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Items: 1 to 20 of 142

1.

Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.

Xi J, Yang X, Zhao Q, Zheng J, An R, Tian S, Huang H, Hu F, Ning P, Xu Y.

Neurosci Lett. 2018 Jan 1;662:181-184. doi: 10.1016/j.neulet.2017.09.029. Epub 2017 Sep 14.

PMID:
28917980
2.

Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese.

Yang X, Zhao Q, An R, Zheng J, Tian S, Xu Y.

Amyotroph Lateral Scler Frontotemporal Degener. 2015;17(1-2):142-7. doi: 10.3109/21678421.2015.1054291. Epub 2015 Aug 24.

PMID:
26313240
3.

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 18;664:128-132. doi: 10.1016/j.neulet.2017.11.015. Epub 2017 Nov 8.

PMID:
29128630
4.

HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort.

Yang X, Zheng J, Tian S, Chen Y, An R, Zhao Q, Xu Y.

J Neurol Sci. 2017 Feb 15;373:124-128. doi: 10.1016/j.jns.2016.12.055. Epub 2016 Dec 28.

PMID:
28131168
5.

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. doi: 10.1016/j.neurobiolaging.2014.07.014. Epub 2014 Jul 18.

PMID:
25129240
6.

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 27;622:113-7. doi: 10.1016/j.neulet.2016.04.060. Epub 2016 Apr 27.

PMID:
27132081
7.

Association studies of MMP-9 in Parkinson's disease and amyotrophic lateral sclerosis.

He X, Zhang L, Yao X, Hu J, Yu L, Jia H, An R, Liu Z, Xu Y.

PLoS One. 2013 Sep 9;8(9):e73777. doi: 10.1371/journal.pone.0073777. eCollection 2013.

8.

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 1;686:205-210. doi: 10.1016/j.neulet.2018.08.024. Epub 2018 Aug 22.

PMID:
30144538
9.

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 15;365:96-100. doi: 10.1016/j.jns.2016.04.003. Epub 2016 Apr 8.

PMID:
27206883
10.

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 Jul 24;10(7):e0133776. doi: 10.1371/journal.pone.0133776. eCollection 2015.

11.

Modulation of disease risk according to a cathepsin D / apolipoprotein E genotype in Parkinson's disease.

Schulte T, Böhringer S, Schöls L, Müller T, Fischer C, Riess O, Przuntek H, Berger K, Epplen JT, Krüger R.

J Neural Transm (Vienna). 2003 Jul;110(7):749-55.

PMID:
12811635
12.

Association of the COQ2 V393A Variant with Parkinson's Disease: A Case-Control Study and Meta-Analysis.

Yang X, Xi J, Zhao Q, Jia H, An R, Liu Z, Xu Y.

PLoS One. 2015 Jun 22;10(6):e0130970. doi: 10.1371/journal.pone.0130970. eCollection 2015.

13.

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. doi: 10.1111/ene.12490. Epub 2014 Jul 12.

PMID:
25040112
14.

Lack of evidence for an association between the V393A variant of COQ2 and amyotrophic lateral sclerosis in a Han Chinese population.

Yang X, Xi J, An R, Yu L, Lin Z, Zhou H, Xu Y.

Neurol Sci. 2015 Jul;36(7):1211-5. doi: 10.1007/s10072-015-2083-7. Epub 2015 Jan 23.

PMID:
25613861
15.

The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease.

Lill CM, Rengmark A, Pihlstrøm L, Fogh I, Shatunov A, Sleiman PM, Wang LS, Liu T, Lassen CF, Meissner E, Alexopoulos P, Calvo A, Chio A, Dizdar N, Faltraco F, Forsgren L, Kirchheiner J, Kurz A, Larsen JP, Liebsch M, Linder J, Morrison KE, Nissbrandt H, Otto M, Pahnke J, Partch A, Restagno G, Rujescu D, Schnack C, Shaw CE, Shaw PJ, Tumani H, Tysnes OB, Valladares O, Silani V, van den Berg LH, van Rheenen W, Veldink JH, Lindenberger U, Steinhagen-Thiessen E; SLAGEN Consortium, Teipel S, Perneczky R, Hakonarson H, Hampel H, von Arnim CAF, Olsen JH, Van Deerlin VM, Al-Chalabi A, Toft M, Ritz B, Bertram L.

Alzheimers Dement. 2015 Dec;11(12):1407-1416. doi: 10.1016/j.jalz.2014.12.009. Epub 2015 Apr 30.

16.

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 15;377:65-71. doi: 10.1016/j.jns.2017.03.028. Epub 2017 Mar 21.

PMID:
28477711
17.

SNP rs356219 of the α-synuclein (SNCA) gene is associated with Parkinson's disease in a Chinese Han population.

Pan F, Dong H, Ding H, Ye M, Liu W, Wu Y, Zhang X, Chen Z, Luo Y, Ding X.

Parkinsonism Relat Disord. 2012 Jun;18(5):632-4. doi: 10.1016/j.parkreldis.2012.01.025. Epub 2012 Feb 19.

PMID:
22349157
18.

Short arm of chromosome 11 and sporadic Alzheimer's disease: catalase and cathepsin D gene polymorphisms.

Capurso C, Solfrizzi V, D'Introno A, Colacicco AM, Capurso SA, Bifaro L, Menga R, Santamato A, Seripa D, Pilotto A, Capurso A, Panza F.

Neurosci Lett. 2008 Feb 27;432(3):237-42. doi: 10.1016/j.neulet.2007.12.026. Epub 2007 Dec 23.

PMID:
18248894
19.

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

Tian S, Yang X, Zhao Q, Zheng J, Huang H, Chen Y, An R, Xu Y.

Neurosci Lett. 2017 Mar 6;642:119-122. doi: 10.1016/j.neulet.2017.02.008. Epub 2017 Feb 6.

PMID:
28179208
20.

Association of DNMT3b gene variants with sporadic Parkinson's disease in a Chinese Han population.

Chen X, Xiao Y, Wei L, Wu Y, Lu J, Guo W, Huang S, Zhou M, Mo M, Li Z, Cen L, Li S, Yang C, Wu Z, Hu S, Pei Z, Yang X, Qu S, Xu P.

J Gene Med. 2017 Nov;19(11):360-365. doi: 10.1002/jgm.2991. Epub 2017 Nov 19.

PMID:
28990350

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