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Items: 1 to 20 of 107

1.

Genetic variation in LINGO-1 (rs9652490) and risk of Parkinson's disease: twelve studies and a meta-analysis.

Wu Y, Wang X, Xu W, Liu W, Fang F, Ding J, Song Y, Chen S.

Neurosci Lett. 2012 Jul 26;522(1):67-72. doi: 10.1016/j.neulet.2012.06.018.

PMID:
22710005
2.

Analysis of LINGO1 (rs9652490) polymorphism in sporadic Parkinson's disease in a Polish population, and a meta-analysis.

Białecka M, Kurzawski M, Tan EK, Drozdzik M.

Neurosci Lett. 2010 Mar 12;472(1):53-5. doi: 10.1016/j.neulet.2010.01.055.

PMID:
20117178
3.

Genetic analysis of "leucine-rich repeat (LRR) and immunoglobulin (Ig) domain-containing, Nogo receptor-interacting protein-1 (LINGO1)" in two independent Chinese parkinson's disease populations.

Wu YR, Tan EK, Chen CM, Kumar PM, Lee-Chen GJ, Chen ST.

Am J Med Genet B Neuropsychiatr Genet. 2011 Jan;156B(1):99-103. doi: 10.1002/ajmg.b.31124.

PMID:
20957646
4.

LINGO1 rs9652490 variant in Parkinson disease patients.

Guo Y, Jankovic J, Song Z, Yang H, Zheng W, Le W, Tang X, Deng X, Yang Y, Deng S, Luo Z, Deng H.

Neurosci Lett. 2011 Jan 7;487(2):174-6. doi: 10.1016/j.neulet.2010.10.016.

PMID:
20951767
5.

Association study between the LINGO1 gene and Parkinson's disease in the Italian population.

Annesi F, De Marco EV, Rocca FE, Nicoletti A, Pugliese P, Nicoletti G, Arabia G, Tarantino P, De Mari M, Lamberti P, Gallerini S, Marconi R, Epifanio A, Morgante L, Cozzolino A, Barone P, Torchia G, Zappia M, Annesi G, Quattrone A.

Parkinsonism Relat Disord. 2011 Sep;17(8):638-41. doi: 10.1016/j.parkreldis.2011.06.020.

PMID:
21752692
6.

Meta-analysis supports association of a functional SNP (rs1801133) in the MTHFR gene with Parkinson's disease.

Zhu ZG, Ai QL, Wang WM, Xiao ZC.

Gene. 2013 Nov 15;531(1):78-83. doi: 10.1016/j.gene.2013.07.034.

PMID:
23916622
7.

Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population.

Zuo X, Jiang H, Guo JF, Yu RH, Sun QY, Hu L, Wang L, Yao LY, Shen L, Pan Q, Yan XX, Xia K, Tang BS.

Neurosci Lett. 2010 Sep 6;481(2):69-72. doi: 10.1016/j.neulet.2010.06.041.

PMID:
20600614
8.

Analysis and meta-analysis of five polymorphisms of the LINGO1 and LINGO2 genes in Parkinson's disease and multiple system atrophy in a Chinese population.

Chen Y, Cao B, Yang J, Wei Q, Ou RW, Zhao B, Song W, Guo X, Shang H.

J Neurol. 2015 Nov;262(11):2478-83. doi: 10.1007/s00415-015-7870-9.

PMID:
26254004
9.

Analysis of Lingo1 variant in sporadic and familial essential tremor among Asians.

Wu YW, Rong TY, Li HH, Xiao Q, Fei QZ, Tan EK, Ding JQ, Chen SD.

Acta Neurol Scand. 2011 Oct;124(4):264-8. doi: 10.1111/j.1600-0404.2010.01466.x.

PMID:
21158743
10.

LINGO1 and risk for essential tremor: results of a meta-analysis of rs9652490 and rs11856808.

Jiménez-Jiménez FJ, García-Martín E, Lorenzo-Betancor O, Pastor P, Alonso-Navarro H, Agúndez JA.

J Neurol Sci. 2012 Jun 15;317(1-2):52-7. doi: 10.1016/j.jns.2012.02.030.

PMID:
22425540
11.
12.

LINGO1 rs9652490 and rs11856808 are not associated with the risk of Parkinson's disease: results of a meta-analysis.

Agúndez JA, Lorenzo-Betancor O, Pastor P, García-Martín E, Luengo A, Alonso-Navarro H, Jiménez-Jiménez FJ.

Parkinsonism Relat Disord. 2012 Jun;18(5):657-9. doi: 10.1016/j.parkreldis.2011.09.005. No abstract available.

PMID:
21955595
13.

GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.

Li NN, Chang XL, Mao XY, Zhang JH, Zhao DM, Tan EK, Peng R.

Hum Genet. 2012 Jul;131(7):1089-93. doi: 10.1007/s00439-011-1133-3.

PMID:
22198721
14.

LINGO1 is not associated with Parkinson's disease in German patients.

Klebe S, Thier S, Lorenz D, Nothnagel M, Schreiber S, Klein C, Hagenah J, Kasten M, Berg D, Srulijes K, Gasser T, Deuschl G, Kuhlenbäumer G.

Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1173-8. doi: 10.1002/ajmg.b.31085.

PMID:
20468067
15.
16.

Association of paraoxonase 1 gene polymorphisms with risk of Parkinson's disease: a meta-analysis.

Zintzaras E, Hadjigeorgiou GM.

J Hum Genet. 2004;49(9):474-81.

PMID:
15368102
17.

Polymorphism in semaphorin 5A (Sema5A) gene is not a marker of Parkinson's disease risk.

Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Tan EK, Drozdzik M.

Neurosci Lett. 2006 May 15;399(1-2):121-3.

PMID:
16481103
18.

Association study of semaphorin 5A with risk of Parkinson's disease in a Chinese Han population.

Ding H, Wang F, Ding X, Song X, Lu X, Zhang K, Xiao H, Ye M, Chen J, Zhang Q.

Brain Res. 2008 Dec 15;1245:126-9. doi: 10.1016/j.brainres.2008.09.080.

PMID:
18950607
19.

COMT gene and risk for Parkinson's disease: a systematic review and meta-analysis.

Jiménez-Jiménez FJ, Alonso-Navarro H, García-Martín E, Agúndez JA.

Pharmacogenet Genomics. 2014 Jul;24(7):331-9. doi: 10.1097/FPC.0000000000000056. Review.

PMID:
24819480
20.

Paraoxonase 1 polymorphisms L55M and Q192R were not risk factors for Parkinson's disease: a HuGE review and meta-analysis.

Liu YL, Yang J, Zheng J, Liu DW, Liu T, Wang JM, Wang CN, Wang MW, Tian QB.

Gene. 2012 Jun 15;501(2):188-92. doi: 10.1016/j.gene.2012.03.067. Review.

PMID:
22521594

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