Please use this identifier to cite or link to this item:
https://doi.org/10.1212/WNL.0b013e3181eccfcd
DC Field | Value | |
---|---|---|
dc.title | Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus | |
dc.contributor.author | Tan, E.-K. | |
dc.contributor.author | Kwok, H.-K. | |
dc.contributor.author | Tan, L.C. | |
dc.contributor.author | Zhao, W.-T. | |
dc.contributor.author | Prakash, K.M. | |
dc.contributor.author | Au, W.-L. | |
dc.contributor.author | Pavanni, R. | |
dc.contributor.author | Ng, Y.-Y. | |
dc.contributor.author | Satake, W. | |
dc.contributor.author | Zhao, Y. | |
dc.contributor.author | Toda, T. | |
dc.contributor.author | Liu, J.-J. | |
dc.date.accessioned | 2014-11-26T09:03:36Z | |
dc.date.available | 2014-11-26T09:03:36Z | |
dc.date.issued | 2010-08-10 | |
dc.identifier.citation | Tan, E.-K., Kwok, H.-K., Tan, L.C., Zhao, W.-T., Prakash, K.M., Au, W.-L., Pavanni, R., Ng, Y.-Y., Satake, W., Zhao, Y., Toda, T., Liu, J.-J. (2010-08-10). Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus. Neurology 75 (6) : 508-512. ScholarBank@NUS Repository. https://doi.org/10.1212/WNL.0b013e3181eccfcd | |
dc.identifier.issn | 00283878 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/110487 | |
dc.description.abstract | Objective: A genome-wide association study (GWAS) in the Japanese population identified 2 new Parkinson disease (PD) susceptibility loci on 1q32 (PARK16) (OMIM 613164) and BST1. We analyzed single nucleotide polymorphism (SNPs) located at the GWAS-linked loci (PARK16, PARK8, PARK1, and BST1) in a Chinese population and also conducted a meta-analysis in Asians by pooling 2 independent replication studies from Japan. Methods: We conducted an analysis of 13 SNPs associated with PD GWAS-linked loci in 2 case-control cohorts comprised of 1,349 ethnic Chinese subjects. Results: PARK16, PARK8, and PARK1 loci but not BST1 were found to be associated with PD. PARK16 SNPs were associated with a decreased risk while PARK1 and PARK8 SNPs were associated with an increased risk of PD. A pooled analysis of our Chinese cohorts and 2 Japanese replication cohorts involving 1,366 subjects with PD and 16,669 controls revealed robust association with these 3 loci and also BST1. There was a trend toward a stronger protective effect of SNPs at the PARK16 locus in sporadic PD compared to familial cases and in older compared to younger subjects. Conclusions: Our study reaffirms the role of GWAS-linked loci in PD in Asian subjects and the strength of association is similar between Chinese and Japanese subjects. Efforts to elucidate the associated gene within PARK16 locus are warranted. © 2010 by AAN Enterprises, Inc. All rights reserved. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1212/WNL.0b013e3181eccfcd | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | DUKE-NUS GRADUATE MEDICAL SCHOOL S'PORE | |
dc.description.doi | 10.1212/WNL.0b013e3181eccfcd | |
dc.description.sourcetitle | Neurology | |
dc.description.volume | 75 | |
dc.description.issue | 6 | |
dc.description.page | 508-512 | |
dc.description.coden | NEURA | |
dc.identifier.isiut | 000280759600006 | |
Appears in Collections: | Staff Publications |
Show simple item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.