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Chunk #17 — Discussion

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Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
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As also noted in earlier CNV studies in ADHD (15–17), we found significant evidence that CNV regions in ADHD patients overlapped with loci implicated by CNVs in autism and schizophrenia. Although schizophrenia and ADHD do not typically co-occur, ADHD and autism co-occur in patients more often than would be expected by chance, and they share heritability (27). The overlap in CNV loci among disorders suggests pleiotropy of genes predisposing to psychiatric disorders (28–31). Additional factors seem to be necessary to explain the specificity of a clinical phenotype. On the other hand, pleiotropy might also imply that the clinical classification tools for psychiatric disorders do not match the biological underpinnings of such disorders (28).