341 related articles for article (PubMed ID: 15792962)
1. Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.
Pittman AM; Myers AJ; Abou-Sleiman P; Fung HC; Kaleem M; Marlowe L; Duckworth J; Leung D; Williams D; Kilford L; Thomas N; Morris CM; Dickson D; Wood NW; Hardy J; Lees AJ; de Silva R
J Med Genet; 2005 Nov; 42(11):837-46. PubMed ID: 15792962
[TBL] [Abstract][Full Text] [Related]
2. Different MAPT haplotypes are associated with Parkinson's disease and progressive supranuclear palsy.
Ezquerra M; Pastor P; Gaig C; Vidal-Taboada JM; Cruchaga C; Muñoz E; Martí MJ; Valldeoriola F; Aguilar M; Calopa M; Hernandez-Vara J; Tolosa E
Neurobiol Aging; 2011 Mar; 32(3):547.e11-6. PubMed ID: 19879020
[TBL] [Abstract][Full Text] [Related]
3. Haplotype-specific MAPT exon 3 expression regulated by common intronic polymorphisms associated with Parkinsonian disorders.
Lai MC; Bechy AL; Denk F; Collins E; Gavriliouk M; Zaugg JB; Ryan BJ; Wade-Martins R; Caffrey TM
Mol Neurodegener; 2017 Oct; 12(1):79. PubMed ID: 29084565
[TBL] [Abstract][Full Text] [Related]
4. The structure of the tau haplotype in controls and in progressive supranuclear palsy.
Pittman AM; Myers AJ; Duckworth J; Bryden L; Hanson M; Abou-Sleiman P; Wood NW; Hardy J; Lees A; de Silva R
Hum Mol Genet; 2004 Jun; 13(12):1267-74. PubMed ID: 15115761
[TBL] [Abstract][Full Text] [Related]
5. 5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.
Cruchaga C; Vidal-Taboada JM; Ezquerra M; Lorenzo E; Martinez-Lage P; Blazquez M; Tolosa E; ; Pastor P
Neurobiol Dis; 2009 Feb; 33(2):164-70. PubMed ID: 19022385
[TBL] [Abstract][Full Text] [Related]
6. Novel haplotypes in 17q21 are associated with progressive supranuclear palsy.
Pastor P; Ezquerra M; Perez JC; Chakraverty S; Norton J; Racette BA; McKeel D; Perlmutter JS; Tolosa E; Goate AM
Ann Neurol; 2004 Aug; 56(2):249-58. PubMed ID: 15293277
[TBL] [Abstract][Full Text] [Related]
7. High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy.
Rademakers R; Melquist S; Cruts M; Theuns J; Del-Favero J; Poorkaj P; Baker M; Sleegers K; Crook R; De Pooter T; Bel Kacem S; Adamson J; Van den Bossche D; Van den Broeck M; Gass J; Corsmit E; De Rijk P; Thomas N; Engelborghs S; Heckman M; Litvan I; Crook J; De Deyn PP; Dickson D; Schellenberg GD; Van Broeckhoven C; Hutton ML
Hum Mol Genet; 2005 Nov; 14(21):3281-92. PubMed ID: 16195395
[TBL] [Abstract][Full Text] [Related]
8. Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype.
Houlden H; Baker M; Morris HR; MacDonald N; Pickering-Brown S; Adamson J; Lees AJ; Rossor MN; Quinn NP; Kertesz A; Khan MN; Hardy J; Lantos PL; St George-Hyslop P; Munoz DG; Mann D; Lang AE; Bergeron C; Bigio EH; Litvan I; Bhatia KP; Dickson D; Wood NW; Hutton M
Neurology; 2001 Jun; 56(12):1702-6. PubMed ID: 11425937
[TBL] [Abstract][Full Text] [Related]
9. Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease.
