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Academic Journal

Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.

Authors : Lionel AC; The Centre for Applied Genomics.; Tammimies K

Subjects: Attention Deficit Disorder with Hyperactivity/Attention Deficit Disorder with Hyperactivity/Attention Deficit Disorder with Hyperactivity/*genetics ; Child Development Disorders, Pervasive/Child Development Disorders, Pervasive/Child Development Disorders, Pervasive/*genetics ; Glycoproteins/Glycoproteins/Glycoproteins/*genetics

Source: Human molecular genetics [Hum Mol Genet] 2014 May 15; Vol. 23 (10), pp. 2752-68. Date of Electronic Publication: 2013 Dec 30.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model:

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Academic Journal

Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.

Authors : Lionel AC; The Centre for Applied Genomics and Program in Genetics and Genome Biology, The Hospital for Sick Children,Toronto, ON, Canada.; Vaags AK

Subjects: Base Sequence* ; Exons* ; Sequence Deletion*

Source: Human molecular genetics [Hum Mol Genet] 2013 May 15; Vol. 22 (10), pp. 2055-66. Date of Electronic Publication: 2013 Feb 07.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model:

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Academic Journal

Individual common variants exert weak effects on the risk for autism spectrum disorders.

Authors : Anney R; Autism Genetics Group, Department of Psychiatry, School of Medicine, Trinity College, Dublin 8, Ireland.; Klei L

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study*; Child Development Disorders, Pervasive/Child Development Disorders, Pervasive/Child Development Disorders, Pervasive/*genetics

Source: Human molecular genetics [Hum Mol Genet] 2012 Nov 01; Vol. 21 (21), pp. 4781-92. Date of Electronic Publication: 2012 Jul 26.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model:

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Academic Journal

A genome-wide scan for common alleles affecting risk for autism.

Authors : Anney R; Department of Psychiatry, School of Medicine, Trinity College, Dublin 8, Ireland.; Klei L

Subjects: Genetic Predisposition to Disease* ; Genome-Wide Association Study* ; Polymorphism, Single Nucleotide*

Source: Human molecular genetics [Hum Mol Genet] 2010 Oct 15; Vol. 19 (20), pp. 4072-82. Date of Electronic Publication: 2010 Jul 27.Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model:

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