Xu Y - Search Results

1

Rare missense variants in the PPP2R5D gene associated with Parkinson's disease in the Han Chinese population.

Ning P, Li K, Ren H, Yang H, Xu Y, Yang X. Ning P, et al. Among authors: xu y. Neurosci Lett. 2022 Apr 17;776:136564. doi: 10.1016/j.neulet.2022.136564. Epub 2022 Mar 4. Neurosci Lett. 2022. PMID: 35257824

2

LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

Zhang Z, Burgunder JM, An X, Wu Y, Chen W, Zhang J, Wang Y, Xu Y, Gou Y, Yuan G, Mao X, Peng R. Zhang Z, et al. Among authors: xu y. Mov Disord. 2009 Oct 15;24(13):1902-5. doi: 10.1002/mds.22371. Mov Disord. 2009. PMID: 19672984

3

LRRK2 R1628P contributes to Parkinson's disease susceptibility in Chinese Han populations from mainland China.

Yu L, Hu F, Zou X, Jiang Y, Liu Y, He X, Xi J, Liu L, Liu Z, He L, Xu Y. Yu L, et al. Among authors: xu y. Brain Res. 2009 Nov 3;1296:113-6. doi: 10.1016/j.brainres.2009.08.047. Epub 2009 Aug 20. Brain Res. 2009. PMID: 19699188

4

SNP rs7684318 of the alpha-synuclein gene is associated with Parkinson's disease in the Han Chinese population.

Yu L, Xu P, He X, Hu F, Lin Z, Zhu M, Liu Z, He L, Xu Y. Yu L, et al. Among authors: xu p, xu y. Brain Res. 2010 Jul 30;1346:262-5. doi: 10.1016/j.brainres.2010.05.069. Epub 2010 Jun 1. Brain Res. 2010. PMID: 20513365

5

Two novel mutations of the GTP cyclohydrolase 1 gene and genotype-phenotype correlation in Chinese Dopa-responsive dystonia patients.

Yu L, Zhou H, Hu F, Xu Y. Yu L, et al. Among authors: xu y. Eur J Hum Genet. 2013 Jul;21(7):731-5. doi: 10.1038/ejhg.2012.239. Epub 2012 Dec 5. Eur J Hum Genet. 2013. PMID: 23211702 Free PMC article.

6

Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.

Yang X, Xu Y. Yang X, et al. Among authors: xu y. Biomed Res Int. 2014;2014:371256. doi: 10.1155/2014/371256. Epub 2014 Aug 14. Biomed Res Int. 2014. PMID: 25197640 Free PMC article. Review.

7

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. Yang X, et al. Among authors: xu y. Neurol Sci. 2015 Jul;36(7):1211-5. doi: 10.1007/s10072-015-2083-7. Epub 2015 Jan 23. Neurol Sci. 2015. PMID: 25613861

8

No evidence of association between polymorphisms in four genes and sporadic amyotrophic lateral sclerosis in Han Chinese.

An R, Xi J, Yang X, Yao X, Xu Y. An R, et al. Among authors: xu y. Amyotroph Lateral Scler Frontotemporal Degener. 2015 Jun;16(3-4):245-8. doi: 10.3109/21678421.2014.999790. Epub 2015 Feb 13. Amyotroph Lateral Scler Frontotemporal Degener. 2015. PMID: 25677198

9

Association of histamine N-methyltransferase Thr105Ile polymorphism with Parkinson's disease and schizophrenia in Han Chinese: a case-control study.

Yang X, Liu C, Zhang J, Han H, Wang X, Liu Z, Xu Y. Yang X, et al. Among authors: xu y. PLoS One. 2015 Mar 13;10(3):e0119692. doi: 10.1371/journal.pone.0119692. eCollection 2015. PLoS One. 2015. PMID: 25768024 Free PMC article.

10

Lack of association between the ATP13A2 A746T variant and Parkinson's disease susceptibility in Han Chinese: a meta-analysis.

Pan LS, Wang Z, Ding D, Zhu XP, Leng HL, Deng XB, Xu YM. Pan LS, et al. Int J Neurosci. 2016;126(7):593-9. doi: 10.3109/00207454.2015.1035377. Epub 2015 Jun 5. Int J Neurosci. 2016. PMID: 26000924

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