-
1
-
-
23344453013
-
Genetics of Parkinson's disease
-
Gasser T. Genetics of Parkinson's disease. Curr Opin Neurol 2005;18:363-369.
-
(2005)
Curr Opin Neurol
, vol.18
, pp. 363-369
-
-
Gasser, T.1
-
2
-
-
0036196860
-
A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1
-
Funayama M, Hasegawa K, Kowa H, Saito M, Tsuji S, Obata F. A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1. Ann Neurol 2002;51:296-301.
-
(2002)
Ann Neurol
, vol.51
, pp. 296-301
-
-
Funayama, M.1
Hasegawa, K.2
Kowa, H.3
Saito, M.4
Tsuji, S.5
Obata, F.6
-
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
-
-
24644486896
-
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
-
Zabetian CP, Samii A, Mosley AD, et al. A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations. Neurology 2005;65:741-744.
-
(2005)
Neurology
, vol.65
, pp. 741-744
-
-
Zabetian, C.P.1
Samii, A.2
Mosley, A.D.3
-
6
-
-
24944449513
-
Analysis of LRRK2 G2019S and I2020T mutations in Parkinson's disease
-
Bialecka M, Hui S, Klodowska-Duda G, Opala G, Tan EK, Drozdzik M. Analysis of LRRK2 G2019S and I2020T mutations in Parkinson's disease. Neurosci Lett 2005;390:1-3.
-
(2005)
Neurosci Lett
, vol.390
, pp. 1-3
-
-
Bialecka, M.1
Hui, S.2
Klodowska-Duda, G.3
Opala, G.4
Tan, E.K.5
Drozdzik, M.6
-
7
-
-
18244394793
-
Clinical features of LRRK2-associated Parkinson's disease in central Norway
-
Aasly JO, Toft M, Fernandez-Mata I, et al. Clinical features of LRRK2-associated Parkinson's disease in central Norway. Ann Neurol 2005;57:762-765.
-
(2005)
Ann Neurol
, vol.57
, pp. 762-765
-
-
Aasly, J.O.1
Toft, M.2
Fernandez-Mata, I.3
-
8
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks WP, Abou-Sleiman PM, Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005;365:415-416.
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
-
9
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson' s disease
-
Di Fonzo A, Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson' s disease. Lancet 2005;365:412-415.
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A.1
Rohe, C.F.2
Ferreira, J.3
-
10
-
-
27644455523
-
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
-
Lesage S, Ibanez P, Lohmann E, et al. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol 2005;58:784-787.
-
(2005)
Ann Neurol
, vol.58
, pp. 784-787
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
-
11
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across European populations
-
Kachergus J, Mata IF, Hulihan M, 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;76:672-680.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
-
13
-
-
24644497562
-
LRRK2 mutations in Parkinson disease
-
Farrer M, Stone J, Mata IF, et al. LRRK2 mutations in Parkinson disease. Neurology 2005;65:738-740.
-
(2005)
Neurology
, vol.65
, pp. 738-740
-
-
Farrer, M.1
Stone, J.2
Mata, I.F.3
-
14
-
-
21144451648
-
LRRK2 R1441G in Spanish patients with Parkinson's disease
-
Mata IF, Taylor JP, Kachergus J, et al. LRRK2 R1441G in Spanish patients with Parkinson's disease. Neurosci Lett 2005;382:309-311.
-
(2005)
Neurosci Lett
, vol.382
, pp. 309-311
-
-
Mata, I.F.1
Taylor, J.P.2
Kachergus, J.3
-
15
-
-
33644822969
-
Type and frequency of mutations in the LRRK2 gene in familiar and sporadic Parkinson's disease
-
Berg D, Schweitzer KJ, Leitner P, et al. Type and frequency of mutations in the LRRK2 gene in familiar and sporadic Parkinson's disease. Brain 2005;128:2760-2762.
-
(2005)
Brain
, vol.128
, pp. 2760-2762
-
-
Berg, D.1
Schweitzer, K.J.2
Leitner, P.3
-
16
-
-
28544441181
-
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: Clinical, pathological, olfactory and functional imaging and genetic data
-
Khan NL, Jain S, Lynch JM, et al. Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. Brain 2005;128(Pt 12):2786-2796.
