Full Name
ERANGA NISHANTHIE VITHANA
Variants
Vithana E.N
Vithana, E.N.
Vithana, Eranga Nishanthie
 
 
 
Email
ophenv@nus.edu.sg
 

Publications

Results 1-20 of 35 (Search time: 0.014 seconds).

Issue DateTitleAuthor(s)
12010Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 geneMehta, J.S.; Tan, D.T. ; Aung, T. ; Vithana, E.N. ; Hemadevi, B.; Sundaresan, P.; Arunkumar, J.; Srinivasan, M.; Prajna, V.
22008Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophyMehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Poh, R.; Beuerman, R.W. ; Aung, T. ; Tan, D.T.H. 
32014Analysis of non-synonymous-coding variants of parkinson's disease-related pathogenic and susceptibility genes in East Asian populationsFoo J.N.; Tan L.C. ; Liany H.; Koh T.H.; Irwan I.D.; Ng Y.Y.; Ahmad-Annuar A.; Au W.-L. ; Aung T. ; Chan A.Y.Y.; Chong S.-A.; Chung S.J.; Jung Y.; Khor C.C. ; Kim J.; Lee J. ; Lim S.-Y.; Mok V.; Prakash K.-M. ; Song K.; Tai E.-S. ; Vithana E.N. ; Wong T.-Y. ; Tan E.-K. ; Liu J. 
42008Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset fuchs endothelial corneal dystrophyMehta, 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.
52008Association analysis of CFH, C2, BF, and HTRA1 gene polymorphisms in Chinese patients with polypoidal choroidal vasculopathyLee, 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.
62008Association of LOXL1 gene polymorphisms with pseudoexfoliation in the JapaneseOzaki, M.; Lee, K.Y.C.; Vithana, E.N. ; Yong, V.H.; Venkatraman, A.; Aung, T. ; Thalamuthu, A.; Mizoguchi, T.
72009Association of LOXL1 polymorphisms with pseudoexfoliation in the ChineseLee, K.Y.C.; Aung, T. ; Ho, S.L.; Pek, D.C.K.; Thalamuthu, A.; Venkatraman, A.; Venkataraman, D.; Vithana, E.N. 
82015Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutantsLakshminarayanan R; Chaurasia S.S ; Murugan E; Venkatraman A; Chai S.-M; Vithana E.N ; Beuerman R.W ; Mehta J.S 
92005Characterization 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. 
1024-May-2013Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell cultureShei, W.; Liu, J.; Htoon, H.M.; Aung, T. ; Vithana, E.N. 
112014Erratum: Atomic layer deposition of a MoS2 film (Nanoscale (2014) 6 (10584-10588))Springelkamp, H; Höhn, R; Mishra, A; Hysi, P.G; Khor, C.-C ; Loomis, S.J; Bailey, J.N.C; Gibson, J; Thorleifsson, G; Janssen, S.F; Luo, X; Ramdas, W.D; Vithana, E ; Nongpiur, M.E ; Montgomery, G.W; Xu, L; Mountain, J.E; Gharahkhani, P; Lu, Y; Amin, N; Karssen, L.C; Sim, K.-S; Van Leeuwen, E.M; Iglesias, A.I; Verhoeven, V.J.M; Hauser, M.A ; Loon, S.