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ERANGA NISHANTHIE VITHANA

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

Publications

Results 1-20 of 30 (Search time: 0.007 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. 
112017Genome-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. 
122007Identification 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.
13Aug-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.
142010Identification 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. 
1517-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 
162013Ion transport function of SLC4A11 in corneal endotheliumJalimarada, S.S.; Ogando, D.G.; Vithana, E.N. ; Bonanno, J.A.
172007Lack 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.
182008Lack 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. 
192015Lens status influences the association between CFH polymorphisms and age-related macular degeneration: Findings from two population-based studies in SingaporeWong, Cheewai; Liao, Jiemin ; Cheung, Chui Ming Gemmy ; Khor, Chiea Chuen; Vithana, Eranga Nishanthie ; Wang, Jiejin; Mitchell, Paul James; Aung Tin ; Wong, Tienyin; Cheng Ching-Yu 
202016Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's diseaseFoo J.N.; Chung S.J.; Tan L.C.; Liany H.; Ryu H.-S.; Hong M.; Koh T.H.; Irwan I.D.; Au W.-L.; Prakash K.-M.; Aung T. ; Cheng C.-Y. ; Chong S.-A. ; Khor C.C. ; Lee J. ; Tai E.-S. ; Vithana E.N. ; Wong T.-Y. ; Song K.; Liu J. ; Tan E.-K.