Liu XO - Search Results

1

[Disease gene screening of known loci in a Chinese family with autosomal dominant retinitis pigmentosa].

Liu W, Lu F, Qia LF, Sha ZQ, Liu XO, Ma S, Tang X, Chang JX, Yang ZL, Ye B. Liu W, et al. Among authors: liu xo. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Feb;26(1):70-3. doi: 10.3760/cma.j.issn.1003-9406.2009.01.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19199256 Chinese.

2

A novel mutation in BBS7 gene causes Bardet-Biedl syndrome in a Chinese family.

Yang Z, Yang Y, Zhao P, Chen K, Chen B, Lin Y, Guo F, Chen Y, Liu X, Lu F, Shi Y, Zhang D, Liao S, Xia Q. Yang Z, et al. Mol Vis. 2008;14:2304-8. Epub 2008 Dec 12. Mol Vis. 2008. PMID: 19093007 Free PMC article.

3

A novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degeneration.

Lu F, Huang L, Lei C, Sha G, Zheng H, Liu X, Yang J, Shi Y, Lin Y, Gong B, Zhu X, Ma S, Qiao L, Lin H, Cheng J, Yang Z. Lu F, et al. PLoS One. 2013 Nov 11;8(11):e78274. doi: 10.1371/journal.pone.0078274. eCollection 2013. PLoS One. 2013. PMID: 24244300 Free PMC article. Clinical Trial.

4

Association study of genetic variants in eight genes/loci with type 2 diabetes in a Han Chinese population.

Lin Y, Li P, Cai L, Zhang B, Tang X, Zhang X, Li Y, Xian Y, Yang Y, Wang L, Lu F, Liu X, Rao S, Chen M, Ma S, Shi Y, Bao M, Wu J, Yang Y, Yang J, Yang Z. Lin Y, et al. BMC Med Genet. 2010 Jun 15;11:97. doi: 10.1186/1471-2350-11-97. BMC Med Genet. 2010. PMID: 20550665 Free PMC article.

5

Mutation in connexin 32 causes Charcot-Marie-Tooth disease in a large Chinese family.

Guo F, Shi Y, Lin Y, Liu X, Liu B, Liu Y, Yang Y, Lu F, Ma S, Yang Z. Guo F, et al. Muscle Nerve. 2010 Nov;42(5):715-21. doi: 10.1002/mus.21756. Muscle Nerve. 2010. PMID: 20730878

6

A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridia.

Liu X, Wu Y, Miao Z, Zhang H, Gong B, Zhu X, Huang L, Shi Y, Hao F, Ma S, Lin H, Wang L, Yang Z. Liu X, et al. Ophthalmic Genet. 2018 Aug;39(4):428-436. doi: 10.1080/13816810.2018.1466336. Epub 2018 Jun 14. Ophthalmic Genet. 2018. PMID: 29902091

7

A genome-wide scan maps a novel autosomal dominant juvenile-onset open-angle glaucoma locus to 2p15-16.

Lin Y, Liu T, Li J, Yang J, Du Q, Wang J, Yang Y, Liu X, Fan Y, Lu F, Chen Y, Pu Y, Zhang K, He X, Yang Z. Lin Y, et al. Mol Vis. 2008 Apr 18;14:739-44. Mol Vis. 2008. PMID: 18432317 Free PMC article.

8

An association study of SERPING1 gene and age-related macular degeneration in a Han Chinese population.

Lu F, Zhao P, Fan Y, Tang S, Hu J, Liu X, Yang X, Chen Y, Li T, Lei C, Yang J, Lin Y, Ma S, Li C, Shi Y, Yang Z. Lu F, et al. Mol Vis. 2010 Jan 10;16:1-6. Mol Vis. 2010. PMID: 20062564 Free PMC article.

9

Single nucleotide polymorphisms at the TRAF1/C5 locus are associated with rheumatoid arthritis in a Han Chinese population.

Zhu J, Zhang D, Wu F, He F, Liu X, Wu L, Zhou B, Liu J, Lu F, Liu J, Luo R, Long W, Yang M, Ma S, Wu X, Shi Y, Wu T, Lin Y, Yang J, Yuan G, Yang Z. Zhu J, et al. BMC Med Genet. 2011 Apr 14;12:53. doi: 10.1186/1471-2350-12-53. BMC Med Genet. 2011. PMID: 21492465 Free PMC article.

10

A genome-wide meta-analysis identifies two novel loci associated with high myopia in the Han Chinese population.

Shi Y, Gong B, Chen L, Zuo X, Liu X, Tam PO, Zhou X, Zhao P, Lu F, Qu J, Sun L, Zhao F, Chen H, Zhang Y, Zhang D, Lin Y, Lin H, Ma S, Cheng J, Yang J, Huang L, Zhang M, Zhang X, Pang CP, Yang Z. Shi Y, et al. Hum Mol Genet. 2013 Jun 1;22(11):2325-33. doi: 10.1093/hmg/ddt066. Epub 2013 Feb 12. Hum Mol Genet. 2013. PMID: 23406873

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