Anthony T. Moore

13.2k total citations · 3 hit papers
107 papers, 8.0k citations indexed

About

Anthony T. Moore is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Anthony T. Moore has authored 107 papers receiving a total of 8.0k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 34 papers in Genetics and 29 papers in Ophthalmology. Recurrent topics in Anthony T. Moore's work include Retinal Development and Disorders (36 papers), Connexins and lens biology (25 papers) and Retinal Diseases and Treatments (16 papers). Anthony T. Moore is often cited by papers focused on Retinal Development and Disorders (36 papers), Connexins and lens biology (25 papers) and Retinal Diseases and Treatments (16 papers). Anthony T. Moore collaborates with scholars based in United Kingdom, United States and Mexico. Anthony T. Moore's co-authors include John R.W. Yates, Shomi S. Bhattacharya, Marcela Votruba, Eamonn R. Maher, Peter J. Francis, Vanita Berry, Donna S. Mackay, M.A. Ferguson‐Smith, Alexander Ionides and Caroline Benjamin and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and Molecular Cell.

In The Last Decade

Anthony T. Moore

106 papers receiving 7.7k 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.

OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28

2000 1.0k citations Anthony T. Moore et al. Nature Genetics profile →
Clinical Features and Natural History of von Hippel-Lindau Disease

1990 675 citations Eamonn R. Maher, Anthony T. Moore et al. profile →
Complement C3 Variant and the Risk of Age-Related Macular Degeneration

