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  1. No Access

    Article

    A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium

    Rare copy number variants contribute significantly to the risk for schizophrenia, with the 22q11.2 locus consistently implicated. Individuals with the 22q11.2 deletion syndrome (22q11DS) have an estimated 25-f...

    R E Gur, A S Bassett, D M McDonald-McGinn, C E Bearden, E Chow… in Molecular Psychiatry (2017)

  2. No Access

    Article

    No support for association between Dyslexia Susceptibility 1 Candidate 1 and developmental dyslexia

    N A Cope, G Hill, M van den Bree, D Harold, V Moskvina, E K Green… in Molecular Psychiatry (2005)

  3. No Access

    Article

    Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD

    Attention deficit hyperactivity disorder (ADHD) is a childhood onset disorder, for which there is good evidence that genetic factors contribute to the aetiology. Recently reported linkage findings suggested ev...

    D Turic, K Langley, S Mills, M Stephens, D Lawson, C Govan… in Molecular Psychiatry (2004)

  4. No Access

    Article

    Linkage disequilibrium map** provides further evidence of a gene for reading disability on chromosome 6p21.3–22

    Linkage disequilibrium (LD) map** was used to follow up reports of linkage between reading disability (RD) and an 18 cM region of chromosome 6p21.3–22. Using a two-stage approach, we tested for association b...

    D Turic, L Robinson, M Duke, D W Morris, V Webb, M Hamshere… in Molecular Psychiatry (2003)