Ligne de temps
19 oct. 2020
publication
Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.
Lire plus14 oct. 2020
publication
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Lire plus11 sept. 2020
11 févr. 2019
publication
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
Lire plus21 janv. 2019
publication
Both rare and common genetic variants contribute to autism in the Faroe Islands.
Lire plus01 mai 2018
publication
Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Lire plus10 mai 2016
publication
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
Lire plus01 déc. 2015
publication
11q24.2-25 micro-rearrangements in autism spectrum disorders: Relation to brain structures.
Lire plus23 sept. 2015
publication
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disability
Lire plus01 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 plus19 janv. 2014
publication
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders
Lire plus03 déc. 2013
07 oct. 2013
09 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