Yang L - Search Results

1

Practice Patterns and Challenges in Managing Inherited Retinal Diseases Across Asia-Pacific: A Survey from the APIED Network.

Wong WM, Tham YC, Ayton LN, Britten-Jones AC, Edwards TL, Grigg J, Simunovic MP, Chen FK, Jin ZB, Shen RJ, Sui R, Yang L, Zhao C, Chen H, Li S, Ding X, Bhende M, Raman R, Sen P, Poornachandra B, Chia V, Manurung F, Sasongko MB, Ikeda H, Fujinami K, Woo SJ, Kim SJ, Bastion MC, Kamalden AT, Lott PP, Fong K, Shunmugam M, Lim A, Thapa R, Ibañez BMB, Koh A, Holder GE, Su X, Chan CM, Fenner BJ, Laude A, Ngo WK, Chen TC, Wang NK, Kang EY, Surawatsatien N, Pisuchpen P, Sujirakul T, Wongchaisuwat N, Apivatthakakul A, Kumaramanickavel G, Leroy B, Michaelides M, Pontikos N, Cheng CY, Pang CP, Chen LJ, Chan HW. Wong WM, et al. Among authors: yang l. Asia Pac J Ophthalmol (Phila). 2024 Sep-Oct;13(5):100098. doi: 10.1016/j.apjo.2024.100098. Epub 2024 Oct 2. Asia Pac J Ophthalmol (Phila). 2024. PMID: 39366638 Free article.

2

Simultaneous expression of two pathogenic genes in four Chinese patients affected with inherited retinal dystrophy.

Liu XZ, Tao TC, Qi H, Feng SN, Chen NN, Zhao L, Ma ZZ, Li GL, Yang LP. Liu XZ, et al. Among authors: yang lp. Int J Ophthalmol. 2020 Feb 18;13(2):220-230. doi: 10.18240/ijo.2020.02.04. eCollection 2020. Int J Ophthalmol. 2020. PMID: 32090030 Free PMC article.

3

Molecular diagnosis based on comprehensive genetic testing in 800 Chinese families with non-syndromic inherited retinal dystrophies.

Liu X, Tao T, Zhao L, Li G, Yang L. Liu X, et al. Among authors: yang l. Clin Exp Ophthalmol. 2021 Jan;49(1):46-59. doi: 10.1111/ceo.13875. Epub 2020 Nov 2. Clin Exp Ophthalmol. 2021. PMID: 33090715

4

Characteristics of genotype and phenotype in Chinese patients with Bardet-Biedl syndrome.

Tao T, Wang L, Chong W, Yang L, Li G. Tao T, et al. Among authors: yang l. Int Ophthalmol. 2020 Sep;40(9):2325-2343. doi: 10.1007/s10792-020-01415-3. Epub 2020 May 24. Int Ophthalmol. 2020. PMID: 32448990

5

Novel mutations of RPGR in Chinese families with X-linked retinitis pigmentosa.

Zhang Z, Dai H, Wang L, Tao T, Xu J, Sun X, Yang L, Li G. Zhang Z, et al. Among authors: yang l. BMC Ophthalmol. 2019 Nov 27;19(1):240. doi: 10.1186/s12886-019-1250-7. BMC Ophthalmol. 2019. PMID: 31775781 Free PMC article.

6

Analysis of RPGR gene mutations in 41 Chinese families affected by X-linked inherited retinal dystrophy.

Liu X, Jia R, Meng X, Wang L, Yang L. Liu X, et al. Among authors: yang l. Front Genet. 2022 Oct 6;13:999695. doi: 10.3389/fgene.2022.999695. eCollection 2022. Front Genet. 2022. PMID: 36276946 Free PMC article.

7

Screening copy number variations in 35 unsolved inherited retinal disease families.

Liu X, Dai H, Li G, Jia R, Meng X, Yu S, Yang L, Hong J. Liu X, et al. Among authors: yang l. Hum Genet. 2024 Feb;143(2):197-210. doi: 10.1007/s00439-023-02631-4. Epub 2024 Jan 29. Hum Genet. 2024. PMID: 38282009 Free PMC article.

8

Allele-specific gene-editing approach for vision loss restoration in RHO-associated retinitis pigmentosa.

Liu X, Qiao J, Jia R, Zhang F, Meng X, Li Y, Yang L. Liu X, et al. Among authors: yang l. Elife. 2023 Jun 5;12:e84065. doi: 10.7554/eLife.84065. Elife. 2023. PMID: 37272616 Free PMC article.

9

Application of Whole Exome and Targeted Panel Sequencing in the Clinical Molecular Diagnosis of 319 Chinese Families with Inherited Retinal Dystrophy and Comparison Study.

Wang L, Zhang J, Chen N, Wang L, Zhang F, Ma Z, Li G, Yang L. Wang L, et al. Among authors: yang l. Genes (Basel). 2018 Jul 19;9(7):360. doi: 10.3390/genes9070360. Genes (Basel). 2018. PMID: 30029497 Free PMC article.

10

In vivo genome editing via CRISPR/Cas9-mediated homology-independent targeted integration for Bietti crystalline corneoretinal dystrophy treatment.

Meng X, Jia R, Zhao X, Zhang F, Chen S, Yu S, Liu X, Dou H, Feng X, Zhang J, Wang N, Xu B, Yang L. Meng X, et al. Among authors: yang l. Nat Commun. 2024 May 6;15(1):3773. doi: 10.1038/s41467-024-48092-9. Nat Commun. 2024. PMID: 38710738 Free PMC article.

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