Dwight Stambolian mainly focuses on Genetics, Genome-wide association study, Macular degeneration, Gene and Genetic association. Dwight Stambolian works mostly in the field of Genome-wide association study, limiting it down to concerns involving Refractive error and, occasionally, Glaucoma, Global health and Visual impairment. The Macular degeneration study combines topics in areas such as Visual acuity, Factor H, Allele frequency and Case-control study.
His research integrates issues of Retinal pigment epithelium and Presenile cataracts in his study of Gene. His work focuses on many connections between Genetic association and other disciplines, such as Mutation, that overlap with his field of interest in Genetic predisposition, Genomics and Age related. His study in the fields of Minor allele frequency and Imputation under the domain of Single-nucleotide polymorphism overlaps with other disciplines such as ABCA1.
Dwight Stambolian mainly investigates Genetics, Macular degeneration, Gene, Genome-wide association study and Ophthalmology. His Locus, Genetic linkage, Single-nucleotide polymorphism, Candidate gene and Genetic association study are his primary interests in Genetics. His Genetic association research is multidisciplinary, relying on both SNP and Haplotype.
The various areas that Dwight Stambolian examines in his Macular degeneration study include Retinal, Factor H, Age related and Bioinformatics. In his study, which falls under the umbrella issue of Gene, Complementary DNA is strongly linked to Molecular biology. His work carried out in the field of Genome-wide association study brings together such families of science as Refractive error and Disease.
The scientist’s investigation covers issues in Genetics, Macular degeneration, Ophthalmology, Age related and Genome-wide association study. His work in Linkage, Exome, Candidate gene, Gene and Locus is related to Genetics. His Exome study incorporates themes from Genetic linkage and Haplotype.
His studies deal with areas such as Visual impairment, Microperimetry, Refractive error and Factor H as well as Macular degeneration. Dwight Stambolian has researched Age related in several fields, including Molecular genetics, Risk variant and Immunology. The study incorporates disciplines such as Disease, TCF4 and Bioinformatics in addition to Genome-wide association study.
Macular degeneration, Genetics, Genome-wide association study, Visual impairment and Disease are his primary areas of study. His Macular degeneration research focuses on subjects like Age related, which are linked to Molecular genetics, Nerve fiber layer and Optical coherence tomography. His biological study focuses on Candidate gene.
Genome-wide association study is a subfield of Single-nucleotide polymorphism that Dwight Stambolian tackles. His Visual impairment research incorporates themes from Global health and Visual acuity. His research in Disease intersects with topics in SNP, Bioinformatics, Transcriptome, Gene and Genetic association.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Next-generation genotype imputation service and methods.
Sayantan Das;Lukas Forer;Sebastian Schönherr;Carlo Sidore;Carlo Sidore.
Nature Genetics (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
Global Causes of Blindness and Distance Vision Impairment 1990-2020: A Systematic Review and Meta-Analysis
Seth R Flaxman;Rupert R A Bourne;Serge Resnikoff;Serge Resnikoff;Peter Ackland.
The Lancet Global Health (2017)
Magnitude, temporal trends, and projections of the global prevalence of blindness and distance and near vision impairment: a systematic review and meta-analysis
Rupert R A Bourne;Seth R Flaxman;Tasanee Braithwaite;Maria V Cicinelli.
The Lancet Global Health (2017)
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche;Wilmar Igl;Jessica N.Cooke Bailey;Felix Grassmann.
Nature Genetics (2016)
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)
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
Wei Chen;Dwight Stambolian;Albert O. Edwards;Kari E. Branham.
Proceedings of the National Academy of Sciences of the United States of America (2010)
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)
Age-Related Macular Degeneration: Genetics and Biology Coming Together
Lars G. Fritsche;Robert N. Fariss;Dwight Stambolian;Gonçalo R. Abecasis.
Annual Review of Genomics and Human Genetics (2014)
Transcriptome analysis and molecular signature of human retinal pigment epithelium
N.V. Strunnikova;A. Maminishkis;J.J. Barb;F. Wang.
Human Molecular Genetics (2010)
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