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rare CNVs risk_factor_for schizophrenia

Subject
rare CNVs
Relation
risk_factor_for
Object
schizophrenia
p-value
Evidence from: primary | all sources

Evidence (8 sources)

Psychiatric Genomics: An Update and an Agenda. (2018) PMID:28969442 cited
Multiple rare CNVs have been implicated; ... all increase risk for several psychiatric disorders ...
confidence: 0.93
Recent genetic findings in schizophrenia and their therapeutic relevance. (2015) PMID:25315827 cited
rare but penetrant large CNVs are associated with schizophrenia and account for ~10% of heritability.
confidence: 0.96
Evaluating historical candidate genes for schizophrenia. (2015) PMID:25754081 cited
Several rare CNVs have genotypic relative risks in the 5–20 range
confidence: 0.90
Copy number variation: what is it and what has it told us about child psychiatric disorders? (2013) PMID:23880486 cited
An increased burden of rare CNVs ... observed ... in schizophrenia
confidence: 0.94
CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited
CNV studies have now established a significant role for rare (<1% in frequency) ... CNVs in risk for schizophrenia.
confidence: 0.96
CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited
A contribution of rare CNVs to disease is evident ... in patients as compared with controls ... schizophrenia.
confidence: 0.95
High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011) PMID:22196331 cited
rare CNVs from large case-controls studies of SCZ ...
confidence: 0.90
Genetics of psychiatric disorders methods: molecular approaches. (2010) PMID:20159337 cited
possible involvement of rare copy number variations in schizophrenia ... has received substantial support
confidence: 0.94