-
1
-
-
84858667775
-
Genetic basis of Parkinson's disease: inheritance, penetrance, and expression
-
Schulte C, Gasser T. Genetic basis of Parkinson's disease: inheritance, penetrance, and expression. Appl Clin Genet 2011;4:67-80.
-
(2011)
Appl Clin Genet
, vol.4
, pp. 67-80
-
-
Schulte, C.1
Gasser, T.2
-
3
-
-
79960210306
-
Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease
-
Aug
-
Bardien S, Lesage S, Brice A, Carr J. Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson's disease. Parkinsonism Relat Disord 2011 Aug;17(7):501-8.
-
(2011)
Parkinsonism Relat Disord
, vol.17
, Issue.7
, pp. 501-508
-
-
Bardien, S.1
Lesage, S.2
Brice, A.3
Carr, J.4
-
4
-
-
81255127582
-
Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson's disease susceptibility?
-
Aug 2 [Epub ahead of print]. doi:10.1016/j.parkreldis.2011.07.001
-
Biernacka JM, Armasu SM, Cunningham JM, Ahlskog JE, Chung SJ, Maraganore DM. Do interactions between SNCA, MAPT, and LRRK2 genes contribute to Parkinson's disease susceptibility? Parkinsonism Relat Disord 2011 Aug 2 [Epub ahead of print]. doi: 10.1016/j.parkreldis.2011.07.001.
-
(2011)
Parkinsonism Relat Disord
-
-
Biernacka, J.M.1
Armasu, S.M.2
Cunningham, J.M.3
Ahlskog, J.E.4
Chung, S.J.5
Maraganore, D.M.6
-
5
-
-
79960265588
-
Subclinical signs in LRRK2 mutation carriers
-
Johansen KK, White LR, Farrer MJ, Aasly JO. Subclinical signs in LRRK2 mutation carriers. Parkinsonism Relat Disord 2011;17(7):528-32.
-
(2011)
Parkinsonism Relat Disord
, vol.17
, Issue.7
, pp. 528-532
-
-
Johansen, K.K.1
White, L.R.2
Farrer, M.J.3
Aasly, J.O.4
-
6
-
-
77956175000
-
Genealogical studies in LRRK2-associated Parkinson's disease in central Norway
-
Johansen KK, Hasselberg K, White LR, Farrer MJ, Aasly JO. Genealogical studies in LRRK2-associated Parkinson's disease in central Norway. Parkinsonism Relat Disord 2010;16(8):527-30.
-
(2010)
Parkinsonism Relat Disord
, vol.16
, Issue.8
, pp. 527-530
-
-
Johansen, K.K.1
Hasselberg, K.2
White, L.R.3
Farrer, M.J.4
Aasly, J.O.5
-
7
-
-
77954957576
-
Fukuoka Kinki Parkinson's Disease Study Group. GST polymorphisms, interaction with smoking and pesticide use, and risk for Parkinson's disease in a Japanese population
-
Kiyohara C, Miyake Y, Koyanagi M; Fukuoka Kinki Parkinson's Disease Study Group. GST polymorphisms, interaction with smoking and pesticide use, and risk for Parkinson's disease in a Japanese population. Parkinsonism Relat Disord 2010;16(7):447-52.
-
(2010)
Parkinsonism Relat Disord
, vol.16
, Issue.7
, pp. 447-452
-
-
Kiyohara, C.1
Miyake, Y.2
Koyanagi, M.3
-
8
-
-
27744446035
-
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
-
Lu CS, Simons EJ, Wu-Chou YH, Fonzo AD, Chang HC, Chen RS, et al. The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism Relat Disord 2005;11:521-2.
-
(2005)
Parkinsonism Relat Disord
, vol.11
, pp. 521-522
-
-
Lu, C.S.1
Simons, E.J.2
Wu-Chou, Y.H.3
Fonzo, A.D.4
Chang, H.C.5
Chen, R.S.6
-
9
-
-
33746079596
-
A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
-
Di Fonzo A, Wu-Chou YH, Lu CS, van Doeselaar M, Simons EJ, Rohé CF, et al. A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 2006;7(3):133-8.
-
(2006)
Neurogenetics
, vol.7
, Issue.3
, pp. 133-138
-
-
Di Fonzo, A.1
Wu-Chou, Y.H.2
Lu, C.S.3
van Doeselaar, M.4
Simons, E.J.5
Rohé, C.F.6
-
10
-
-
77951876814
-
Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study
-
Tan EK, Peng R, Teo YY, Tan LC, Angeles D, Ho P, et al. Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study. Hum Mutat 2010;31(5):561-8.
-
(2010)
Hum Mutat
, vol.31
, Issue.5
, pp. 561-568
-
-
Tan, E.K.1
Peng, R.2
Teo, Y.Y.3
Tan, L.C.4
Angeles, D.5
Ho, P.6
-
11
-
-
33847267765
-
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, et al. Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. Parkinsonism Relat Disord 2007;13(2):89-92.
