Anthony T. Moore

21.9k citations
267 papers · 11.0k · 1 hit paper · h-index 56

Impact in

  • Ophthalmology top 0.05%
    • Retinal Diseases and Treatments
    • Glaucoma and retinal disorders
  • Molecular Biology top 0.5%
    • Retinal Development and Disorders
    • CRISPR and Genetic Engineering
    • Connexins and lens biology

Papers in

  • Molecular Biology 161
    • Retinal Development and Disorders 131
    • Connexins and lens biology 19
    • RNA regulation and disease 7
  • Ophthalmology 65
    • Retinal Diseases and Treatments 45
    • Retinal and Optic Conditions 8
Co-authors
Michel Michaelides (127 shared papers)Andrew R. Webster (121 shared papers)Graham E. Holder (75 shared papers)Anthony G. Robson (67 shared papers)David M. Hunt (26 shared papers)Alan C. Bird (20 shared papers)Fred W. Fitzke (7 shared papers)Panagiotis I. Sergouniotis (24 shared papers)
Journals
Investigative Ophthalmology & Visual Science (57 papers)Ophthalmology (24 papers)British Journal of Ophthalmology (23 papers)Eye (15 papers)Ophthalmic Genetics (11 papers)
Partner nations
United KingdomUnited StatesMexico

In The Last Decade

Anthony T. Moore

265 papers receiving 10.8k citations

Anthony T. Moore's Hit Papers

Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis 2008 · 1.5k citations
1.5k0+6+12Years since publication4008001.2k
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

  • it has ≥500 total citations;
  • it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
  • it reaches the top citation threshold in at least one of its specific research topics.
  1. 2008 New England Journal of Medicine

Peers

Anthony T. Moore
Comparison fields: 5 of 148
  • Ophthalmology 3.5k
  • Molecular Biology 7.5k
  • Cellular and Molecular Neuroscience 1.2k
  • Genetics 1.5k
  • Radiology, Nuclear Medicine and Imaging 1.1k
Replace Richard G. Weleber with:
Richard G. Weleber United States
Michel Michaelides United Kingdom
Andrew R. Webster United Kingdom
Stephen H. Tsang United States
Shomi S. Bhattacharya United Kingdom
Paul A. Sieving United States
Bo Chang United States
Elise Héon Canada
Birgit Lorenz Germany
Thomas Rosenberg Denmark
Anthony T. Moore relative to Richard G. Weleber United States Richard G. Weleber's profile →
Citations per field
00.5×1.5×1.8×
Richard G. Weleber · 1×
Citations per year

