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| | Issue Date | Title | Author(s) |
| 1 | 2010 | Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene | Mehta, J.S.; Tan, D.T. ; Aung, T. ; Vithana, E.N. ; Hemadevi, B.; Sundaresan, P.; Arunkumar, J.; Srinivasan, M.; Prajna, V. |
| 2 | 2008 | Analysis of conjunctival fibroblasts from a proband with Schnyder corneal dystrophy | Mehta, J.S.; Vithana, E.N. ; Venkataraman, D.; Venkatraman, A.; Poh, R.; Beuerman, R.W. ; Aung, T. ; Tan, D.T.H. |
| 3 | 2014 | Analysis of non-synonymous-coding variants of parkinson's disease-related pathogenic and susceptibility genes in East Asian populations | Foo 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. |
| 4 | 2008 | Analysis of the posterior polymorphous corneal dystrophy 3 gene, TCF8, in late-onset fuchs endothelial corneal dystrophy | 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. |
| 5 | 2008 | Association analysis of CFH, C2, BF, and HTRA1 gene polymorphisms in Chinese patients with polypoidal choroidal vasculopathy | 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. |
| 6 | 2008 | Association of LOXL1 gene polymorphisms with pseudoexfoliation in the Japanese | Ozaki, M.; Lee, K.Y.C.; Vithana, E.N. ; Yong, V.H.; Venkatraman, A.; Aung, T. ; Thalamuthu, A.; Mizoguchi, T. |
| 7 | 2009 | Association of LOXL1 polymorphisms with pseudoexfoliation in the Chinese | Lee, K.Y.C.; Aung, T. ; Ho, S.L.; Pek, D.C.K.; Thalamuthu, A.; Venkatraman, A.; Venkataraman, D.; Vithana, E.N. |
| 8 | 2015 | Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutants | Lakshminarayanan R; Chaurasia S.S ; Murugan E; Venkatraman A; Chai S.-M; Vithana E.N ; Beuerman R.W ; Mehta J.S |
| 9 | 2005 | Characterization of Bietti crystalline dystrophy patients with CYP4V2 mutations | Lee, K.Y.C.; Koh, A.H.C.; Aung, T. ; Ang, C.-L.; Yong, V.H.K.; Yeung, K.; Vithana, E.N. |
| 10 | 24-May-2013 | Differential expression of the Slc4 bicarbonate transporter family in murine corneal endothelium and cell culture | Shei, W.; Liu, J.; Htoon, H.M.; Aung, T. ; Vithana, E.N. |
| 11 | 2019 | Erratum to: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (Nature Communications, (2018), 9, 1, (1864), 10.1038/s41467-018-03646-6) | Iglesias, A.I.; Mishra, A.; Vitart, V.; Bykhovskaya, Y.; Höhn, R.; Springelkamp, H.; Cuellar-Partida, G.; Gharahkhani, P.; Bailey, J.N.C.; Willoughby, C.E.; Li, X.; Yazar, S.; Nag, A.; Khawaja, A.P.; Polašek, O.; Siscovick, D.; Mitchell, P.; Tham, Y.C. ; Haines, J.L.; Kearns, L.S.; Hayward, C.; Shi, Y. ; van Leeuwen, E.M.; Taylor, K.D.; Wang, J.J.; Rochtchina, E.; Attia, J.; Scott, R.; Holliday, E.G.; Wong, T.Y. ; Baird, P.N.; Xie, J.; Inouye, M.; Viswanathan, A.; Sim, X. ; Bonnemaijer, P.; Rotter, J.I.; Martin, N.G.; Zeller, T.; Mills, R.A.; Souzeau, E.; Staffieri, S.E.; Jonas, J.B.; Schmidtmann, I.; Boutin, T.; Kang, J.H.; Lucas, S.E.M.; Beutel, M.E.; Wilson, J.F.; Donnelly, P.; 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.; 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.; 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.; Allingham, R.R.; Brilliant, M.H.; Budenz, D.L.; Christen, W.G.; Fingert, J.; Friedman, D.S.; Gaasterland, D.; Gaasterland, T.; Hauser, M.A.; Kraft, P.; Lee, R.K.; Lichter, P.R.; Liu, Y.; Loomis, S.J.; 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.; Weinreb, R.N.; Wollstein, G.; Zack, D.J.; Zhang, K.; Uitterlinden, A.G.; Vithana, E.N. ; Foster, P.J.; Hysi, P.G.; Hewitt, A.W.; Khor, C.C. ; Pasquale, L.R.; Montgomery, G.W.; Klaver, C.C.W.; Aung, T. ; Pfeiffer, N.; Mackey, D.A.; Hammond, C.J.; Cheng, C.-Y. ; Craig, J.E.; Rabinowitz, Y.S.; Wiggs, J.L.; Burdon, K.P.; van Duijn, C.M.; MacGregor, S. |
| 12 | 2014 | Erratum: 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 |
| 13 | 2015 | Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium | Li 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 |
| 14 | 2017 | Genome-wide association study of Parkinson's disease in East Asians | Foo 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. |
| 15 | 2007 | Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa | Alvarez, 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. |
| 16 | Aug-2007 | Identification and characterization of a novel mutation in the carbonic anhydrase IV gene that causes retinitis pigmentosa | 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. |
| 17 | 2010 | Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population | Vithana, E.N. ; Nongpiur, M.E.; Venkataraman, D.; Chan, S.H.; Mavinahalli, J.; Aung, T. |
| 18 | 17-May-2019 | In-utero epigenetic factors are associated with early-onset myopia in young children | Seow 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 |
| 19 | 2013 | Ion transport function of SLC4A11 in corneal endothelium | Jalimarada, S.S.; Ogando, D.G.; Vithana, E.N. ; Bonanno, J.A. |
| 20 | 2007 | Lack of association between interleukin-1 gene cluster polymorphisms and glaucoma in Chinese subjects | 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. |