-C ; Despriet, D.D.G; Nag, A; Venturini, C; Sanfilippo, P.G; Schillert, A; Kang, J.H; Landers, J; Jonasson, F; Cree, A.J; Van Koolwijk, L.M.E; Rivadeneira, F; Souzeau, E; Jonsson, V; Menon, G; Mitchell, P; Wang, J.J; Rochtchina, E; Attia, J; Scott, R; Holliday, E.G; Baird, P.N; Xie, J; Inouye, M; Viswanathan, A; Sim, X ; Weinreb, R.N; De Jong, P.T.V.M; Oostra, B.A; Uitterlinden, A.G; Hofman, A; Ennis, S; Thorsteinsdottir, U; Burdon, K.P; Allingham, R.R ; Brilliant, M.H; Budenz, D.L; Christen, W.G; Fingert, J; Friedman, D.S; Gaasterland, D; Gaasterland, T; Haines, J.L; Kang, J.H; Kraft, P; Lee, R.K; Lichter, P.R; Liu, Y; Moroi, S.E; Pericak-Vance, M.A; Realini, A; Richards, J.E; Schuman, J.S; Scott, W.K; Singh, K; Sit, A.J; Vollrath, D; Wollstein, G; Zack, D.J; Zhang, K; Barroso, I; Blackwell, J.M; Bramon, E; Brown, M.A; Casas, J.P; Corvin, A; Deloukas, P; Duncanson, A; Jankowski, J; Markus, H.S; Mathew, C.G; Palmer, C.N.A; Plomin, R; Rautanen, A; Sawcer, S.J; Trembath, R.C; Viswanathan, A.C; Wood, N.W; Spencer, C.C.A; Band, G; Bellenguez, C; Freeman, C; Hellenthal, G; Giannoulatou, E; Pirinen, M; Pearson, R; Strange, A; Su, Z; Vukcevic, D; Donnelly, P; Langford, C; Hunt, S.E; Edkins, S; Gwilliam, R; Blackburn, H; Bumpstead, S.J; Dronov, S; Gillman, M; Gray, E; Hammond, N; Jayakumar, A; McCann, O.T; Liddle, J; Potter, S.C; Ravindrarajah, R; Ricketts, M; Waller, M; Weston, P; Widaa, S; Whittaker, P; Spector, T.D; Mirshahi, A; Saw, S.-M ; Vingerling, J.R; Teo, Y.-Y ; Wolfs, R.C.W; Lemij, H.G; Tai, E.-S ; Jansonius, N.M; Jonas, J.B; Cheng, C.-Y ; Aung, T ; Klaver, C.C.W; Craig, J.E; MacGregor, S; MacKey, D.A; Lotery, A.J; Stefansson, K; Bergen, A.A.B; Young, T.L; Wiggs, J.L; Pfeiffer, N; Wong, T.-Y ; Pasquale, L.R; Hewitt, A.W; Van Duijn, C.M; Hammond, C.J; Blue Mountains Eye Study-GWAS groupw; NEIGHBORHOOD Consortiumz; Wellcome Trust Case Control Consortium 2 (WTCCC2); Data and Analysis Group; DNA, Genotyping, Data QC and Informatics Group; Publications Committee; Tan, L.K ; Liu, B ; Teng, J.H; Guo, S; Low, H.Y; Loh, K.P 
122015Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortiumLi Q.; Wojciechowski R.; Simpson C.L.; Hysi P.G.; Verhoeven V.J.M.; Ikram M.K. ; Höhn R.; Vitart V.; Hewitt A.W.; Oexle K.; Mäkelä K.-M.; MacGregor S.; Pirastu M.; Fan Q. ; Cheng C.-Y. ; St Pourcain B.; McMahon G.; Kemp J.P.; Northstone K.; Rahi J.S.; Cumberland P.M.; Martin N.G.; Sanfilippo P.G.; Lu Y.; Wang Y.X.; Hayward C.; Polašek O.; Campbell H.; Bencic G.; Wright A.F.; Wedenoja J.; Zeller T.; Schillert A.; Mirshahi A.; Lackner K.; Yip S.P.; Yap M.K.H.; Ried J.S.; Gieger C.; Murgia F.; Wilson J.F.; Fleck B.; Yazar S.; Vingerling J.R.; Hofman A.; Uitterlinden A.; Rivadeneira F.; Amin N.; Karssen L.; Oostra B.A.; Zhou X. ; Teo Y.-Y. ; Tai E.S. ; Vithana E. ; Barathi V. ; Zheng Y.; Siantar R.G.; Neelam K.; Shin Y.; Lam J.; Yonova-Doing E.; Venturini C.; Hosseini S.M.; Wong H.