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.
Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
20081.5k citationsJames Bainbridge, Graham E. Holder et al.profile →
Peers — A (Enhanced Table)
Peers by citation overlap · career bar shows stage (early→late)
cites ·
hero ref
Countries citing papers authored by Anthony T. Moore
Since
Specialization
Citations
This map shows the geographic impact of Anthony T. Moore'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 Anthony T. Moore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Anthony T. Moore more than expected).
Fields of papers citing papers by Anthony T. Moore
This network shows the impact of papers produced by Anthony T. Moore. 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 Anthony T. Moore. The network helps show where Anthony T. Moore may publish in the future.
Co-authorship network of co-authors of Anthony T. Moore
This figure shows the co-authorship network connecting the top 25 collaborators of Anthony T. Moore.
A scholar is included among the top collaborators of Anthony T. Moore 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 Anthony T. Moore. Anthony T. Moore is excluded from
the visualization to improve readability, since they are connected to all nodes in the network.
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
7.
Tracey‐White, Dhani, Clare E. Futter, Anthony T. Moore, et al.. (2014). Translational bypass therapy using ataluren to treat nonsense-mediated choroideremia. Investigative Ophthalmology & Visual Science. 55(13). 3302–3302.2 indexed citations
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
10.
Lenassi, Eva, Zubin Saihan, Zheng Li, et al.. (2013). A comprehensive screen of the USH2A gene in 185 patients with autosomal recessive retinal disease. Investigative Ophthalmology & Visual Science. 54(15). 677–677.1 indexed citations
11.
Webster, Andrew R., Anthony G. Robson, Philip Hykin, et al.. (2011). Unilateral Retinitis Pigmentosa? A Retrospective Case Series Of Unilateral Pigmentary Retinopathy. Investigative Ophthalmology & Visual Science. 52(14). 4995–4995.1 indexed citations
12.
Carroll, Joseph, Eyal Banin, David M. Hunt, et al.. (2010). Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM). Investigative Ophthalmology & Visual Science. 51(13). 2935–2935.3 indexed citations
13.
Rha, Jungtae, Melissa Wagner-Schuman, Anthony T. Moore, et al.. (2010). Adaptive Optics Imaging of the Cone Mosaic in Oligocone Trichromacy. Investigative Ophthalmology & Visual Science. 51(13). 6296–6296.1 indexed citations
Puech, Virginie, Bernard Puech, Andrew R. Webster, et al.. (2008). A Molecular Genetic Investigation of Two Families With Macular Dysplasia in Association With Digit Abnormalities. Investigative Ophthalmology & Visual Science. 49(13). 456–456.1 indexed citations
Wu, Huimin, Michel Michaelides, S. Wilkie, et al.. (2006). Exclusion of the Cone cGMP Phosphodiesterase Subunit Gene as a Cause of Cone Dystrophy With Supernormal Rod ERG. Investigative Ophthalmology & Visual Science. 47(13). 3289–3289.1 indexed citations
Michaelides, Michel, G.E. Holder, Keith Bradshaw, David M. Hunt, & Anthony T. Moore. (2005). Cone–Rod Dystrophy, Intra–Familial Variability and Incomplete Penetrance Associated With the R172W Mutation in the Peripherin/RDS Gene. Investigative Ophthalmology & Visual Science. 46(13). 1791–1791.2 indexed citations
20.
Audo, Isabelle, M. Neveu, Anthony G. Robson, et al.. (2004). CHARACTERIZATION OF ENHANCED S–CONE SYNDROME (ESCS).. Investigative Ophthalmology & Visual Science. 45(13). 5117–5117.1 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.