Vithana E - Search Results

1

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. Han S, et al. Among authors: vithana e. Hum Mol Genet. 2011 Sep 15;20(18):3693-8. doi: 10.1093/hmg/ddr269. Epub 2011 Jun 10. Hum Mol Genet. 2011. PMID: 21665993

2

Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucoma.

Aung T, Yong VH, Chew PT, Seah SK, Gazzard G, Foster PJ, Vithana EN. Aung T, et al. Invest Ophthalmol Vis Sci. 2005 Apr;46(4):1303-6. doi: 10.1167/iovs.04-1163. Invest Ophthalmol Vis Sci. 2005. PMID: 15790895

3

Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations.

Lee KY, Koh AH, Aung T, Yong VH, Yeung K, Ang CL, Vithana EN. Lee KY, et al. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3812-6. doi: 10.1167/iovs.05-0378. Invest Ophthalmol Vis Sci. 2005. PMID: 16186368

4

Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjects.

How AC, Aung T, Chew X, Yong VH, Lim MC, Lee KY, Toh JY, Li Y, Liu J, Vithana EN. How AC, et al. Invest Ophthalmol Vis Sci. 2007 May;48(5):2123-6. doi: 10.1167/iovs.06-1213. Invest Ophthalmol Vis Sci. 2007. PMID: 17460270

5

Bradyopsia in an Asian man.

Cheng JY, Luu CD, Yong VH, Mathur R, Aung T, Vithana EN. Cheng JY, et al. Arch Ophthalmol. 2007 Aug;125(8):1138-40. doi: 10.1001/archopht.125.8.1138. Arch Ophthalmol. 2007. PMID: 17698770 No abstract available.

6

SLC4A11 mutations in Fuchs endothelial corneal dystrophy.

Vithana EN, Morgan PE, Ramprasad V, Tan DT, Yong VH, Venkataraman D, Venkatraman A, Yam GH, Nagasamy S, Law RW, Rajagopal R, Pang CP, Kumaramanickevel G, Casey JR, Aung T. Vithana EN, et al. Hum Mol Genet. 2008 Mar 1;17(5):656-66. doi: 10.1093/hmg/ddm337. Epub 2007 Nov 16. Hum Mol Genet. 2008. PMID: 18024964

7

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese.

Ozaki M, Lee KY, Vithana EN, Yong VH, Thalamuthu A, Mizoguchi T, Venkatraman A, Aung T. Ozaki M, et al. Invest Ophthalmol Vis Sci. 2008 Sep;49(9):3976-80. doi: 10.1167/iovs.08-1805. Epub 2008 Apr 30. Invest Ophthalmol Vis Sci. 2008. PMID: 18450598

8

Association analysis of CFH, C2, BF, and HTRA1 gene polymorphisms in Chinese patients with polypoidal choroidal vasculopathy.

Lee KY, Vithana EN, Mathur R, Yong VH, Yeo IY, Thalamuthu A, Lee MW, Koh AH, Lim MC, How AC, Wong DW, Aung T. Lee KY, et al. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2613-9. doi: 10.1167/iovs.07-0860. Invest Ophthalmol Vis Sci. 2008. PMID: 18515590

9

Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in Singaporean subjects.

Aung T, Yong VH, Lim MC, Venkataraman D, Toh JY, Chew PT, Vithana EN. Aung T, et al. J Glaucoma. 2008 Jun-Jul;17(4):257-8. doi: 10.1097/IJG.0b013e31815c3aa5. J Glaucoma. 2008. PMID: 18552608

10

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy.

Mehta JS, Vithana EN, Venkataraman D, Venkatraman A, Poh R, Beuerman RW, Aung T, Tan DT. Mehta JS, et al. Mol Vis. 2008 Jul 9;14:1277-81. Mol Vis. 2008. PMID: 18618004 Free PMC article.

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