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Sharma, M.* ; Lichtner, P. ; Kruger, R.* ; Berg, D.* ; Schulte, C.* ; Illig, T. ; Riess, O.* ; Gasser, T.*

Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.

Neurobiol. Aging 30, 1706-1709 (2009)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
A recently published whole genome association study showed the involvement of 13 SNPs in the pathogenesis of Parkinson disease (PD). We performed a replication study to assess their involvement in our sporadic cohort consisting of 663 cases and 1002 controls ascertained from Germany. One of the previously reported SNP, rs7723605, showed evidence of association (p value 0.04) in our sample. We further refined the signal by genotyping additional 22 SNPs around SNP rs7723605. Our refinement analysis, however, did not provide evidence for association in our sample after adjusting for multiple testing by permutation procedure. In conclusion, our study did not lend support to the finding that the reported SNPs are directly influencing the susceptibility to sporadic form of PD at least in our population.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Parkinson disease; Whole genome association; Linkage disequilibrium (LD)
ISSN (print) / ISBN 0197-4580
e-ISSN 1558-1497
Quellenangaben Volume: 30, Issue: 10, Pages: 1706-1709 Article Number: , Supplement: ,
Publisher Elsevier
Publishing Place New York, NY [u.a.]
Non-patent literature Publications
Reviewing status Peer reviewed