Vandrovcova J; Pittman AM; Malzer E; Abou-Sleiman PM; Lees AJ; Wood NW; de Silva R
Neurobiol Aging; 2009 Sep; 30(9):1477-82. PubMed ID: 18162161
[TBL] [Abstract][Full Text] [Related]
10. H1 haplotype of the MAPT gene is associated with lower regional gray matter volume in healthy carriers.
Canu E; Boccardi M; Ghidoni R; Benussi L; Testa C; Pievani M; Bonetti M; Binetti G; Frisoni GB
Eur J Hum Genet; 2009 Mar; 17(3):287-94. PubMed ID: 18854867
[TBL] [Abstract][Full Text] [Related]
11. Haplotype-specific expression of exon 10 at the human MAPT locus.
Caffrey TM; Joachim C; Paracchini S; Esiri MM; Wade-Martins R
Hum Mol Genet; 2006 Dec; 15(24):3529-37. PubMed ID: 17085483
[TBL] [Abstract][Full Text] [Related]
12. Linkage disequilibrium and haplotype tagging polymorphisms in the Tau H1 haplotype.
Oliveira SA; Scott WK; Zhang F; Stajich JM; Fujiwara K; Hauser M; Scott BL; Pericak-Vance MA; Vance JM; Martin ER
Neurogenetics; 2004 Sep; 5(3):147-55. PubMed ID: 15459824
[TBL] [Abstract][Full Text] [Related]
13. Functional MAPT haplotypes: bridging the gap between genotype and neuropathology.
Caffrey TM; Wade-Martins R
Neurobiol Dis; 2007 Jul; 27(1):1-10. PubMed ID: 17555970
[TBL] [Abstract][Full Text] [Related]
14. An association study of common variation at the MAPT locus with late-onset Alzheimer's disease.
Abraham R; Sims R; Carroll L; Hollingworth P; O'Donovan MC; Williams J; Owen MJ
Am J Med Genet B Neuropsychiatr Genet; 2009 Dec; 150B(8):1152-5. PubMed ID: 19308965
[TBL] [Abstract][Full Text] [Related]
15. Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting.
Scaravilli T; Tolosa E; Ferrer I
Mov Disord; 2005 Aug; 20 Suppl 12():S21-8. PubMed ID: 16092076
[TBL] [Abstract][Full Text] [Related]
16. Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders.
Webb A; Miller B; Bonasera S; Boxer A; Karydas A; Wilhelmsen KC
Arch Neurol; 2008 Nov; 65(11):1473-8. PubMed ID: 19001166
[TBL] [Abstract][Full Text] [Related]
17. Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy.
de Silva R; Weiler M; Morris HR; Martin ER; Wood NW; Lees AJ
Neurosci Lett; 2001 Oct; 311(3):145-8. PubMed ID: 11578815
[TBL] [Abstract][Full Text] [Related]
18. Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.
Koga S; Kouri N; Walton RL; Ebbert MTW; Josephs KA; Litvan I; Graff-Radford N; Ahlskog JE; Uitti RJ; van Gerpen JA; Boeve BF; Parks A; Ross OA; Dickson DW
Acta Neuropathol; 2018 Sep; 136(3):389-404. PubMed ID: 29926172
[TBL] [Abstract][Full Text] [Related]
19. The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.
Camuzat A; Romana M; Dürr A; Feingold J; Brice A; Ruberg M; Lannuzel A
Mov Disord; 2008 Dec; 23(16):2384-91. PubMed ID: 18785640
[TBL] [Abstract][Full Text] [Related]
20. Associations of mitochondrial genomic variation with corticobasal degeneration, progressive supranuclear palsy, and neuropathological tau measures.
Valentino RR; Tamvaka N; Heckman MG; Johnson PW; Soto-Beasley AI; Walton RL; Koga S; Uitti RJ; Wszolek ZK; Dickson DW; Ross OA
Acta Neuropathol Commun; 2020 Sep; 8(1):162. PubMed ID: 32943110
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
