Zhu X - Search Results

1

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.

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

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.

4

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.

5

Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma.

Chen Y, Lin Y, Vithana EN, Jia L, Zuo X, Wong TY, Chen LJ, Zhu X, Tam PO, Gong B, Qian S, Li Z, Liu X, Mani B, Luo Q, Guzman C, Leung CK, Li X, Cao W, Yang Q, Tham CC, Cheng Y, Zhang X, Wang N, Aung T, Khor CC, Pang CP, Sun X, Yang Z. Chen Y, et al. Among authors: zhu x. Nat Genet. 2014 Oct;46(10):1115-9. doi: 10.1038/ng.3078. Epub 2014 Aug 31. Nat Genet. 2014. PMID: 25173107

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

A short N-terminal domain of HDAC4 preserves photoreceptors and restores visual function in retinitis pigmentosa.

Guo X, Wang SB, Xu H, Ribic A, Mohns EJ, Zhou Y, Zhu X, Biederer T, Crair MC, Chen B. Guo X, et al. Among authors: zhu x. Nat Commun. 2015 Aug 14;6:8005. doi: 10.1038/ncomms9005. Nat Commun. 2015. PMID: 26272629 Free PMC article.

9

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.

10

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.

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