These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
220 related articles for article (PubMed ID: 23387289)
1. Insights into keratoconus from a genetic perspective. Burdon KP; Vincent AL Clin Exp Optom; 2013 Mar; 96(2):146-54. PubMed ID: 23387289 [TBL] [Abstract][Full Text] [Related]
2. Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification. Karolak JA; Polakowski P; Szaflik J; Szaflik JP; Gajecka M Ophthalmic Genet; 2016; 37(1):37-43. PubMed ID: 24940934 [TBL] [Abstract][Full Text] [Related]
3. A new perspective on the genetics of keratoconus: why have we not been more successful? Valgaeren H; Koppen C; Van Camp G Ophthalmic Genet; 2018 Apr; 39(2):158-174. PubMed ID: 29111844 [TBL] [Abstract][Full Text] [Related]
4. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation. Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324 [TBL] [Abstract][Full Text] [Related]
5. [Search for genetic markers for precise diagnostics of keratoconus]. Skorodumova LO; Belodedova AV; Sharova EI; Malyugin BE Biomed Khim; 2019 Jan; 65(1):9-20. PubMed ID: 30816092 [TBL] [Abstract][Full Text] [Related]
6. Visual System Homeobox 1 (VSX1) Gene Analysis in Keratoconus: Design of Specific Primers and DNA Amplification Protocols for Accurate Molecular Characterization. Ng JB; Poh RY; Lee KR; Subrayan V; Deva JP; Lau AY; Tan JA Clin Lab; 2016 Sep; 62(9):1731-1737. PubMed ID: 28164597 [TBL] [Abstract][Full Text] [Related]
7. Mutational screening of VSX1, SPARC, SOD1, LOX, and TIMP3 in keratoconus. De Bonis P; Laborante A; Pizzicoli C; Stallone R; Barbano R; Longo C; Mazzilli E; Zelante L; Bisceglia L Mol Vis; 2011; 17():2482-94. PubMed ID: 21976959 [TBL] [Abstract][Full Text] [Related]
8. A comprehensive molecular genetic analysis of keratoconus patients from assam, a northeastern state of India. Chakravarty M; Ponnam SPG; Bardoloi N; Kumar S; Saikia P Eur J Ophthalmol; 2022 May; 32(3):1361-1369. PubMed ID: 35296157 [TBL] [Abstract][Full Text] [Related]
9. Absence of significant genetic alterations in the Lopes AG; de Almeida GC; Miola MP; Teixeira RM; Pires FCBL; Miani RA; de Mattos LC; Brandão CC; Castiglioni L Ophthalmic Genet; 2022 Feb; 43(1):73-79. PubMed ID: 34802378 [TBL] [Abstract][Full Text] [Related]
10. Genetics and clinical characteristics of keratoconus. Stabuc-Silih M; Strazisar M; Ravnik-Glavac M; Hawlina M; Glavac D Acta Dermatovenerol Alp Pannonica Adriat; 2010; 19(2):3-10. PubMed ID: 20664914 [TBL] [Abstract][Full Text] [Related]
11. Genomic strategies to understand causes of keratoconus. Karolak JA; Gajecka M Mol Genet Genomics; 2017 Apr; 292(2):251-269. PubMed ID: 28032277 [TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of VSX1 and SOD1 in Iranian patients with keratoconus. Saee-Rad S; Hashemi H; Miraftab M; Noori-Daloii MR; Chaleshtori MH; Raoofian R; Jafari F; Greene W; Fakhraie G; Rezvan F; Heidari M Mol Vis; 2011; 17():3128-36. PubMed ID: 22171159 [TBL] [Abstract][Full Text] [Related]
13. Polymorphism Analysis of VSX1 and SOD1 Genes in Greek Patients with Keratoconus. Moschos MM; Kokolakis N; Gazouli M; Chatziralli IP; Droutsas D; Anagnou NP; Ladas ID Ophthalmic Genet; 2015; 36(3):213-7. PubMed ID: 24099280 [TBL] [Abstract][Full Text] [Related]
14. Absence of pathogenic mutations in VSX1 and SOD1 genes in patients with keratoconus. Stabuc-Silih M; Strazisar M; Hawlina M; Glavac D Cornea; 2010 Feb; 29(2):172-6. PubMed ID: 20023586 [TBL] [Abstract][Full Text] [Related]
15. VSX1 mutational analysis in a series of Italian patients affected by keratoconus: detection of a novel mutation. Bisceglia L; Ciaschetti M; De Bonis P; Campo PA; Pizzicoli C; Scala C; Grifa M; Ciavarella P; Delle Noci N; Vaira F; Macaluso C; Zelante L Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):39-45. PubMed ID: 15623752 [TBL] [Abstract][Full Text] [Related]
16. VSX1 gene variants are associated with keratoconus in unrelated Korean patients. Mok JW; Baek SJ; Joo CK J Hum Genet; 2008; 53(9):842-849. PubMed ID: 18626569 [TBL] [Abstract][Full Text] [Related]
17. The Genetics of Keratoconus: A Review. Wheeler J; Hauser MA; Afshari NA; Allingham RR; Liu Y Reprod Syst Sex Disord; 2012 Jun; (Suppl 6):. PubMed ID: 23795306 [TBL] [Abstract][Full Text] [Related]
18. Screening the visual system homeobox 1 gene in keratoconus and posterior polymorphous dystrophy cohorts identifies a novel variant. Vincent AL; Jordan C; Sheck L; Niederer R; Patel DV; McGhee CN Mol Vis; 2013; 19():852-60. PubMed ID: 23592923 [TBL] [Abstract][Full Text] [Related]
19. Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32. Gajecka M; Radhakrishna U; Winters D; Nath SK; Rydzanicz M; Ratnamala U; Ewing K; Molinari A; Pitarque JA; Lee K; Leal SM; Bejjani BA Invest Ophthalmol Vis Sci; 2009 Apr; 50(4):1531-9. PubMed ID: 19011015 [TBL] [Abstract][Full Text] [Related]
20. Rare, potentially pathogenic variants in 21 keratoconus candidate genes are not enriched in cases in a large Australian cohort of European descent. Lucas SEM; Zhou T; Blackburn NB; Mills RA; Ellis J; Leo P; Souzeau E; Ridge B; Charlesworth JC; Lindsay R; Craig JE; Burdon KP PLoS One; 2018; 13(6):e0199178. PubMed ID: 29924831 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]