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Items: 1 to 20 of 85

1.

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. doi: 10.1007/s00439-012-1201-3. Epub 2012 Jul 20.

PMID:
22814818
2.

Collagen-related genes influence the glaucoma risk factor, central corneal thickness.

Vithana EN, Aung T, Khor CC, Cornes BK, Tay WT, Sim X, Lavanya R, Wu R, Zheng Y, Hibberd ML, Chia KS, Seielstad M, Goh LK, Saw SM, Tai ES, Wong TY.

Hum Mol Genet. 2011 Feb 15;20(4):649-58. doi: 10.1093/hmg/ddq511. Epub 2010 Nov 23.

PMID:
21098505
3.

Distribution of COL8A2 and COL8A1 gene variants in Caucasian primary open angle glaucoma patients with thin central corneal thickness.

Desronvil T, Logan-Wyatt D, Abdrabou W, Triana M, Jones R, Taheri S, Del Bono E, Pasquale LR, Olivier M, Haines JL, Fan BJ, Wiggs JL.

Mol Vis. 2010 Oct 29;16:2185-91.

4.

A genome-wide association study of central corneal thickness in Latinos.

Gao X, Gauderman WJ, Liu Y, Marjoram P, Torres M, Haritunians T, Kuo JZ, Chen YD, Allingham RR, Hauser MA, Taylor KD, Rotter JI, Varma R.

Invest Ophthalmol Vis Sci. 2013 Apr 1;54(4):2435-43. doi: 10.1167/iovs.13-11692.

5.

New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8.

Vitart V, Bencić G, Hayward C, Skunca Herman J, Huffman J, Campbell S, Bućan K, Navarro P, Gunjaca G, Marin J, Zgaga L, Kolcić I, Polasek O, Kirin M, Hastie ND, Wilson JF, Rudan I, Campbell H, Vatavuk Z, Fleck B, Wright A.

Hum Mol Genet. 2010 Nov 1;19(21):4304-11. doi: 10.1093/hmg/ddq349. Epub 2010 Aug 18.

PMID:
20719862
6.

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. doi: 10.1007/s00439-009-0729-3. Epub 2009 Aug 28.

PMID:
19714363
7.

Genome-wide analysis of central corneal thickness in primary open-angle glaucoma cases in the NEIGHBOR and GLAUGEN consortia.

Ulmer M, Li J, Yaspan BL, Ozel AB, Richards JE, Moroi SE, Hawthorne F, Budenz DL, Friedman DS, Gaasterland D, Haines J, Kang JH, Lee R, Lichter P, Liu Y, Pasquale LR, Pericak-Vance M, Realini A, Schuman JS, Singh K, Vollrath D, Weinreb R, Wollstein G, Zack DJ, Zhang K, Young T, Allingham RR, Wiggs JL, Ashley-Koch A, Hauser MA.

Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4468-74. doi: 10.1167/iovs.12-9784.

8.

Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.

Igo RP Jr, Kopplin LJ, Joseph P, Truitt B, Fondran J, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser M, Lass JH, Iyengar SK; FECD Genetics Multi-center Study Group.

PLoS One. 2012;7(10):e46742. doi: 10.1371/journal.pone.0046742. Epub 2012 Oct 23.

9.

Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations.

Cornes BK, Khor CC, Nongpiur ME, Xu L, Tay WT, Zheng Y, Lavanya R, Li Y, Wu R, Sim X, Wang YX, Chen P, Teo YY, Chia KS, Seielstad M, Liu J, Hibberd ML, Cheng CY, Saw SM, Tai ES, Jonas JB, Vithana EN, Wong TY, Aung T.

Hum Mol Genet. 2012 Jan 15;21(2):437-45. doi: 10.1093/hmg/ddr463. Epub 2011 Oct 7. Erratum in: Hum Mol Genet. 2012 Oct 1;21(19):4365.

PMID:
21984434
10.

Genetic association of COL5A1 variants in keratoconus patients suggests a complex connection between corneal thinning and keratoconus.

Li X, Bykhovskaya Y, Canedo AL, Haritunians T, Siscovick D, Aldave AJ, Szczotka-Flynn L, Iyengar SK, Rotter JI, Taylor KD, Rabinowitz YS.

Invest Ophthalmol Vis Sci. 2013 Apr 12;54(4):2696-704. doi: 10.1167/iovs.13-11601.

11.

Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness.