-
(2007)
Parkinsonism Relat Disord
, vol.13
, Issue.2
, pp. 89-92
-
-
Farrer, M.J.1
Stone, J.T.2
Lin, C.H.3
Dächsel, J.C.4
Hulihan, M.M.5
Haugarvoll, K.6
-
12
-
-
79551495766
-
Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease
-
Lin CH, Wu RM, Tai CH, Chen ML, Hu FC. Lrrk2 S1647T and BDNF V66M interact with environmental factors to increase risk of Parkinson's disease. Parkinsonism Relat Disord 2011;17(2):84-8.
-
(2011)
Parkinsonism Relat Disord
, vol.17
, Issue.2
, pp. 84-88
-
-
Lin, C.H.1
Wu, R.M.2
Tai, C.H.3
Chen, M.L.4
Hu, F.C.5
-
13
-
-
80052967403
-
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
-
Aug 30 [Epub ahead of print]. doi:10.1016/S1474-4422(11)70175-2
-
Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. Lancet Neurol 2011 Aug 30 [Epub ahead of print]. doi: 10.1016/S1474-4422(11)70175-2.
-
(2011)
Lancet Neurol
-
-
Ross, O.A.1
Soto-Ortolaza, A.I.2
Heckman, M.G.3
Aasly, J.O.4
Abahuni, N.5
Annesi, G.6
-
14
-
-
28744453588
-
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, et al. Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Hum Mol Genet 2005;14(23): 3549-56.
-
(2005)
Hum Mol Genet
, vol.14
, Issue.23
, pp. 3549-3556
-
-
Skipper, L.1
Li, Y.2
Bonnard, C.3
Pavanni, R.4
Yih, Y.5
Chua, E.6
-
15
-
-
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, Hirota Y, Ito C, Kubo M, et al. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. Nat Genet 2009;41(12):1303-7.
-
(2009)
Nat Genet
, vol.41
, Issue.12
, pp. 1303-1307
-
-
Satake, W.1
Nakabayashi, Y.2
Mizuta, I.3
Hirota, Y.4
Ito, C.5
Kubo, M.6
-
16
-
-
77955462116
-
Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus
-
Tan EK, Kwok HH, Tan LC, Zhao WT, Prakash KM, Au WL, et al. Analysis of GWAS-linked loci in Parkinson disease reaffirms PARK16 as a susceptibility locus. Neurology 2010;75(6):508-12.
-
(2010)
Neurology
, vol.75
, Issue.6
, pp. 508-512
-
-
Tan, E.K.1
Kwok, H.H.2
Tan, L.C.3
Zhao, W.T.4
Prakash, K.M.5
Au, W.L.6
-
17
-
-
70549088602
-
Genomewide association study reveals genetic risk underlying Parkinson's disease
-
Simon-Sanchez J, Schulte C, Bras JM, Sharma M, Gibbs JR, Berg D, et al. Genomewide association study reveals genetic risk underlying Parkinson's disease. Nat Genet 2009;41(12):1308-12.
-
(2009)
Nat Genet
, vol.41
, Issue.12
, pp. 1308-1312
-
-
Simon-Sanchez, J.1
Schulte, C.2
Bras, J.M.3
Sharma, M.4
Gibbs, J.R.5
Berg, D.6
-
18
-
-
79951811351
-
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
-
International Parkinson Disease Genomics Consortium
-
International Parkinson Disease Genomics Consortium, Nalls MA, Plagnol V, Hernandez DG, Sharma M, Sheerin UM, et al. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. Lancet 2011;377(9766):641-9.
-
(2011)
Lancet
, vol.377
, Issue.9766
, pp. 641-649
-
-
Nalls, M.A.1
Plagnol, V.2
Hernandez, D.G.3
Sharma, M.4
Sheerin, U.M.5
-
19
-
-
80052328932
-
Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee
-
Hamza TH, Chen H, Hill-Burns EM, Rhodes SL, Montimurro J, Kay DM, et al. Genome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffee. PLoS Genet 2011;7(8):e1002237.
-
(2011)
PLoS Genet
, vol.7
, Issue.8
-
-
Hamza, T.H.1
Chen, H.2
Hill-Burns, E.M.3
Rhodes, S.L.4
Montimurro, J.5
Kay, D.M.6
-
20
-
-
77956646167
-
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease
-
Hamza TH, Zabetian CP, Tenesa A, Laederach A, Montimurro J, Yearout D, et al. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nat Genet 2010;42(9):781-5.
-
(2010)
Nat Genet
, vol.42
, Issue.9
, pp. 781-785
-
-
Hamza, T.H.1
Zabetian, C.P.2
Tenesa, A.3
Laederach, A.4
Montimurro, J.5
Yearout, D.6
-
21
-
-
79959841853
-
Webbased genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease
-
Do CB, Tung JY, Dorfman E, Kiefer AK, Drabant EM, Francke U, et al. Webbased genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease. PLoS Genet 2011;7(6):e1002141.
-
(2011)
PLoS Genet
, vol.7
, Issue.6
-
-
Do, C.B.1
Tung, J.Y.2
Dorfman, E.3
Kiefer, A.K.4
Drabant, E.M.5
Francke, U.6
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