Gender differences in health and health expectancies of older adults in Singapore: An examination of diseases, impairments, and functional disabilities

by Yong, V., Saito, Y., Chan, A.
Published 2014

Changes in the prevalence of mobility limitations and mobile life expectancy of older adults in Singapore, 1995-2005

by Yong, V., Saito, Y., Chan, A.
Published 2016

Microglial reaction in some CNS nuclei following nerves transection in BALB/c and interferon-γ gene knockout mice

by Ng, Y.-K., Ling, E.-A., Yong, V.-W.
Published 2012

In vitro transscleral penetration of ganciclovir in the pig eye

by Heng, W.J., Lim, A.T.H., Lee, H.S., Chew, P.T.K., Yong, V.S.H.
Published 2016

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

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

Subjective visual experience during phacoemulsification and intraocular lens implantation under topical anesthesia

by Au Eong, K.-G., Low, C.-H., Heng, W.-J., Aung, T., Lim, T.-H., Ho, S.-H., Yong, V.S.H.
Published 2014

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

by Aung, T., Lim, M.C.C., Yong, V.H.K., Venkataraman, D., Toh, J.-Y., Vithana, E.N., Chew, P.T.K.
Published 2011

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

by Aung, T., Yong, V.H.K., Chew, P.T.K., Seah, S.K.L., Gazzard, G., Foster, P.J., Vithana, E.N.
Published 2016

Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations

by Lee, K.Y.C., Koh, A.H.C., Aung, T., Ang, C.-L., Yong, V.H.K., Yeung, K., Vithana, E.N.
Published 2011

Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset fuchs endothelial corneal dystrophy

by Mehta, J.S., Vithana, E.N., Tan, D.T.H., Yong, V.H.K., Aung, T., Yam, G.H.F., Law, R.W.K., Pang, C.P.
Published 2011

Visually significant opacification of hydrophilic acrylic intraocular lenses - A clinico-pathological analysis

by Yong, V.K.Y., Netto, P.A., Heng, W.-J., Yap, E.-Y., Lee, H.-M., Ng, M.M.L., Au Eong, K.-G.
Published 2016

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

Systemic autonomic function in subjects with primary angle-closure glaucoma: A comparative study of symptomatic and asymptomatic disease presentation

by Yong, V.K.Y., Lee, J.-J., Liew, G.-C., Yip, C.-C., Umapathi, T., Tan, N.C.K., Aung, T., Foster, P.J., Chew, P.T.K.
Published 2011

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

by How, A.C.S., Aung, T., Lim, M.C.C., Lee, K.Y.C., Chew, X., Yong, V.H.K., Toh, J.-Y., Vithana, E.N., Li, Y., Liu, J.
Published 2011

Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa

by Alvarez, B.V., Vithana, E.N., Yang, Z., Koh, A.H., Yeung, K., Yong, V., Shandro, H.J., Chen, Y., Kolatkar, P., Palasingam, P., Zhang, K., Aung, T., Casey, J.R.
Published 2016

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

by Lee, K.Y., Mathur, R., Yeo, I.Y., Lee, M.-W., Koh, A.H., Lim, M.C., How, A.C., Wong, D.W., Aung, T., Vithana, E.N., Yong, V.H., Thalamuthu, A.
Published 2011

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

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

by Vithana, E.N., Tan, D.T.H., Yong, V.H.K., Morgan, P., Casey, J.R., Sundaresan, P., Hemadevi, B., Srinivasan, M., Prajna, V., Ebenezer, N.D., Mohamed, M.D., Inglehearn, C.F., Anand, S., Khine, K.O., Khine, M., Salto-Tellez, M., Guo, K., Aung Tin
Published 2012

Erratum to: For vidaillac et al. “sex steroids induce membrane stress responses and virulence properties in pseudomonas aeruginosa” (mbio, 11, 5, e01774-20, 2020, 10.1128/mBio.0177...

by Vidaillac, C., Yong, V.F.L., Aschtgen, M.-S., Qu, J., Yang, S., Xu, G., Seng, Z.J., Brown, A.C., Ali, M.K., Jaggi, T.K., Sankaran, J., Foo, Y.H., Righetti, F., Nedumaran, A.M., Aogáin, M.M., Roizman, D., Richard, J.-A., Rogers, T.R., Toyofuku, M., Luo, D., Loh, E., Wohland, T., Czarny, B., Horvat, J.C., Hansbro, P.M., Yang, L., Li, L., Normark, S., Henriques-Normark, B., Chotirmall, S.H.
Published 2021