181 related articles for article (PubMed ID: 32562694)
1. Evaluation of the genetic association between early-onset primary angle-closure glaucoma and retinitis pigmentosa.
Liu X; Li J; Lin S; Xiao X; Luo J; Wei W; Ling Y; Fang L; Xiao H; Chen L; Huang J; Zhong Y; Zhang Q
Exp Eye Res; 2020 Aug; 197():108118. PubMed ID: 32562694
[TBL] [Abstract][Full Text] [Related]
2. Clinical and Genetic Analysis of Retinitis Pigmentosa with Primary Angle Closure Glaucoma in the Chinese Population.
Wang DD; Gao FJ; Hu FY; Cao WJ; Xu P; Huang Y; Sun XH; Wu JH
Curr Eye Res; 2022 Sep; 47(9):1339-1345. PubMed ID: 35924323
[TBL] [Abstract][Full Text] [Related]
3. Ocular Biometry in Primary Angle-Closure Glaucoma Associated with Retinitis Pigmentosa.
Xu J; Ouyang Z; Yang Y; Cai X; Wang Z; Lin M; Zhang X; Liu X; Yu M
J Ophthalmol; 2017; 2017():9164846. PubMed ID: 29464115
[TBL] [Abstract][Full Text] [Related]
4. Prevalence of primary angle-closure disease in retinitis pigmentosa.
Pradhan ZS; Shroff S; Bansod A; Poornachandra B; Shetty A; Devi S; Rao DAS; Puttaiah NK; Rao HL
Indian J Ophthalmol; 2022 Jul; 70(7):2449-2451. PubMed ID: 35791130
[TBL] [Abstract][Full Text] [Related]
5. Genetic and clinical findings of panel-based targeted exome sequencing in a northeast Chinese cohort with retinitis pigmentosa.
Sun Y; Li W; Li JK; Wang ZS; Bai JY; Xu L; Xing B; Yang W; Wang ZW; Wang LS; He W; Chen F
Mol Genet Genomic Med; 2020 Apr; 8(4):e1184. PubMed ID: 32100970
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation in the PRPH2 gene in a Chinese pedigree with retinitis pigmentosa and angle-closure glaucoma.
Li WN; Du XJ; Zhang YT; Wang LY; Zhu J
BMC Ophthalmol; 2021 Aug; 21(1):302. PubMed ID: 34399712
[TBL] [Abstract][Full Text] [Related]
7. Molecular Epidemiology in 591 Italian Probands With Nonsyndromic Retinitis Pigmentosa and Usher Syndrome.
Colombo L; Maltese PE; Castori M; El Shamieh S; Zeitz C; Audo I; Zulian A; Marinelli C; Benedetti S; Costantini A; Bressan S; Percio M; Ferri P; Abeshi A; Bertelli M; Rossetti L
Invest Ophthalmol Vis Sci; 2021 Feb; 62(2):13. PubMed ID: 33576794
[TBL] [Abstract][Full Text] [Related]
8. Frequent mutations of RetNet genes in eoHM: Further confirmation in 325 probands and comparison with late-onset high myopia based on exome sequencing.
Zhou L; Xiao X; Li S; Jia X; Zhang Q
Exp Eye Res; 2018 Jun; 171():76-91. PubMed ID: 29453956
[TBL] [Abstract][Full Text] [Related]
9. Application of targeted panel sequencing and whole exome sequencing for 76 Chinese families with retinitis pigmentosa.
Dan H; Huang X; Xing Y; Shen Y
Mol Genet Genomic Med; 2020 Mar; 8(3):e1131. PubMed ID: 31960602
[TBL] [Abstract][Full Text] [Related]
10. Coding Variants in
Qiao C; Jia H; Zhang H; Wang H; Liang J; Song J; Li L; Duan X; Cao K; Hu J
DNA Cell Biol; 2020 Jun; 39(6):949-957. PubMed ID: 32397755
[TBL] [Abstract][Full Text] [Related]
11. Whole-exome sequencing identified genes known to be responsible for retinitis pigmentosa in 28 Chinese families.
Shen C; You B; Chen YN; Li Y; Li W; Wei WB
Mol Vis; 2022; 28():96-113. PubMed ID: 35814500
[TBL] [Abstract][Full Text] [Related]
12. Mutations of 60 known causative genes in 157 families with retinitis pigmentosa based on exome sequencing.
Xu Y; Guan L; Shen T; Zhang J; Xiao X; Jiang H; Li S; Yang J; Jia X; Yin Y; Guo X; Wang J; Zhang Q
Hum Genet; 2014 Oct; 133(10):1255-71. PubMed ID: 24938718
[TBL] [Abstract][Full Text] [Related]
13. In-depth analysis of eight susceptibility loci of primary angle closure glaucoma in Han Chinese.
Shi H; Chen Y; Lu H; Zhu R; Zhang J; He M; Guan H
Exp Eye Res; 2021 Jan; 202():108350. PubMed ID: 33227294
[TBL] [Abstract][Full Text] [Related]
14. Variants in Nebulin (NEB) Are Linked to the Development of Familial Primary Angle Closure Glaucoma in Basset Hounds.
Ahram DF; Grozdanic SD; Kecova H; Henkes A; Collin RW; Kuehn MH
PLoS One; 2015; 10(5):e0126660. PubMed ID: 25938837
[TBL] [Abstract][Full Text] [Related]
15. Whole Exome Sequencing Reveals Novel Candidate Genes in Familial Forms of Glaucomatous Neurodegeneration.
Narta K; Teltumbade MR; Vishal M; Sadaf S; Faruq M; Jama H; Waseem N; Rao A; Sen A; Ray K; Mukhopadhyay A
Genes (Basel); 2023 Feb; 14(2):. PubMed ID: 36833422
[TBL] [Abstract][Full Text] [Related]
16. Association between retinitis pigmentosa and an increased risk of primary angle closure glaucoma: A population-based cohort study.
Hung MC; Chen YY
PLoS One; 2022; 17(9):e0274066. PubMed ID: 36083972
[TBL] [Abstract][Full Text] [Related]
17. Association of Genes implicated in primary angle-closure Glaucoma and the ocular biometric parameters of anterior chamber depth and axial length in a northern Chinese population.
Wang S; Zhuang W; Ma J; Xu M; Piao S; Hao J; Zhang W; Chi H; Xue Z; Ha S
BMC Ophthalmol; 2018 Oct; 18(1):271. PubMed ID: 30348125
[TBL] [Abstract][Full Text] [Related]
18. Distinct iris gene expression profiles of primary angle closure glaucoma and primary open angle glaucoma and their interaction with ocular biometric parameters.
Seet LF; Narayanaswamy A; Finger SN; Htoon HM; Nongpiur ME; Toh LZ; Ho H; Perera SA; Wong TT
Clin Exp Ophthalmol; 2016 Nov; 44(8):684-692. PubMed ID: 26988898
[TBL] [Abstract][Full Text] [Related]
19. Biallelic variants in
Li X; Sun W; Xiao X; Fang L; Li S; Liu X; Zhang Q
Br J Ophthalmol; 2022 Dec; 106(12):1710-1715. PubMed ID: 34154991
[TBL] [Abstract][Full Text] [Related]
20. Anterior Segment Biometry in Primary Angle Closure Glaucoma Patients with Visual Field Progression: Comparison between Malays and Chinese.
Neoh FP; Y A; Siti AA; Liza-Sharmini AT
J Curr Glaucoma Pract; 2023; 17(1):3-8. PubMed ID: 37228307
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
