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rare CNVs risk_factor_for autism

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

Evidence (3 sources)

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 ... autism.
confidence: 0.95
Pathway analysis of genomic data: concepts, methods, and prospects for future development. (2012) PMID:22480918 cited
identification of a synaptogenesis gene network affected by rare CNVs in autism
confidence: 0.95
Genetics of psychiatric disorders methods: molecular approaches. (2010) PMID:20159337 cited
possible involvement of rare copy number variations in ... autism, a possibility that has received substantial support
confidence: 0.94