430 related articles for article (PubMed ID: 25525168)
1. Detection of mutations in LRPAP1, CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2 in 298 families with early-onset high myopia by exome sequencing.
Jiang D; Li J; Xiao X; Li S; Jia X; Sun W; Guo X; Zhang Q
Invest Ophthalmol Vis Sci; 2014 Dec; 56(1):339-45. PubMed ID: 25525168
[TBL] [Abstract][Full Text] [Related]
2. Mutational screening of SLC39A5, LEPREL1 and LRPAP1 in a cohort of 187 high myopia patients.
Feng CY; Huang XQ; Cheng XW; Wu RH; Lu F; Jin ZB
Sci Rep; 2017 Apr; 7(1):1120. PubMed ID: 28442722
[TBL] [Abstract][Full Text] [Related]
3. Mutation screening of 17 candidate genes in a cohort of 67 probands with early-onset high myopia.
Liu F; Wang J; Xing Y; Li T
Ophthalmic Physiol Opt; 2020 May; 40(3):271-280. PubMed ID: 32215939
[TBL] [Abstract][Full Text] [Related]
4. Mutational screening of
Zheng YH; Cai XB; Xia LQ; Zhou FY; Wen XR; Chen DF; Han F; Zhou KJ; Jin ZB; Zhuang WJ; Lin B
Mol Vis; 2021; 27():706-717. PubMed ID: 35002215
[TBL] [Abstract][Full Text] [Related]
5. Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China.
Ye M; Ma Y; Qin YX; Cai B; Ma LM; Ma Z; Liu Y; Jin ZB; Zhuang WJ
Mol Genet Genomics; 2023 May; 298(3):669-682. PubMed ID: 36964802
[TBL] [Abstract][Full Text] [Related]
6. Association between SCO2 mutation and extreme myopia in Japanese patients.
Wakazono T; Miyake M; Yamashiro K; Yoshikawa M; Yoshimura N
Jpn J Ophthalmol; 2016 Jul; 60(4):319-25. PubMed ID: 27052445
[TBL] [Abstract][Full Text] [Related]
7. Mutations in LRPAP1 are associated with severe myopia in humans.
Aldahmesh MA; Khan AO; Alkuraya H; Adly N; Anazi S; Al-Saleh AA; Mohamed JY; Hijazi H; Prabakaran S; Tacke M; Al-Khrashi A; Hashem M; Reinheckel T; Assiri A; Alkuraya FS
Am J Hum Genet; 2013 Aug; 93(2):313-20. PubMed ID: 23830514
[TBL] [Abstract][Full Text] [Related]
8. Novel mutations of the X-linked genes associated with early-onset high myopia in five Chinese families.
Zi F; Li Z; Cheng W; Huang X; Sheng X; Rong W
BMC Med Genomics; 2023 Sep; 16(1):223. PubMed ID: 37749571
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing identifies ZNF644 mutations in high myopia.
Shi Y; Li Y; Zhang D; Zhang H; Li Y; Lu F; Liu X; He F; Gong B; Cai L; Li R; Liao S; Ma S; Lin H; Cheng J; Zheng H; Shan Y; Chen B; Hu J; Jin X; Zhao P; Chen Y; Zhang Y; Lin Y; Li X; Fan Y; Yang H; Wang J; Yang Z
PLoS Genet; 2011 Jun; 7(6):e1002084. PubMed ID: 21695231
[TBL] [Abstract][Full Text] [Related]
10. New ZNF644 mutations identified in patients with high myopia.
Xiang X; Wang T; Tong P; Li Y; Guo H; Wan A; Xia L; Liu Y; Li Y; Tian Q; Shen L; Cai X; Tian L; Jin X; Xia K; Hu Z
Mol Vis; 2014; 20():939-46. PubMed ID: 24991186
[TBL] [Abstract][Full Text] [Related]
11. SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia.
Guo H; Jin X; Zhu T; Wang T; Tong P; Tian L; Peng Y; Sun L; Wan A; Chen J; Liu Y; Li Y; Tian Q; Xia L; Zhang L; Pan Y; Lu L; Liu Q; Shen L; Li Y; Xiong W; Li J; Tang B; Feng Y; Zhang X; Zhang Z; Pan Q; Hu Z; Xia K
J Med Genet; 2014 Aug; 51(8):518-25. PubMed ID: 24891338
[TBL] [Abstract][Full Text] [Related]
12. Evaluation of 12 myopia-associated genes in Chinese patients with high myopia.
Li J; Jiang D; Xiao X; Li S; Jia X; Sun W; Guo X; Zhang Q
Invest Ophthalmol Vis Sci; 2015 Jan; 56(2):722-9. PubMed ID: 25587058
[TBL] [Abstract][Full Text] [Related]
13. Exome Sequence Analysis of 14 Families With High Myopia.
Kloss BA; Tompson SW; Whisenhunt KN; Quow KL; Huang SJ; Pavelec DM; Rosenberg T; Young TL
Invest Ophthalmol Vis Sci; 2017 Apr; 58(4):1982-1990. PubMed ID: 28384719
[TBL] [Abstract][Full Text] [Related]
14. A novel deep intronic COL2A1 mutation in a family with early-onset high myopia/ocular-only Stickler syndrome.
Sun W; Xiao X; Li S; Jia X; Zhang Q
Ophthalmic Physiol Opt; 2020 May; 40(3):281-288. PubMed ID: 32196734
[TBL] [Abstract][Full Text] [Related]
15. The Genetic Confirmation and Clinical Characterization of LOXL3-Associated MYP28: A Common Type of Recessive Extreme High Myopia.
Jiang Y; Zhou L; Wang Y; Ouyang J; Li S; Xiao X; Jia X; Wang J; Yi Z; Sun W; Jiao X; Wang P; Hejtmancik JF; Zhang Q
Invest Ophthalmol Vis Sci; 2023 Mar; 64(3):14. PubMed ID: 36917121
[TBL] [Abstract][Full Text] [Related]
16. Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia.
Yang E; Yu J; Liu X; Chu H; Li L
Invest Ophthalmol Vis Sci; 2023 May; 64(5):10. PubMed ID: 37191617
[TBL] [Abstract][Full Text] [Related]
17. X-linked heterozygous mutations in
Xiao X; Li S; Jia X; Guo X; Zhang Q
Mol Vis; 2016; 22():1257-1266. PubMed ID: 27829781
[TBL] [Abstract][Full Text] [Related]
18. Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes.
Sun W; Huang L; Xu Y; Xiao X; Li S; Jia X; Gao B; Wang P; Guo X; Zhang Q
Invest Ophthalmol Vis Sci; 2015 Dec; 56(13):8365-72. PubMed ID: 26747767
[TBL] [Abstract][Full Text] [Related]
19. Exome sequencing identified null mutations in LOXL3 associated with early-onset high myopia.
Li J; Gao B; Xiao X; Li S; Jia X; Sun W; Guo X; Zhang Q
Mol Vis; 2016; 22():161-7. PubMed ID: 26957899
[TBL] [Abstract][Full Text] [Related]
20. Homozygous loss-of-function mutation of the LEPREL1 gene causes severe non-syndromic high myopia with early-onset cataract.
Guo H; Tong P; Peng Y; Wang T; Liu Y; Chen J; Li Y; Tian Q; Hu Y; Zheng Y; Xiao L; Xiong W; Pan Q; Hu Z; Xia K
Clin Genet; 2014 Dec; 86(6):575-9. PubMed ID: 24172257
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
