252 related articles for article (PubMed ID: 26244290)
1. Molecular Characterization of FZD4, LRP5, and TSPAN12 in Familial Exudative Vitreoretinopathy.
Seo SH; Yu YS; Park SW; Kim JH; Kim HK; Cho SI; Park H; Lee SJ; Seong MW; Park SS; Kim JY
Invest Ophthalmol Vis Sci; 2015 Aug; 56(9):5143-51. PubMed ID: 26244290
[TBL] [Abstract][Full Text] [Related]
2. Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Rao FQ; Cai XB; Cheng FF; Cheng W; Fang XL; Li N; Huang XF; Li LH; Jin ZB
Invest Ophthalmol Vis Sci; 2017 May; 58(5):2623-2629. PubMed ID: 28494495
[TBL] [Abstract][Full Text] [Related]
3. The characteristics of digenic familial exudative vitreoretinopathy.
Li Y; Peng J; Li J; Zhang Q; Li J; Zhang X; Fei P; She K; Zhao P
Graefes Arch Clin Exp Ophthalmol; 2018 Nov; 256(11):2149-2156. PubMed ID: 30097784
[TBL] [Abstract][Full Text] [Related]
4. Mutation Spectrum of the LRP5, NDP, and TSPAN12 Genes in Chinese Patients With Familial Exudative Vitreoretinopathy.
Tang M; Sun L; Hu A; Yuan M; Yang Y; Peng X; Ding X
Invest Ophthalmol Vis Sci; 2017 Nov; 58(13):5949-5957. PubMed ID: 29181528
[TBL] [Abstract][Full Text] [Related]
5. Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
Mao J; Chen Y; Fang Y; Shao Y; Xiang Z; Li H; Zhao S; Chen Y; Shen L
Ann Med; 2022 Dec; 54(1):3286-3298. PubMed ID: 36411543
[TBL] [Abstract][Full Text] [Related]
6. Next-Generation Sequencing in the Familial Exudative Vitreoretinopathy-Associated Rhegmatogenous Retinal Detachment.
Chen C; Wang Z; Sun L; Huang S; Li S; Zhang A; Luo X; Huang L; Ding X
Invest Ophthalmol Vis Sci; 2019 Jun; 60(7):2659-2666. PubMed ID: 31237656
[TBL] [Abstract][Full Text] [Related]
7. Mutation spectrum in a cohort with familial exudative vitreoretinopathy.
Qu N; Li W; Han DM; Gao JY; Yang ZT; Jiang L; Liu TB; Chen YX; Jiang XS; Zhou L; Wu JH; Huang X
Mol Genet Genomic Med; 2022 Sep; 10(9):e2021. PubMed ID: 35876299
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetical features of probands and affected family members with familial exudative vitreoretinopathy in a large Chinese cohort.
Wang S; Zhang X; Hu Y; Fei P; Xu Y; Peng J; Zhao P
Br J Ophthalmol; 2021 Jan; 105(1):83-86. PubMed ID: 32238352
[TBL] [Abstract][Full Text] [Related]
9. Whole exome sequencing revealed 14 variants in NDP, FZD4, LRP5, and TSPAN12 genes for 20 families with familial exudative vitreoretinopathy.
Dan H; Wang D; Huang Z; Shi Q; Zheng M; Xiao Y; Song Z
BMC Med Genomics; 2022 Mar; 15(1):54. PubMed ID: 35277167
[TBL] [Abstract][Full Text] [Related]
10. Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.
Li JK; Li Y; Zhang X; Chen CL; Rao YQ; Fei P; Zhang Q; Zhao P; Li J
Invest Ophthalmol Vis Sci; 2018 Nov; 59(13):5368-5381. PubMed ID: 30452590
[TBL] [Abstract][Full Text] [Related]
11. A Survey of Multigenic Protein-Altering Variant Frequency in Familial Exudative Vitreo-Retinopathy (FEVR) Patients by Targeted Sequencing of Seven FEVR-Linked Genes.
Cicerone AP; Dailey W; Sun M; Santos A; Jeong D; Jones L; Koustas K; Drekh M; Schmitz K; Haque N; Felisky JA; Guzman AE; Mellert K; Trese MT; Capone A; Drenser KA; Mitton KP
Genes (Basel); 2022 Mar; 13(3):. PubMed ID: 35328049
[TBL] [Abstract][Full Text] [Related]
12. Large Deletions of TSPAN12 Cause Familial Exudative Vitreoretinopathy (FEVR).
Seo SH; Kim MJ; Park SW; Kim JH; Yu YS; Song JY; Cho SI; Ahn JH; Oh YH; Lee JS; Lee S; Seong MW; Park SS; Kim JY
Invest Ophthalmol Vis Sci; 2016 Dec; 57(15):6902-6908. PubMed ID: 28002565
[TBL] [Abstract][Full Text] [Related]
13. Whole exome sequencing revealed novel pathogenic variants in Vietnamese patients with FEVR.
Trang DT; Phu NM; Hung DM; Nhung VP; Ha NN; Thuong MTH; Ngoc TTB; Hiep NX; Ton ND; Hai NV; Ha NH
Mol Vis; 2022; 28():480-491. PubMed ID: 37089697
[TBL] [Abstract][Full Text] [Related]
14. Mutation spectrum of the FZD-4, TSPAN12 AND ZNF408 genes in Indian FEVR patients.
Musada GR; Syed H; Jalali S; Chakrabarti S; Kaur I
BMC Ophthalmol; 2016 Jun; 16():90. PubMed ID: 27316669
[TBL] [Abstract][Full Text] [Related]
15. Symmetry of folds in FEVR: A genotype-phenotype correlation study.
Wang Z; Chen C; Sun L; Zhang A; Liu C; Huang L; Ding X
Exp Eye Res; 2019 Sep; 186():107720. PubMed ID: 31299183
[TBL] [Abstract][Full Text] [Related]
16. Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy.
Tao T; Xu N; Li J; Li H; Qu J; Yin H; Liang J; Zhao M; Li X; Huang L
Invest Ophthalmol Vis Sci; 2021 Dec; 62(15):4. PubMed ID: 34860240
[TBL] [Abstract][Full Text] [Related]
17. Variable Familial Exudative Vitreoretinopathy in a family harbouring variants in both FZD4 and TSPAN12.
Schatz P; Khan AO
Acta Ophthalmol; 2017 Nov; 95(7):705-709. PubMed ID: 28211206
[TBL] [Abstract][Full Text] [Related]
18. Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.
Zhang L; Yang Y; Li S; Tai Z; Huang L; Liu Y; Zhu X; Di Y; Qu C; Jiang Z; Li Y; Zhang G; Kim R; Sundaresan P; Yang Z; Zhu X
Genet Test Mol Biomarkers; 2016 Jul; 20(7):346-51. PubMed ID: 27228167
[TBL] [Abstract][Full Text] [Related]
19. Genetic Characteristics and Clinical Manifestations of Foveal Hypoplasia in Familial Exudative Vitreoretinopathy.
Ju Y; Zhang L; Gao F; Zong Y; Chen T; Ruan L; Chang Q; Zhang T; Huang X
Am J Ophthalmol; 2024 Jun; 262():73-85. PubMed ID: 38280677
[TBL] [Abstract][Full Text] [Related]
20. Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy.
Huang XY; Zhuang H; Wu JH; Li JK; Hu FY; Zheng Y; Tellier LCAM; Zhang SH; Gao FJ; Zhang JG; Xu GZ
Mol Vis; 2017; 23():605-613. PubMed ID: 28867931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
