Ligne de temps

Julien Buratti
Ingénieur(e) de Recherche
21 janv. 2019
publication

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

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01 janv. 2017
publication

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

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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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23 sept. 2015
publication

A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability

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01 déc. 2014
team

Génétique Humaine et Fonctions Cognitives

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