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Lack of association between the LRRK2 A419V variant and Asian Parkinson's disease.
Gopalai AA, Lim SY, Aziz ZA, Lim SK, Tan LP, Chong YB, Tan CT, Puvanarajah S, Viswanathan S, Kuppusamy R, Tan AH, Lim TT, Eow GB, Norlinah MI, Li HH, Zhao Y, Ahmad-Annuar A. Gopalai AA, et al. Among authors: eow gb. Ann Acad Med Singap. 2013 May;42(5):237-40. Ann Acad Med Singap. 2013. PMID: 23771111 Free article.
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case-control association study for Parkinson's disease.
Gopalai AA, Lim JL, Li HH, Zhao Y, Lim TT, Eow GB, Puvanarajah S, Viswanathan S, Norlinah MI, Abdul Aziz Z, Lim SK, Tan CT, Tan AH, Lim SY, Tan EK, Ahmad Annuar A. Gopalai AA, et al. Among authors: eow gb. Mol Genet Genomic Med. 2019 Nov;7(11):e604. doi: 10.1002/mgg3.604. Epub 2019 Sep 5. Mol Genet Genomic Med. 2019. PMID: 31487119 Free PMC article.
LRRK2 G2385R and R1628P mutations are associated with an increased risk of Parkinson's disease in the Malaysian population.
Gopalai AA, Lim SY, Chua JY, Tey S, Lim TT, Mohamed Ibrahim N, Tan AH, Eow GB, Abdul Aziz Z, Puvanarajah SD, Viswanathan S, Looi I, Lim SK, Tan LP, Chong YB, Tan CT, Zhao Y, Tan EK, Ahmad-Annuar A. Gopalai AA, et al. Among authors: eow gb. Biomed Res Int. 2014;2014:867321. doi: 10.1155/2014/867321. Epub 2014 Aug 28. Biomed Res Int. 2014. PMID: 25243190 Free PMC article.
Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
Lim JL, Ng EY, Lim SY, Tan AH, Abdul-Aziz Z, Ibrahim KA, Gopalai AA, Tay YW, Vijayanathan Y, Toh TS, Lim SK, Bee PC, Puvanarajah SD, Viswanathan S, Looi I, Lim TT, Eow GB, Cheah WK, Tan EK, Ahmad-Annuar A. Lim JL, et al. Among authors: eow gb. Neurol Sci. 2021 Oct;42(10):4203-4207. doi: 10.1007/s10072-021-05056-x. Epub 2021 Feb 8. Neurol Sci. 2021. PMID: 33559030
PARK16 is associated with PD in the Malaysian population.
Gopalai AA, Ahmad-Annuar A, Li HH, Zhao Y, Lim SY, Tan AH, Lim TT, Eow GB, Santhi P, Shanthi V, Norlinah MI, Aziz ZA, Lim SK, Tan CT, Tan EK. Gopalai AA, et al. Among authors: eow gb. Am J Med Genet B Neuropsychiatr Genet. 2016 Sep;171(6):839-47. doi: 10.1002/ajmg.b.32454. Epub 2016 May 13. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27174169
A previously misdiagnosed cohort of aquaporin 4 antibody-positive neuromyelitis optica spectrum disorder with disease duration of >10 years in multi-ethnic Penang, Malaysia: Clinical features and disease course.
Hor JY, Lim TT, Chow HB, Tan K, Cheah CF, Ching YM, Arip M, Easaw PE, Eow GB. Hor JY, et al. Among authors: eow gb. Mult Scler Relat Disord. 2016 Jan;5:89-90. doi: 10.1016/j.msard.2015.11.008. Epub 2015 Nov 14. Mult Scler Relat Disord. 2016. PMID: 26856950 No abstract available.
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