Jiang Z - Search Results

1

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

Zhang L, Yang Y, Li S, Tai Z, Huang L, Liu Y, Zhu X, Di Y, Qu C, Jiang Z, Li Y, Zhang G, Kim R, Sundaresan P, Yang Z, Zhu X. Zhang L, et al. Among authors: jiang z. Genet Test Mol Biomarkers. 2016 Jul;20(7):346-51. doi: 10.1089/gtmb.2015.0322. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27228167

2

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: jiang z. 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

3

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: jiang z. Sci Rep. 2015 Nov 4;5:16120. doi: 10.1038/srep16120. Sci Rep. 2015. PMID: 26530129 Free PMC article.

4

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: jiang z. Sci Rep. 2016 Jan 20;6:19432. doi: 10.1038/srep19432. Sci Rep. 2016. PMID: 26787102 Free PMC article.

5

Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa.

Yang Y, Yang Y, Huang L, Zhai Y, Li J, Jiang Z, Gong B, Fang H, Kim R, Yang Z, Sundaresan P, Zhu X, Zhou Y. Yang Y, et al. Among authors: jiang z. Sci Rep. 2016 Sep 27;6:33681. doi: 10.1038/srep33681. Sci Rep. 2016. PMID: 27670293 Free PMC article.

6

Loss of Tmem30a leads to photoreceptor degeneration.

Zhang L, Yang Y, Li S, Zhang S, Zhu X, Tai Z, Yang M, Liu Y, Guo X, Chen B, Jiang Z, Lu F, Zhu X. Zhang L, et al. Among authors: jiang z. Sci Rep. 2017 Aug 24;7(1):9296. doi: 10.1038/s41598-017-09506-5. Sci Rep. 2017. PMID: 28839191 Free PMC article.

7

Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa.

Yang M, Li S, Liu W, Yang Y, Zhang L, Zhang S, Jiang Z, Yang Z, Zhu X. Yang M, et al. Among authors: jiang z. Genet Test Mol Biomarkers. 2018 Mar;22(3):165-169. doi: 10.1089/gtmb.2017.0248. Epub 2018 Feb 13. Genet Test Mol Biomarkers. 2018. PMID: 29437494

8

A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa.

Zhou Y, Li S, Huang L, Yang Y, Zhang L, Yang M, Liu W, Ramasamy K, Jiang Z, Sundaresan P, Zhu X, Yang Z. Zhou Y, et al. Among authors: jiang z. Hum Mol Genet. 2018 Jul 15;27(14):2563-2572. doi: 10.1093/hmg/ddy165. Hum Mol Genet. 2018. PMID: 29726989

9

Genetic Association Study Between the COL11A1 and COL18A1 Genes and High Myopia in a Han Chinese Population.

Wu H, Jiang L, Zheng R, Luo D, Liu X, Hao F, Jiang Z, Gong B, Yang Z, Shi Y. Wu H, et al. Among authors: jiang l, jiang z. Genet Test Mol Biomarkers. 2018 Jun;22(6):359-365. doi: 10.1089/gtmb.2017.0235. Epub 2018 May 21. Genet Test Mol Biomarkers. 2018. PMID: 29781737

10

A splicing mutation in aryl hydrocarbon receptor associated with retinitis pigmentosa.

Zhou Y, Li S, Huang L, Yang Y, Zhang L, Yang M, Liu W, Ramasamy K, Jiang Z, Sundaresan P, Zhu X, Yang Z. Zhou Y, et al. Among authors: jiang z. Hum Mol Genet. 2018 Jul 15;27(14):2587. doi: 10.1093/hmg/ddy228. Hum Mol Genet. 2018. PMID: 29931334 No abstract available.

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