Zhang X - Search Results

1

Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.

Zhang L, Sun Z, Zhao P, Huang L, Xu M, Yang Y, Chen X, Lu F, Zhang X, Wang H, Zhang S, Liu W, Jiang Z, Ma S, Chen R, Zhao C, Yang Z, Sui R, Zhu X. Zhang L, et al. Among authors: zhang s, zhang x. Hum Mol Genet. 2018 Dec 1;27(23):4157-4168. doi: 10.1093/hmg/ddy281. Hum Mol Genet. 2018. PMID: 30085091 Free PMC article.

2

Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis.

Li JK, Fei P, Li Y, Huang QJ, Zhang Q, Zhang X, Rao YQ, Li J, Zhao P. Li JK, et al. Among authors: zhang q, zhang x. Sci Rep. 2016 May 23;6:26564. doi: 10.1038/srep26564. Sci Rep. 2016. PMID: 27212378 Free PMC article.

3

Clinical and genetic characteristics of Leber congenital amaurosis with novel mutations in known genes based on a Chinese eastern coast Han population.

Wang S, Zhang Q, Zhang X, Wang Z, Zhao P. Wang S, et al. Among authors: zhang q, zhang x. Graefes Arch Clin Exp Ophthalmol. 2016 Nov;254(11):2227-2238. doi: 10.1007/s00417-016-3428-5. Epub 2016 Jul 16. Graefes Arch Clin Exp Ophthalmol. 2016. PMID: 27422788

4

Comprehensive analysis of genetic variations in strictly-defined Leber congenital amaurosis with whole-exome sequencing in Chinese.

Wang SY, Zhang Q, Zhang X, Zhao PQ. Wang SY, et al. Among authors: zhang q, zhang x. Int J Ophthalmol. 2016 Sep 18;9(9):1260-4. doi: 10.18240/ijo.2016.09.04. eCollection 2016. Int J Ophthalmol. 2016. PMID: 27672588 Free PMC article.

5

Evaluating inner retinal dimples after inner limiting membrane removal using multimodal imaging of optical coherence tomography.

Liu J, Chen Y, Wang S, Zhang X, Zhao P. Liu J, et al. Among authors: zhang x. BMC Ophthalmol. 2018 Jun 27;18(1):155. doi: 10.1186/s12886-018-0828-9. BMC Ophthalmol. 2018. PMID: 29945560 Free PMC article.

6

Long-term surgical outcomes of multiple parfoveolar curvilinear internal limiting membrane peeling for myopic foveoschisis.

Tian T, Jin H, Zhang Q, Zhang X, Zhang H, Zhao P. Tian T, et al. Among authors: zhang q, zhang x, zhang h. Eye (Lond). 2018 Nov;32(11):1783-1789. doi: 10.1038/s41433-018-0178-0. Epub 2018 Jul 30. Eye (Lond). 2018. PMID: 30061650 Free PMC article.

7

The characteristics of digenic familial exudative vitreoretinopathy.

Li Y, Peng J, Li J, Zhang Q, Li J, Zhang X, Fei P, She K, Zhao P. Li Y, et al. Among authors: zhang q, zhang x. Graefes Arch Clin Exp Ophthalmol. 2018 Nov;256(11):2149-2156. doi: 10.1007/s00417-018-4076-8. Epub 2018 Aug 10. Graefes Arch Clin Exp Ophthalmol. 2018. PMID: 30097784

8

Clinical features of posterior microphthalmic and nanophthalmic eyes.

Liu JJ, Chen YY, Zhang X, Zhao PQ. Liu JJ, et al. Among authors: zhang x. Int J Ophthalmol. 2018 Nov 18;11(11):1829-1834. doi: 10.18240/ijo.2018.11.15. eCollection 2018. Int J Ophthalmol. 2018. PMID: 30450315 Free PMC article.

9

Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.

Li JK, Li Y, Zhang X, Chen CL, Rao YQ, Fei P, Zhang Q, Zhao P, Li J. Li JK, et al. Among authors: zhang q, zhang x. Invest Ophthalmol Vis Sci. 2018 Nov 1;59(13):5368-5381. doi: 10.1167/iovs.17-23541. Invest Ophthalmol Vis Sci. 2018. PMID: 30452590

10

Prenatal diagnosis of familial exudative vitreoretinopathy and Norrie disease.

Liu J, Zhu J, Yang J, Zhang X, Zhang Q, Zhao P. Liu J, et al. Among authors: zhang q, zhang x. Mol Genet Genomic Med. 2019 Jan;7(1):e00503. doi: 10.1002/mgg3.503. Epub 2018 Nov 25. Mol Genet Genomic Med. 2019. PMID: 30474316 Free PMC article.

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