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CNV risk_factor_for psychiatric disorders

Subject
CNV
Relation
risk_factor_for
Object
psychiatric disorders
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 growing body of research on CNV provides a compelling rationale ... to psychiatric disease ... increase the proportion of genetic risk that can be explained.
confidence: 0.90
Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) PMID:19339359 cited
initial set of ... CNV associations for psychiatric disorders
confidence: 0.95
Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) PMID:19339359 cited
studies of CNVs and rare SNPs will also be critical in elucidating disease mechanisms
confidence: 0.88