-
1
-
-
67749118059
-
LRRK2 gene variation and its contribution to Parkinson disease
-
Paisan-Ruiz C. LRRK2 gene variation and its contribution to Parkinson disease. Hum Mutat 2009;30:1153-60.
-
(2009)
Hum Mutat
, vol.30
, pp. 1153-1160
-
-
Paisan-Ruiz, C.1
-
2
-
-
68949125734
-
Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease
-
Biskup S, West AB. Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease. Biochim Biophys Acta 2009;1792:625-33.
-
(2009)
Biochim Biophys Acta
, vol.1792
, pp. 625-633
-
-
Biskup, S.1
West, A.B.2
-
3
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: A case-control study
-
Healy DG, Falchi M, O'Sullivan SS, Bonifati V, Durr A, Bressman S, et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008;7:583-90.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
-
4
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across European populations
-
DOI 10.1086/429256
-
Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, et al. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am J Hum Genet 2005;76:672-80. (Pubitemid 40432174)
-
(2005)
American Journal of Human Genetics
, vol.76
, Issue.4
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
Taylor, J.P.4
Lincoln, S.5
Aasly, J.6
Gibson, J.M.7
Ross, O.A.8
Lynch, T.9
Wiley, J.10
Payami, H.11
Nutt, J.12
Maraganore, D.M.13
Czyzewski, K.14
Styczynska, M.15
Wszolek, Z.K.16
Farrer, M.J.17
Toft, M.18
-
5
-
-
33845453622
-
Frequency of LRRK2 mutations in early- and late-onset Parkinson disease
-
DOI 10.1212/01.wnl.0000244345.49809.36, PII 0000611420061128000016
-
Clark LN, Wang Y, Karlins E, Saito L, Mejia-Santana H, Harris J, et al. Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Neurology 2006;67:1786-91. (Pubitemid 44900754)
-
(2006)
Neurology
, vol.67
, Issue.10
, pp. 1786-1791
-
-
Clark, L.N.1
Wang, Y.2
Karlins, E.3
Saito, L.4
Mejia-Santana, H.5
Harris, J.6
Louis, E.D.7
Cote, L.J.8
Andrews, H.9
Fahn, S.10
Waters, C.11
Ford, B.12
Frucht, S.13
Ottman, R.14
Marder, K.15
-
6
-
-
33645160640
-
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor
-
Goldwurm S, Di Fonzo A, Simons EJ, Rohé CF, Zini M, Canesi M, et al. The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor. J Med Genet 2005;42:e65.
-
(2005)
J Med Genet
, vol.42
-
-
Goldwurm, S.1
Di Fonzo, A.2
Simons, E.J.3
Rohé, C.F.4
Zini, M.5
Canesi, M.6
-
7
-
-
79958116682
-
Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries
-
Bar-Shira A, Hutter CM, Giladi N, Zabetian CP, Orr-Urtreger A. Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. Neurogenetics 2009;10:355-8.
-
(2009)
Neurogenetics
, vol.10
, pp. 355-358
-
-
Bar-Shira, A.1
Hutter, C.M.2
Giladi, N.3
Zabetian, C.P.4
Orr-Urtreger, A.5
-
8
-
-
33749021352
-
LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: Evidence of two distinct founding events beginning two millennia ago
-
DOI 10.1086/508025
-
Zabetian CP, Hutter CM, Yearout D, Lopez AN, Factor SA, Griffith A, et al. LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. Am J Hum Genet 2006;79:752-8. (Pubitemid 44452754)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.4
, pp. 752-758
-
-
Zabetian, C.P.1
Hutter, C.M.2
Yearout, D.3
Lopez, A.N.4
Factor, S.A.5
Griffith, A.6
Leis, B.C.7
Bird, T.D.8
Nutt, J.G.9
Higgins, D.S.10
Roberts, J.W.11
Kay, D.M.12
Edwards, K.L.13
Samii, A.14
Payami, H.15
-
9
-
-
76549094100
-
Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India
-
Vinish M, Prabhakar S, Khullar M, Verma I, Anand A. Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India. J Neurol Neurosurg Psychiatry 2010;81:166-70.
