Zhang J - Search Results

1

Molecular genetic testing in clinical diagnostic assessments that demonstrate correlations in patients with autosomal recessive inherited retinal dystrophy.

Liu X, Xiao J, Huang H, Guan L, Zhao K, Xu Q, Zhang X, Pan X, Gu S, Chen Y, Zhang J, Shen Y, Jiang H, Gao X, Kang X, Sheng X, Chen X, Zhao C. Liu X, et al. Among authors: zhang j, zhang x. JAMA Ophthalmol. 2015 Apr;133(4):427-36. doi: 10.1001/jamaophthalmol.2014.5831. JAMA Ophthalmol. 2015. PMID: 25611614

2

Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.

Xu Y, Guan L, Shen T, Zhang J, Xiao X, Jiang H, Li S, Yang J, Jia X, Yin Y, Guo X, Wang J, Zhang Q. Xu Y, et al. Among authors: zhang q, zhang j. Hum Genet. 2014 Oct;133(10):1255-71. doi: 10.1007/s00439-014-1460-2. Epub 2014 Jun 18. Hum Genet. 2014. PMID: 24938718

3

Mutation analysis of Leber congenital amaurosis‑associated genes in patients with retinitis pigmentosa.

Shen T, Guan L, Li S, Zhang J, Xiao X, Jiang H, Yang J, Guo X, Wang J, Zhang Q. Shen T, et al. Among authors: zhang q, zhang j. Mol Med Rep. 2015 Mar;11(3):1827-32. doi: 10.3892/mmr.2014.2894. Epub 2014 Nov 7. Mol Med Rep. 2015. PMID: 25377065

4

Mutation analysis in 129 genes associated with other forms of retinal dystrophy in 157 families with retinitis pigmentosa based on exome sequencing.

Xu Y, Guan L, Xiao X, Zhang J, Li S, Jiang H, Jia X, Yang J, Guo X, Yin Y, Wang J, Zhang Q. Xu Y, et al. Among authors: zhang q, zhang j. Mol Vis. 2015 Apr 28;21:477-86. eCollection 2015. Mol Vis. 2015. PMID: 25999675 Free PMC article.

5

Unique Variants in OPN1LW Cause Both Syndromic and Nonsyndromic X-Linked High Myopia Mapped to MYP1.

Li J, Gao B, Guan L, Xiao X, Zhang J, Li S, Jiang H, Jia X, Yang J, Guo X, Yin Y, Wang J, Zhang Q. Li J, et al. Among authors: zhang q, zhang j. Invest Ophthalmol Vis Sci. 2015 Jun;56(6):4150-5. doi: 10.1167/iovs.14-16356. Invest Ophthalmol Vis Sci. 2015. PMID: 26114493

6

Identification of MFRP Mutations in Chinese Families with High Hyperopia.

Xu Y, Guan L, Xiao X, Zhang J, Li S, Jiang H, Jia X, Yin Y, Guo X, Yang Z, Zhang Q. Xu Y, et al. Among authors: zhang q, zhang j. Optom Vis Sci. 2016 Jan;93(1):19-26. doi: 10.1097/OPX.0000000000000751. Optom Vis Sci. 2016. PMID: 26583794

7

Exome sequencing reveals CHM mutations in six families with atypical choroideremia initially diagnosed as retinitis pigmentosa.

Li S, Guan L, Fang S, Jiang H, Xiao X, Yang J, Wang P, Yin Y, Guo X, Wang J, Zhang J, Zhang Q. Li S, et al. Among authors: zhang q, zhang j. Int J Mol Med. 2014 Aug;34(2):573-7. doi: 10.3892/ijmm.2014.1797. Epub 2014 Jun 6. Int J Mol Med. 2014. PMID: 24913019

8

Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosis.

Chen Y, Zhang Q, Shen T, Xiao X, Li S, Guan L, Zhang J, Zhu Z, Yin Y, Wang P, Guo X, Wang J, Zhang Q. Chen Y, et al. Among authors: zhang q, zhang j. Invest Ophthalmol Vis Sci. 2013 Jun 26;54(6):4351-7. doi: 10.1167/iovs.13-11606. Invest Ophthalmol Vis Sci. 2013. PMID: 23661368

9

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

Wang H, Wang X, He C, Li H, Qing J, Grati M, Hu Z, Li J, Hu Y, Xia K, Mei L, Wang X, Yu J, Chen H, Jiang L, Liu Y, Men M, Zhang H, Guan L, Xiao J, Zhang J, Liu X, Feng Y. Wang H, et al. Among authors: zhang j, zhang h. J Hum Genet. 2015 Mar;60(3):119-126. doi: 10.1038/jhg.2014.114. Epub 2015 Jan 15. J Hum Genet. 2015. PMID: 25589040 Free PMC article.

10

Exome sequencing of 47 chinese families with cone-rod dystrophy: mutations in 25 known causative genes.

Huang L, Zhang Q, Li S, Guan L, Xiao X, Zhang J, Jia X, Sun W, Zhu Z, Gao Y, Yin Y, Wang P, Guo X, Wang J, Zhang Q. Huang L, et al. Among authors: zhang q, zhang j. PLoS One. 2013 Jun 11;8(6):e65546. doi: 10.1371/journal.pone.0065546. Print 2013. PLoS One. 2013. PMID: 23776498 Free PMC article.

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