Ligne de temps

Alexandre Mathieu
Ingénieur(e) de Recherche
26 juin 2023
publication

Phenotypic effects of genetic variants associated with autism.

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13 juin 2022
project

Étude des facteurs génétiques impliqués dans l’autisme et les troubles apparentés (projet “C07/C16”)

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11 juin 2020
project

PARIS: Paris Autism Research International Sib-Pair Study

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21 janv. 2019
publication

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

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09 janv. 2019
publication

Synesthesia & Autistic Features in a Large Family:evidence for spatial imagery as a common factor

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04 oct. 2018
publication

Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology

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01 mai 2018
publication

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.

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27 févr. 2018
project

EU-AIMS

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01 janv. 2017
publication

A framework to identify contributing genes in patients with Phelan-McDermid syndrome.

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14 nov. 2016
project

Background on the genetics of ASD

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14 nov. 2016
software

GRAVITY

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10 mai 2016
publication

CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders

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22 févr. 2016
project

Le syndrome de Phelan-McDermid : des mécanismes aux traitements

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01 déc. 2015
publication

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

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16 juil. 2015
project

The serotonin-NAS-melatonin pathway and susceptibility to ASD

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01 déc. 2014
team

Génétique Humaine et Fonctions Cognitives

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01 sept. 2014
publication

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

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