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Items: 1 to 20 of 65

1.

Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism.

Fan Q, Zhou X, Khor CC, Cheng CY, Goh LK, Sim X, Tay WT, Li YJ, Ong RT, Suo C, Cornes B, Ikram MK, Chia KS, Seielstad M, Liu J, Vithana E, Young TL, Tai ES, Wong TY, Aung T, Teo YY, Saw SM.

PLoS Genet. 2011 Dec;7(12):e1002402. doi: 10.1371/journal.pgen.1002402. Epub 2011 Dec 1.

2.

Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore.

Han S, Chen P, Fan Q, Khor CC, Sim X, Tay WT, Ong RT, Suo C, Goh LK, Lavanya R, Zheng Y, Wu R, Seielstad M, Vithana E, Liu J, Chia KS, Lee JJ, Tai ES, Wong TY, Aung T, Teo YY, Saw SM.

Hum Mol Genet. 2011 Sep 15;20(18):3693-8. doi: 10.1093/hmg/ddr269. Epub 2011 Jun 10.

3.

A genome-wide association study for corneal curvature identifies the platelet-derived growth factor receptor α gene as a quantitative trait locus for eye size in white Europeans.

Guggenheim JA, McMahon G, Kemp JP, Akhtar S, St Pourcain B, Northstone K, Ring SM, Evans DM, Smith GD, Timpson NJ, Williams C.

Mol Vis. 2013;19:243-53. Epub 2013 Jan 3.

4.

Interrogation of the platelet-derived growth factor receptor alpha locus and corneal astigmatism in Australians of Northern European ancestry: results of a genome-wide association study.

Yazar S, Mishra A, Ang W, Kearns LS, Mountain JA, Pennell C, Montgomery GW, Young TL, Hammond CJ, Macgregor S, Mackey DA, Hewitt AW.

Mol Vis. 2013 Jun 6;19:1238-46. Print 2013.

5.

Genetic variants near PDGFRA are associated with corneal curvature in Australians.

Mishra A, Yazar S, Hewitt AW, Mountain JA, Ang W, Pennell CE, Martin NG, Montgomery GW, Hammond CJ, Young TL, Macgregor S, Mackey DA.

Invest Ophthalmol Vis Sci. 2012 Oct 11;53(11):7131-6. doi: 10.1167/iovs.12-10489.

6.

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Li Q, Wojciechowski R, Simpson CL, Hysi PG, Verhoeven VJ, Ikram MK, Höhn R, Vitart V, Hewitt AW, Oexle K, Mäkelä KM, MacGregor S, Pirastu M, Fan Q, Cheng CY, St Pourcain B, McMahon G, Kemp JP, Northstone K, Rahi JS, Cumberland PM, Martin NG, Sanfilippo PG, Lu Y, Wang YX, Hayward C, Polašek O, Campbell H, Bencic G, Wright AF, Wedenoja J, Zeller T, Schillert A, Mirshahi A, Lackner K, Yip SP, Yap MK, Ried JS, Gieger C, Murgia F, Wilson JF, Fleck B, Yazar S, Vingerling JR, Hofman A, Uitterlinden A, Rivadeneira F, Amin N, Karssen L, Oostra BA, Zhou X, Teo YY, Tai ES, Vithana E, Barathi V, Zheng Y, Siantar RG, Neelam K, Shin Y, Lam J, Yonova-Doing E, Venturini C, Hosseini SM, Wong HS, Lehtimäki T, Kähönen M, Raitakari O, Timpson NJ, Evans DM, Khor CC, Aung T, Young TL, Mitchell P, Klein B, van Duijn CM, Meitinger T, Jonas JB, Baird PN, Mackey DA, Wong TY, Saw SM, Pärssinen O, Stambolian D, Hammond CJ, Klaver CC, Williams C, Paterson AD, Bailey-Wilson JE, Guggenheim JA; CREAM Consortium.

Hum Genet. 2015 Feb;134(2):131-46. doi: 10.1007/s00439-014-1500-y. Epub 2014 Nov 4.

7.

CMPK1 and RBP3 are associated with corneal curvature in Asian populations.

Chen P, Miyake M, Fan Q, Liao J, Yamashiro K, Ikram MK, Chew M, Vithana EN, Khor CC, Aung T, Tai ES, Wong TY, Teo YY, Yoshimura N, Saw SM, Cheng CY.

Hum Mol Genet. 2014 Nov 15;23(22):6129-36. doi: 10.1093/hmg/ddu322. Epub 2014 Jun 24.

8.

Identification of a candidate gene for astigmatism.

Lopes MC, Hysi PG, Verhoeven VJ, Macgregor S, Hewitt AW, Montgomery GW, Cumberland P, Vingerling JR, Young TL, van Duijn CM, Oostra B, Uitterlinden AG, Rahi JS, Mackey DA, Klaver CC, Andrew T, Hammond CJ.

