ADHD case subjects had a 1.49‑fold excess of CNVs located at the eight loci previously implicated in schizophrenia relative to comparison subjects (5.4% vs 3.6%, p=0.03).

confidence: 0.90

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

CNV regions in ADHD patients overlapped with loci implicated by CNVs in autism and schizophrenia.

confidence: 0.90

CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012) PMID:22424231 cited

findings of CNV studies in ... schizophrenia ...

confidence: 0.94

High frequencies of de novo CNVs in bipolar disorder and schizophrenia. (2011) PMID:22196331 cited

null hypothesis CNV sets each for the ... schizophrenia ... de novo CNV sets

confidence: 0.90

Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) PMID:19339359 cited

large GWAS analyses (for ... CNV associations) ... schizophrenia ... samples

confidence: 0.90

Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) PMID:19339359 cited

For schizophrenia, four genomewide studies of CNVs ... have produced two types of replicated findings

confidence: 0.95

Genomewide association studies: history, rationale, and prospects for psychiatric disorders. (2009) PMID:19339359 cited

replicated CNV associations for schizophrenia

confidence: 0.95

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

excess of de novo CNV events ... in that disorder

confidence: 0.90