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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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De novo mutations in schizophrenia implicate synaptic networks.
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Strong association of de novo copy number mutations with sporadic schizophrenia.
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
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Strong association of de novo copy number mutations with autism.
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Microduplications of 16p11.2 are associated with schizophrenia.
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The autism and schizophrenia associated gene CYFIP1 is critical for the maintenance of dendritic complexity and the stabilization of mature spines.
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Common variants conferring risk of schizophrenia.
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.