Invest Ophthalmol Vis Sci. 2013 Feb 1;54(2):1260-7. doi: 10.1167/iovs.12-10463.

9.

The genetic effect on refractive error and anterior corneal aberration: twin eye study.

Yeh LK, Chiu CJ, Fong CF, Wang IJ, Chen WL, Hsiao CK, Huang SC, Shih YF, Hu FR, Lin LL.

J Refract Surg. 2007 Mar;23(3):257-65.

PMID:
17385291
10.

Corneal power and astigmatism in Down syndrome.

Little JA, Woodhouse JM, Saunders KJ.

Optom Vis Sci. 2009 Jun;86(6):748-54. doi: 10.1097/OPX.0b013e3181a59d5d.

PMID:
19390470
11.

Dominant genetic effects on corneal astigmatism: the genes in myopia (GEM) twin study.

Dirani M, Islam A, Shekar SN, Baird PN.

Invest Ophthalmol Vis Sci. 2008 Apr;49(4):1339-44. doi: 10.1167/iovs.07-1011.

PMID:
18385047
12.

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.

13.

Visual outcome in corneal grafts: a preliminary analysis of the Swedish Corneal Transplant Register.

Claesson M, Armitage WJ, Fagerholm P, Stenevi U.

Br J Ophthalmol. 2002 Feb;86(2):174-80.

14.

Coordinated genetic scaling of the human eye: shared determination of axial eye length and corneal curvature.

Guggenheim JA, Zhou X, Evans DM, Timpson NJ, McMahon G, Kemp JP, St Pourcain B, Northstone K, Ring SM, Fan Q, Wong TY, Cheng CY, Khor CC, Aung T, Saw SM, Williams C.

Invest Ophthalmol Vis Sci. 2013 Mar 7;54(3):1715-21. doi: 10.1167/iovs.12-10560.

15.

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Stambolian D, Wojciechowski R, Oexle K, Pirastu M, Li X, Raffel LJ, Cotch MF, Chew EY, Klein B, Klein R, Wong TY, Simpson CL, Klaver CC, van Duijn CM, Verhoeven VJ, Baird PN, Vitart V, Paterson AD, Mitchell P, Saw SM, Fossarello M, Kazmierkiewicz K, Murgia F, Portas L, Schache M, Richardson A, Xie J, Wang JJ, Rochtchina E; DCCT/EDIC Research Group, Viswanathan AC, Hayward C, Wright AF, Polasek O, Campbell H, Rudan I, Oostra BA, Uitterlinden AG, Hofman A, Rivadeneira F, Amin N, Karssen LC, Vingerling JR, Hosseini SM, Döring A, Bettecken T, Vatavuk Z, Gieger C, Wichmann HE, Wilson JF, Fleck B, Foster PJ, Topouzis F, McGuffin P, Sim X, Inouye M, Holliday EG, Attia J, Scott RJ, Rotter JI, Meitinger T, Bailey-Wilson JE.

Hum Mol Genet. 2013 Jul 1;22(13):2754-64. doi: 10.1093/hmg/ddt116. Epub 2013 Mar 7.

16.

[The analysis of the axises of corneal astigmatism and total astigmatism in astigmatic patients].

Dai Z, Yu R, Gong X, Wang S.

Yan Ke Xue Bao. 2000 Dec;16(4):279-80. Chinese.

PMID:
12579790
18.

Refractive and corneal astigmatism in white school children in northern ireland.

O'Donoghue L, Rudnicka AR, McClelland JF, Logan NS, Owen CG, Saunders KJ.

Invest Ophthalmol Vis Sci. 2011 Jun 8;52(7):4048-53. doi: 10.1167/iovs.10-6100.

PMID:
21372019
19.

A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.

Yamazaki K, Umeno J, Takahashi A, Hirano A, Johnson TA, Kumasaka N, Morizono T, Hosono N, Kawaguchi T, Takazoe M, Yamada T, Suzuki Y, Tanaka H, Motoya S, Hosokawa M, Arimura Y, Shinomura Y, Matsui T, Matsumoto T, Iida M, Tsunoda T, Nakamura Y, Kamatani N, Kubo M.

Gastroenterology. 2013 Apr;144(4):781-8. doi: 10.1053/j.gastro.2012.12.021. Epub 2012 Dec 22.

PMID:
23266558
20.

Association between single-nucleotide polymorphisms on chromosome 1p22 and 20q12 and nonsyndromic cleft lip with or without cleft palate: new data in Han Chinese and meta-analysis.

Huang E, Cheng H, Xu M, Shu S, Tang S.

Birth Defects Res A Clin Mol Teratol. 2012 Jun;94(6):469-76. doi: 10.1002/bdra.23013. Epub 2012 Apr 21.

PMID:
22522387
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