Timeline

19 Oct 2020
publication

Mutations associated with neuropsychiatric conditions delineate functional brain connectivity dimensions contributing to autism and schizophrenia.

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14 Oct 2020
publication

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.

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11 Sep 2020
publication

Effect Sizes of Deletions and Duplications on Autism Risk Across the Genome.

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11 Feb 2019
publication

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

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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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01 May 2018
publication

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

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10 May 2016
publication

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

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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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23 Sep 2015
publication

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

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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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19 Jan 2014
publication

Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders

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03 Dec 2013
publication

Heterozygous FA2H mutations in autism spectrum disorders

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07 Oct 2013
publication

The emerging role of SHANK genes in neuropsychiatric 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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