195 related articles for article (PubMed ID: 29756641)
21. Parkinson's Disease Genetic Loci in Rapid Eye Movement Sleep Behavior Disorder.
Gan-Or Z; Girard SL; Noreau A; Leblond CS; Gagnon JF; Arnulf I; Mirarchi C; Dauvilliers Y; Desautels A; Mitterling T; Cochen De Cock V; Frauscher B; Monaca C; Hogl B; Dion PA; Postuma RB; Montplaisir JY; Rouleau GA
J Mol Neurosci; 2015 Jul; 56(3):617-22. PubMed ID: 25929833
[TBL] [Abstract][Full Text] [Related]
22. Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study.
Tobin JE; Latourelle JC; Lew MF; Klein C; Suchowersky O; Shill HA; Golbe LI; Mark MH; Growdon JH; Wooten GF; Racette BA; Perlmutter JS; Watts R; Guttman M; Baker KB; Goldwurm S; Pezzoli G; Singer C; Saint-Hilaire MH; Hendricks AE; Williamson S; Nagle MW; Wilk JB; Massood T; Laramie JM; DeStefano AL; Litvan I; Nicholson G; Corbett A; Isaacson S; Burn DJ; Chinnery PF; Pramstaller PP; Sherman S; Al-hinti J; Drasby E; Nance M; Moller AT; Ostergaard K; Roxburgh R; Snow B; Slevin JT; Cambi F; Gusella JF; Myers RH
Neurology; 2008 Jul; 71(1):28-34. PubMed ID: 18509094
[TBL] [Abstract][Full Text] [Related]
23. REM Sleep Behavior Disorder in Parkinson's Disease and Other Synucleinopathies.
St Louis EK; Boeve AR; Boeve BF
Mov Disord; 2017 May; 32(5):645-658. PubMed ID: 28513079
[TBL] [Abstract][Full Text] [Related]
24. Microtubule-associated protein tau (MAPT) influences the risk of Parkinson's disease among Indians.
Das G; Misra AK; Das SK; Ray K; Ray J
Neurosci Lett; 2009 Aug; 460(1):16-20. PubMed ID: 19450659
[TBL] [Abstract][Full Text] [Related]
25. LRRK2 protective haplotype and full sequencing study in REM sleep behavior disorder.
Ouled Amar Bencheikh B; Ruskey JA; Arnulf I; Dauvilliers Y; Monaca CC; De Cock VC; Gagnon JF; Spiegelman D; Hu MTM; Högl B; Stefani A; Ferini-Strambi L; Plazzi G; Antelmi E; Young P; Heidbreder A; Mollenhauer B; Sixel-Döring F; Trenkwalder C; Oertel W; Montplaisir JY; Postuma RB; Rouleau GA; Gan-Or Z
Parkinsonism Relat Disord; 2018 Jul; 52():98-101. PubMed ID: 29576439
[TBL] [Abstract][Full Text] [Related]
26. DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E in vitro.
Coupland KG; Mellick GD; Silburn PA; Mather K; Armstrong NJ; Sachdev PS; Brodaty H; Huang Y; Halliday GM; Hallupp M; Kim WS; Dobson-Stone C; Kwok JB
Mov Disord; 2014 Nov; 29(13):1606-14. PubMed ID: 24375821
[TBL] [Abstract][Full Text] [Related]
27. The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.
Williams-Gray CH; Evans JR; Goris A; Foltynie T; Ban M; Robbins TW; Brayne C; Kolachana BS; Weinberger DR; Sawcer SJ; Barker RA
Brain; 2009 Nov; 132(Pt 11):2958-69. PubMed ID: 19812213
[TBL] [Abstract][Full Text] [Related]
28. Tau haplotypes regulate transcription and are associated with Parkinson's disease.
Kwok JB; Teber ET; Loy C; Hallupp M; Nicholson G; Mellick GD; Buchanan DD; Silburn PA; Schofield PR
Ann Neurol; 2004 Mar; 55(3):329-34. PubMed ID: 14991810
[TBL] [Abstract][Full Text] [Related]
29. Blood RNA biomarkers in prodromal PARK4 and rapid eye movement sleep behavior disorder show role of complexin 1 loss for risk of Parkinson's disease.
Lahut S; Gispert S; Ömür Ö; Depboylu C; Seidel K; Domínguez-Bautista JA; Brehm N; Tireli H; Hackmann K; Pirkevi C; Leube B; Ries V; Reim K; Brose N; den Dunnen WF; Johnson M; Wolf Z; Schindewolf M; Schrempf W; Reetz K; Young P; Vadasz D; Frangakis AS; Schröck E; Steinmetz H; Jendrach M; Rüb U; Başak AN; Oertel W; Auburger G
Dis Model Mech; 2017 May; 10(5):619-631. PubMed ID: 28108469
[TBL] [Abstract][Full Text] [Related]
30. Correlation of tau gene polymorphism with age at onset of Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Neurosci Lett; 2006 Sep; 405(3):202-6. PubMed ID: 16876320
[TBL] [Abstract][Full Text] [Related]
31. Association of tau haplotype-tagging polymorphisms with Parkinson's disease in diverse ethnic Parkinson's disease cohorts.
