Han X - Search Results

1

Clinical and Molecular Features of a Chinese Cohort With Syndromic and Nonsyndromic Retinal Dystrophies Related to the CEP290 Gene.

Zhu T, Shen Y, Sun Z, Han X, Wei X, Li W, Lu C, Cheng T, Zou X, Li H, Cao Z, Gao H, Ma X, Luo M, Sui R. Zhu T, et al. Among authors: han x. Am J Ophthalmol. 2023 Apr;248:96-106. doi: 10.1016/j.ajo.2022.11.023. Epub 2022 Dec 7. Am J Ophthalmol. 2023. PMID: 36493848

2

Rep1 copy number variation is an important genetic cause of choroideremia in Chinese patients.

Zhou Q, Yao F, Han X, Li H, Yang L, Sui R. Zhou Q, et al. Among authors: han x. Exp Eye Res. 2017 Nov;164:64-73. doi: 10.1016/j.exer.2017.07.016. Epub 2017 Jul 31. Exp Eye Res. 2017. PMID: 28774736

3

CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIA.

Han X, Wu S, Li H, Zhu T, Wei X, Zhou Q, Sui R. Han X, et al. Retina. 2020 Nov;40(11):2240-2253. doi: 10.1097/IAE.0000000000002743. Retina. 2020. PMID: 31922496

4

Genetic and clinical characterization of mainland Chinese patients with sialidosis type 1.

Han X, Wu S, Wang M, Li H, Huang Y, Sui R. Han X, et al. Mol Genet Genomic Med. 2020 Aug;8(8):e1316. doi: 10.1002/mgg3.1316. Epub 2020 May 26. Mol Genet Genomic Med. 2020. PMID: 32453490 Free PMC article.

5

Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutations.

Wu S, Zhu T, Sun Z, Wei X, Han X, Zou X, Sui R. Wu S, et al. Among authors: han x. Stem Cell Res. 2021 May;53:102330. doi: 10.1016/j.scr.2021.102330. Epub 2021 Apr 7. Stem Cell Res. 2021. PMID: 33857831 Free article.

6

Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variants.

Zhu T, Wu S, Sun Z, Wei X, Han X, Zou X, Sui R. Zhu T, et al. Among authors: han x. Stem Cell Res. 2021 Aug;55:102502. doi: 10.1016/j.scr.2021.102502. Epub 2021 Aug 12. Stem Cell Res. 2021. PMID: 34419747 Free article.

7

Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutation.

Han X, Wu S, Sun Z, Zhu T, Wei X, Zou X, Sui R. Han X, et al. Stem Cell Res. 2022 Mar;59:102661. doi: 10.1016/j.scr.2022.102661. Epub 2022 Jan 10. Stem Cell Res. 2022. PMID: 35032821 Free article.

8

Generation of a human induced pluripotent stem cell line PUMCHi019-A from a dominant optic atrophy patient with an OPA1 mutation.

Sun Z, Wu S, Zhu T, Wei X, Han X, Zou X, Sui R. Sun Z, et al. Among authors: han x. Stem Cell Res. 2022 Apr;60:102705. doi: 10.1016/j.scr.2022.102705. Epub 2022 Feb 8. Stem Cell Res. 2022. PMID: 35152176 Free article.

9

Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy.

Li H, Wei X, Wu S, Zhu T, Sun Z, Li H, Han X, Zou X, Yao F, Sui R. Li H, et al. Among authors: han x. Graefes Arch Clin Exp Ophthalmol. 2024 Jan;262(1):337-351. doi: 10.1007/s00417-023-06178-y. Epub 2023 Aug 16. Graefes Arch Clin Exp Ophthalmol. 2024. PMID: 37584790

10

A Novel Risk Stratification-Based Immunomodulatory Treatment Strategy for Vogt-Koyanagi-Harada Disease.

Jin K, Liang A, Song H, Xiao F, Gao F, Han X, Zhang M, Zhao C. Jin K, et al. Among authors: han x. Am J Ophthalmol. 2024 Jun;262:25-33. doi: 10.1016/j.ajo.2024.01.035. Epub 2024 Feb 16. Am J Ophthalmol. 2024. PMID: 38369223

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