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Please use this identifier to cite or link to this item: http://hdl.handle.net/2262/60879

Title: Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.
Author: GILL, MICHAEL
CORVIN, AIDEN PETER
MORRIS, DEREK
Sponsor: 
Name Grant Number
242167

Author's Homepage: http://people.tcd.ie/mgill
http://people.tcd.ie/acorvin
http://people.tcd.ie/morrisdw
Keywords: Genetics
Neuroscience
Schizophrenia
Issue Date: 2012
Citation: Lips ES, Cornelisse LN, Toonen RF, Min JL, Hultman CM, Holmans PA, O'Donovan MC, Purcell SM, Smit AB, Verhage M, Sullivan PF, Visscher PM, Posthuma D, Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia., Molecular Psychiatry, 17, 10, 2012, 996-1006
Series/Report no.: Molecular Psychiatry
17
10
Abstract: Schizophrenia is a highly heritable disorder with a polygenic pattern of inheritance and a population prevalence of _1%. Previous studies have implicated synaptic dysfunction in schizophrenia. We tested the accumulated association of genetic variants in expert-curated synaptic gene groups with schizophrenia in 4673 cases and 4965 healthy controls, using functional gene group analysis. Identifying groups of genes with similar cellular function rather than genes in isolation may have clinical implications for finding additional drug targets. We found that a group of 1026 synaptic genes was significantly associated with the risk of schizophrenia (P=7.6 _ 10(-11)) and more strongly associated than 100 randomly drawn, matched control groups of genetic variants (P<0.01). Subsequent analysis of synaptic subgroups suggested that the strongest association signals are derived from three synaptic gene groups: intracellular signal transduction (P=2.0 _ 10(-4)), excitability (P=9.0 _ 10(-4)) and cell adhesion and trans-synaptic signaling (P=2.4 _ 10(-3)). These results are consistent with a role of synaptic dysfunction in schizophrenia and imply that impaired intracellular signal transduction in synapses, synaptic excitability and cell adhesion and trans-synaptic signaling play a role in the pathology of schizophrenia.
Description: PUBLISHED
URI: http://hdl.handle.net/2262/60879
Related links: http://dx.doi.org/10.1038/mp.2011.117
Access: OpenAccess
Appears in Collections:Psychiatry (Scholarly Publications)

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