Andrew R. Webster

22.2k total citations · 1 hit paper
341 papers, 10.1k citations indexed

About

Andrew R. Webster is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Andrew R. Webster has authored 341 papers receiving a total of 10.1k indexed citations (citations by other indexed papers that have themselves been cited), including 273 papers in Molecular Biology, 208 papers in Ophthalmology and 55 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Andrew R. Webster's work include Retinal Development and Disorders (240 papers), Retinal Diseases and Treatments (179 papers) and Glaucoma and retinal disorders (47 papers). Andrew R. Webster is often cited by papers focused on Retinal Development and Disorders (240 papers), Retinal Diseases and Treatments (179 papers) and Glaucoma and retinal disorders (47 papers). Andrew R. Webster collaborates with scholars based in United Kingdom, United States and Mexico. Andrew R. Webster's co-authors include Anthony T. Moore, Michel Michaelides, Graham E. Holder, Anthony G. Robson, Panagiotis I. Sergouniotis, Alan C. Bird, Graeme C. Black, Gavin Arno, Genevieve Wright and Anthony T. Moore and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Andrew R. Webster

324 papers receiving 9.9k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Retinal gene therapy in patients with choroideremia: initial findings from a phase 1/2 clinical trial

2014 622 citations Graeme C. Black, Andrew R. Webster et al. profile →

Peers

Andrew R. Webster

OPHTH

RNMI

GENET

CMN

Stephen H. Tsang United States

Shomi S. Bhattacharya United Kingdom

Anneke I. den Hollander Netherlands

Eric A. Pierce United States

James Bainbridge United Kingdom

Arthur A. Bergen Netherlands

Elise Héon Canada

Ernst R. Tamm Germany

Anthony T. Moore United Kingdom

Stephen H. Tsang United States

Andrew R. Webster

8.5k ×1.1

5.4k ×1.0

OPHTH

1.7k ×1.0

RNMI

1.2k ×0.7

GENET

1.8k ×1.5

CMN

Citations per year, relative to Andrew R. Webster Andrew R. Webster (= 1×) peers Stephen H. Tsang

Countries citing papers authored by Andrew R. Webster

Since Specialization

Citations

This map shows the geographic impact of Andrew R. Webster's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Andrew R. Webster with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrew R. Webster more than expected).

Fields of papers citing papers by Andrew R. Webster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew R. Webster. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Andrew R. Webster. The network helps show where Andrew R. Webster may publish in the future.

Co-authorship network of co-authors of Andrew R. Webster

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew R. Webster. A scholar is included among the top collaborators of Andrew R. Webster based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Andrew R. Webster. Andrew R. Webster is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Schiff, Elena, Siying Lin, José S. Pulido, et al.. (2025). Comparison of inherited retinal disease genes covered by two comprehensive genetic testing panels and a widely used online resource. Eye. 39(5). 1009–1010. 1 indexed citations

Lin, Siying, Anthony G. Robson, Dorothy Thompson, et al.. (2024). Non‐syndromic retinal dystrophy associated with biallelic variation of SUMF1 and reduced leukocyte sulfatase activity. Clinical Genetics. 106(4). 505–511. 1 indexed citations

Lee, Sang‐Eun, Kalyan Dulla, Wouter Beumer, et al.. (2023). Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>C. Molecular Therapy — Nucleic Acids. 31. 674–688. 24 indexed citations

Varela, Malena Daich, Emma Duignan, Samantha R. De Silva, et al.. (2023). CERKL-Associated Retinal Dystrophy. Ophthalmology Retina. 7(10). 918–931. 3 indexed citations

Georgiou, Michalis, Kaoru Fujinami, Anthony G. Robson, et al.. (2023). RBP3-Retinopathy—Inherited High Myopia and Retinal Dystrophy: Genetic Characterization, Natural History, and Deep Phenotyping. American Journal of Ophthalmology. 258. 119–129. 2 indexed citations

