Andrew R. Webster mostly deals with Genetics, Retinitis pigmentosa, Ophthalmology, Visual acuity and Electroretinography. His Retinitis pigmentosa study incorporates themes from Nonsense mutation, Dystrophy, Genetic heterogeneity and Locus. His study in Retinal and Macular degeneration is carried out as part of his Ophthalmology studies.
His work in Retinal tackles topics such as Retina which are related to areas like Photoreceptor Connecting Cilium. His Visual acuity study integrates concerns from other disciplines, such as Retinopathy, Optometry and Foveal. His Electroretinography research is multidisciplinary, incorporating perspectives in Ophthalmoscopy, Photopic vision, Retinal Rod Photoreceptor Cells, Pathology and Fundus.
His main research concerns Ophthalmology, Genetics, Retinitis pigmentosa, Retinal and Visual acuity. His Ophthalmology study frequently links to related topics such as Retinopathy. His research related to Missense mutation, Gene, Mutation, Retinal degeneration and Allele might be considered part of Genetics.
The Retinitis pigmentosa study which covers Exon that intersects with Molecular biology. His work carried out in the field of Retinal brings together such families of science as Exome sequencing, Retina and Disease. His Visual acuity study combines topics from a wide range of disciplines, such as Ophthalmoscopy, Maculopathy, Nyctalopia and Optical coherence tomography.
Andrew R. Webster focuses on Ophthalmology, Genetics, Retinal, Retinitis pigmentosa and Visual acuity. While the research belongs to areas of Ophthalmology, Andrew R. Webster spends his time largely on the problem of Retinopathy, intersecting his research to questions surrounding Retinitis pigmentosa GTPase regulator. His Retinal study combines topics in areas such as Disease gene, Consanguinity, Retina and Proband.
His Retinitis pigmentosa study combines topics from a wide range of disciplines, such as Internal medicine and Visual field. His Visual acuity study integrates concerns from other disciplines, such as Clinical trial, Adverse effect, Erg, Choroideremia and Cohort. His Electroretinography study deals with Achromatopsia intersecting with Foveal.
Andrew R. Webster spends much of his time researching Ophthalmology, Retinitis pigmentosa, Genetics, Retinal and Visual acuity. His Ophthalmology study combines topics in areas such as Retinopathy, Prospective cohort study and Atrophy. Andrew R. Webster incorporates Retinitis pigmentosa and In patient in his research.
The various areas that Andrew R. Webster examines in his Retinal study include Missense mutation, Retina and Cell biology. His Visual acuity research incorporates elements of Visual field and Clinical trial. His Electroretinography research includes elements of Ophthalmoscopy, Achromatopsia and Fundus.
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Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial
Robert E MacLaren;Robert E MacLaren;Markus Groppe;Markus Groppe;Alun R Barnard;Charles L Cottriall.
The Lancet (2014)
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)
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan.
Berton Zbar;Takeshi Kishida;Fan Chen;Laura Schmidt.
Human Mutation (1996)
Genetic influence on early age-related maculopathy: a twin study.
Christopher J Hammond;Andrew R Webster;Harold Snieder;Harold Snieder;Alan C Bird.
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 Bolz;Leen Abu-Safieh.
Human Molecular Genetics (2002)
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.
A H Prowse;A R Webster;F M Richards;S Richard.
American Journal of Human Genetics (1997)
Biallelic Mutation of BEST1 Causes a Distinct Retinopathy in Humans
Rosemary Burgess;Rosemary Burgess;Ian D. Millar;Bart P. Leroy;Jill E. Urquhart;Jill E. Urquhart.
American Journal of Human Genetics (2008)
Phenotypic expression in von Hippel-Lindau disease: correlations with germline VHL gene mutations.
E R Maher;A R Webster;F M Richards;J S Green.
Journal of Medical Genetics (1996)
Clinical characteristics of ocular angiomatosis in von Hippel-Lindau disease and correlation with germline mutation.
Andrew R. Webster;Eamonn R. Maher;Anthony T. Moore.
Archives of Ophthalmology (1999)
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease
K J Carss;G Arno;M Erwood;J Stephens.
American Journal of Human Genetics (2017)
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