-
(2010)
J Neurol Neurosurg Psychiatry
, vol.81
, pp. 166-170
-
-
Vinish, M.1
Prabhakar, S.2
Khullar, M.3
Verma, I.4
Anand, A.5
-
10
-
-
33646712143
-
Parkin mutations in familial and sporadic Parkinson's disease among Indians
-
DOI 10.1016/j.parkreldis.2005.12.004, PII S1353802006000022
-
Chaudhary S, Behari M, Dihana M, Swaminath PV, Govindappa ST, Jayaram S, et al. Parkin mutations in familial and sporadic Parkinson's disease among Indians. Parkinsonism Relat Disord 2006;12:239-45. (Pubitemid 43737242)
-
(2006)
Parkinsonism and Related Disorders
, vol.12
, Issue.4
, pp. 239-245
-
-
Chaudhary, S.1
Behari, M.2
Dihana, M.3
Swaminath, P.V.4
Govindappa, S.T.5
Jayaram, S.6
Goyal, V.7
Maitra, A.8
Muthane, U.B.9
Juyal, R.C.10
Thelma, B.K.11
-
11
-
-
27444434729
-
Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease
-
DOI 10.1136/jnnp.2004.046888
-
Madegowda RH, Kishore A, Anand A. Mutational screening of the parkin gene among South Indians with early onset Parkinson's disease. J Neurol Neurosurg Psychiatry 2005;76:1588-90. (Pubitemid 41531714)
-
(2005)
Journal of Neurology, Neurosurgery and Psychiatry
, vol.76
, Issue.11
, pp. 1588-1590
-
-
Madegowda, R.H.1
Kishore, A.2
Anand, A.3
-
12
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: A clinico-pathological study of 100 cases
-
Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992;55:181-4.
-
(1992)
J Neurol Neurosurg Psychiatry
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
13
-
-
28544446980
-
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
-
Bras JM, Guerreiro RJ, Ribeiro MH, Januario C, Morgadinho A, Oliveira CR, et al. G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. Mov Disord 2005;20:1653-5.
-
(2005)
Mov Disord
, vol.20
, pp. 1653-1655
-
-
Bras, J.M.1
Guerreiro, R.J.2
Ribeiro, M.H.3
Januario, C.4
Morgadinho, A.5
Oliveira, C.R.6
-
14
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Krawetz S, Misener S, editors, Totowa, New Jersey: Humana Press
-
Rozen S, Skaletsky H. Primer3 on the WWW for general users and for biologist programmers. In: Krawetz S, Misener S, editors. Bioinformatics Methods and Protocols: Methods in Molecular Biology. Totowa, New Jersey: Humana Press; 2000. p. 365-86.
-
(2000)
Bioinformatics Methods and Protocols: Methods in Molecular Biology
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
-
15
-
-
33750406222
-
Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients
-
DOI 10.1016/j.neulet.2006.04.052, PII S0304394006004460
-
Punia S, Behari M, Govindappa ST, Swaminath PV, Jayaram S, Goyal V, et al. Absence/rarity of commonly reported LRRK2 mutations in Indian Parkinson's disease patients. Neurosci Lett 2006;409:83-8. (Pubitemid 44637251)
-
(2006)
Neuroscience Letters
, vol.409
, Issue.2
, pp. 83-88
-
-
Punia, S.1
Behari, M.2
Govindappa, S.T.3
Swaminath, P.V.4
Jayaram, S.5
Goyal, V.6
Muthane, U.B.7
Juyal, R.C.8
Thelma, B.K.9
-
16
-
-
33747701497
-
Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease
-
DOI 10.1212/01.wnl.0000227732.37801.d4, PII 0000611420060822000037
-
Zabetian CP, Morino H, Ujike H, Yamamoto M, Oda M, Maruyama H, et al. Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease. Neurology 2006;67:697-9. (Pubitemid 44273625)
-
(2006)
Neurology
, vol.67
, Issue.4
, pp. 697-699
-
-
Zabetian, C.P.1
Morino, H.2
Ujike, H.3
Yamamoto, M.4
Oda, M.5
Maruyama, H.6
Izumi, Y.7
Kaji, R.8
Griffith, A.9
Leis, B.C.10
Roberts, J.W.11
Yearout, D.12
Samii, A.13
Kawakami, H.14
-
17
-
-
48449089238
-
Is the G2019S LRRK2 mutation common in all southern European populations?
