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Family-based genome-wide copy number scan identifies five new genes of dyslexia involved in dendritic spinal plasticity

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Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31

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Large, rare chromosomal deletions associated with severe early-onset obesity

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De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot

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Linkage, Association, and Gene-Expression Analyses Identify CNTNAP2 as an Autism-Susceptibility Gene

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Structural Variation of Chromosomes in Autism Spectrum Disorder

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Subunit-Selective Modulation of GABA Type A Receptor Neurotransmission and Cognition in Schizophrenia

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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures

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Strong association of de novo copy number mutations with sporadic schizophrenia

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Photolysis of a caged peptide reveals rapid action of N-ethylmaleimide sensitive factor before neurotransmitter release

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Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

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