192 related articles for article (PubMed ID: 19672984)
1. 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; 24(13):1902-5. PubMed ID: 19672984
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 18201193
[TBL] [Abstract][Full Text] [Related]
3. LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China.
Yu L; Hu F; Zou X; Jiang Y; Liu Y; He X; Xi J; Liu L; Liu Z; He L; Xu Y
Brain Res; 2009 Nov; 1296():113-6. PubMed ID: 19699188
[TBL] [Abstract][Full Text] [Related]
4. Association of LRRK2 R1628P variant with Parkinson's disease in Ethnic Han-Chinese and subgroup population.
Zhang P; Wang Q; Jiao F; Yan J; Chen L; He F; Zhang Q; Tian B
Sci Rep; 2016 Nov; 6():35171. PubMed ID: 27812003
[TBL] [Abstract][Full Text] [Related]
5. 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. PubMed ID: 19854095
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 18412265
[TBL] [Abstract][Full Text] [Related]
7. Confirmation of the association between LRRK2 R1628P variant and susceptibility to Parkinson's disease in the Thai population.
Pulkes T; Papsing C; Thakkinstian A; Pongpakdee S; Kulkantrakorn K; Hanchaiphiboolkul S; Tiamkao S; Boonkongchuen P
Parkinsonism Relat Disord; 2014 Sep; 20(9):1018-21. PubMed ID: 24997548
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 23624603
[TBL] [Abstract][Full Text] [Related]
9. Relationship between LRRK2 R1628P polymorphism and Parkinson's disease in Asian populations.
Zhao H; Kong Z
Oncotarget; 2016 Jul; 7(30):46890-46898. PubMed ID: 27384489
[TBL] [Abstract][Full Text] [Related]
10. Lrrk2 R1628P variant is a risk factor for essential tremor.
Chao YX; Ng EY; Tan L; Prakash KM; Au WL; Zhao Y; Tan EK
Sci Rep; 2015 Mar; 5():9029. PubMed ID: 25761573
[TBL] [Abstract][Full Text] [Related]
11. Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China.
Mao XY; Burgunder JM; Zhang ZJ; An XK; Zhang JH; Yang Y; Li T; Wang YC; Chang XL; Peng R
Neurosci Lett; 2010 Jan; 469(2):256-9. PubMed ID: 20004703
[TBL] [Abstract][Full Text] [Related]
12. A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.
Fung HC; Chen CM; Hardy J; Singleton AB; Wu YR
BMC Neurol; 2006 Dec; 6():47. PubMed ID: 17187665
[TBL] [Abstract][Full Text] [Related]
13. An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.
Yuan X; Chen Y; Cao B; Zhao B; Wei Q; Guo X; Yang Y; Yuan L; Shang H
Parkinsonism Relat Disord; 2015 Feb; 21(2):147-9. PubMed ID: 25511328
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 18688798
[No Abstract] [Full Text] [Related]
15. 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. PubMed ID: 18781329
[TBL] [Abstract][Full Text] [Related]
16. 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. PubMed ID: 22981185
[No Abstract] [Full Text] [Related]
17. Confirmation of LRRK2 S1647T variant as a risk factor for Parkinson's disease in southern China.
Zheng Y; Liu Y; Wu Q; Hong H; Zhou H; Chen J; Wang H; Xian W; Li J; Liu Z; Pei Z; Chen L
Eur J Neurol; 2011 Mar; 18(3):538-40. PubMed ID: 20629711
[TBL] [Abstract][Full Text] [Related]
18. 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; 17(18):1859-62. PubMed ID: 17179858
[TBL] [Abstract][Full Text] [Related]
19. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.
Tan EK; Zhao Y; Skipper L; Tan MG; Di Fonzo A; Sun L; Fook-Chong S; Tang S; Chua E; Yuen Y; Tan L; Pavanni R; Wong MC; Kolatkar P; Lu CS; Bonifati V; Liu JJ
Hum Genet; 2007 Feb; 120(6):857-63. PubMed ID: 17019612
[TBL] [Abstract][Full Text] [Related]
20. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study.
Ross OA; Soto-Ortolaza AI; Heckman MG; Aasly JO; Abahuni N; Annesi G; Bacon JA; Bardien S; Bozi M; Brice A; Brighina L; Van Broeckhoven C; Carr J; Chartier-Harlin MC; Dardiotis E; Dickson DW; Diehl NN; Elbaz A; Ferrarese C; Ferraris A; Fiske B; Gibson JM; Gibson R; Hadjigeorgiou GM; Hattori N; Ioannidis JP; Jasinska-Myga B; Jeon BS; Kim YJ; Klein C; Kruger R; Kyratzi E; Lesage S; Lin CH; Lynch T; Maraganore DM; Mellick GD; Mutez E; Nilsson C; Opala G; Park SS; Puschmann A; Quattrone A; Sharma M; Silburn PA; Sohn YH; Stefanis L; Tadic V; Theuns J; Tomiyama H; Uitti RJ; Valente EM; van de Loo S; Vassilatis DK; Vilariño-Güell C; White LR; Wirdefeldt K; Wszolek ZK; Wu RM; Farrer MJ;
Lancet Neurol; 2011 Oct; 10(10):898-908. PubMed ID: 21885347
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]