Eranga N. Vithana
Eranga N. Vithana
Singapore Eye Research Institute, National University of Singapore, Duke-NUS Graduate Medical School
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Cited by
Cited by
Seven new loci associated with age-related macular degeneration
AMD Gene Consortium
Nature genetics 45 (4), 433, 2013
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
VJM Verhoeven, PG Hysi, R Wojciechowski, Q Fan, JA Guggenheim, ...
Nature genetics 45 (3), 314-318, 2013
A human homolog of yeast pre-mRNA splicing gene, PRP31, underlies autosomal dominant retinitis pigmentosa on chromosome 19q13. 4 (RP11)
EN Vithana, L Abu-Safieh, MJ Allen, A Carey, M Papaioannou, ...
Molecular cell 8 (2), 375-381, 2001
Mapping of a familial essential tremor gene, FET1, to chromosome 3q13
JR Gulcher, Ŝ Jónsson, A Kong, K Kristjánsson, ML Frigge, A Kárason, ...
Nature genetics 17 (1), 84-87, 1997
Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: same or different disease?
A Laude, PD Cackett, EN Vithana, IY Yeo, D Wong, AH Koh, TY Wong, ...
Progress in retinal and eye research 29 (1), 19-29, 2010
Alpha-B crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
V Berry, P Francis, MA Reddy, D Collyer, E Vithana, I MacKay, G Dawson, ...
The American Journal of Human Genetics 69 (5), 1141-1145, 2001
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus
Y Lu, V Vitart, KP Burdon, CC Khor, Y Bykhovskaya, A Mirshahi, ...
Nature genetics 45 (2), 155, 2013
Mutations in HPRP3, a third member ofpre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
CF Chakarova, MM Hims, H Bolz, L Abu-Safieh, RJ Patel, ...
Human molecular genetics 11 (1), 87-92, 2002
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
N Kato, M Loh, F Takeuchi, N Verweij, X Wang, W Zhang, TN Kelly, ...
Nature genetics 47 (11), 1282-1293, 2015
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
JD French, M Ghoussaini, SL Edwards, KB Meyer, K Michailidou, ...
The American Journal of Human Genetics 92 (4), 489-503, 2013
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
EN Vithana, P Morgan, P Sundaresan, ND Ebenezer, DTH Tan, ...
Nature genetics 38 (7), 755-757, 2006
SLC4A11 mutations in Fuchs endothelial corneal dystrophy
EN Vithana, PE Morgan, V Ramprasad, DTH Tan, VHK Yong, ...
Human molecular genetics 17 (5), 656-666, 2008
Genome-wide association analyses identify three new susceptibility loci for primary angle closure glaucoma
EN Vithana, CC Khor, C Qiao, ME Nongpiur, R George, LJ Chen, T Do, ...
Nature genetics 44 (10), 1142-1146, 2012
Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma
PG Hysi, CY Cheng, H Springelkamp, S Macgregor, JNC Bailey, ...
Nature genetics 46 (10), 1126-1130, 2014
Collagen-related genes influence the glaucoma risk factor, central corneal thickness
EN Vithana, T Aung, CC Khor, BK Cornes, WT Tay, X Sim, R Lavanya, ...
Human molecular genetics 20 (4), 649-658, 2011
Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma
JNC Bailey, SJ Loomis, JH Kang, RR Allingham, P Gharahkhani, CC Khor, ...
Nature genetics 48 (2), 189-194, 2016
Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma
Y Chen, Y Lin, EN Vithana, L Jia, X Zuo, TY Wong, LJ Chen, X Zhu, ...
Nature genetics 46 (10), 1115, 2014
New loci and coding variants confer risk for age-related macular degeneration in East Asians
CY Cheng, K Yamashiro, LJ Chen, J Ahn, L Huang, L Huang, ...
Nature communications 6 (1), 1-10, 2015
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error
CY Cheng, M Schache, MK Ikram, TL Young, JA Guggenheim, V Vitart, ...
The American Journal of Human Genetics 93 (2), 264-277, 2013
Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese
YJ Li, L Goh, CC Khor, Q Fan, M Yu, S Han, X Sim, RTH Ong, TY Wong, ...
Ophthalmology 118 (2), 368-375, 2011
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