Georgiou, Michalis, Anthony G. Robson, Sami H. Uwaydat, et al.. (2023). RP2-Associated X-linked Retinopathy: Clinical Findings, Molecular Genetics, and Natural History in a Large Cohort of Female Carriers. American Journal of Ophthalmology. 261. 112–120. 2 indexed citations

Obolensky, Alexey, Mingchu Xu, Yumei Li, et al.. (2022). Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily. Genetics in Medicine. 24(7). 1523–1535. 7 indexed citations

Hayes, Nicole, Lisa K. Akison, Elizabeth Elliott, et al.. (2022). Key Stakeholder Priorities for the Review and Update of the Australian Guide to Diagnosis of Fetal Alcohol Spectrum Disorder: A Qualitative Descriptive Study. International Journal of Environmental Research and Public Health. 19(10). 5823–5823. 9 indexed citations

Pontikos, Nikolas, et al.. (2021). Collaborative Research and Development of a Novel, Patient-Centered Digital Platform (MyEyeSite) for Rare Inherited Retinal Disease Data: Acceptability and Feasibility Study. JMIR Formative Research. 6(1). e21341–e21341. 4 indexed citations

10.

Georgiou, Michalis, Lucia Finocchio, Kaoru Fujinami, et al.. (2021). X-Linked Retinoschisis. Ophthalmology. 129(5). 542–551. 19 indexed citations

11.

Petrushkin, Harry, Andrew R. Webster, Elena Moraitis, et al.. (2021). A Novel Pathogenic NOD2 Variant in a Mother and Daughter with Blau Syndrome. Ophthalmic Genetics. 42(6). 753–764. 3 indexed citations

12.

Low, Sancy, Alice E. Davidson, Maria Papadopoulos, et al.. (2019). A new paradigm for delivering personalised care: integrating genetics with surgical interventions in BEST1 mutations. Eye. 34(3). 577–583. 7 indexed citations

13.

Plant, Gordon T., et al.. (2019). Light adaptation of the photopic electroretinogram in healthy subjects, and in patients with diseases affecting ganglion cells, the retinal pigment epithelium and the rod system. Investigative Ophthalmology & Visual Science. 60(9). 2501–2501.

14.

Scheidecker, Sophie, Sarah Hull, Valérie Pelletier, et al.. (2015). Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome. American Journal of Ophthalmology. 160(2). 364–372.e1. 19 indexed citations

15.

Dubis, Adam M., Christopher S. Langlo, Alfredo Dubra, et al.. (2015). Residual Foveal Cone Structure in CNGB3 Achromatopsia: Factors for gene therapy candidate selection. Investigative Ophthalmology & Visual Science. 56(7). 4264–4264. 1 indexed citations

16.

Ba‐Abbad, Rola, Jonathan Aboshiha, Yusufu N. Sulai, et al.. (2014). Outer Retinal Changes Associated with the RPGR Carrier Phenotype: Insights from high-resolution imaging. Investigative Ophthalmology & Visual Science. 55(13). 274–274. 1 indexed citations

17.

Wattam-Bell, John, Koji Nishiguchi, Vanita Sundaram, et al.. (2013). Cortical visual processing in patients with congenital achromatopsia: coherent form, motion and biological motion perception. Journal of Vision. 13(9). 21–21. 1 indexed citations

18.

Mehta, Hemal, et al.. (2012). AUTOFLUORESCENCE AND SPECTRAL-DOMAIN OCT FINDINGS IN AN ATROPHIC MACULOPATHY ASSOCIATED WITH PSEUDOXANTHOMA ELASTICUM. UCL Discovery (University College London). 2 indexed citations

19.

Mackay, Donna S., Arundhati Dev Borman, Phillip Moradi, et al.. (2011). RDH12 retinopathy: novel mutations and phenotypic description.. PubMed. 17. 2706–16. 49 indexed citations

20.

Sergouniotis, Panagiotis I., Donna S. Mackay, Alexander Day, et al.. (2010). A detailed phenotypic assessment of individuals affected by MFRP-related oculopathy.. PubMed. 16. 540–8. 33 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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