Ye Z - Search Results

1

Evaluation of four genetic variants in han chinese subjects with high myopia.

Ye Z, Luo H, Gong B, Lin Y, Shuai P, Wang P, Ye C, Yang Z, Wang W, Shi Y. Ye Z, et al. Among authors: ye c. J Ophthalmol. 2015;2015:729463. doi: 10.1155/2015/729463. Epub 2015 Jan 5. J Ophthalmol. 2015. PMID: 25628894 Free PMC article.

2

Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma.

Yang Y, Shi Y, Huang X, Li X, Ye Z, Shuai P, Qu C, Chen R, Xu J, Yang Z, Lu F, Gong B. Yang Y, et al. Among authors: ye z. Gene. 2015 Oct 25;571(2):188-93. doi: 10.1016/j.gene.2015.06.042. Epub 2015 Jun 19. Gene. 2015. PMID: 26095806

3

Evaluation of the Association Between Common Genetic Variants Near the ABCA1 Gene and Primary Angle Closure Glaucoma in a Han Chinese Population.

Luo H, Chen Y, Ye Z, Sun X, Shi Y, Luo Q, Gong B, Shuai P, Yang J, Zhou Y, Liu X, Zhang K, Tan C, Li Y, Lin Y, Yang Z. Luo H, et al. Among authors: ye z. Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6248-54. doi: 10.1167/iovs.15-16741. Invest Ophthalmol Vis Sci. 2015. PMID: 26431478

4

Novel Compound Heterozygous CBS Mutations Cause Homocystinuria in a Han Chinese Family.

Gong B, Liu L, Li Z, Ye Z, Xiao Y, Zeng G, Shi Y, Wang Y, Feng X, Li X, Hao F, Liu X, Qu C, Li Y, Mu G, Yang Z. Gong B, et al. Among authors: ye z. Sci Rep. 2015 Dec 15;5:17947. doi: 10.1038/srep17947. Sci Rep. 2015. PMID: 26667307 Free PMC article.

5

Associations of 6p21.3 Region with Age-related Macular Degeneration and Polypoidal Choroidal Vasculopathy.

Ye Z, Shuai P, Zhai Y, Li F, Jiang L, Lu F, Wen F, Huang L, Zhang D, Liu X, Lin Y, Luo H, Zhang H, Zhu X, Wu Z, Yang Z, Gong B, Shi Y. Ye Z, et al. Sci Rep. 2016 Feb 10;6:20914. doi: 10.1038/srep20914. Sci Rep. 2016. PMID: 26861912 Free PMC article.

6

Association of IGF1 and IGF1R gene polymorphisms with high myopia in a Han Chinese population.

Wang P, Liu X, Ye Z, Gong B, Yang Y, Zhang D, Wu X, Zheng H, Li Y, Yang Z, Shi Y. Wang P, et al. Among authors: ye z. Ophthalmic Genet. 2017 Mar-Apr;38(2):122-126. doi: 10.3109/13816810.2016.1145699. Epub 2016 Apr 4. Ophthalmic Genet. 2017. PMID: 27044882

7

A novel deleterious mutation in the COMP gene that causes pseudoachondroplasia.

Luo H, Yu S, Lin Y, Guo Q, Ma R, Ye Z, Di Y, Li N, Miao Y, Zhou Y, Li Y, Yang J, Yang Z. Luo H, et al. Among authors: ye z. Hum Genome Var. 2016 Jun 9;3:16009. doi: 10.1038/hgv.2016.9. eCollection 2016. Hum Genome Var. 2016. PMID: 27330822 Free PMC article.

8

Association between SKIV2L polymorphism rs429608 and age-related macular degeneration: A meta-analysis.

Shuai P, Ye Z, Liu Y, Qu C, Liu X, Luo H, Feng X, Li X, Shi Y, Gong B. Shuai P, et al. Among authors: ye z. Ophthalmic Genet. 2017 May-Jun;38(3):245-251. doi: 10.1080/13816810.2016.1210650. Epub 2016 Aug 2. Ophthalmic Genet. 2017. PMID: 27484132

9

Genetic association of COL1A1 polymorphisms with high myopia in Asian population: a Meta-analysis.

Gong B, Qu C, Huang XF, Ye ZM, Zhang DD, Shi Y, Chen R, Liu YP, Shuai P. Gong B, et al. Int J Ophthalmol. 2016 Aug 18;9(8):1187-93. doi: 10.18240/ijo.2016.08.16. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27588274 Free PMC article.

10

Effects of dexamethasone and HA1077 on actin cytoskeleton and β-catenin in cultured human trabecular meshwork cells.

Peng J, Feng XY, Ye ZM, Luo Q, Cheng YL, Wu ZZ, Lei CT, Gong B. Peng J, et al. Int J Ophthalmol. 2016 Oct 18;9(10):1376-1380. doi: 10.18240/ijo.2016.10.02. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27803851 Free PMC article.

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