2007 650 citations Alan C. Bird, Anthony T. Moore et al. profile →

Peers

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-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.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Identification and Correction of Mechanisms Underlying Inherited Blindness in Human iPSC-Derived Optic Cups 2016 ·Cell stem cell ·David A. Parfitt, Amelia Lane, Conor M. Ramsden, Amanda‐Jayne F. Carr, Peter Munro, Katarina Jovanović, Nele Schwarz, Naheed Kanuga, Manickam Nick Muthiah, Sarah Hull, Jean‐Marc Gallo, Lyndon da Cruz, Anthony T. Moore, Alison J. Hardcastle, Peter Coffey, Michael E. Cheetham	233
2	Developing robust and cost-effective methods for estimating the national recreational catch of Southern Bluefin Tuna in Australia 2015 ·eCite Digital Repository (University of Tasmania) ·Anthony T. Moore, Karina C. Hall, (unknown), S Tracey, Scott P. Hansen, Peter Ward, Ilona Stobutzki, John C. Andrews, Simon Nicol, Paul Brown	4
3	Mutations in TUBGCP4 Alter Microtubule Organization via the γ-Tubulin Ring Complex in Autosomal-Recessive Microcephaly with Chorioretinopathy 2015 ·The American Journal of Human Genetics ·Sophie Scheidecker, Christelle Etard, Laurence Haren, Corinne Stoetzel, Sarah Hull, Gavin Arno, Vincent Plagnol, Séverine Drunat, Sandrine Passemard, Annick Toutain, Cathy Obringer, Mériam Koob, Véronique Geoffroy, Vincent Marion, Uwe Strähle, Pia Østergaard, Alain Verloès, Andreas Merdes, Anthony T. Moore, Hélène Dollfus	50
4	Natural History and Retinal Structure in Patients with Usher Syndrome Type 1 Owing to MYO7A Mutation 2013 ·Ophthalmology ·Eva Lenassi, Zubin Saihan, Valentina Cipriani, Polona Le Quesne Stabej, Anthony T. Moore, Linda Luxon, Maria Bitner‐Glindzicz, Andrew R. Webster	27
5	A clinical molecular genetic service for United Kingdom families with choroideraemia 2013 ·European Journal of Medical Genetics ·Simon Ramsden, Anna O’Grady, Tracy Fletcher, James O’Sullivan, (unknown), Stephanie Barton, Georgina Hall, Anthony T. Moore, Andrew R. Webster, Graeme C. Black	16
6	Understanding the expectations of patients with inherited retinal dystrophies 2013 ·British Journal of Ophthalmology ·Ryan Combs, Georgina Hall, Katherine Payne, (unknown), Sophie Devery, Susan M. Downes, Anthony T. Moore, Simon Ramsden, Graeme C. Black, Marion McAllister	23
7	Biallelic Mutations in PLA2G5, Encoding Group V Phospholipase A2, Cause Benign Fleck Retina 2011 ·The American Journal of Human Genetics ·Panagiotis I. Sergouniotis, Alice E. Davidson, Donna S. Mackay, Eva Lenassi, Zheng Li, Anthony G. Robson, Xu Yang, Jaimie Hoh Kam, Timothy Isaacs, Graham E. Holder, Glen Jeffery, Jonathan Beck, Anthony T. Moore, Vincent Plagnol, Andrew R. Webster	34
8	Biallelic mutation of protocadherin-21 (PCDH21) causes retinal degeneration in humans. 2010 ·PubMed Central ·Robert Henderson, Zheng Li, (unknown), Donna S. Mackay, (unknown), (unknown), Anthony T. Moore, Shomi S. Bhattacharya, Andrew R. Webster	45
9	Bornholm Eye Disease Arises From a Specific Combination of Amino Acid Changes Encoded by Exon 3 of the L/M Cone Opsin Gene 2010 ·Investigative Ophthalmology & Visual Science ·Michelle E. McClements, Maureen Neitz, Anthony T. Moore, David M. Hunt	4
10	Childhood macular dystrophies 2009 ·Current Opinion in Ophthalmology ·Anthony T. Moore	4
11	X-linked cataract and Nance-Horan syndrome are allelic disorders 2009 ·Human Molecular Genetics ·Margherita Coccia, Simon P. Brooks, Tom R. Webb, (unknown), (unknown), Victoria Murday, (unknown), (unknown), Teresia Wangensteen, Ruth Riise, Anand Saggar, Soo‐Mi Park, Naheed Kanuga, Peter J. Francis, Eamonn R. Maher, Anthony T. Moore, Isabelle Russell‐Eggitt, Alison J. Hardcastle	50
12	Mutation in Rab3 GTPase-Activating Protein (RAB3GAP) Noncatalytic Subunit in a Kindred with Martsolf Syndrome 2006 ·The American Journal of Human Genetics ·Irene A. Aligianis, Neil V. Morgan, Marina Mione, Colin A. Johnson, Elisabeth Rosser, Raoul C. M. Hennekam, Gill Adams, Richard C. Trembath, Daniela T. Pilz, Neil Stoodley, Anthony T. Moore, Steve Wilson, Eamonn R. Maher	78
13	Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations 2005 ·Human Genetics ·Tim Forshew, Colin A. Johnson, Shagufta Khaliq, Shanaz Pasha, Catherine Willis, (unknown), Louise Tee, (unknown), Richard C. Trembath, S. Qasim Mehdi, Anthony T. Moore, Eamonn R. Maher	66
14	Mutations of VMD2 Splicing Regulators Cause Nanophthalmos and Autosomal Dominant Vitreoretinochoroidopathy (ADVIRC) 2004 ·Investigative Ophthalmology & Visual Science ·(unknown), Bart P. Leroy, Niki Hart‐Holden, B. A. Lafaut, Bart Loeys, Ludwine Messiaen, Rahat Perveen, M. Ashwin Reddy, Shomi S. Bhattacharya, Elias I. Traboulsi, Diana Baralle, Jean‐Jacques De Laey, Bernard Puech, Philippe Kestelyn, Anthony T. Moore, Forbes Manson, Graeme C. Black	163
15	A CRYGD mutation is associated with familial coralliform cataract 2004 ·Investigative Ophthalmology & Visual Science ·Anita Arora, (unknown), Peter J. Francis, Alexander Ionides, Vanita Berry, Anthony T. Moore, S.S. Bhattacharya	0
16	Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q 2000 ·Nature Genetics ·(unknown), Peter J. Francis, Shalesh Kaushal, Anthony T. Moore, (unknown)	238
17	A clinical and molecular genetic analysis of solitary ocular angioma 1999 ·Ophthalmology ·Andrew R. Webster, Eamonn R. Maher, Alan C. Bird, Zdeněk Gregor, Anthony T. Moore	40
18	A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q 1998 ·The American Journal of Human Genetics ·Alan Shiels, Donna S. Mackay, Alexander Ionides, Vanita Berry, Anthony T. Moore, Shomi S. Bhattacharya	275
19	An Analysis of Phenotypic Variation in the Familial Cancer Syndrome von Hippel–Lindau Disease: Evidence for Modifier Effects 1998 ·The American Journal of Human Genetics ·Andrew R. Webster, Frances M. Richards, (unknown), Anthony T. Moore, Eamonn R. Maher	76
20	Clinical features and molecular genetics of Von Hippel-Lindau disease 1995 ·Ophthalmic Genetics ·Eamonn R. Maher, Andrew R. Webster, Anthony T. Moore	38

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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