-
Papapetropoulos S, Adi N, Shehadeh L, Bishopric N, Singer C, Argyriou AA, et al. Is the G2019S LRRK2 mutation common in all southern European populations? J Clin Neurosci 2008;15:1027-30.
-
(2008)
J Clin Neurosci
, vol.15
, pp. 1027-1030
-
-
Papapetropoulos, S.1
Adi, N.2
Shehadeh, L.3
Bishopric, N.4
Singer, C.5
Argyriou, A.A.6
-
18
-
-
67651166905
-
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients
-
Shojaee S, Sina F, Farboodi N, Fazlali Z, Ghazavi F, Ghorashi SA, et al. A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients. Mov Disord 2009;24:1023-7.
-
(2009)
Mov Disord
, vol.24
, pp. 1023-1027
-
-
Shojaee, S.1
Sina, F.2
Farboodi, N.3
Fazlali, Z.4
Ghazavi, F.5
Ghorashi, S.A.6
-
19
-
-
22544465257
-
LRRK2 haplotype analyses in European and North African families with Parkinson disease: A common founder for the G2019S mutation dating from the 13th century [2]
-
DOI 10.1086/432422
-
Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, et al. LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet 2005;77:330-2. (Pubitemid 41022715)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.2
, pp. 330-332
-
-
Lesage, S.1
Leutenegger, A.-L.2
Ibanez, P.3
Janin, S.4
Lohmann, E.5
Durr, A.6
Brice, A.7
-
20
-
-
38349189767
-
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease
-
Warren L, Gibson R, Ishihara L, Elango R, Xue Z, Akkari A, et al. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism Relat Disord 2008;14:77-80.
-
(2008)
Parkinsonism Relat Disord
, vol.14
, pp. 77-80
-
-
Warren, L.1
Gibson, R.2
Ishihara, L.3
Elango, R.4
Xue, Z.5
Akkari, A.6
-
21
-
-
67349203890
-
LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay
-
Mata IF, Cosentino C, Marca V, Torres L, Mazzetti P, Ortega O, et al. LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay. Parkinsonism Relat Disord 2009;15:370-3.
-
(2009)
Parkinsonism Relat Disord
, vol.15
, pp. 370-373
-
-
Mata, I.F.1
Cosentino, C.2
Marca, V.3
Torres, L.4
Mazzetti, P.5
Ortega, O.6
-
22
-
-
34347253600
-
Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease
-
DOI 10.1002/mds.21477
-
Huang Y, Halliday GM, Vandebona H, Mellick GD, Mastaglia F, Stevens J, et al. Prevalence and clinical features of common LRRK2 mutations in Australians with Parkinson's disease. Mov Disord 2007;22:982-9. (Pubitemid 46999295)
-
(2007)
Movement Disorders
, vol.22
, Issue.7
, pp. 982-989
-
-
Huang, Y.1
Halliday, G.M.2
Vandebona, H.3
Mellick, G.D.4
Mastaglia, F.5
Stevens, J.6
Kwok, J.7
Garlepp, M.8
Silburn, P.A.9
Horne, M.K.10
Kotschet, K.11
Venn, A.12
Rowe, D.B.13
Rubio, J.P.14
Sue, C.M.15
-
23
-
-
48849095698
-
The ancestry of LRRK2 Gly2019Ser Parkinsonism
-
Benamer HT. The ancestry of LRRK2 Gly2019Ser Parkinsonism. Lancet Neurol 2008;7:769-70.
-
(2008)
Lancet Neurol
, vol.7
, pp. 769-770
-
-
Benamer, H.T.1
-
24
-
-
70249150754
-
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype
-
Pirkevi C, Lesage S, Condroyer C, Tomiyama H, Hattori N, Ertan S, et al. A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype. Neurogenetics 2009;10:271-3.
