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.
142 related articles for article (PubMed ID: 20360993)
1. Candidate gene study to investigate the genetic determinants of normal variation in central corneal thickness. Dimasi DP; Burdon KP; Hewitt AW; Savarirayan R; Healey PR; Mitchell P; Mackey DA; Craig JE Mol Vis; 2010 Mar; 16():562-9. PubMed ID: 20360993 [TBL] [Abstract][Full Text] [Related]
2. Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. Iglesias AI; Mishra A; Vitart V; Bykhovskaya Y; Höhn R; Springelkamp H; Cuellar-Partida G; Gharahkhani P; Bailey JNC; Willoughby CE; Li X; Yazar S; Nag A; Khawaja AP; Polašek O; Siscovick D; Mitchell P; Tham YC; Haines JL; Kearns LS; Hayward C; Shi Y; van Leeuwen EM; Taylor KD; ; Bonnemaijer P; Rotter JI; Martin NG; Zeller T; Mills RA; Souzeau E; Staffieri SE; Jonas JB; Schmidtmann I; Boutin T; Kang JH; Lucas SEM; Wong TY; Beutel ME; Wilson JF; ; ; Uitterlinden AG; Vithana EN; Foster PJ; Hysi PG; Hewitt AW; Khor CC; Pasquale LR; Montgomery GW; Klaver CCW; Aung T; Pfeiffer N; Mackey DA; Hammond CJ; Cheng CY; Craig JE; Rabinowitz YS; Wiggs JL; Burdon KP; van Duijn CM; MacGregor S Nat Commun; 2018 May; 9(1):1864. PubMed ID: 29760442 [TBL] [Abstract][Full Text] [Related]
3. Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes. Dimasi DP; Chen JY; Hewitt AW; Klebe S; Davey R; Stirling J; Thompson E; Forbes R; Tan TY; Savarirayan R; Mackey DA; Healey PR; Mitchell P; Burdon KP; Craig JE Hum Genet; 2010 Jan; 127(1):33-44. PubMed ID: 19714363 [TBL] [Abstract][Full Text] [Related]
4. The effect of haplotype variation in the bovine PAX6 gene. Huang YZ; Jing YJ; Wei TB; Lan XY; Lei CZ; Zhang CL; Chen H Mol Biol Rep; 2013 Dec; 40(12):6775-84. PubMed ID: 24072657 [TBL] [Abstract][Full Text] [Related]
5. PAX6 haplotypes are associated with high myopia in Han chinese. Jiang B; Yap MK; Leung KH; Ng PW; Fung WY; Lam WW; Gu YS; Yip SP PLoS One; 2011 May; 6(5):e19587. PubMed ID: 21589860 [TBL] [Abstract][Full Text] [Related]
6. Association of PAX6 polymorphisms with high myopia in Han Chinese nuclear families. Han W; Leung KH; Fung WY; Mak JY; Li YM; Yap MK; Yip SP Invest Ophthalmol Vis Sci; 2009 Jan; 50(1):47-56. PubMed ID: 19124844 [TBL] [Abstract][Full Text] [Related]
7. Ten SNPs of PAX6, Lumican, and MYOC genes are not associated with high myopia in Han Chinese. Dai L; Li Y; Du CY; Gong LM; Han CC; Li XG; Fan P; Fu SB Ophthalmic Genet; 2012 Sep; 33(3):171-8. PubMed ID: 22809227 [TBL] [Abstract][Full Text] [Related]
8. Exploring functional candidate genes for genetic association in german patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma. Krumbiegel M; Pasutto F; Mardin CY; Weisschuh N; Paoli D; Gramer E; Zenkel M; Weber BH; Kruse FE; Schlötzer-Schrehardt U; Reis A Invest Ophthalmol Vis Sci; 2009 Jun; 50(6):2796-801. PubMed ID: 19182256 [TBL] [Abstract][Full Text] [Related]
9. Association study of common variations of FBN1 gene and essential hypertension in Han Chinese population. Chen J; Yang S; Zhao X; Shen J; Wang H; Chen Y; Ji Y; Wang W; Zhou W; Wang X; Tang J; Lu X; Chen S; Wang L; Li H; Shen C; Zhao Y Mol Biol Rep; 2014; 41(4):2257-64. PubMed ID: 24413999 [TBL] [Abstract][Full Text] [Related]
10. A functional polymorphism at 3'UTR of the PAX6 gene may confer risk for extreme myopia in the Chinese. Liang CL; Hsi E; Chen KC; Pan YR; Wang YS; Juo SH Invest Ophthalmol Vis Sci; 2011 Jun; 52(6):3500-5. PubMed ID: 21421876 [TBL] [Abstract][Full Text] [Related]
11. Novel genetic variation in exon 28 of FBN1 gene is associated with essential hypertension. Shen C; Lu X; Wang L; Chen S; Li Y; Liu X; Li J; Huang J; Gu D Am J Hypertens; 2011 Jun; 24(6):687-93. PubMed ID: 21331051 [TBL] [Abstract][Full Text] [Related]
13. Association of paired box 6 with high myopia in Japanese. Miyake M; Yamashiro K; Nakanishi H; Nakata I; Akagi-Kurashige Y; Tsujikawa A; Moriyama M; Ohno-Matsui K; Mochizuki M; Yamada R; Matsuda F; Yoshimura N Mol Vis; 2012; 18():2726-35. PubMed ID: 23213273 [TBL] [Abstract][Full Text] [Related]
14. Association of fibrillin 1 single-nucleotide polymorphism haplotypes with systemic sclerosis in Choctaw and Japanese populations. Tan FK; Wang N; Kuwana M; Chakraborty R; Bona CA; Milewicz DM; Arnett FC Arthritis Rheum; 2001 Apr; 44(4):893-901. PubMed ID: 11315929 [TBL] [Abstract][Full Text] [Related]
15. Population-based meta-analysis in Caucasians confirms association with COL5A1 and ZNF469 but not COL8A2 with central corneal thickness. Hoehn R; Zeller T; Verhoeven VJ; Grus F; Adler M; Wolfs RC; Uitterlinden AG; Castagne R; Schillert A; Klaver CC; Pfeiffer N; Mirshahi A Hum Genet; 2012 Nov; 131(11):1783-93. PubMed ID: 22814818 [TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant cornea plana is not associated with pathogenic mutations in DCN, DSPG3, FOXC1, KERA, LUM, or PITX2. Aldave AJ; Sonmez B; Bourla N; Schultz G; Papp JC; Salem AK; Rayner SA; Yellore VS Ophthalmic Genet; 2007 Jun; 28(2):57-67. PubMed ID: 17558846 [TBL] [Abstract][Full Text] [Related]
17. A genetic epidemiologic study of candidate genes involved in the optic nerve head morphology. Gasten AC; Ramdas WD; Broer L; van Koolwijk LM; Ikram MK; de Jong PT; Aulchenko YS; Wolfs RC; Hofman A; Rivadeneira F; Uitterlinden AG; Oostra BA; Lemij HG; Klaver CC; Jansonius NM; Vingerling JR; van Duijn CM Invest Ophthalmol Vis Sci; 2012 Mar; 53(3):1485-91. PubMed ID: 22266513 [TBL] [Abstract][Full Text] [Related]
18. PAX6 gene associated with high myopia: a meta-analysis. Tang SM; Rong SS; Young AL; Tam PO; Pang CP; Chen LJ Optom Vis Sci; 2014 Apr; 91(4):419-29. PubMed ID: 24637479 [TBL] [Abstract][Full Text] [Related]