Aung T - 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: aung t. Hum Mol Genet. 2017 Jan 1;26(1):226-232. doi: 10.1093/hmg/ddw379. Hum Mol Genet. 2017. PMID: 28011712

2

A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene.

Aung T, Ocaka L, Ebenezer ND, Morris AG, Krawczak M, Thiselton DL, Alexander C, Votruba M, Brice G, Child AH, Francis PJ, Hitchings RA, Lehmann OJ, Bhattacharya SS. Aung T, et al. Hum Genet. 2002 Jan;110(1):52-6. doi: 10.1007/s00439-001-0645-7. Epub 2001 Nov 23. Hum Genet. 2002. PMID: 11810296

3

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

4

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

5

Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2).

Vithana EN, Morgan P, Sundaresan P, Ebenezer ND, Tan DT, Mohamed MD, Anand S, Khine KO, Venkataraman D, Yong VH, Salto-Tellez M, Venkatraman A, Guo K, Hemadevi B, Srinivasan M, Prajna V, Khine M, Casey JR, Inglehearn CF, Aung T. Vithana EN, et al. Among authors: aung t. Nat Genet. 2006 Jul;38(7):755-7. doi: 10.1038/ng1824. Epub 2006 Jun 11. Nat Genet. 2006. PMID: 16767101

6

Myopia, axial length, and OCT characteristics of the macula in Singaporean children.

Luo HD, Gazzard G, Fong A, Aung T, Hoh ST, Loon SC, Healey P, Tan DT, Wong TY, Saw SM. Luo HD, et al. Among authors: aung t. Invest Ophthalmol Vis Sci. 2006 Jul;47(7):2773-81. doi: 10.1167/iovs.05-1380. Invest Ophthalmol Vis Sci. 2006. PMID: 16799013

7

An outbreak of Fusarium keratitis associated with contact lens wear in Singapore.

Khor WB, Aung T, Saw SM, Wong TY, Tambyah PA, Tan AL, Beuerman R, Lim L, Chan WK, Heng WJ, Lim J, Loh RS, Lee SB, Tan DT. Khor WB, et al. Among authors: aung t. JAMA. 2006 Jun 28;295(24):2867-73. doi: 10.1001/jama.295.24.2867. JAMA. 2006. PMID: 16804153

8

Rationale and methodology for a population-based study of eye diseases in Malay people: The Singapore Malay eye study (SiMES).

Foong AW, Saw SM, Loo JL, Shen S, Loon SC, Rosman M, Aung T, Tan DT, Tai ES, Wong TY. Foong AW, et al. Among authors: aung t. Ophthalmic Epidemiol. 2007 Jan-Feb;14(1):25-35. doi: 10.1080/09286580600878844. Ophthalmic Epidemiol. 2007. PMID: 17365815

9

Novel SLC4A11 mutations in patients with recessive congenital hereditary endothelial dystrophy (CHED2). Mutation in brief #958. Online.

Ramprasad VL, Ebenezer ND, Aung T, Rajagopal R, Yong VH, Tuft SJ, Viswanathan D, El-Ashry MF, Liskova P, Tan DT, Bhattacharya SS, Kumaramanickavel G, Vithana EN. Ramprasad VL, et al. Among authors: aung t. Hum Mutat. 2007 May;28(5):522-3. doi: 10.1002/humu.9487. Hum Mutat. 2007. PMID: 17397048

10

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

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