Whole-exome sequencing in obsessive-compulsive disorder identifies rare mutations in immunological and neurodevelopmental pathways

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An Inherited Small Microdeletion at 15q13.3 in a Patient with Early- Onset Obsessive-Compulsive Disorder

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De novo mutations revealed by whole-exome sequencing are strongly associated with autism

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Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

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Functional studies and rare variant screening of SLC1A1/EAAC1 in males with obsessive–compulsive disorder

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Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism

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Exome sequencing supports a de novo mutational paradigm for schizophrenia

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Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

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