Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophy

by Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Yong, V.H.K., Aung, T., Tan, D.T.H.
Published 2011

Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutants

by Lakshminarayanan R, Chaurasia S.S, Murugan E, Venkatraman A, Chai S.-M, Vithana E.N, Beuerman R.W, Mehta J.S
Published 2016

Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese

by Ozaki, M., Lee, K.Y.C., Vithana, E.N., Yong, V.H., Venkatraman, A., Aung, T., Thalamuthu, A., Mizoguchi, T.
Published 2011

Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy

by Mehta, J.S., Vithana, E.N., Venkataraman, D., Venkatraman, A., Poh, R., Beuerman, R.W., Aung, T., Tan, D.T.H.
Published 2011

Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese

by Lee, K.Y.C., Aung, T., Ho, S.L., Pek, D.C.K., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Vithana, E.N.
Published 2011

Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyes

by Aung, T., Lim, M.C.C., Wong, T.T.L., Yong, V.H.K., Venkataraman, D., Venkatraman, A., Vithana, E.N., Chew, P.T.K., Thalamuthu, A.
Published 2011

A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy

by Lakshminarayanan, R., Vithana, E.N., Chai, S.-M., Chaurasia, S.S., Saraswathi, P., Venkatraman, A., Rojare, C., Venkataraman, D., Tan, D., Aung, T., Beuerman, R.W., Mehta, J.S.
Published 2014

Toll-like receptor 3 polymorphism rs3775291 is not associated with choroidal neovascularization or polypoidal choroidal vasculopathy in Chinese subjects

by Sng, C.C.A., Cackett, P.D., Yeo, I.Y., Thalamuthu, A., Venkatraman, A., Venkataraman, D., Koh, A.H., Tai, E.-S., Wong, T.Y., Aung, T., Vithana, E.N.
Published 2014

PH Induced Conformational Transitions in the Transforming Growth Factor ?-Induced Protein (TGF?IP) Associated Corneal Dystrophy Mutants

by Murugan, E, Venkatraman, A, Lei, Z, Mouvet, V, Rui Yi Lim, R, Muruganantham, N, Goh, E, Swee Lim Peh, G, Beuerman, R.W, Chaurasia, S.S, Rajamani, L, Mehta, J.S
Published 2020

SLC4A11 mutations in Fuchs endothelial corneal dystrophy

by Vithana, E.N., Tan, D.T.H., Venkataraman, D., Venkatraman, A., Aung, T., Morgan, P.E., Casey, J.R., Ramprasad, V., Nagasamy, S., Kumaramanickevel, G., Rajagopal, R., Yam, G.H.F., Law, R.W.K., Pang, C.P., Yong, V.H.K
Published 2011