Xu Y - Search Results

1

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. He X, et al. Among authors: xu y. PLoS One. 2013 Sep 9;8(9):e73777. doi: 10.1371/journal.pone.0073777. eCollection 2013. PLoS One. 2013. PMID: 24040066 Free PMC article.

2

[A new point mutation on exon 2 of parkin gene in Parkinson's disease].

Xu Y, Liu Z, Wang Y, Tao E, Chen G, Chen B. Xu Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002 Oct;19(5):409-11. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2002. PMID: 12362318 Chinese.

3

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

4

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

5

Structural and functional changes mapped in the brains of amyotrophic lateral sclerosis patients with/without dysphagia: a pilot study.

Li S, Chen Q, Yu B, Xue K, Luo C, Xu Y, Gong Q, He C, Zhou D, He L, Yao D. Li S, et al. Among authors: xu y. Amyotroph Lateral Scler. 2009 Oct-Dec;10(5-6):280-7. doi: 10.3109/17482960902893342. Amyotroph Lateral Scler. 2009. PMID: 19922114

6

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

7

Novel human pathological mutations. Gene symbol: GCH1. Disease: dystonia, dopa-responsive.

Hu F, Xu Y, Zhou D, He X, Yu L. Hu F, et al. Among authors: xu y. Hum Genet. 2010 Apr;127(4):482. Hum Genet. 2010. PMID: 21488304 No abstract available.

8

The C(-1562)T polymorphism of matrix metalloproteinase-9 gene is associated with schizophrenia in China.

Han H, He X, Tang J, Liu W, Liu K, Zhang J, Wang X, Xu Y, Chen X. Han H, et al. Among authors: xu y. Psychiatry Res. 2011 Nov 30;190(1):163-4. doi: 10.1016/j.psychres.2011.04.026. Epub 2011 May 26. Psychiatry Res. 2011. PMID: 21620482 No abstract available.

9

The functional SNP rs4376531 in the ARHGEF gene is a risk factor for the atherothrombotic stroke in Han Chinese.

Yin YY, Zhang B, Zhou MK, Guo J, Lei L, He XH, Xu YM, He L. Yin YY, et al. Neurol India. 2011 May-Jun;59(3):408-12. doi: 10.4103/0028-3886.82755. Neurol India. 2011. PMID: 21743172 Free article.

10

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.

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