What have the genomics ever done for the psychoses?

• Published in: Psychological medicine 2010-04, Vol.40 (4), p.529-540
• Main Authors: Gill, M., Donohoe, G., Corvin, A.
• Format: Article
• Language: English
• Subjects: Adult and adolescent clinical studies; Autistic Disorder - genetics; Biological and medical sciences; Carrier Proteins - genetics; Cell Adhesion Molecules, Neuronal - genetics; Cognition; Cognition Disorders - epidemiology; Cognition Disorders - genetics; Copy number variation; DNA variants; Dysbindin; Dystrophin-Associated Proteins; Genes; Genetic Predisposition to Disease; genetics; Genome, Human; Genomics; Humans; Liability; Medical sciences; Mental disorders; Nerve Net - physiology; Nerve Tissue Proteins - genetics; Neuregulin-1 - genetics; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Psychoses; psychosis; Psychotic Disorders - epidemiology; Psychotic Disorders - genetics; Schizophrenia; Schizophrenia - epidemiology; Schizophrenia - genetics; Variants
• ISSN: 0033-2917; 1469-8978
• DOI: 10.1017/S0033291709991139

Despite the substantial heritability of the psychoses and their genuine public health burden, the applicability of the genomic approach in psychiatry has been strongly questioned or prematurely dismissed. selective review of the recent literature on molecular genetic and genomic approaches to the psychoses including the early output from genome-wide association studies and the genomic analysis of DNA structural variation. Susceptibility variants at strong candidate genes have been identified including neuregulin, dysbindin, DISC1 and neurexin 1. Rare but highly penetrant copy number variants and new mutations affecting genes involved in neurodevelopment, cell signalling and synaptic function have been described showing some overlapping genetic architecture with other developmental disorders including autism. The de-novo mutations described offer an explanation for the familial sporadic divide and the persistence of schizophrenia in the population. The functional effects of risk variants at the level of cognition and connectivity has been described and recently, ZNF804A has been identified, and the MHC re-identified as risk loci, and it has been shown that at least a third of the variation in liability is due to multiple common risk variants of small effect with a substantial shared genetic liability between schizophrenia and bipolar affective disorder. The genomics have done much for the psychoses to date and more is anticipated.