Browsing by Author Yong, V.H.K.

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Showing results 2 to 11 of 11 < previous 
Issue DateTitleAuthor(s)
2005Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutationsLee, K.Y.C.; Koh, A.H.C.; Aung, T. ; Ang, C.-L.; Yong, V.H.K.; Yeung, K.; Vithana, E.N. 
Oct-2012Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucomaVithana, E.N.; Khor, C.-C. ; Qiao, C.; Nongpiur, M.E.; George, R.; Chen, L.-J.; Do, T.; Abu-Amero, K.; Huang, C.K.; Low, S.; Tajudin, L.-S.A.; Perera, S.A.; Cheng, C.-Y. ; Xu, L.; Jia, H.; Ho, C.-L.; Sim, K.S.; Wu, R.-Y.; Tham, C.C.Y.; Chew, P.T.K.; Su, D.H.; Oen, F.T.; Sarangapani, S.; Soumittra, N.; Osman, E.A.; Wong, H.-T.; Tang, G.; Fan, S.; Meng, H.; Huong, D.T.L.; Wang, H.; Feng, B.; Baskaran, M.; Shantha, B.; Ramprasad, V.L.; Kumaramanickavel, G.; Iyengar, S.K.; How, A.C.; Lee, K.Y.; Sivakumaran, T.A.; Yong, V.H.K.; Ting, S.M.L.; Li, Y.; Wang, Y.-X.; Tay, W.-T.; Sim, X. ; Lavanya, R.; Cornes, B.K.; Zheng, Y.-F.; Wong, T.T.; Loon, S.-C.; Yong, V.K.Y.; Waseem, N.; Yaakub, A.; Chia, K.-S. ; Rand Allingham, R.; Hauser, M.A.; Lam, D.S.C.; Hibberd, M.L. ; Bhattacharya, S.S.; Zhang, M.; Teo, Y.Y. ; Tan, D.T.; Jonas, J.B.; Tai, E.-S.; Saw, S.-M. ; Hon, D.N.; Al-Obeidan, S.A.; Liu, J. ; Chau, T.N.B.; Simmons, C.P.; Bei, J.-X.; Zeng, Y.-X.; Foster, P.J.; Vijaya, L.; Wong, T.-Y. ; Pang, C.-P.; Wang, N.; Aung, T.
2007Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjectsHow, 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.
2008Lack of association between the rs2664538 polymorphism in the MMP-9 gene and primary angle closure glaucoma in singaporean subjectsAung, T. ; Lim, M.C.C.; Aung, T. ; Yong, V.H.K.; Venkataraman, D.; Toh, J.-Y.; Vithana, E.N. ; Chew, P.T.K. 
2008Molecular analysis of CHX10 and MFRP in Chinese subjects with primary angle closure glaucoma and short axial length eyesAung, 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.
2005Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaAung, T. ; Chew, P.T.K. ; Seah, S.K.L.; Gazzard, G.; Foster, P.J.; Yong, V.H.K.; Vithana, E.N.
Apr-2005Molecular analysis of the myocilin gene in Chinese subjects with chronic primary-angle closure glaucomaAung, T. ; Yong, V.H.K.; Chew, P.T.K. ; Seah, S.K.L.; Gazzard, G.; Foster, P.J.; Vithana, E.N.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)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.
2006Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Vithana, E.N. ; Tan, D.T.H. ; Venkataraman, D.; Yong, V.H.K.; Aung, T. ; 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.; Salto-Tellez, M. ; Guo, K.
2009Surgical management and genetic analysis of a Chinese family with the S171P mutation in the UBIAD1 gene, the gene for Schnyder corneal dystrophyMehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Yong, V.H.K.; Aung, T. ; Tan, D.T.H.