Yang ZL - Search Results

1

[Advances in molecular genetic study of myopia].

Zhang DD, Yang ZL. Zhang DD, et al. Among authors: yang zl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Aug;26(4):414-8. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 20017306 Review. Chinese.

2

[A novel GJA8 mutation in a Chinese family with autosomal dominant congenital cataract].

Lin Y, Liu NN, Lei CT, Fan YC, Liu XQ, Yang Y, Wang JF, Liu B, Yang ZL. Lin Y, et al. Among authors: yang zl, yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Feb;25(1):59-62. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18247306 Chinese.

3

[Linkage analysis of one family with autosomal dominant high myopia].

Chang JX, Zhang DD, Lin Y, Liu B, Lu F, Tang X, Yang Y, Chen B, Zhang CJ, Yang ZL. Chang JX, et al. Among authors: yang zl, yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008 Aug;25(4):424-6. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2008. PMID: 18683142 Chinese.

4

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.

5

[Linkage analysis of a family with familial hypertriglyceridemia].

Tang X, Lin Y, Liu B, Ma S, Yang Y, Yang ZL. Tang X, et al. Among authors: yang zl, yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):499-503. doi: 10.3760/cma.j.issn.1003-9406.2009.05.004. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806567 Chinese.

6

[Mutation analysis of the PAX6 gene in a family with congenital aniridia and cataract].

Lin Y, Li J, Yang Y, Yang JY, Zhang B, Tang X, Liu XQ, Lu F, Yang ZL. Lin Y, et al. Among authors: yang zl, yang jy, yang y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Oct;26(5):542-5. doi: 10.3760/cma.j.issn.1003-9406.2009.05.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009. PMID: 19806578 Chinese.

7

Association study of complement factor H, C2, CFB, and C3 and age-related macular degeneration in a Han Chinese population.

Liu X, Zhao P, Tang S, Lu F, Hu J, Lei C, Yang X, Lin Y, Ma S, Yang J, Zhang D, Shi Y, Li T, Chen Y, Fan Y, Yang Z. Liu X, et al. Retina. 2010 Sep;30(8):1177-84. doi: 10.1097/IAE.0b013e3181cea676. Retina. 2010. PMID: 20523265

8

[Association study on single nucleotide polymorphisms in HTRA1 gene and rheumatoid arthritis].

Luo RJ, Zhang DD, Zhu J, Zhou B, Ma S, Lu F, Liu J, Long WB, Yang ZL, Zhang CJ. Luo RJ, et al. Among authors: yang zl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010 Jun;27(3):305-9. doi: 10.3760/cma.j.issn.1003-9406.2010.0.015. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2010. PMID: 20533271 Chinese.

9

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.

10

Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population.

Shi Y, Qu J, Zhang D, Zhao P, Zhang Q, Tam POS, Sun L, Zuo X, Zhou X, Xiao X, Hu J, Li Y, Cai L, Liu X, Lu F, Liao S, Chen B, He F, Gong B, Lin H, Ma S, Cheng J, Zhang J, Chen Y, Zhao F, Yang X, Chen Y, Yang C, Lam DSC, Li X, Shi F, Wu Z, Lin Y, Yang J, Li S, Ren Y, Xue A, Fan Y, Li D, Pang CP, Zhang X, Yang Z. Shi Y, et al. Am J Hum Genet. 2011 Jun 10;88(6):805-813. doi: 10.1016/j.ajhg.2011.04.022. Epub 2011 Jun 6. Am J Hum Genet. 2011. PMID: 21640322 Free PMC article.

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