paris Autism Research International Sib-Pair Study

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21 Jan 2019
publication

Both rare and common genetic variants contribute to autism in the Faroe Islands

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27 Feb 2018
project

EU-AIMS

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14 Nov 2016
project

Background on the genetics of ASD

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22 Feb 2016
project

Le syndrome de Phelan-McDermid : des mécanismes aux traitements

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01 Dec 2015
publication

11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.

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16 Jul 2015
project

The serotonin-NAS-melatonin pathway and susceptibility to ASD

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01 Dec 2014
team

Génétique Humaine et Fonctions Cognitives

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01 Sep 2014
publication

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments.

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03 Mar 2014
publication

Heterogeneous pattern of selective pressure for PRRT2 in human populations, but no association with autism spectrum disorders

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09 Jul 2012
publication

Crystal structure and functional mapping of human ASMT, the last enzyme of the melatonin synthesis pathway

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09 Feb 2012
publication

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.

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01 Nov 2011
publication

Genetic variations of the melatonin pathway in patients with attention-deficit and hyperactivity disorders.

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04 Mar 2011
publication

Variations of the candidate SEZ6L2 gene on Chromosome 16p11.2 in patients with autism spectrum disorders and in human populations.

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15 Jul 2010
publication

Identification of pathway-biased and deleterious melatonin receptor mutants in autism spectrum disorders and in the general population

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