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Items: 1 to 20 of 100

1.

Lrrk2 R1628P in non-Chinese Asian races.

Tan EK, Tang M, Tan LC, Wu YR, Wu RM, Ross OA, Zhao Y.

Ann Neurol. 2008 Oct;64(4):472-3. doi: 10.1002/ana.21467. No abstract available.

PMID:
18688798
2.

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

Zhang Z, Burgunder JM, An X, Wu Y, Chen W, Zhang J, Wang Y, Xu Y, Gou Y, Yuan G, Mao X, Peng R.

Mov Disord. 2009 Oct 15;24(13):1902-5. doi: 10.1002/mds.22371.

PMID:
19672984
3.

Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant.

Tan EK, Schapira AH.

Eur J Neurol. 2008 Mar;15(3):203-4. doi: 10.1111/j.1468-1331.2007.02053.x. No abstract available. Erratum in: Eur J Neurol. 2008 Apr;15(4):434.

PMID:
18290841
4.

LRRK2 G2385R and LRRK2 R1628P increase risk of Parkinson's disease in a Han Chinese population from Southern Mainland China.

Fu X, Zheng Y, Hong H, He Y, Zhou S, Guo C, Liu Y, Xian W, Zeng J, Li J, Liu Z, Chen L, Pei Z.

Parkinsonism Relat Disord. 2013 Mar;19(3):397-8. doi: 10.1016/j.parkreldis.2012.08.007. No abstract available.

PMID:
22981185
5.

Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.

Ross OA, Wu YR, Lee MC, Funayama M, Chen ML, Soto AI, Mata IF, Lee-Chen GJ, Chen CM, Tang M, Zhao Y, Hattori N, Farrer MJ, Tan EK, Wu RM.

Ann Neurol. 2008 Jul;64(1):88-92. doi: 10.1002/ana.21405.

PMID:
18412265
6.

LRRK2 G2019S founder haplotype in the Chinese population.

Tan EK, Skipper L, Tan L, Liu JJ.

Mov Disord. 2007 Jan;22(1):105-7.

PMID:
17083102
7.

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.

Hum Mutat. 2010 May;31(5):561-8. doi: 10.1002/humu.21225.

PMID:
20186690
8.

LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

An XK, Peng R, Li T, Burgunder JM, Wu Y, Chen WJ, Zhang JH, Wang YC, Xu YM, Gou YR, Yuan GG, Zhang ZJ.

Eur J Neurol. 2008 Mar;15(3):301-5. doi: 10.1111/j.1468-1331.2007.02052.x.

PMID:
18201193
9.

LRRK2 R1398H polymorphism is associated with decreased risk of Parkinson's disease in a Han Chinese population.

Chen L, Zhang S, Liu Y, Hong H, Wang H, Zheng Y, Zhou H, Chen J, Xian W, He Y, Li J, Liu Z, Pei Z, Zeng J.

Parkinsonism Relat Disord. 2011 May;17(4):291-2. doi: 10.1016/j.parkreldis.2010.11.012. No abstract available.

PMID:
21159540
10.

Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia.

Farrer MJ, Stone JT, Lin CH, Dächsel JC, Hulihan MM, Haugarvoll K, Ross OA, Wu RM.

Parkinsonism Relat Disord. 2007 Mar;13(2):89-92.

PMID:
17222580
11.

Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.

Wang C, Cai Y, Zheng Z, Tang BS, Xu Y, Wang T, Ma J, Chen SD, Langston JW, Tanner CM, Chan P; Chinese Parkinson Study Group (CPSG)..

Parkinsonism Relat Disord. 2012 Sep;18(8):958-63.

PMID:
22658533
12.

Association between G2385R and R1628P polymorphism of LRRK2 gene and sporadic Parkinson's disease in a Han-Chinese population in south-eastern China.

Cai J, Lin Y, Chen W, Lin Q, Cai B, Wang N, Zheng W.

Neurol Sci. 2013 Nov;34(11):2001-6. doi: 10.1007/s10072-013-1436-3.

PMID:
23624603
13.

Comparing LRRK2 Gly2385Arg carriers with noncarriers.

Tan EK, Fook-Chong S, Yi Z.

Mov Disord. 2007 Apr 15;22(5):749-50. No abstract available.

PMID:
17290460
14.

A study of six point mutation analysis of LRRK2 gene in Chinese mainland patients with Parkinson's disease.

Hu ZX, Peng DT, Cai M, Pu JL, Lei XG, Yin XZ, Ou-Yang ZY, Luo W, Zhang BR.

Neurol Sci. 2011 Aug;32(4):741-2. doi: 10.1007/s10072-010-0453-8. No abstract available.

PMID:
21234781
15.

A novel P755L mutation in LRRK2 gene associated with Parkinson's disease.

Wu T, Zeng Y, Ding X, Li X, Li W, Dong H, Chen S, Zhang X, Ma G, Yao J, Deng X.

Neuroreport. 2006 Dec 18;17(18):1859-62.

PMID:
17179858
16.

The LRRK2 G2385R variant is a risk factor for sporadic Parkinson's disease in the Korean population.

Kim JM, Lee JY, Kim HJ, Kim JS, Shin ES, Cho JH, Park SS, Jeon BS.

Parkinsonism Relat Disord. 2010 Feb;16(2):85-8. doi: 10.1016/j.parkreldis.2009.10.004.

PMID:
19854095
17.

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.

Hum Genet. 2008 Oct;124(3):287-8. doi: 10.1007/s00439-008-0544-2.

PMID:
18781329
18.

The LRRK2 R1628P variant plays a protective role in Han Chinese population with Alzheimer's disease.

Li HL, Lu SJ, Sun YM, Guo QH, Sadovnick AD, Wu ZY.

CNS Neurosci Ther. 2013 Apr;19(4):207-15. doi: 10.1111/cns.12062.

PMID:
23421816
19.

A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease.

Wang L, Guo JF, Nie LL, Xu Q, Zuo X, Sun QY, Yan XX, Tang BS.

Neurosci Lett. 2010 Jan 14;468(3):198-201. doi: 10.1016/j.neulet.2009.10.080.

PMID:
19879329
20.

New LRRK2 variants identified in Parkinson's disease.

Tan EK, Schapira AH.

Eur J Neurol. 2011 Mar;18(3):369-70. doi: 10.1111/j.1468-1331.2010.03163.x. No abstract available.

PMID:
20629720
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