D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics and Molecular Biology D-index 65 Citations 12,568 192 World Ranking 1850 National Ranking 209

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

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 most cited work include:

  • Seven new loci associated with age-related macular degeneration (584 citations)
  • Seven new loci associated with age-related macular degeneration (584 citations)
  • Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial (531 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Ophthalmology (60.65%)
  • Genetics (58.49%)
  • Retinitis pigmentosa (39.20%)

What were the highlights of his more recent work (between 2017-2021)?

  • Ophthalmology (60.65%)
  • Genetics (58.49%)
  • Retinal (32.72%)

In recent papers he was focusing on the following fields of study:

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.

Between 2017 and 2021, his most popular works were:

  • Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia (72 citations)
  • Beneficial effects on vision in patients undergoing retinal gene therapy for choroideremia (72 citations)
  • Whole-genome sequencing of patients with rare diseases in a national health system. (70 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Internal medicine

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.

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.

Best Publications

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)

699 Citations

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)

656 Citations

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)

589 Citations

Genetic influence on early age-related maculopathy: a twin study.

Christopher J Hammond;Andrew R Webster;Harold Snieder;Harold Snieder;Alan C Bird.
Ophthalmology (2002)

296 Citations

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)

277 Citations

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)

270 Citations

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)

263 Citations

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)

259 Citations

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)

250 Citations

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)

234 Citations

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