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  Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11

Francks, C., DeLisi, L. E., Shaw, S. H., Fisher, S. E., Richardson, A. J., Stein, J. F., et al. (2003). Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human Molecular Genetics, 12(24), 3225-3230. doi:10.1093/hmg/ddg362.

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Francks_Parent_of_origin_effects_Hum_Mol_Gen_2003.pdf (Publisher version), 93KB
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Francks_Parent_of_origin_effects_Hum_Mol_Gen_2003.pdf
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Francks, Clyde1, Author           
DeLisi, Lynn E., Author
Shaw, Sarah H., Author
Fisher, Simon E.1, Author           
Richardson, Alex J., Author
Stein, John F., Author
Monaco, Anthony P., Author
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1Wellcome Trust Centre for Human Genetics, University of Oxford, UK, ou_persistent22              

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 Abstract: Schizophrenia and non-right-handedness are moderately associated, and both traits are often accompanied by abnormalities of asymmetrical brain morphology or function. We have found linkage previously of chromosome 2p12-q11 to a quantitative measure of handedness, and we have also found linkage of schizophrenia/schizoaffective disorder to this same chromosomal region in a separate study. Now, we have found that in one of our samples (191 reading-disabled sibling pairs), the relative hand skill of siblings was correlated more strongly with paternal than maternal relative hand skill. This led us to re-analyse 2p12-q11 under parent-of-origin linkage models. We found linkage of relative hand skill in the RD siblings to 2p12-q11 with P=0.0000037 for paternal identity-by-descent sharing, whereas the maternally inherited locus was not linked to the trait (P>0.2). Similarly, in affected-sib-pair analysis of our schizophrenia dataset (241 sibling pairs), we found linkage to schizophrenia for paternal sharing with LOD=4.72, P=0.0000016, within 3 cM of the peak linkage to relative hand skill. Maternal linkage across the region was weak or non-significant. These similar paternal-specific linkages suggest that the causative genetic effects on 2p12-q11 are related. The linkages may be due to a single maternally imprinted influence on lateralized brain development that contains common functional polymorphisms.

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Language(s): eng - English
 Dates: 2003
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1093/hmg/ddg362
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Title: Human Molecular Genetics
Source Genre: Journal
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Publ. Info: Oxford, England : IRL Press
Pages: - Volume / Issue: 12 (24) Sequence Number: - Start / End Page: 3225 - 3230 Identifier: Other: 954925581153
Other: 0964-6906
CoNE: https://pure.mpg.de/cone/journals/resource/954925581153