Author details

Full Name

Eranga N Vithana

Affiliation

ORCID

Career Start Year

1996

Papers

118

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37418643	RETINITIS PIGMENTOSA ASSOCIATED WITH THE EYS C2139Y VARIANT : An Important Cause of Blindness in East Asian Populations.	Retina	2023
35729796	Comparison of machine learning approaches for structure-function modeling in glaucoma.	Ann N Y Acad Sci	2022
36048435	Evaluation of Generative Adversarial Networks for High-Resolution Synthetic Image Generation of Circumpapillary Optical Coherence Tomography Images for Glaucoma.	JAMA Ophthalmol	2022
32682838	Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci for Estimating Angle Closure Disease Severity.	Ophthalmology	2021
32371412	Factors affecting the diagnostic performance of circumpapillary retinal nerve fibre layer measurement in glaucoma.	Br J Ophthalmol	2021
34230538	Association of peripheral anterior synechiae with anterior segment parameters in eyes with primary angle closure glaucoma.	Scientific Reports	2021
33627673	Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.	Nat Commun	2021
33311586	Common variants in SOX-2 and congenital cataract genes contribute to age-related nuclear cataract.	Commun Biol	2020
31895154	Primary angle closure glaucoma genomic associations and disease mechanism.	Current Opinion in Ophthalmology	2020
31100065	In-utero epigenetic factors are associated with early-onset myopia in young children.	PLoS ONE	2019
30682148	Trinucleotide repeat expansion length as a predictor of the clinical progression of Fuchs' Endothelial Corneal Dystrophy.	PLoS One	2019
31377279	Integration of Genetic and Biometric Risk Factors for Detection of Primary Angle Closure Glaucoma.	Am J Ophthalmol	2019
29452408	Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.	Hum Mol Genet	2018
28621876	Social, health and ocular factors associated with primary open-angle glaucoma amongst Chinese Singaporeans.	Clin Exp Ophthalmol	2018
29310965	Evaluation of Primary Angle-Closure Glaucoma Susceptibility Loci in Patients with Early Stages of Angle-Closure Disease.	Ophthalmology	2018
28011712	Genome-wide association study of Parkinson's disease in East Asians.	Hum Mol Genet	2017
29016860	Primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 encodes a novel Rac1/Cdc42 GAP that modulates cell migration and blood-aqueous barrier function.	Human Molecular Genetics	2017
28553957	Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.	Nat Genet	2017
28073927	New insights into the genetics of primary open-angle glaucoma based on meta-analyses of intraocular pressure and optic disc characteristics.	Hum Mol Genet	2017
26687033	Linking a genome-wide association study signal to a LRRK2 coding variant in Parkinson's disease.	Mov Disord	2016
27064256	Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma.	Nat Genet	2016
27020472	Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error.	Nat Commun	2016
26752265	Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.	Nat Genet	2016
26550974	CYP1B1 and MYOC Mutations in Vietnamese Primary Congenital Glaucoma Patients.	Journal of Glaucoma	2016
25168388	Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk.	Hum Mol Genet	2015
25631615	Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology.	Genet Epidemiol	2015
25706626	A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.	Nat Genet	2015
25629512	New loci and coding variants confer risk for age-related macular degeneration in East Asians.	Nat Commun	2015
25367360	Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.	Hum Genet	2015
25786237	Lens status influences the association between CFH polymorphisms and age-related macular degeneration: findings from two population-based studies in Singapore.	PLoS One	2015
25745874	Aggregate Effects of Intraocular Pressure and Cup-to-Disc Ratio Genetic Variants on Glaucoma in a Multiethnic Asian Population.	Ophthalmology	2015
25861811	A common variant near TGFBR3 is associated with primary open angle glaucoma.	Hum Mol Genet	2015
25817435	Corrigendum: New loci and coding variants confer risk for age-related macular degeneration in East Asians.	Nat Commun	2015
25557343	Biochemical properties and aggregation propensity of transforming growth factor-induced protein (TGFBIp) and the amyloid forming mutants.	Ocul Surf	2015
26307087	Genetic variants and cellular stressors associated with exfoliation syndrome modulate promoter activity of a lncRNA within the LOXL1 locus.	Hum Mol Genet	2015
26390057	Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.	Nat Genet	2015
26383992	A Genetic Variant in TGFBR3-CDC7 Is Associated with Visual Field Progression in Primary Open-Angle Glaucoma Patients from Singapore.	Ophthalmology	2015
26018902	Corrigendum: a common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome.	Nat Genet	2015
24954895	Gene-age interactions in blood pressure regulation: a large-scale investigation with the CHARGE, Global BPgen, and ICBP Consortia.	Am J Hum Genet	2014
25284770	Clinical and genetic aspects of the TGFBI-associated corneal dystrophies.	Ocul Surf	2014
25537207	Association of common SIX6 polymorphisms with peripapillary retinal nerve fiber layer thickness: the Singapore Chinese Eye Study.	Invest Ophthalmol Vis Sci	2014
25298419	Transethnic replication of association of CTG18.1 repeat expansion of TCF4 gene with Fuchs' corneal dystrophy in Chinese implies common causal variant.	Invest Ophthalmol Vis Sci	2014
24474268	Genotype-phenotype correlation analysis for three primary angle closure glaucoma-associated genetic polymorphisms.	Investigative Ophthalmology and Visual Science	2014
24951543	Meta-analysis of genome-wide association studies in multiethnic Asians identifies two loci for age-related nuclear cataract.	Hum Mol Genet	2014
25173106	Genome-wide analysis of multi-ancestry cohorts identifies new loci influencing intraocular pressure and susceptibility to glaucoma.	Nat Genet	2014
25173107	Common variants near ABCA1 and in PMM2 are associated with primary open-angle glaucoma.	Nat Genet	2014
24801512	Expression of the primary angle closure glaucoma (PACG) susceptibility gene PLEKHA7 in endothelial and epithelial cell junctions in the eye.	Investigative Ophthalmology and Visual Science	2014
24565865	Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.	Hum Mol Genet	2014
24963161	CMPK1 and RBP3 are associated with corneal curvature in Asian populations.	Hum Mol Genet	2014
24647736	Multiple nonglycemic genomic loci are newly associated with blood level of glycated hemoglobin in East Asians.	Diabetes	2014