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

The 25 scholars most cited alongside Anthony T. Moore, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anthony T. Moore Line = papers co-authored together Anthony T. Moore links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 267 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Effect of Gene Therapy on Visual Function in Leber's Congenital Amaurosis
New England Journal of Medicine ·James Bainbridge, Alexander J. Smith, Susie S. Barker, Scott Robbie, Robert Henderson, Kamaljit S. Balaggan, Ananth C. Viswanathan, Graham E. Holder, Andrew Stockman, Nick Tyler, Simon M. Petersen‐Jones, Shomi S. Bhattacharya, Adrian J. Thrasher, Fred W. Fitzke, Barrie J. Carter, Gary S. Rubin, Anthony T. Moore, Robin R. Ali
Hit paper breakdown →		20081490
2
Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
British Journal of Ophthalmology ·Neruban Kumaran, Anthony T. Moore, Richard G. Weleber, Michel Michaelides
2017232
3
Two infant vision screening programmes: Prediction and prevention of strabismus and amblyopia from photo- and videorefractive screening
Eye ·Janette Atkinson, Oliver Braddick, Bill Bobier, Shirley Anker, D L Ehrlich, John A. King, Peter Watson, Anthony T. Moore
1996193
4
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans
Nature Genetics ·Sanjay M. Sisodiya, S. L. Free, Kathleen A. Williamson, Tejal N. Mitchell, Catherine Willis, John Stevens, B. E. Kendall, Simon Shorvon, Isabel M. Hanson, Anthony T. Moore, Veronica van Heyningen
2001187
5
Mutations in the Retinal Guanylate Cyclase (RETGC-1) Gene in Dominant Cone-Rod Dystrophy
Human Molecular Genetics ·Rosemary E. Kelsell, Kevin Gregory-Evans, Annette Payne, Isabelle Perrault, Josseline Kaplan, Ruey‐Bing Yang, David L. Garbers, Alan C. Bird, Anthony T. Moore, David M. Hunt
1998187
6
Progressive Cone and Cone-Rod Dystrophies: Phenotypes and Underlying Molecular Genetic Basis
Survey of Ophthalmology ·Michel Michaelides, Alison J. Hardcastle, David M. Hunt, Anthony T. Moore
2006173
7
Differentiating drusen: Drusen and drusen-like appearances associated with ageing, age-related macular degeneration, inherited eye disease and other pathological processes
Progress in Retinal and Eye Research ·Kamron N. Khan, Omar A. Mahroo, Rehna Khan, Moin Mohamed, Martin McKibbin, Alan C. Bird, Michel Michaelides, Adnan Tufail, Anthony T. Moore
2016166
8
Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom
Ophthalmology ·Nikolas Pontikos, Gavin Arno, Neringa Jurkutė, Elena Schiff, Rola Ba‐Abbad, Samantha Malka, Ainoa Gimenez, Michalis Georgiou, Genevieve Wright, Monica Armengol, Hannah Knight, Menachem Katz, Mariya Moosajee, Patrick Yu‐Wai‐Man, Anthony T. Moore, Michel Michaelides, Andrew R. Webster, Omar A. Mahroo
2020164
9
Complement Factor H Variant Y402H Is a Major Risk Determinant for Geographic Atrophy and Choroidal Neovascularization in Smokers and Nonsmokers
Investigative Ophthalmology & Visual Science ·Tiina Sepp, Jane C. Khan, Deborah A. Thurlby, Humma Shahid, David Clayton, Anthony T. Moore, Alan C. Bird, John R.W. Yates
2006148
10
Recessive Mutations of the Gene TRPM1 Abrogate ON Bipolar Cell Function and Cause Complete Congenital Stationary Night Blindness in Humans
The American Journal of Human Genetics ·Zheng Li, Panagiotis I. Sergouniotis, Michel Michaelides, Donna S. Mackay, Genevieve Wright, Sophie Devery, Anthony T. Moore, Graham E. Holder, Anthony G. Robson, Andrew R. Webster
2009143
11
Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease
Ophthalmology ·Kaoru Fujinami, Jana Zernant, Ravinder Chana, Genevieve Wright, Kazushige Tsunoda, Yoko Ozawa, Kazuo Tsubota, Anthony G. Robson, Graham E. Holder, Rando Allikmets, Michel Michaelides, Anthony T. Moore
2014130
12
Retinal Structure and Function in Achromatopsia
Ophthalmology ·Venki Sundaram, Caroline Wilde, Jonathan Aboshiha, Jill A. Cowing, Colin Han, Christopher S. Langlo, Ravinder Chana, Alice E. Davidson, Panagiotis I. Sergouniotis, James Bainbridge, Robin R. Ali, Alfredo Dubra, Gary S. Rubin, Andrew R. Webster, Anthony T. Moore, Marko Nardini, Joseph Carroll, Michel Michaelides
2013129
13
Progressive cone and cone-rod dystrophies: clinical features, molecular genetics and prospects for therapy
British Journal of Ophthalmology ·Jasdeep Gill, Michalis Georgiou, Angelos Kalitzeos, Anthony T. Moore, Michel Michaelides
2019126
14
Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta
The American Journal of Human Genetics ·David Parry, Alan J. Mighell, Walid El‐Sayed, (unknown), I K Jalili, Hélène Dollfus, Agnès Bloch‐Zupan, Román Carlos, Ian Carr, Louise Downey, Katharine M. Blain, David Mansfield, Mehdi Shahrabi, Mansour Heidari, Parissa Aref, Mohsen Abbasi, Michel Michaelides, Anthony T. Moore, Jennifer Kirkham, Chris F. Inglehearn
2009121
15
A Longitudinal Study of Stargardt Disease: Clinical and Electrophysiologic Assessment, Progression, and Genotype Correlations
American Journal of Ophthalmology ·Kaoru Fujinami, Noemi Lois, Alice E. Davidson, Donna S. Mackay, Chris R. Hogg, Edwin M. Stone, Kazushige Tsunoda, Kazuo Tsubota, Catey Bunce, Anthony G. Robson, Anthony T. Moore, Andrew R. Webster, Graham E. Holder, Michel Michaelides
2013116
16
Functional characteristics of patients with retinal dystrophy that manifest abnormal parafoveal annuli of high density fundus autofluorescence; a review and update
Documenta Ophthalmologica ·Anthony G. Robson, Michel Michaelides, Zubin Saihan, Alan C. Bird, Andrew R. Webster, Anthony T. Moore, Fred W. Fitzke, Graham E. Holder
2007116
17
A Longitudinal Study of Stargardt Disease: Quantitative Assessment of Fundus Autofluorescence, Progression, and Genotype Correlations
Investigative Ophthalmology & Visual Science ·Kaoru Fujinami, Noemi Lois, Rajarshi Mukherjee, Vikki A. McBain, Kazushige Tsunoda, Kazuo Tsubota, Edwin M. Stone, Fred W. Fitzke, Catey Bunce, Anthony T. Moore, Andrew R. Webster, Michel Michaelides
2013114
18
Organization of the Visual Cortex in Human Albinism
Journal of Neuroscience ·Michael B. Hoffmann, D.J. Tolhurst, Anthony T. Moore, Antony B. Morland
2003100
19
Mutations in the Gene KCNV2 Encoding a Voltage-Gated Potassium Channel Subunit Cause “Cone Dystrophy with Supernormal Rod Electroretinogram” in Humans
The American Journal of Human Genetics ·Huimin Wu, Jill A. Cowing, Michel Michaelides, Susan E. Wilkie, Glen Jeffery, Sharon Jenkins, Viktória Mester, Alan C. Bird, Anthony G. Robson, Graham E. Holder, Anthony T. Moore, David M. Hunt, Andrew R. Webster
2006100
20
Human Cone Visual Pigment Deletions Spare Sufficient Photoreceptors to Warrant Gene Therapy
Human Gene Therapy ·Artur V. Cideciyan, Robert B. Hufnagel, Joseph Carroll, Alexander Sumaroka, Xunda Luo, Sharon Schwartz, Alfredo Dubra, Megan Land, Michel Michaelides, Jessica C. Gardner, Alison J. Hardcastle, Anthony T. Moore, Robert A. Sisk, Zubair M. Ahmed, Susanne Kohl, Bernd Wissinger, Samuel G. Jacobson
201394

