Yih Y - Search Results

1

Analysis of PINK1 in Asian patients with familial parkinsonism.

Tan EK, Yew K, Chua E, Shen H, Jamora RD, Lee E, Puong KY, Zhao Y, Pavanni R, Wong MC, Puvan K, Yih Y, Tan LC. Tan EK, et al. Among authors: yih y. Clin Genet. 2005 Nov;68(5):468-70. doi: 10.1111/j.1399-0004.2005.00500.x. Clin Genet. 2005. PMID: 16207217 No abstract available.

2

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

Tan EK, Shen H, Tan LC, Farrer M, Yew K, Chua E, Jamora RD, Puvan K, Puong KY, Zhao Y, Pavanni R, Wong MC, Yih Y, Skipper L, Liu JJ. Tan EK, et al. Among authors: yih y. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.

3

Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort.

Tan EK, Zhao Y, Puong KY, Law HY, Chan LL, Yew K, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Ng IS. Tan EK, et al. Among authors: yih y. Neurology. 2004 Jul 27;63(2):362-3. doi: 10.1212/01.wnl.0000130199.57181.7b. Neurology. 2004. PMID: 15277639

4

Monoamine oxidase B polymorphism, cigarette smoking and risk of Parkinson's disease: a study in an Asian population.

Tan EK, Chai A, Lum SY, Shen H, Tan C, Teoh ML, Yih Y, Wong MC, Zhao Y. Tan EK, et al. Among authors: yih y. Am J Med Genet B Neuropsychiatr Genet. 2003 Jul 1;120B(1):58-62. doi: 10.1002/ajmg.b.20035. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12815741

5

Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.

Skipper L, Li Y, Bonnard C, Pavanni R, Yih Y, Chua E, Sung WK, Tan L, Wong MC, Tan EK, Liu J. Skipper L, et al. Among authors: yih y. Hum Mol Genet. 2005 Dec 1;14(23):3549-56. doi: 10.1093/hmg/ddi376. Epub 2005 Nov 3. Hum Mol Genet. 2005. PMID: 16269443

6

LRRK2 R1628P increases risk of Parkinson's disease: replication evidence.

Tan EK, Tan LC, Lim HQ, Li R, Tang M, Yih Y, Pavanni R, Prakash KM, Fook-Chong S, Zhao Y. Tan EK, et al. Among authors: yih y. Hum Genet. 2008 Oct;124(3):287-8. doi: 10.1007/s00439-008-0544-2. Epub 2008 Sep 10. Hum Genet. 2008. PMID: 18781329

7

DRD3 variant and risk of essential tremor.

Tan EK, Prakash KM, Fook-Chong S, Yih Y, Chua E, Lum SY, Wong MC, Pavanni R, Zhao Y. Tan EK, et al. Among authors: yih y. Neurology. 2007 Mar 6;68(10):790-1. doi: 10.1212/01.wnl.0000256773.87498.2f. Neurology. 2007. PMID: 17339592 No abstract available.

8

Glucocerebrosidase mutations and risk of Parkinson disease in Chinese patients.

Tan EK, Tong J, Fook-Chong S, Yih Y, Wong MC, Pavanni R, Zhao Y. Tan EK, et al. Among authors: yih y. Arch Neurol. 2007 Jul;64(7):1056-8. doi: 10.1001/archneur.64.7.1056. Arch Neurol. 2007. PMID: 17620502 No abstract available.

9

Exploring an interaction of adenosine A2A receptor variability with coffee and tea intake in Parkinson's disease.

Tan EK, Lu ZY, Fook-Chong SM, Tan E, Shen H, Chua E, Yih Y, Teo YY, Zhao Y. Tan EK, et al. Among authors: yih y. Am J Med Genet B Neuropsychiatr Genet. 2006 Sep 5;141B(6):634-6. doi: 10.1002/ajmg.b.30359. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16823803

10

Alpha-synuclein haplotypes implicated in risk of Parkinson's disease.

Tan EK, Chai A, Teo YY, Zhao Y, Tan C, Shen H, Chandran VR, Teoh ML, Yih Y, Pavanni R, Wong MC, Puvan K, Lo YL, Yap E. Tan EK, et al. Among authors: yih y. Neurology. 2004 Jan 13;62(1):128-31. doi: 10.1212/01.wnl.0000101721.25345.dc. Neurology. 2004. PMID: 14718715

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