Liu JJ - Search Results

1

Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study.

Tan EK, Peng R, Teo YY, Tan LC, Angeles D, Ho P, Chen ML, Lin CH, Mao XY, Chang XL, Prakash KM, Liu JJ, Au WL, Le WD, Jankovic J, Burgunder JM, Zhao Y, Wu RM. Tan EK, et al. Among authors: liu jj. Hum Mutat. 2010 May;31(5):561-8. doi: 10.1002/humu.21225. Hum Mutat. 2010. PMID: 20186690

2

Analysis of EIF4G1 in Parkinson's disease among Asians.

Zhao Y, Ho P, Prakash KM, Foo JN, Liu JJ, Au WL, Tan LC, Tan EK. Zhao Y, et al. Among authors: liu jj. Neurobiol Aging. 2013 Apr;34(4):1311.e5-6. doi: 10.1016/j.neurobiolaging.2012.09.003. Epub 2012 Oct 23. Neurobiol Aging. 2013. PMID: 23092605

3

SLC1A2 variant associated with essential tremor but not Parkinson disease in Chinese subjects.

Tan EK, Foo JN, Tan L, Au WL, Prakash KM, Ng E, Ikram MK, Wong TY, Liu JJ, Zhao Y. Tan EK, et al. Among authors: liu jj. Neurology. 2013 Apr 23;80(17):1618-9. doi: 10.1212/WNL.0b013e31828f1903. Epub 2013 Apr 17. Neurology. 2013. PMID: 23596072

4

LRRK2 G2019S founder haplotype in the Chinese population.

Tan EK, Skipper L, Tan L, Liu JJ. Tan EK, et al. Among authors: liu jj. Mov Disord. 2007 Jan;22(1):105-7. doi: 10.1002/mds.21206. Mov Disord. 2007. PMID: 17083102

5

Analysis of LRRK2 Gly2385Arg genetic variant in non-Chinese Asians.

Tan EK, Zhao Y, Tan L, Lim HQ, Lee J, Yuen Y, Pavanni R, Wong MC, Fook-Chong S, Liu JJ. Tan EK, et al. Among authors: liu jj. Mov Disord. 2007 Sep 15;22(12):1816-8. doi: 10.1002/mds.21658. Mov Disord. 2007. PMID: 17659642

6

Absence of A673T amyloid-β precursor protein variant in Alzheimer's disease and other neurological diseases.

Ting SK, Chong MS, Kandiah N, Hameed S, Tan L, Au WL, Prakash KM, Pavanni R, Lee TS, Foo JN, Bei JX, Yu XQ, Liu JJ, Zhao Y, Lee WL, Tan EK. Ting SK, et al. Among authors: liu jj. Neurobiol Aging. 2013 Oct;34(10):2441.e7-8. doi: 10.1016/j.neurobiolaging.2013.04.012. Epub 2013 May 4. Neurobiol Aging. 2013. PMID: 23652020

7

Identification of a novel risk variant in the FUS gene in essential tremor.

Wu YR, Foo JN, Tan LC, Chen CM, Prakash KM, Chen YC, Bei JX, Au WL, Chang CW, Wong TY, Liu JJ, Zhao Y, Tan EK. Wu YR, et al. Among authors: liu jj. Neurology. 2013 Aug 6;81(6):541-4. doi: 10.1212/WNL.0b013e31829e700c. Epub 2013 Jul 3. Neurology. 2013. PMID: 23825177

8

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: liu jj. Neurosci Lett. 2005 Aug 26;384(3):327-9. doi: 10.1016/j.neulet.2005.04.103. Neurosci Lett. 2005. PMID: 15955629 Clinical Trial.

9

Analysis of 14 LRRK2 mutations in Parkinson's plus syndromes and late-onset Parkinson's disease.

Tan EK, Skipper L, Chua E, Wong MC, Pavanni R, Bonnard C, Kolatkar P, Liu JJ. Tan EK, et al. Among authors: liu jj. Mov Disord. 2006 Jul;21(7):997-1001. doi: 10.1002/mds.20875. Mov Disord. 2006. PMID: 16602113

10

Polymorphisms in candidate genes: implications for the current treatment of Parkinson's disease.

Skipper L, Liu JJ, Tan EK. Skipper L, et al. Among authors: liu jj. Expert Opin Pharmacother. 2006 May;7(7):849-55. doi: 10.1517/14656566.7.7.849. Expert Opin Pharmacother. 2006. PMID: 16634708 Review.

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