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Potential genetic variants in schizophrenia : A Bayesian analysis

Hall, Hakan (author)
Lawyer, Glenn (author)
Sillen, Anna (author)
Karolinska Institutet
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Jonsson, Erik G. (author)
Karolinska Institutet
Agartz, Ingrid (author)
Karolinska Institutet
Terenius, Lars (author)
Karolinska Institutet
Arnborg, Stefan (author)
KTH,Numerisk Analys och Datalogi, NADA
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 (creator_code:org_t)
2009-07-12
2007
English.
In: World Journal of Biological Psychiatry. - : Informa UK Limited. - 1562-2975 .- 1814-1412. ; 8:1, s. 12-22
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • A number of different gene polymorphisms have been found to dispose for the development of schizophrenia. However, no single gene polymorphism is sufficient for the precipitation of schizophrenia. Swedish psychosis patients (n = 103) and control subjects (n = 89) were analyzed for 36 single nucleotide polymorphisms in 30 candidate genes for schizophrenia. Evidence of association was analyzed with Bayesian statistical methods. Variants in the genes coding for dopamine-D-2 receptor, brain-derived neurotrophic factor (BDNF), neuropeptide Y (NPY), neuregulin 1, reelin and synapsin 3 showed association with schizophrenia, although few subjects were found in the minority allele for the two latter variants. The six gene variants, all with suspected connection to schizophrenia, were found to be risk factors when considered in combination, but not separately. The results indicate that the Bayesian statistical method gives additional possibilities in the search for risk factors for schizophrenia or other complex disorders.

Keyword

BDNE
dopamine-D2 receptor
neuregulin 1
neuropeptide Y
schizophrenia
d2 receptor gene
neuropeptide-y polymorphism
brain morphology
bdnf gene
association
metaanalysis
expression
risk
population
alleles

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ref (subject category)
art (subject category)

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