Zhu X - Search Results

1

Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy.

Li S, Yang M, Zhao R, Peng L, Liu W, Jiang X, He Y, Dai E, Zhang L, Yang Y, Shi Y, Zhao P, Yang Z, Zhu X. Li S, et al. Among authors: zhu x. Genes Dis. 2022 Oct 11;10(6):2572-2585. doi: 10.1016/j.gendis.2022.10.003. eCollection 2023 Nov. Genes Dis. 2022. PMID: 37554197 Free PMC article.

2

A genetic variant in the SKIV2L gene is significantly associated with age-related macular degeneration in a Han Chinese population.

Lu F, Shi Y, Qu C, Zhao P, Liu X, Gong B, Ma S, Zhou Y, Zhang Q, Fei P, Xu Y, Hu J, Fan Y, Lin Y, Zhu X, Yang Z. Lu F, et al. Among authors: zhu x. Invest Ophthalmol Vis Sci. 2013 Apr 26;54(4):2911-7. doi: 10.1167/iovs.12-11381. Invest Ophthalmol Vis Sci. 2013. PMID: 23557739

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. Among authors: zhu x. 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

Exome sequencing analysis identifies compound heterozygous mutation in ABCA4 in a Chinese family with Stargardt disease.

Zhou Y, Tao S, Chen H, Huang L, Zhu X, Li Y, Wang Z, Lin H, Hao F, Yang Z, Wang L, Zhu X. Zhou Y, et al. Among authors: zhu x. PLoS One. 2014 Mar 14;9(3):e91962. doi: 10.1371/journal.pone.0091962. eCollection 2014. PLoS One. 2014. PMID: 24632595 Free PMC article.

5

Genetic variants in PVRL2-TOMM40-APOE region are associated with human longevity in a Han Chinese population.

Lu F, Guan H, Gong B, Liu X, Zhu R, Wang Y, Qian J, Zhou T, Lan X, Wang P, Lin Y, Ma S, Lin H, Zhu X, Chen R, Zhu X, Shi Y, Yang Z. Lu F, et al. Among authors: zhu r, zhu x. PLoS One. 2014 Jun 12;9(6):e99580. doi: 10.1371/journal.pone.0099580. eCollection 2014. PLoS One. 2014. PMID: 24924924 Free PMC article.

6

Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.

Xu Y, Huang L, Li J, Zhang Q, Fei P, Zhu X, Tai Z, Ma S, Gong B, Li Y, Zang W, Zhu X, Zhao P, Yang Z. Xu Y, et al. Among authors: zhu x. Mol Vis. 2014 Sep 20;20:1296-306. eCollection 2014. Mol Vis. 2014. PMID: 25352738 Free PMC article.

7

Whole-exome sequencing reveals a novel frameshift mutation in the FAM161A gene causing autosomal recessive retinitis pigmentosa in the Indian population.

Zhou Y, Saikia BB, Jiang Z, Zhu X, Liu Y, Huang L, Kim R, Yang Y, Qu C, Hao F, Gong B, Tai Z, Niu L, Yang Z, Sundaresan P, Zhu X. Zhou Y, et al. Among authors: zhu x. J Hum Genet. 2015 Oct;60(10):625-30. doi: 10.1038/jhg.2015.92. Epub 2015 Aug 6. J Hum Genet. 2015. PMID: 26246154

8

Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy.

Fei P, Zhu X, Jiang Z, Ma S, Li J, Zhang Q, Zhou Y, Xu Y, Tai Z, Zhang L, Huang L, Yang Z, Zhao P, Zhu X. Fei P, et al. Among authors: zhu x. Sci Rep. 2015 Nov 4;5:16120. doi: 10.1038/srep16120. Sci Rep. 2015. PMID: 26530129 Free PMC article.

9

Whole-exome Sequencing Analysis Identifies Mutations in the EYS Gene in Retinitis Pigmentosa in the Indian Population.

Di Y, Huang L, Sundaresan P, Li S, Kim R, Ballav Saikia B, Qu C, Zhu X, Zhou Y, Jiang Z, Zhang L, Lin Y, Zhang D, Li Y, Zhang H, Yin Y, Lu F, Zhu X, Yang Z. Di Y, et al. Among authors: zhu x. Sci Rep. 2016 Jan 20;6:19432. doi: 10.1038/srep19432. Sci Rep. 2016. PMID: 26787102 Free PMC article.

10

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. Among authors: zhu x. Sci Rep. 2016 Feb 10;6:20914. doi: 10.1038/srep20914. Sci Rep. 2016. PMID: 26861912 Free PMC article.

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