-
(2009)
Neurogenetics
, vol.10
, pp. 271-273
-
-
Pirkevi, C.1
Lesage, S.2
Condroyer, C.3
Tomiyama, H.4
Hattori, N.5
Ertan, S.6
-
25
-
-
20644455323
-
The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
-
DOI 10.1016/j.neulet.2005.04.103, PII S030439400500594X
-
Tan EK, Shen H, Tan LC, Farrer M, Yew K, Chua E, et al. The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients. Neurosci Lett 2005;384:327-9. (Pubitemid 40836023)
-
(2005)
Neuroscience Letters
, vol.384
, Issue.3
, pp. 327-329
-
-
Tan, E.K.1
Shen, H.2
Tan, L.C.S.3
Farrer, M.4
Yew, K.5
Chua, E.6
Jamora, R.D.7
Puvan, K.8
Puong, K.Y.9
Zhao, Y.10
Pavanni, R.11
Wong, M.C.12
Yih, Y.13
Skipper, L.14
Liu, J.-J.15
-
26
-
-
33645130652
-
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinsons's disease patients from 18 countries
-
DOI 10.1002/mds.20886
-
Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, et al. Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries. Mov Disord 2006;21:1102-8. (Pubitemid 44336593)
-
(2006)
Movement Disorders
, vol.21
, Issue.8
, pp. 1102-1108
-
-
Tomiyama, H.1
Li, Y.2
Funayama, M.3
Hasegawa, K.4
Yoshino, H.5
Kubo, S.-I.6
Sato, K.7
Hattori, T.8
Lu, C.-S.9
Inzelberg, R.10
Djaldetti, R.11
Melamed, E.12
Amouri, R.13
Gouider-Khouja, N.14
Hentati, F.15
Hatano, Y.16
Wang, M.17
Imamichi, Y.18
Mizoguchi, K.19
Miyajima, H.20
Obata, F.21
Toda, T.22
Farrer, M.J.23
Mizuno, Y.24
Hattori, N.25
more..
-
27
-
-
73449090031
-
The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease and multiple system atrophy
-
Cho JW, Kim SY, Park SS, Jeon BS. The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease and multiple system atrophy. J Clin Neurol 2009;5:29-32.
-
(2009)
J Clin Neurol
, vol.5
, pp. 29-32
-
-
Cho, J.W.1
Kim, S.Y.2
Park, S.S.3
Jeon, B.S.4
-
28
-
-
52649172690
-
Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease
-
Choi JM, Woo MS, Ma HI, Kang SY, Sung YH, Yong SW, et al. Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. Neurogenetics 2008;9:263-9.
-
(2008)
Neurogenetics
, vol.9
, pp. 263-269
-
-
Choi, J.M.1
Woo, M.S.2
Ma, H.I.3
Kang, S.Y.4
Sung, Y.H.5
Yong, S.W.6
-
29
-
-
33745862378
-
Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease
-
DOI 10.1002/mds.20814
-
Fung HC, Chen CM, Hardy J, Hernandez D, Singleton A, Wu YR. Lack of G2019S LRRK2 mutation in a cohort of Taiwanese with sporadic Parkinson's disease. Mov Disord 2006;21:880-1. (Pubitemid 44028316)
-
(2006)
Movement Disorders
, vol.21
, Issue.6
, pp. 880-881
-
-
Fung, H.-C.1
Chen, C.-M.2
Hardy, J.3
Hernandez, D.4
Singleton, A.5
Wu, Y.-R.6
-
30
-
-
27744446035
-
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
-
DOI 10.1016/j.parkreldis.2005.09.003, PII S1353802005001884
-
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. (Pubitemid 41627846)
-
(2005)
Parkinsonism and Related Disorders
, vol.11
, Issue.8
, 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
Weng, Y.-H.7
Rohe, C.F.8
Breedveld, G.J.9
Hattori, N.10
Gasser, T.11
Oostra, B.A.12
Bonifati, V.13
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