Eranga N. Vithana spends much of his time researching Genetics, Genome-wide association study, Polymorphism, Glaucoma and Odds ratio. His work blends Genetics and Chromatin immunoprecipitation studies together. His biological study spans a wide range of topics, including SNP, Enhancer RNAs and Candidate gene.
His Polymorphism course of study focuses on Case-control study and Macular degeneration, Primary angle-closure glaucoma, Susceptibility locus, Age related and Cohort study. His Odds ratio research integrates issues from Keratoconus and Exome. His study on Haplotype is often connected to CpG site as part of broader study in Genotype.
His primary areas of study are Genetics, Genome-wide association study, Ophthalmology, Glaucoma and Single-nucleotide polymorphism. Genetics is frequently linked to Molecular biology in his study. Eranga N. Vithana has researched Genome-wide association study in several fields, including Odds ratio, SNP, Polymorphism, Case-control study and Genetic association.
His research in Polymorphism intersects with topics in Minor allele frequency and Bioinformatics. His Glaucoma research incorporates elements of Intraocular pressure and Cornea. The study incorporates disciplines such as Internal medicine and Genotyping in addition to Single-nucleotide polymorphism.
Eranga N. Vithana focuses on Glaucoma, Ophthalmology, Genome-wide association study, Genetics and Primary angle-closure glaucoma. Eranga N. Vithana has included themes like Odds ratio and Internal medicine in his Glaucoma study. His work on Retinal as part of his general Ophthalmology study is frequently connected to Closure, thereby bridging the divide between different branches of science.
His Genome-wide association study study incorporates themes from Disease, Genetic association and Candidate gene. His work focuses on many connections between Genetic association and other disciplines, such as Polymorphism, that overlap with his field of interest in Candidate Disease Gene, Case-control study and Genetic architecture. His research links Cell biology with Genetics.
His main research concerns Genome-wide association study, Genetics, Glaucoma, Candidate gene and Intraocular pressure. His work carried out in the field of Genome-wide association study brings together such families of science as Odds ratio and Disease. Eranga N. Vithana studies Genetics, focusing on Genetic association in particular.
The concepts of his Genetic association study are interwoven with issues in Candidate Disease Gene, Case-control study, Polymorphism and Genetic architecture. His Candidate gene research is multidisciplinary, incorporating elements of Quantitative trait locus, Corneal Diseases, Keratoconus and Mendelian Randomization Analysis. His Intraocular pressure research is multidisciplinary, relying on both Genetic variation, Optic disk and Bioinformatics.
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Seven new loci associated with age-related macular degeneration
Lars G. Fritsche;Lars G. Fritsche;Wei Chen;Wei Chen;Matthew Schu;Brian L. Yaspan.
Nature Genetics (2013)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J M Verhoeven;Pirro G Hysi;Robert Wojciechowski;Robert Wojciechowski;Qiao Fan.
Nature Genetics (2013)
A Human Homolog of Yeast Pre-mRNA Splicing Gene, PRP31, Underlies Autosomal Dominant Retinitis Pigmentosa on Chromosome 19q13.4 (RP11)
Eranga N. Vithana;Leen Abu-Safieh;Maxine J. Allen;Alisoun Carey.
Molecular Cell (2001)
Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: same or different disease?
Augustinus Laude;Peter D. Cackett;Eranga N. Vithana;Ian Y. Yeo.
Progress in Retinal and Eye Research (2010)
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.
Yi Lu;Veronique Vitart;Kathryn P. Burdon;Chiea Chuen Khor.
Nature Genetics (2013)
Alpha-b crystallin gene (CRYAB) mutation causes dominant congenital posterior polar cataract in humans
Vanita Berry;Peter Francis;M. Ashwin Reddy;Dean Collyer.
American Journal of Human Genetics (2001)
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation
Norihiro Kato;Marie Loh;Marie Loh;Marie Loh;Fumihiko Takeuchi;Niek Verweij.
Nature Genetics (2015)
Mutations in HPRP3, a third member of pre-mRNA splicing factor genes, implicated in autosomal dominant retinitis pigmentosa
Christina F Chakarova;Matthew M Hims;Hanno Jörn Bolz;Leen Abu-Safieh.
Human Molecular Genetics (2002)
Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers
Juliet D. French;Maya Ghoussaini;Stacey L. Edwards;Kerstin B. Meyer.
American Journal of Human Genetics (2013)
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)
Eranga N Vithana;Patricio Morgan;Periasamy Sundaresan;Neil D Ebenezer.
Nature Genetics (2006)
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