201 related articles for article (PubMed ID: 26589003)
1. Genome-wide estimate of the heritability of Multiple System Atrophy.
Federoff M; Price TR; Sailer A; Scholz S; Hernandez D; Nicolas A; Singleton AB; Nalls M; Houlden H
Parkinsonism Relat Disord; 2016 Jan; 22():35-41. PubMed ID: 26589003
[TBL] [Abstract][Full Text] [Related]
2. Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson's Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population.
Chen Y; Wei QQ; Ou R; Cao B; Chen X; Zhao B; Guo X; Yang Y; Chen K; Wu Y; Song W; Shang HF
PLoS One; 2015; 10(7):e0133776. PubMed ID: 26208350
[TBL] [Abstract][Full Text] [Related]
3. The relationship between four GWAS-identified loci in Alzheimer's disease and the risk of Parkinson's disease, amyotrophic lateral sclerosis, and multiple system atrophy.
Chen Y; Cao B; Chen X; Ou R; Wei Q; Zhao B; Wu Y; Yuan L; Shang HF
Neurosci Lett; 2018 Nov; 686():205-210. PubMed ID: 30144538
[TBL] [Abstract][Full Text] [Related]
4. No association of GPNMB rs156429 polymorphism with Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in Chinese population.
Xu Y; Chen Y; Ou R; Wei QQ; Cao B; Chen K; Shang HF
Neurosci Lett; 2016 May; 622():113-7. PubMed ID: 27132081
[TBL] [Abstract][Full Text] [Related]
5. SLC1A2 rs3794087 are associated with susceptibility to Parkinson's disease, but not essential tremor, amyotrophic lateral sclerosis or multiple system atrophy in a Chinese population.
Xu Y; Cao B; Chen Y; Ou R; Wei Q; Yang J; Zhao B; Song W; Shang HF
J Neurol Sci; 2016 Jun; 365():96-100. PubMed ID: 27206883
[TBL] [Abstract][Full Text] [Related]
6. Investigating ELOVL7 coding variants in multiple system atrophy.
Wernick AI; Walton RL; Soto-Beasley AI; Koga S; Ren Y; Heckman MG; Milanowski LM; Valentino RR; Kondru N; Uitti RJ; Cheshire WP; Wszolek ZK; Dickson DW; Ross OA
Neurosci Lett; 2021 Apr; 749():135723. PubMed ID: 33600908
[TBL] [Abstract][Full Text] [Related]
7. Multiple system atrophy: the application of genetics in understanding etiology.
Federoff M; Schottlaender LV; Houlden H; Singleton A
Clin Auton Res; 2015 Feb; 25(1):19-36. PubMed ID: 25687905
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Association analysis of SNP rs11868035 in SREBF1 with sporadic Parkinson's disease, sporadic amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
Yuan X; Cao B; Wu Y; Chen Y; Wei Q; Ou R; Yang J; Chen X; Zhao B; Song W; Shang H
Neurosci Lett; 2018 Jan; 664():128-132. PubMed ID: 29128630
[TBL] [Abstract][Full Text] [Related]
10. An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China.
Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF
Eur J Neurol; 2014 Oct; 21(10):1337-43. PubMed ID: 25040112
[TBL] [Abstract][Full Text] [Related]
11. Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy.
Al-Chalabi A; Dürr A; Wood NW; Parkinson MH; Camuzat A; Hulot JS; Morrison KE; Renton A; Sussmuth SD; Landwehrmeyer BG; Ludolph A; Agid Y; Brice A; Leigh PN; Bensimon G;
PLoS One; 2009 Sep; 4(9):e7114. PubMed ID: 19771175
[TBL] [Abstract][Full Text] [Related]
12. GBA variation and susceptibility to multiple system atrophy.
Wernick AI; Walton RL; Koga S; Soto-Beasley AI; Heckman MG; Gan-Or Z; Ren Y; Rademakers R; Uitti RJ; Wszolek ZK; Cheshire WP; Dickson DW; Ross OA
Parkinsonism Relat Disord; 2020 Aug; 77():64-69. PubMed ID: 32623306
[TBL] [Abstract][Full Text] [Related]
13. Determining the Effect of the HNMT, STK39, and NMD3 Polymorphisms on the Incidence of Parkinson's Disease, Amyotrophic Lateral Sclerosis, and Multiple System Atrophy in Chinese Populations.
