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.
237 related articles for article (PubMed ID: 21998696)
1. Influence of ROBO1 and RORA on risk of age-related macular degeneration reveals genetically distinct phenotypes in disease pathophysiology. Jun G; Nicolaou M; Morrison MA; Buros J; Morgan DJ; Radeke MJ; Yonekawa Y; Tsironi EE; Kotoula MG; Zacharaki F; Mollema N; Yuan Y; Miller JW; Haider NB; Hageman GS; Kim IK; Schaumberg DA; Farrer LA; DeAngelis MM PLoS One; 2011; 6(10):e25775. PubMed ID: 21998696 [TBL] [Abstract][Full Text] [Related]
2. Prospective study of common variants in the retinoic acid receptor-related orphan receptor α gene and risk of neovascular age-related macular degeneration. Schaumberg DA; Chasman D; Morrison MA; Adams SM; Guo Q; Hunter DJ; Hankinson SE; DeAngelis MM Arch Ophthalmol; 2010 Nov; 128(11):1462-71. PubMed ID: 21060049 [TBL] [Abstract][Full Text] [Related]
3. Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: a systems biology based approach. Silveira AC; Morrison MA; Ji F; Xu H; Reinecke JB; Adams SM; Arneberg TM; Janssian M; Lee JE; Yuan Y; Schaumberg DA; Kotoula MG; Tsironi EE; Tsiloulis AN; Chatzoulis DZ; Miller JW; Kim IK; Hageman GS; Farrer LA; Haider NB; DeAngelis MM Vision Res; 2010 Mar; 50(7):698-715. PubMed ID: 19786043 [TBL] [Abstract][Full Text] [Related]
4. Metallothionein polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration. García M; Álvarez L; Fernández Á; González-Iglesias H; Escribano J; Fernández-Vega B; Villota E; Fernández-Vega Cueto L; Fernández-Vega Á; Coca-Prados M Ophthalmic Genet; 2017; 38(5):451-458. PubMed ID: 28635422 [TBL] [Abstract][Full Text] [Related]
5. CFH polymorphisms in a Northern Spanish population with neovascular and dry forms of age-related macular degeneration. García M; Álvarez L; Nogacka AM; González-Iglesias H; Escribano J; Fernández-Vega B; Fernández-Vega Á; Fernández-Vega L; Coca-Prados M Acta Ophthalmol; 2015 Dec; 93(8):e658-66. PubMed ID: 26152901 [TBL] [Abstract][Full Text] [Related]
6. Association between polymorphisms of the DNA base excision repair genes MUTYH and hOGG1 and age-related macular degeneration. Synowiec E; Blasiak J; Zaras M; Szaflik J; Szaflik JP Exp Eye Res; 2012 May; 98():58-66. PubMed ID: 22469746 [TBL] [Abstract][Full Text] [Related]
7. Retinoic acid related orphan receptor α is a genetic modifier that rescues retinal degeneration in a mouse model of Stargardt disease and Dry AMD. Akula M; McNamee SM; Love Z; Nasraty N; Chan NPM; Whalen M; Avola MO; Olivares AM; Leehy BD; Jelcick AS; Singh P; Upadhyay AK; Chen DF; Haider NB Gene Ther; 2024 Jul; 31(7-8):413-421. PubMed ID: 38755404 [TBL] [Abstract][Full Text] [Related]
8. [Genetic and risk factors for exudative AMD]. Dietzel M; Farwick A; Hense HW Ophthalmologe; 2010 Dec; 107(12):1103-8. PubMed ID: 20878164 [TBL] [Abstract][Full Text] [Related]
9. Rare Genetic Variants Associated With Development of Age-Related Macular Degeneration. Saksens NT; Geerlings MJ; Bakker B; Schick T; Daha MR; Fauser S; Boon CJ; de Jong EK; Hoyng CB; den Hollander AI JAMA Ophthalmol; 2016 Mar; 134(3):287-93. PubMed ID: 26767664 [TBL] [Abstract][Full Text] [Related]
10. Association of C-Reactive Protein Genetic Polymorphisms With Late Age-Related Macular Degeneration. Cipriani V; Hogg RE; Sofat R; Moore AT; Webster AR; Yates JRW; Fletcher AE; JAMA Ophthalmol; 2017 Sep; 135(9):909-916. PubMed ID: 28750115 [TBL] [Abstract][Full Text] [Related]
11. Association of polymorphisms in complement component 3 with age-related macular degeneration in an Iranian population. Bonyadi M; Mohammadian T; Jabbarpoor Bonyadi MH; Fotouhi N; Soheilian M; Javadzadeh A; Moein H; Yaseri M Ophthalmic Genet; 2017; 38(1):61-66. PubMed ID: 27029644 [TBL] [Abstract][Full Text] [Related]
12. Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes. Sobrin L; Ripke S; Yu Y; Fagerness J; Bhangale TR; Tan PL; Souied EH; Buitendijk GH; Merriam JE; Richardson AJ; Raychaudhuri S; Reynolds R; Chin KA; Lee AY; Leveziel N; Zack DJ; Campochiaro P; Smith RT; Barile GR; Hogg RE; Chakravarthy U; Behrens TW; Uitterlinden AG; van Duijn CM; Vingerling JR; Brantley MA; Baird PN; Klaver CC; Allikmets R; Katsanis N; Graham RR; Ioannidis JP; Daly MJ; Seddon JM Ophthalmology; 2012 Sep; 119(9):1874-85. PubMed ID: 22705344 [TBL] [Abstract][Full Text] [Related]
13. Influence of TIMP3/SYN3 polymorphisms on the phenotypic presentation of age-related macular degeneration. Ardeljan D; Meyerle CB; Agron E; Wang JJ; Mitchell P; Chew EY; Zhao J; Maminishkis A; Chan CC; Tuo J Eur J Hum Genet; 2013 Oct; 21(10):1152-7. PubMed ID: 23422939 [TBL] [Abstract][Full Text] [Related]
14. HIF1A as a major vascular endothelial growth factor regulator: do its polymorphisms have an association with age-related macular degeneration? Okur V; Cetin O; Cetin E; Tepeli E; Bulgu Y; Yildirim C Clin Exp Ophthalmol; 2015; 43(1):47-53. PubMed ID: 24995509 [TBL] [Abstract][Full Text] [Related]
15. Single nucleotide polymorphism in the cholesterol-24S-hydroxylase (CYP46A1) gene and its association with CFH and LOC387715 gene polymorphisms in age-related macular degeneration. Fourgeux C; Dugas B; Richard F; Björkhem I; Acar N; Bron AM; Korobelnik JF; Leveziel N; Zerbib J; Puche N; Creuzot-Garcher CP; Souied E; Bretillon L Invest Ophthalmol Vis Sci; 2012 Oct; 53(11):7026-33. PubMed ID: 22977134 [TBL] [Abstract][Full Text] [Related]
16. Reliability and diagnostic performance of a novel mobile app for hyperacuity self-monitoring in patients with age-related macular degeneration. Schmid MK; Thiel MA; Lienhard K; Schlingemann RO; Faes L; Bachmann LM Eye (Lond); 2019 Oct; 33(10):1584-1589. PubMed ID: 31043690 [TBL] [Abstract][Full Text] [Related]
17. Genetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficits. Bates TC; Luciano M; Medland SE; Montgomery GW; Wright MJ; Martin NG Behav Genet; 2011 Jan; 41(1):50-7. PubMed ID: 20949370 [TBL] [Abstract][Full Text] [Related]