Vithana EN - Search Results

1

Genome-wide association study of Parkinson's disease in East Asians.

Foo JN, Tan LC, Irwan ID, Au WL, Low HQ, Prakash KM, Ahmad-Annuar A, Bei J, Chan AY, Chen CM, Chen YC, Chung SJ, Deng H, Lim SY, Mok V, Pang H, Pei Z, Peng R, Shang HF, Song K, Tan AH, Wu YR, Aung T, Cheng CY, Chew FT, Chew SH, Chong SA, Ebstein RP, Lee J, Saw SM, Seow A, Subramaniam M, Tai ES, Vithana EN, Wong TY, Heng KK, Meah WY, Khor CC, Liu H, Zhang F, Liu J, Tan EK. Foo JN, et al. Among authors: vithana en. Hum Mol Genet. 2017 Jan 1;26(1):226-232. doi: 10.1093/hmg/ddw379. Hum Mol Genet. 2017. PMID: 28011712

2

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. Among authors: vithana en. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3812-6. doi: 10.1167/iovs.05-0378. Invest Ophthalmol Vis Sci. 2005. PMID: 16186368

3

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. Among authors: vithana en. Invest Ophthalmol Vis Sci. 2007 May;48(5):2123-6. doi: 10.1167/iovs.06-1213. Invest Ophthalmol Vis Sci. 2007. PMID: 17460270

4

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

5

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. Among authors: vithana en. 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

6

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. Among authors: vithana en. Invest Ophthalmol Vis Sci. 2008 Jun;49(6):2613-9. doi: 10.1167/iovs.07-0860. Invest Ophthalmol Vis Sci. 2008. PMID: 18515590

7

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. Among authors: vithana en. J Glaucoma. 2008 Jun-Jul;17(4):257-8. doi: 10.1097/IJG.0b013e31815c3aa5. J Glaucoma. 2008. PMID: 18552608

8

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. Among authors: vithana en. Mol Vis. 2008 Jul 9;14:1277-81. Mol Vis. 2008. PMID: 18618004 Free PMC article.

9

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese.

Lee KY, Ho SL, Thalamuthu A, Venkatraman A, Venkataraman D, Pek DC, Aung T, Vithana EN. Lee KY, et al. Among authors: vithana en. Mol Vis. 2009 Jun 4;15:1120-6. Mol Vis. 2009. PMID: 19503743 Free PMC article.

10

Novel human pathological mutations. Gene symbol: SLC4A11. Disease: Corneal endothelial dystrophy 2.

Chai SM, Vithana EN, Venkataraman D, Saleh H, Chekkalichintavida NP, al-Sayyed F, Aung T. Chai SM, et al. Among authors: vithana en. Hum Genet. 2010 Jan;127(1):110. Hum Genet. 2010. PMID: 20108384 No abstract available.

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