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Similarity
3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
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Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
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Microdeletions of 3q29 confer high risk for schizophrenia.
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Association between microdeletion and microduplication at 16p11.2 and autism.
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Large recurrent microdeletions associated with schizophrenia.
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Structural variation of chromosomes in autism spectrum disorder.
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A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.
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Microduplications of 16p11.2 are associated with schizophrenia.
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Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.
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Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2.
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Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
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Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
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Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
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Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
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Strong association of de novo copy number mutations with autism.
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Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.
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De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
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1.3 Mb de novo deletion in chromosome band 3q29 associated with normal intelligence in a child.
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Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
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15q13.3 microdeletions increase risk of idiopathic generalized epilepsy.
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Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
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3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.
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Deletion 17q12 is a recurrent copy number variant that confers high risk of autism and schizophrenia.
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Population analysis of large copy number variants and hotspots of human genetic disease.
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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
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CNVs conferring risk of autism or schizophrenia affect cognition in controls.
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10
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.