SCOPUS 정보 검색 플랫폼

Volumn 10, Issue 17, 2001, Pages 1847-1851

α-synuclein gene haplotypes are associated with Parkinson's disease

(10) Farrer, Matt a Maraganore, Demetrius M b Lockhart, Paul a Singleton, Andrew a Lesnick, T G b De Andrade, Mariza b West, Andrew a De Silva, Rohan c Hardy, John a Hernandez, Dena a

a MAYO GRADUATE SCHOOL (United States)

b MAYO CLINIC (United States)

c UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA SYNUCLEIN; TAU PROTEIN;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DNA POLYMORPHISM; ETIOLOGY; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC PREDISPOSITION; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; PARKINSON DISEASE; PATHOGENESIS; PRIORITY JOURNAL; PROGRESSIVE SUPRANUCLEAR PALSY; PROMOTER REGION; RISK FACTOR; SYNUCLEINOPATHY; TAUOPATHY;

EID: 0035880458 PISSN: 09646906 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (313)

References (18)

1
- 0032937059
- Diagnostic criteria for Parkinson disease
- (1999) Arch. Neurol. , vol.56 , pp. 33-39
- Gelb, D.J.¹ Oliver, E.² Gilman, S.³

2
- 0032568534
- α-synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies
- (1998) Proc. Natl Acad. Sci. USA , vol.95 , pp. 6469-6473
- Spillantini, M.G.¹ Crowther, R.A.² Jakes, R.³ Hasegawa, M.⁴ Goedert, M.⁵

3
- 0030744876
- Mutation in the α-synuclein gene identified in families with Parkinson's disease
- (1997) Science , vol.276 , pp. 2045-2047
- Polymeropoulos, M.H.¹ Lavedan, C.² Leroy, E.³ Ide, S.E.⁴ Dehejia, A.⁵ Dutra, A.⁶ Pike, B.⁷ Root, H.⁸ Rubenstein, J.⁹ Boyer, R.¹⁰

4
- 0034649710
- Familial aggregation of Parkinson's disease in Iceland
- (2000) N. Engl. J. Med. , vol.343 , pp. 1765-1770
- Sveinbjornsdottir, S.¹ Hicks, A.A.² Jonsson, T.³ Petursson, H.⁴ Guomundsson, G.⁵ Frigge, M.L.⁶ Kong, A.⁷ Gulcher, J.R.⁸ Stefansson, K.⁹

5
- 0032862949
- The genetics of disorders with synuclein pathology and parkinsonism
- (1999) Hum. Mol. Genet. , vol.8 , pp. 1901-1905
- Farrer, M.¹ Gwinn-Hardy, K.² Hutton, M.³ Hardy, J.⁴

6
- 9444298408
- Genetic studies in Alzheimer's disease with an NACP/α-synuclein polymorphism
- (1996) Ann. Neurol. , vol.40 , pp. 207-215
- Xia, Y.¹ De Silva, R.H.A.² Rosi, B.L.³ Yamaoka, L.H.⁴ Rimmler, J.B.⁵ Pericak-Vance, M.A.⁶ Roses, A.D.⁷ Chen, X.⁸ Masliah, E.⁹ DeTeresa, R.¹⁰

7
- 0342950666
- Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype
- (1999) Ann. Neurol. , vol.45 , pp. 611-617
- Kruger, R.¹ Vieira-Saecker, A.M.² Kuhn, W.³ Berg, D.⁴ Muller, T.⁵ Kuhnl, N.⁶ Fuchs, G.A.⁷ Storch, A.⁸ Hungs, M.⁹ Woitalla, D.¹⁰

8
- 0034646346
- Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?
- (2000) Neurology , vol.54 , pp. 1195-1198
- Tan, E.K.¹ Matsuura, T.² Nagamitsu, S.³ Khajavi, M.⁴ Jankovic, J.⁵ Ashizawa, T.⁶

9
- 0031678048
- Mutation, sequence analysis, and association studies of α-synuclein in Parkinson's disease
- (1998) Neurology , vol.51 , pp. 1757-1759
- Parsian, A.¹ Racette, B.² Zhang, Z.H.³ Chakraverty, S.⁴ Rundle, M.⁵ Goate, A.⁶ Perlmutter, J.S.⁷

10
- 0035831303
- Genetic studies in Parkinson's disease with an α-synuclein/NACP gene polymorphism in Japan
- (2001) Neurosci. Lett. , vol.300 , pp. 125-127
- Izumi, Y.¹ Morino, H.² Oda, M.³ Maruyama, H.⁴ Udaka, F.⁵ Kameyama, M.⁶ Nakamura, S.⁷ Kawakami, H.⁸

11
- 18544406092
- Parkinson's disease is not associated with the combined -synuclein/apolipoprotein E susceptibility genotype
- (2001) Ann. Neurol. , vol.49 , pp. 665-668
- Khan, N.¹ Graham, E.² Dixon, P.³ Morris, C.⁴ Mander, A.⁵ Clayton, D.⁶ Vaughan, J.⁷ Quinn, N.⁸ Lees, A.⁹ Daniel, S.¹⁰

12
- 0001200144
- Testing linkage disequilibrium between a disease gene and marker loci
- (1993) Am. J. Hum. Genet. , vol.53 , pp. 1107
- Xie, X.¹ Ott, J.²

13
- 0033990339
- Model-free analysis and permutation tests for allelic associations
- (2000) Hum. Hered. , vol.50 , pp. 133-139
- Zhao, J.H.¹ Curtis, D.² Sham, P.C.³

14
- 0033041179
- Association of an extended haplotype in the tau gene with progressive supranuclear palsy
- (1999) Hum. Mol. Genet. , vol.8 , pp. 711-715
- Baker, M.¹ Litvan, I.² Houlden, H.³ Adamson, J.⁴ Dickson, D.⁵ Perez-Tur, J.⁶ Hardy, J.⁷ Lynch, T.⁸ Bigio, E.⁹ Hutton, M.¹⁰

15
- 0035153594
- Human and mouse α-synuclein genes: Comparative genomic sequence analysis and identification of a novel gene regulatory element
- (2001) Genome Res. , vol.11 , pp. 78-86
- Touchman, J.W.¹ Dehejia, A.² Chiba-Falek, O.³ Cabin, D.E.⁴ Schwartz, J.R.⁵ Orrison, B.M.⁶ Polymeropoulos, M.H.⁷ Nussbaum, R.L.⁸

16
- 0033544368
- Case-control study of the ubiquitin carboxy-terminal hydrolase L1 gene in Parkinson's disease
- (1999) Neurology , vol.53 , pp. 1858-1860
- Maraganore, D.M.¹ Farrer, M.J.² Hardy, J.A.³ Lincoln, S.J.⁴ McDonnell, S.K.⁵ Rocca, W.A.⁶

17
- 0030872838
- PolyPhred: Automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing
- (1997) Nucleic Acids Res. , vol.25 , pp. 2745-2751
- Nickerson, D.A.¹ Tobe, V.O.² Taylor, S.L.³

18
- 0031612929
- Recommendations for a nomenclature system for human gene mutations
- Nomenclature Working Group
- (1998) Hum. Mutat. , vol.11 , pp. 1-3
- Antonarakis, S.E.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.