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CNVs: Harbingers of a Rare Variant Revolution in Psychiatric Genetics

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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

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Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

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2p15–p16.1 microdeletion syndrome: molecular characterization and association of the OTX1 and XPO1 genes with autism spectrum disorders

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Investigation of the serum levels of anterior pituitary hormones in male children with autism

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Novel Proteins Regulated by mTOR in Subependymal Giant Cell Astrocytomas of Patients with Tuberous Sclerosis Complex and New Therapeutic Implications

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The immune systemʼs role in the biology of autism

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Annexin A1: A Central Player in the Anti-Inflammatory and Neuroprotective Role of Microglia

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Mutation spectrum revealed by breakpoint sequencing of human germline CNVs

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A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

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A genome-wide association study of alcohol dependence

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Comparing cortisol, stress, and sensory sensitivity in children with autism

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Kinesin Family Member 6 Variant Trp719Arg Does Not Associate With Angiographically Defined Coronary Artery Disease in the Ottawa Heart Genomics Study

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A genome-wide linkage and association scan reveals novel loci for autism

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Common genetic variants on 5p14.1 associate with autism spectrum disorders

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Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

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Origins and functional impact of copy number variation in the human genome

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Human Splicing Finder: an online bioinformatics tool to predict splicing signals

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Familial aggregation of quantitative autistic traits in multiplex versus simplex autism

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Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history

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Copy-number variations associated with neuropsychiatric conditions

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Advances in autism genetics: on the threshold of a new neurobiology

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