-
1
-
-
34447289622
-
Pathogenic mutations in Parkinson disease
-
Tan EK, Skipper LM. Pathogenic mutations in Parkinson disease. Hum Mutat 2007; 28: 641-653.
-
(2007)
Hum Mutat
, vol.28
, pp. 641-653
-
-
Tan, E.K.1
Skipper, L.M.2
-
2
-
-
33748619215
-
The importance of LRRK2 mutations in Parkinson disease
-
Schapira AH. The importance of LRRK2 mutations in Parkinson disease. Arch Neurol 2006; 63: 1225-1228.
-
(2006)
Arch Neurol
, vol.63
, pp. 1225-1228
-
-
Schapira, A.H.1
-
3
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology
-
Zimprich A, Biskup S, Leitner P, et al. Mutations in LRRK2 cause autosomal-dominant Parkinsonism with pleomorphic pathology. Neuron 2004; 44: 601-607.
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
-
4
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz C, Jain S, Evans EW, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004; 44: 595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
-
5
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
-
Healy DG, Falchi M, O'Sullivan SS, et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008; 7: 583-590.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
-
6
-
-
44949148980
-
The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson's disease
-
Möller JC, Rissling I, Mylius V, Höft C, Eggert KM, Oertel WH. The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson's disease. Eur J Neurol 2008; 15: 743-745.
-
(2008)
Eur J Neurol
, vol.15
, pp. 743-745
-
-
Möller, J.C.1
Rissling, I.2
Mylius, V.3
Höft, C.4
Eggert, K.M.5
Oertel, W.H.6
-
7
-
-
33846358949
-
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence
-
Tan EK, Zhao Y, Skipper L, et al. The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence. Hum Genet 2007; 120: 857-863.
-
(2007)
Hum Genet
, vol.120
, pp. 857-863
-
-
Tan, E.K.1
Zhao, Y.2
Skipper, L.3
-
8
-
-
39149133173
-
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, et al. LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han Chinese from mainland China. Eur J Neurol 2008; 15: 301-305.
-
(2008)
Eur J Neurol
, vol.15
, pp. 301-305
-
-
An, X.K.1
Peng, R.2
Li, T.3
Burgunder, J.M.4
-
9
-
-
48949092066
-
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
-
Ross OA, Wu YR, Lee MC, et al. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann Neurol 2008; 64: 88-92.
-
(2008)
Ann Neurol
, vol.64
, pp. 88-92
-
-
Ross, O.A.1
Wu, Y.R.2
Lee, M.C.3
-
10
-
-
39149123182
-
Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant
-
Tan EK, Schapira AH. Uniting Chinese across Asia: the LRRK2 Gly2385Arg risk variant. Eur J Neurol 2008; 15: 203-204.
-
(2008)
Eur J Neurol
, vol.15
, pp. 203-204
-
-
Tan, E.K.1
Schapira, A.H.2
-
11
-
-
33746079596
-
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
-
Di Fonzo A, Wu-Chou YH, et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 2006; 7: 133-138.
-
(2006)
Neurogenetics
, vol.7
, pp. 133-138
-
-
Di Fonzo, A.1
Wu-Chou, Y.H.2
-
12
-
-
77951876814
-
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study
-
Tan EK, Peng R, Teo YY, et al. Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study. Hum Mutat 2010; 31: 561-568.
-
(2010)
Hum Mutat
, vol.31
, pp. 561-568
-
-
Tan, E.K.1
Peng, R.2
Teo, Y.Y.3
-
13
-
-
79951653866
-
Confirmation of LRRK2 S1647T as a risk factor for Parkinson's disease in Southern China
-
Zheng Y, Liu Y, Wu Q, et al. Confirmation of LRRK2 S1647T as a risk factor for Parkinson's disease in Southern China. Eur J Neurol 2010; 18: 538-540.
-
(2010)
Eur J Neurol
, vol.18
, pp. 538-540
-
-
Zheng, Y.1
Liu, Y.2
Wu, Q.3
-
14
-
-
70549084415
-
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
-
Satake W, Nakabayashi Y, Mizuta I, et al. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009; 41: 1303-1307.
-
(2009)
Nat Genet
, vol.41
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
-
15
-
-
70549088602
-
Genome-wide association study reveals genetic risk underlying Parkinson's disease
-
Simón-Sánchez J, Schulte C, Bras JM, et al. Genome-wide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009; 41: 1308-1312.
-
(2009)
Nat Genet
, vol.41
, pp. 1308-1312
-
-
Simón-Sánchez, J.1
Schulte, C.2
Bras, J.M.3
-
16
-
-
35348820061
-
The role of common genetic risk variants in Parkinson disease
-
Tan EK. The role of common genetic risk variants in Parkinson disease. Clin Genet 2007; 72: 387-393.
-
(2007)
Clin Genet
, vol.72
, pp. 387-393
-
-
Tan, E.K.1
-
17
-
-
70349329841
-
LRRK2 G2385R modulates age at onset in Parkinson's disease: a multi-center pooled analysis
-
Tan EK, Peng R, Wu YR, et al. LRRK2 G2385R modulates age at onset in Parkinson's disease: a multi-center pooled analysis. Am J Med Genet B Neuropsychiatr Genet 2009; 7: 1022-1023.
-
(2009)
Am J Med Genet B Neuropsychiatr Genet
, vol.7
, pp. 1022-1023
-
-
Tan, E.K.1
Peng, R.2
Wu, Y.R.3
-
18
-
-
70350319531
-
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease
-
Sidransky E, Nalls MA, Aasly JO, et al. Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. N Engl J Med 2009; 361: 1651-1661.
-
(2009)
N Engl J Med
, vol.361
, pp. 1651-1661
-
-
Sidransky, E.1
Nalls, M.A.2
Aasly, J.O.3
-
19
-
-
70349103837
-
Parkin protects against LRRK2 G2019S mutant-induced dopaminergic neurodegeneration in Drosophila
-
Ng CH, Mok SZ, Koh C, et al. Parkin protects against LRRK2 G2019S mutant-induced dopaminergic neurodegeneration in Drosophila. J Neurosci 2009; 29: 11257-11262.
-
(2009)
J Neurosci
, vol.29
, pp. 11257-11262
-
-
Ng, C.H.1
Mok, S.Z.2
Koh, C.3
-
20
-
-
70349235644
-
Perspectives on recent advances in the understanding and treatment of Parkinson's disease
-
Schapira AH, Agid Y, Barone P, et al. Perspectives on recent advances in the understanding and treatment of Parkinson's disease. Eur J Neurol 2009; 16: 1090-1099.
-
(2009)
Eur J Neurol
, vol.16
, pp. 1090-1099
-
-
Schapira, A.H.1
Agid, Y.2
Barone, P.3
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