Fung HC; Xiromerisiou G; Gibbs JR; Wu YR; Eerola J; Gourbali V; Hellström O; Chen CM; Duckworth J; Papadimitriou A; Tienari PJ; Hadjigeorgiou GM; Hardy J; Singleton AB
Neurodegener Dis; 2006; 3(6):327-33. PubMed ID: 17192721
[TBL] [Abstract][Full Text] [Related]
32. Association of MAPT H1 subhaplotypes with neuropathology of lewy body disease.
Heckman MG; Kasanuki K; Brennan RR; Labbé C; Vargas ER; Soto AI; Murray ME; Koga S; Dickson DW; Ross OA
Mov Disord; 2019 Sep; 34(9):1325-1332. PubMed ID: 31234228
[TBL] [Abstract][Full Text] [Related]
33. MAPT rs242562 and GSK3B rs334558 are associated with Parkinson's Disease in central China.
Yu L; Huang J; Zhai D; Liu L; Guo K; Long X; Xiong J; Zhang Z; Wang Y; Zhao Y; Wu P; Wang D; Lin Z; Wu J; Xiong N; Wang T
BMC Neurosci; 2014 Apr; 15():54. PubMed ID: 24779391
[TBL] [Abstract][Full Text] [Related]
34. Screening non-MAPT genes of the Chr17q21 H1 haplotype in Parkinson's disease.
Soto-Beasley AI; Walton RL; Valentino RR; Hook PW; Labbé C; Heckman MG; Johnson PW; Goff LA; Uitti RJ; McLean PJ; Springer W; McCallion AS; Wszolek ZK; Ross OA
Parkinsonism Relat Disord; 2020 Sep; 78():138-144. PubMed ID: 32829096
[TBL] [Abstract][Full Text] [Related]
35. The nasal and gut microbiome in Parkinson's disease and idiopathic rapid eye movement sleep behavior disorder.
Heintz-Buschart A; Pandey U; Wicke T; Sixel-Döring F; Janzen A; Sittig-Wiegand E; Trenkwalder C; Oertel WH; Mollenhauer B; Wilmes P
Mov Disord; 2018 Jan; 33(1):88-98. PubMed ID: 28843021
[TBL] [Abstract][Full Text] [Related]
36. Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals.
Winder-Rhodes SE; Hampshire A; Rowe JB; Peelle JE; Robbins TW; Owen AM; Barker RA
Neurobiol Aging; 2015 Mar; 36(3):1519-28. PubMed ID: 25577413
[TBL] [Abstract][Full Text] [Related]
37. MAPT haplotype diversity in multiple system atrophy.
Labbé C; Heckman MG; Lorenzo-Betancor O; Murray ME; Ogaki K; Soto-Ortolaza AI; Walton RL; Fujioka S; Koga S; Uitti RJ; van Gerpen JA; Petersen RC; Graff-Radford NR; Younkin SG; Boeve BF; Cheshire WP; Low PA; Sandroni P; Coon EA; Singer W; Wszolek ZK; Dickson DW; Ross OA
Parkinsonism Relat Disord; 2016 Sep; 30():40-5. PubMed ID: 27374978
[TBL] [Abstract][Full Text] [Related]
38. MAPT H1 Haplotype is Associated with Late-Onset Alzheimer's Disease Risk in APOEɛ4 Noncarriers: Results from the Dementia Genetics Spanish Consortium.
Pastor P; Moreno F; Clarimón J; Ruiz A; Combarros O; Calero M; López de Munain A; Bullido MJ; de Pancorbo MM; Carro E; Antonell A; Coto E; Ortega-Cubero S; Hernandez I; Tárraga L; Boada M; Lleó A; Dols-Icardo O; Kulisevsky J; Vázquez-Higuera JL; Infante J; Rábano A; Fernández-Blázquez MÁ; Valentí M; Indakoetxea B; Barandiarán M; Gorostidi A; Frank-García A; Sastre I; Lorenzo E; Pastor MA; Elcoroaristizabal X; Lennarz M; Maier W; Rámirez A; Serrano-Ríos M; Lee SE; Sánchez-Juan P;
J Alzheimers Dis; 2016; 49(2):343-52. PubMed ID: 26444794
[TBL] [Abstract][Full Text] [Related]
39. Glucocerebrosidase gene variants are accumulated in idiopathic REM sleep behavior disorder.
Gámez-Valero A; Iranzo A; Serradell M; Vilas D; Santamaria J; Gaig C; Álvarez R; Ariza A; Tolosa E; Beyer K
Parkinsonism Relat Disord; 2018 May; 50():94-98. PubMed ID: 29487000
[TBL] [Abstract][Full Text] [Related]
40. CD4+ T-cell Transcription Factors in Idiopathic REM Sleep Behavior Disorder and Parkinson's Disease.
De Francesco E; Terzaghi M; Storelli E; Magistrelli L; Comi C; Legnaro M; Mauri M; Marino F; Versino M; Cosentino M
Mov Disord; 2021 Jan; 36(1):225-229. PubMed ID: 32649001
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]