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  1. Article

    Open Access

    CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems

    The chromodomain helicase DNA binding domain (CHD) proteins modulate gene expression via their ability to remodel chromatin structure and influence histone acetylation. Recent studies have shown that CHD2 prot...

    Sébastien Chénier, Grace Yoon, Bob Argiropoulos in Journal of Neurodevelopmental Disorders (2014)

  2. Article

    Open Access

    NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders

    Microdeletions in the NRXN1 gene have been associated with a range of neurodevelopmental disorders, including autism spectrum disorders, schizophrenia, intellectual disability, speech and language delay, epile...

    Sarah Curran, Joo Wook Ahn, Hannah Grayton in Journal of Molecular Psychiatry (2013)