-
(2005)
Brain
, vol.128
, Issue.PART 12
, pp. 2786-2796
-
-
Khan, N.L.1
Jain, S.2
Lynch, J.M.3
-
17
-
-
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
-
Lesage S, Leutenegger AL, Ibanez P, 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;77:330-332.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 330-332
-
-
Lesage, S.1
Leutenegger, A.L.2
Ibanez, P.3
-
18
-
-
28744453588
-
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease
-
Skipper L, Li Y, Bonnard C, et al. Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease. Hum Mol Genet 2005;14:3549-3556.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3549-3556
-
-
Skipper, L.1
Li, Y.2
Bonnard, C.3
-
19
-
-
31344432937
-
LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs
-
Lesage S, Durr A, Tazir M, et al. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med 2006;354:422-423.
-
(2006)
N Engl J Med
, vol.354
, pp. 422-423
-
-
Lesage, S.1
Durr, A.2
Tazir, M.3
-
20
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius LJ, Senthil G, Saunders-Pullman R, et al. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N Engl J Med 2006;354:424-425.
-
(2006)
N Engl J Med
, vol.354
, pp. 424-425
-
-
Ozelius, L.J.1
Senthil, G.2
Saunders-Pullman, R.3
-
21
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Wszolek ZK, Pfeiffer RF, Tsuboi Y, et al. Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 2004;62:1619-1622.
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Tsuboi, Y.3
-
22
-
-
20444420103
-
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
-
Funayama M, Hasegawa K, Ohta E, et al. An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family. Ann Neurol 2005;57:918-921.
-
(2005)
Ann Neurol
, vol.57
, pp. 918-921
-
-
Funayama, M.1
Hasegawa, K.2
Ohta, E.3
-
24
-
-
0034053093
-
Clinical and genetic study of familial Parkinson's disease in Tunisia
-
Gouider-Khouja N, Belal S, Hamida MB, Hentati F. Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology 2000;54:1603-1609.
-
(2000)
Neurology
, vol.54
, pp. 1603-1609
-
-
Gouider-Khouja, N.1
Belal, S.2
Hamida, M.B.3
Hentati, F.4
-
25
-
-
0026629509
-
What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study
-
Hughes AJ, Ben Shlomo Y, Daniel SE, Lees AJ. What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. Neurology 1992;42:1142-1146.
-
(1992)
Neurology
, vol.42
, pp. 1142-1146
-
-
Hughes, A.J.1
Ben Shlomo, Y.2
Daniel, S.E.3
Lees, A.J.4
-
27
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
28
-
-
0037340869
-
-
Hakonarson H, Gulcher JR, Stefansson K. deCODE genetics, Inc. Pharmacogenomics 2003;4:209-215.
-
Hakonarson H, Gulcher JR, Stefansson K. deCODE genetics, Inc. Pharmacogenomics 2003;4:209-215.
-
-
-
-
29
-
-
0035092024
-
Flow cytometric platform for high-throughput single nucleotide polymorphism analysis
-
Taylor JD, Briley D, Nguyen Q, et al. Flow cytometric platform for high-throughput single nucleotide polymorphism analysis. Biotechniques 2001;30:661-669.
-
(2001)
Biotechniques
, vol.30
, pp. 661-669
-
-
Taylor, J.D.1
Briley, D.2
Nguyen, Q.3
-
30
-
-
0036338150
-
Merlin-rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis GR, Cherny SS, Cookson WO, Cardon LR. Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat Genet 2002;30:97-101.
-
(2002)
Nat Genet
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
32
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 2005;365:410-412.
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
-
33
-
-
20444414834
-
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
-
Deng H, Le W, Guo Y, Hunter CB, Xie W, Jankovic J. Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation. Ann Neurol 2005;57:933-934.
-
(2005)
Ann Neurol
, vol.57
, pp. 933-934
-
-
Deng, H.1
Le, W.2
Guo, Y.3
Hunter, C.B.4
Xie, W.5
Jankovic, J.6
-
34
-
-
33646192015
-
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes
-
Fendri K, Kefi M, Hentati F, Amouri R. Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes. Neuromuscul Disord 2006;16:316-320.
-
(2006)
Neuromuscul Disord
, vol.16
, pp. 316-320
-
-
Fendri, K.1
Kefi, M.2
Hentati, F.3
Amouri, R.4
-
35
-
-
27144517403
-
Analysis of LRRK2 functional domains in nondominant Parkinson disease
-
Skipper L, Shen H, Chua E, et al. Analysis of LRRK2 functional domains in nondominant Parkinson disease. Neurology 2005;65:1319-1321.
-
(2005)
Neurology
, vol.65
, pp. 1319-1321
-
-
Skipper, L.1
Shen, H.2
Chua, E.3
|