CNV risk_factor_for schizophrenia
Evidence from:
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Evidence (6 sources)
Recent genetic findings in schizophrenia and their therapeutic relevance.
(2015)
PMID:25315827
cited
Both act as risk factors for schizophrenia.
confidence: 0.96
Recent genetic findings in schizophrenia and their therapeutic relevance.
(2015)
PMID:25315827
cited
CNVs ... are associated with an increased risk of schizophrenia.
confidence: 0.95
Copy number variation: what is it and what has it told us about child psychiatric disorders?
(2013)
PMID:23880486
cited
CNVs as risks for psychiatric disorders ... disorders such as ... schizophrenia.
confidence: 0.95
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
(2012)
PMID:22420048
cited
CNVs ... were significantly enriched for loci previously implicated in schizophrenia
confidence: 0.90
rare CNVs contribute to genetic risk for schizophrenia
confidence: 0.96
Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk.
(2009)
PMID:19065143
cited
and an excess of de novo CNV events in that disorder have raised the possibility of a significant contribution from rare events.
confidence: 0.94