About Anthony T. Moore

Anthony T. Moore is a scholar working on Molecular Biology, Ophthalmology, Genetics, Radiology, Nuclear Medicine and Imaging and Cell Biology, having authored 267 papers that have together received 11.0k indexed citations. Recurring topics across this work include Retinal Development and Disorders (131 papers), Retinal Diseases and Treatments (45 papers), Connexins and lens biology (19 papers), Photoreceptor and optogenetics research (10 papers), melanin and skin pigmentation (9 papers), Retinopathy of Prematurity Studies (8 papers), Retinal and Optic Conditions (8 papers) and RNA regulation and disease (7 papers). The work is most often cited by research in Ophthalmology (3.5k citations), Molecular Biology (7.5k citations), Cellular and Molecular Neuroscience (1.2k citations), Genetics (1.5k citations) and Radiology, Nuclear Medicine and Imaging (1.1k citations). Anthony T. Moore has collaborated with scholars based in United Kingdom, United States and Mexico. Frequent co-authors include Michel Michaelides, Andrew R. Webster, Graham E. Holder, Anthony G. Robson, David M. Hunt, Alan C. Bird, Fred W. Fitzke, Panagiotis I. Sergouniotis, Andrew Stockman and Shomi S. Bhattacharya. Their work appears in journals such as Investigative Ophthalmology & Visual Science, Ophthalmology, British Journal of Ophthalmology, Eye and Ophthalmic Genetics.

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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