Ouyang J - Search Results

1

Different Phenotypes Represent Advancing Stages of ABCA4-Associated Retinopathy: A Longitudinal Study of 212 Chinese Families From a Tertiary Center.

Wang Y, Sun W, Zhou J, Li X, Jiang Y, Li S, Jia X, Xiao X, Ouyang J, Wang Y, Zhou L, Long Y, Liu M, Li Y, Yi Z, Wang P, Zhang Q. Wang Y, et al. Among authors: ouyang j. Invest Ophthalmol Vis Sci. 2022 May 2;63(5):28. doi: 10.1167/iovs.63.5.28. Invest Ophthalmol Vis Sci. 2022. PMID: 35608843 Free PMC article.

2

Metalloproteinase Adamts16 Is Required for Proper Closure of the Optic Fissure.

Cao M, Ouyang J, Guo J, Lin S, Chen S. Cao M, et al. Among authors: ouyang j. Invest Ophthalmol Vis Sci. 2018 Mar 1;59(3):1167-1177. doi: 10.1167/iovs.17-22827. Invest Ophthalmol Vis Sci. 2018. PMID: 29625437

3

Regional Gene Expression Profile Comparison Reveals the Unique Transcriptome of the Optic Fissure.

Cao M, Ouyang J, Liang H, Guo J, Lin S, Yang S, Xie T, Chen S. Cao M, et al. Among authors: ouyang j. Invest Ophthalmol Vis Sci. 2018 Dec 3;59(15):5773-5784. doi: 10.1167/iovs.18-23962. Invest Ophthalmol Vis Sci. 2018. PMID: 30521666

4

Biallelic mutations in USP45, encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosis.

Yi Z, Ouyang J, Sun W, Xiao X, Li S, Jia X, Wang P, Zhang Q. Yi Z, et al. Among authors: ouyang j. J Med Genet. 2019 May;56(5):325-331. doi: 10.1136/jmedgenet-2018-105709. Epub 2018 Dec 20. J Med Genet. 2019. PMID: 30573563

5

CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection.

Ouyang J, Sun W, Xiao X, Li S, Jia X, Zhou L, Wang P, Zhang Q. Ouyang J, et al. Hum Mol Genet. 2019 Jun 15;28(12):1959-1970. doi: 10.1093/hmg/ddz029. Hum Mol Genet. 2019. PMID: 30689892 Free PMC article.

6

Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12-q13.3.

Xiao X, Sun W, Ouyang J, Li S, Jia X, Tan Z, Hejtmancik JF, Zhang Q. Xiao X, et al. Among authors: ouyang j. Hum Genet. 2019 Oct;138(10):1077-1090. doi: 10.1007/s00439-019-02039-z. Epub 2019 Jun 6. Hum Genet. 2019. PMID: 31172260 Free PMC article.

7

Rare variants in novel and known genes associated with primary angle closure glaucoma based on whole exome sequencing of 549 probands.

Sun W, Xiao X, Li S, Ouyang J, Li X, Jia X, Liu X, Zhang Q. Sun W, et al. Among authors: ouyang j. J Genet Genomics. 2019 Jul 20;46(7):353-357. doi: 10.1016/j.jgg.2019.06.004. Epub 2019 Jul 10. J Genet Genomics. 2019. PMID: 31377238 No abstract available.

8

Comparative exome sequencing reveals novel candidate genes for retinitis pigmentosa.

Yi Z, Ouyang J, Sun W, Li S, Xiao X, Zhang Q. Yi Z, et al. Among authors: ouyang j. EBioMedicine. 2020 Jun;56:102792. doi: 10.1016/j.ebiom.2020.102792. Epub 2020 May 23. EBioMedicine. 2020. PMID: 32454406 Free PMC article.

9

Confirming and expanding the phenotypes of FZD5 variants: Coloboma, inferior chorioretinal hypoplasia, and high myopia.

Jiang Y, Ouyang J, Li S, Xiao X, Sun W, Zhang Q. Jiang Y, et al. Among authors: ouyang j. Mol Vis. 2021 Jan 20;27:50-60. eCollection 2021. Mol Vis. 2021. PMID: 33633439 Free PMC article.

10

DNAH17 is essential for rat spermatogenesis and fertility.

Chen L, Ouyang J, Li X, Xiao X, Sun W, Li S, Zhou L, Liao Y, Zhang Q. Chen L, et al. Among authors: ouyang j. J Genet. 2021;100:14. J Genet. 2021. PMID: 33764336 Free article.

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