Zhaotian Zhang - Search Results

Year	Number of Results
2005	1
2007	1
2013	2
2015	2
2016	1
2017	5
2018	7
2019	9
2020	8
2021	9
2022	11
2023	5
2024	1

1

Ocular toxocariasis presenting as leukocoria.

Xie Y, Sun L, Chen Y, Zhou X, Zhang Z, Ding X. Xie Y, et al. Among authors: zhang z. Lancet Infect Dis. 2022 Mar;22(3):426. doi: 10.1016/S1473-3099(21)00704-0. Lancet Infect Dis. 2022. PMID: 35218757 No abstract available.

2

CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis.

Yang M, Li S, Huang L, Zhao R, Dai E, Jiang X, He Y, Lu J, Peng L, Liu W, Zhang Z, Jiang D, Zhang Y, Jiang Z, Yang Y, Zhao P, Zhu X, Ding X, Yang Z. Yang M, et al. Among authors: zhang z. JCI Insight. 2022 Jul 22;7(14):e158428. doi: 10.1172/jci.insight.158428. JCI Insight. 2022. PMID: 35700046 Free PMC article.

3

Mathematics in biomedical imaging.

Jiang M, Louis AK, Wolf D, Zhao H, Daul C, Zhang Z, Zhou T. Jiang M, et al. Among authors: zhang z. Int J Biomed Imaging. 2007;2007:64954. doi: 10.1155/2007/64954. Int J Biomed Imaging. 2007. PMID: 18274655 Free PMC article. No abstract available.

4

NDP-related retinopathies: clinical phenotype of female carriers.

Huang L, Sun L, Li X, Li S, Zhang T, Zhang Z, Ding X. Huang L, et al. Among authors: zhang z. Br J Ophthalmol. 2023 Aug;107(8):1151-1155. doi: 10.1136/bjophthalmol-2021-320084. Epub 2022 Mar 31. Br J Ophthalmol. 2023. PMID: 35361573 Free PMC article.

5

Whole-Gene Deletions of FZD4 Cause Familial Exudative Vitreoretinopathy.

Huang L, Lu J, Zhang L, Zhang Z, Sun L, Li S, Zhang T, Chen L, Cao L, Ding X. Huang L, et al. Among authors: zhang z. Genes (Basel). 2021 Jun 27;12(7):980. doi: 10.3390/genes12070980. Genes (Basel). 2021. PMID: 34199009 Free PMC article.

6

Scleral remodeling in early adulthood: the role of FGF-2.

Qin Y, Liu T, Zhang Z, Xing S, Gong L, Ni Y. Qin Y, et al. Among authors: zhang z. Sci Rep. 2023 Nov 27;13(1):20779. doi: 10.1038/s41598-023-48264-5. Sci Rep. 2023. PMID: 38012225 Free PMC article.

7

Ocular findings and genetic test in Alström syndrome in childhood.

Wang Y, Huang L, Sun L, Li S, Zhang Z, Zhang T, Lai Y, Ding X. Wang Y, et al. Among authors: zhang z. Exp Eye Res. 2022 Dec;225:109277. doi: 10.1016/j.exer.2022.109277. Epub 2022 Oct 4. Exp Eye Res. 2022. PMID: 36206858

8

Update on the Phenotypic and Genotypic Spectrum of KIF11-Related Retinopathy.

Wang Y, Zhang Z, Huang L, Sun L, Li S, Zhang T, Ding X. Wang Y, et al. Among authors: zhang z. Genes (Basel). 2022 Apr 18;13(4):713. doi: 10.3390/genes13040713. Genes (Basel). 2022. PMID: 35456519 Free PMC article.

9

Construction of immune-related risk signature for uveal melanoma.

Zhang Z, Ni Y, Chen G, Wei Y, Peng M, Zhang S. Zhang Z, et al. Artif Cells Nanomed Biotechnol. 2020 Dec;48(1):912-919. doi: 10.1080/21691401.2020.1773480. Artif Cells Nanomed Biotechnol. 2020. PMID: 32496920

10

Knobloch Syndrome Associated with Novel COL18A1 Variants in Chinese Population.

Li S, Wang Y, Sun L, Yan W, Huang L, Zhang Z, Zhang T, Ding X. Li S, et al. Among authors: zhang z. Genes (Basel). 2021 Sep 26;12(10):1512. doi: 10.3390/genes12101512. Genes (Basel). 2021. PMID: 34680907 Free PMC article.

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