-S.; Lehtimäki T.; Kähönen M.; Raitakari O.; Timpson N.J.; Evans D.M.; Khor C.-C. ; Aung T. ; Young T.L. ; Mitchell P.; Klein B.; van Duijn C.M.; Meitinger T.; Jonas J.B.; Baird P.N.; Mackey D.A.; Wong T.Y. ; Saw S.-M. ; Pärssinen O.; Stambolian D.; Hammond C.J.; Klaver C.C.W.; Williams C.; Paterson A.D.; Bailey-Wilson J.E.; Guggenheim J.A.; Meguro A.; Young A.L.; Veluchamy A.B.; Metspalu A.; Döring A.; Khawaja A.P.; Klein B.E.; Pourcain B.S.; Delcourt C.; Maubaret C.; Pang C.P.; Ho D.W.H.; Chew E.; Mihailov E.; Smith G.D.; Biino G.; Rudan I.; Seppala I.; Kaprio J.; Craig J.E.; Polling J.R.; Tideman J.-W.; Fondran J.R.; Wang J.J.; Liao J.; Zhao J.H.; Xie J.; Bailey Wilson J.E.; Burdon K.P.; Khaw K.-T.; Yamashiro K.; Portas L.; Farrer L.; Raffel L.J.; Chen L.J.; Xu L.; Deangelis M.M.; Morrison M.; Schache M.; Cotch M.-F.; Miyake M.; Fossarello M.; He M.; Yoshimura N.; Wareham N.J.; Mizuki N.; Pfeiffer N.; Polasek O.; Tam P.O.; Foster P.J.; Chen P.; Gharahkhani P.; Fogarty R.D.; Luben R.N.; Igo R.P.; Jr.; Klein R.; Mohsen Hosseini S.; Janmahasatian S.; Feng S.; Panda-Jonas S.; Iyengar S.K.; Lass J.H.; Rantanen T.; Haller T.; Nangia V.; Jhanji V.; Chen W.; Zhou X.; Guo X.; Li X.; Vatavuk Z.; The CREAM consortium
132017Genome-wide association study of Parkinson's disease in East AsiansFoo J.N.; Tan L.C. ; Irwan I.D.; Au W.-L. ; Low H.Q.; Prakash K.-M. ; Ahmad-Annuar A.; Bei J.; Chan A.Y.; Chen C.M.; Chen Y.-C.; Chung S.J.; Deng H.; Lim S.-Y.; Mok V.; Pang H.; Pei Z.; Peng R.; Shang H.-F.; Song K.; Tan A.H.; Wu Y.-R.; Aung T. ; Cheng C.-Y. ; Chew F.T. ; Chew S.-H.; Chong S.-A. ; Ebstein R.P. ; Lee J. ; Saw S.-M. ; Seow A. ; Subramaniam M. ; Tai E.-S. ; Vithana E.N. ; Wong T.-Y. ; Heng K.K.; Meah W.-Y. ; Khor C.C. ; Liu H.; Zhang F.; Liu J. ; Tan E.-K. 
142007Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosaAlvarez, B.V.; Casey, J.R.; Shandro, H.J.; Vithana, E.N. ; Yeung, K.; Yong, V.; Aung, T. ; Yang, Z.; Chen, Y.; Zhang, K.; Koh, A.H.; Kolatkar, P.; Palasingam, P.
15Aug-2007Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosaAlvarez, 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.
162010Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese populationVithana, E.N. ; Nongpiur, M.E.; Venkataraman, D.; Chan, S.H.; Mavinahalli, J.; Aung, T. 
1717-May-2019In-utero epigenetic factors are associated with early-onset myopia in young childrenSeow WJ ; Ngo CS ; Pan H; Barathi VA ; Tompson SW ; Whisenhunt KN; Vithana E ; Chong YS ; Juo SH; Hysi P; Young TL ; Karnani N ; Saw SM 
182013Ion transport function of SLC4A11 in corneal endotheliumJalimarada, S.S.; Ogando, D.G.; Vithana, E.N. ; Bonanno, J.A.
192007Lack 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.
202008Lack 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.