Chen Y; Cao B; Ou R; Wei Q; Chen X; Zhao B; Wu Y; Song W; Shang HF
J Mol Neurosci; 2018 Apr; 64(4):574-580. PubMed ID: 29564728
[TBL] [Abstract][Full Text] [Related]
14. SNCA variants rs2736990 and rs356220 as risk factors for Parkinson's disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population.
Guo XY; Chen YP; Song W; Zhao B; Cao B; Wei QQ; Ou RW; Yang Y; Yuan LX; Shang HF
Neurobiol Aging; 2014 Dec; 35(12):2882.e1-2882.e6. PubMed ID: 25129240
[TBL] [Abstract][Full Text] [Related]
15. Association analysis of polymorphisms in VMAT2 and TMEM106B genes for Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy.
Hu T; Chen Y; Ou R; Wei Q; Cao B; Zhao B; Wu Y; Song W; Chen X; Shang HF
J Neurol Sci; 2017 Jun; 377():65-71. PubMed ID: 28477711
[TBL] [Abstract][Full Text] [Related]
16. SNCA variants are associated with increased risk for multiple system atrophy.
Scholz SW; Houlden H; Schulte C; Sharma M; Li A; Berg D; Melchers A; Paudel R; Gibbs JR; Simon-Sanchez J; Paisan-Ruiz C; Bras J; Ding J; Chen H; Traynor BJ; Arepalli S; Zonozi RR; Revesz T; Holton J; Wood N; Lees A; Oertel W; Wüllner U; Goldwurm S; Pellecchia MT; Illig T; Riess O; Fernandez HH; Rodriguez RL; Okun MS; Poewe W; Wenning GK; Hardy JA; Singleton AB; Del Sorbo F; Schneider S; Bhatia KP; Gasser T
Ann Neurol; 2009 May; 65(5):610-4. PubMed ID: 19475667
[TBL] [Abstract][Full Text] [Related]
17. Association of the COQ2 V393A variant with risk of multiple system atrophy in East Asians: a case-control study and meta-analysis of the literature.
Zhao Q; Yang X; Tian S; An R; Zheng J; Xu Y
Neurol Sci; 2016 Mar; 37(3):423-30. PubMed ID: 26590992
[TBL] [Abstract][Full Text] [Related]
18. Multiple system atrophy and CAG repeat length: A genetic screening of polyglutamine disease genes in Italian patients.
Mongelli A; Sarro L; Rizzo E; Nanetti L; Meucci N; Pezzoli G; Goldwurm S; Taroni F; Mariotti C; Gellera C
Neurosci Lett; 2018 Jun; 678():37-42. PubMed ID: 29715545
[TBL] [Abstract][Full Text] [Related]
19. Assessment of TREM2 rs75932628 association with Parkinson's disease and multiple system atrophy in a Chinese population.
Chen Y; Chen X; Guo X; Song W; Cao B; Wei Q; Ou R; Zhao B; Shang HF
Neurol Sci; 2015 Oct; 36(10):1903-6. PubMed ID: 26058955
[TBL] [Abstract][Full Text] [Related]
20. Genome-wide analysis of the heritability of amyotrophic lateral sclerosis.
Keller MF; Ferrucci L; Singleton AB; Tienari PJ; Laaksovirta H; Restagno G; Chiò A; Traynor BJ; Nalls MA
JAMA Neurol; 2014 Sep; 71(9):1123-34. PubMed ID: 25023141
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
