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Evolutionary and functional data power search for obsessive-compulsive disorder genes

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Cortico-striatal synaptic defects and OCD-like behaviours in Sapap3-mutant mice
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Microduplications of 16p11.2 are associated with schizophrenia
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Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease
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Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9
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Slitrk5 deficiency impairs corticostriatal circuitry and leads to obsessive-compulsive–like behaviors in mice
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Variation in the Gene Encoding the Serotonin 2A Receptor Is Associated with Outcome of Antidepressant Treatment
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Disruption of the neurexin 1 gene is associated with schizophrenia
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Repeated Cortico-Striatal Stimulation Generates Persistent OCD-Like Behavior
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The genetics of obsessive-compulsive disorder: a review
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