Lu Y, Dimasi DP, Hysi PG, Hewitt AW, Burdon KP, Toh T, Ruddle JB, Li YJ, Mitchell P, Healey PR, Montgomery GW, Hansell N, Spector TD, Martin NG, Young TL, Hammond CJ, Macgregor S, Craig JE, Mackey DA.

PLoS Genet. 2010 May 13;6(5):e1000947. doi: 10.1371/journal.pgen.1000947.

12.

Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian population.

Sahebjada S, Schache M, Richardson AJ, Snibson G, MacGregor S, Daniell M, Baird PN.

Invest Ophthalmol Vis Sci. 2013 Dec 17;54(13):8224-8. doi: 10.1167/iovs.13-12982.

PMID:
24265017
13.

Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area.

Khor CC, Ramdas WD, Vithana EN, Cornes BK, Sim X, Tay WT, Saw SM, Zheng Y, Lavanya R, Wu R, Wang JJ, Mitchell P, Uitterlinden AG, Rivadeneira F, Teo YY, Chia KS, Seielstad M, Hibberd M, Vingerling JR, Klaver CC, Jansonius NM, Tai ES, Wong TY, van Duijn CM, Aung T.

Hum Mol Genet. 2011 May 1;20(9):1864-72. doi: 10.1093/hmg/ddr060. Epub 2011 Feb 9.

PMID:
21307088
14.

Central corneal thickness and glaucoma in East Asian people.

Day AC, Machin D, Aung T, Gazzard G, Husain R, Chew PT, Khaw PT, Seah SK, Foster PJ.

Invest Ophthalmol Vis Sci. 2011 Oct 28;52(11):8407-12. doi: 10.1167/iovs.11-7927.

PMID:
21917940
15.

Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population.

Axenovich T, Zorkoltseva I, Belonogova N, van Koolwijk LM, Borodin P, Kirichenko A, Babenko V, Ramdas WD, Amin N, Despriet DD, Vingerling JR, Lemij HG, Oostra BA, Klaver CC, Aulchenko Y, van Duijn CM.

J Med Genet. 2011 Dec;48(12):802-9. doi: 10.1136/jmedgenet-2011-100436. Epub 2011 Nov 5. Erratum in: J Med Genet. 2012 Mar;49(3):220. van Koolwijk, Leonike [corrected to van Koolwijk, Leonike M E]; Ramdas, Wishal [corrected to Ramdas, Wishal D]; Despriet, Dominiec [corrected to Despriet, Dominiec D G];Vingerling, Johannes [corrected to Vingerling, Johannes R]; Lemij, Hans [corrected to Lemij, Hans G]; Klaver, Caroline [corrected to Klaver, Caroline C W];Aulchenko, Yurii [corrected to Aulchenko, Yurii S]; van Duijn, Cornelia [corrected to van Duijn, Cornelia M].

PMID:
22058429
16.

Intraocular pressure, central corneal thickness, and glaucoma in chinese adults: the liwan eye study.

Wang D, Huang W, Li Y, Zheng Y, Foster PJ, Congdon N, He M.

Am J Ophthalmol. 2011 Sep;152(3):454-462.e1. doi: 10.1016/j.ajo.2011.03.005. Epub 2011 Jun 16.

PMID:
21679915
17.

Replication study of the association of SNPs in the LHX3-QSOX2 and IGF1 loci with adult height in the Japanese population; wide-ranging comparison of each SNP genotype distribution.

Fujihara J, Takeshita H, Kimura-Kataoka K, Yuasa I, Iida R, Ueki M, Nagao M, Kominato Y, Yasuda T.

Leg Med (Tokyo). 2012 Jul;14(4):205-8. doi: 10.1016/j.legalmed.2012.02.001. Epub 2012 Apr 12.

PMID:
22503243
18.

A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.

Osman W, Low SK, Takahashi A, Kubo M, Nakamura Y.

Hum Mol Genet. 2012 Jun 15;21(12):2836-42. doi: 10.1093/hmg/dds103. Epub 2012 Mar 13.

PMID:
22419738
19.

Mutations in the zinc finger protein gene, ZNF469, contribute to the pathogenesis of keratoconus.

Vincent AL, Jordan CA, Cadzow MJ, Merriman TR, McGhee CN.

Invest Ophthalmol Vis Sci. 2014 Aug 5;55(9):5629-35. doi: 10.1167/iovs.14-14532.

PMID:
25097247
20.

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