Richard A. Lewis

24.7k total citations · 1 hit paper
255 papers, 13.1k citations indexed

About

Richard A. Lewis is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Richard A. Lewis has authored 255 papers receiving a total of 13.1k indexed citations (citations by other indexed papers that have themselves been cited), including 110 papers in Molecular Biology, 106 papers in Ophthalmology and 69 papers in Genetics. Recurrent topics in Richard A. Lewis's work include Glaucoma and retinal disorders (59 papers), Retinal Development and Disorders (57 papers) and Retinal Diseases and Treatments (55 papers). Richard A. Lewis is often cited by papers focused on Glaucoma and retinal disorders (59 papers), Retinal Development and Disorders (57 papers) and Retinal Diseases and Treatments (55 papers). Richard A. Lewis collaborates with scholars based in United States, United Kingdom and Canada. Richard A. Lewis's co-authors include James R. Lupski, Nicholas Katsanis, Vincent M. Riccardi, José L. Badano, Philip L. Beales, Noah F. Shroyer, Stephen J. Ansley, Robert L. Nussbaum, Chris A. Johnson and Erica R. Eichers and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Richard A. Lewis

249 papers receiving 12.7k 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.

Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular Degeneration

1997 687 citations Richard A. Lewis, James R. Lupski et al. Science profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Richard A. Lewis United States	62	7.1k	4.9k	3.9k	2.4k	1.3k	255	13.1k
Michael A. Hauser United States	45	4.4k 0.6×	4.0k 0.8×	1.4k 0.4×	2.3k 0.9×	580 0.5×	174	9.4k
Daniel F. Schorderet Switzerland	49	5.7k 0.8×	2.3k 0.5×	1.9k 0.5×	1.7k 0.7×	1.4k 1.1×	253	9.4k
Ursula Schlötzer‐Schrehardt Germany	63	3.6k 0.5×	6.6k 1.3×	1.0k 0.3×	5.3k 2.2×	1.3k 1.1×	308	13.4k
Ernst R. Tamm Germany	56	4.8k 0.7×	4.4k 0.9×	862 0.2×	2.2k 0.9×	1.4k 1.1×	200	8.9k
Lieve Moons Belgium	62	9.9k 1.4×	1.9k 0.4×	1.1k 0.3×	1.3k 0.5×	1.6k 1.3×	270	19.5k
Carmen Ayuso Spain	50	5.7k 0.8×	1.9k 0.4×	2.2k 0.6×	707 0.3×	783 0.6×	351	9.0k
Birgit Lorenz Germany	40	4.8k 0.7×	3.0k 0.6×	1.1k 0.3×	1.6k 0.7×	711 0.6×	249	6.8k
Jamie E. Craig Australia	49	3.2k 0.5×	5.1k 1.0×	1.0k 0.3×	2.7k 1.1×	656 0.5×	311	8.7k
Abbot F. Clark United States	64	6.4k 0.9×	9.0k 1.8×	655 0.2×	3.2k 1.3×	2.1k 1.6×	232	12.7k
Thomas Rosenberg Denmark	52	5.3k 0.7×	2.3k 0.5×	1.8k 0.5×	1.0k 0.4×	954 0.8×	205	7.7k

Countries citing papers authored by Richard A. Lewis

Since Specialization

Citations

This map shows the geographic impact of Richard A. Lewis'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 Richard A. Lewis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Richard A. Lewis more than expected).

Fields of papers citing papers by Richard A. Lewis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard A. Lewis. 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 Richard A. Lewis. The network helps show where Richard A. Lewis may publish in the future.

Co-authorship network of co-authors of Richard A. Lewis

This figure shows the co-authorship network connecting the top 25 collaborators of Richard A. Lewis. A scholar is included among the top collaborators of Richard A. Lewis 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 Richard A. Lewis. Richard A. Lewis 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

Lewis, Richard A., et al.. (2022). Police ethics committees in England and Wales: Exploratory online and web surveys. Policing A Journal of Policy and Practice. 17.

Cao, Ye, Eva Fung, Soledad Kleppe, et al.. (2022). Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy. American Journal of Medical Genetics Part A. 191(3). 776–785. 2 indexed citations

Brubaker, Jacob W., et al.. (2020). One Year of Netarsudil and Latanoprost Fixed-Dose Combination for Elevated Intraocular Pressure. Ophthalmology Glaucoma. 3(5). 327–338. 20 indexed citations

Lewis, Richard A., et al.. (2020). Four-Year Outcomes of Two Second-Generation Trabecular Micro-Bypass Stents in Patients with Open-Angle Glaucoma on One Medication. Dove Medical Press (Taylor and Francis Group).

Serle, Janet B., Malik Y. Kahook, Richard A. Lewis, et al.. (2018). Long-term Safety and Ocular Hypotensive Efficacy of Netarsudil Ophthalmic Solution: The ROCKET-2 Study. Investigative Ophthalmology & Visual Science. 59(9). 1242–1242. 1 indexed citations

Pan, Calvin, et al.. (2016). GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism. PLoS ONE. 11(9). e0162273–e0162273. 3 indexed citations

Granadillo, Jorge L., et al.. (2014). Early onset and severe clinical course associated with the m.5540G>A mutation in MT-TW. Molecular Genetics and Metabolism Reports. 1. 61–65. 3 indexed citations

Cecchi, Alana C., Naomi Ogawa, Hugo R. Martinez, et al.. (2013). Missense mutations in FBN1 exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome. American Journal of Medical Genetics Part A. 161(9). 2305–2310. 33 indexed citations

Lewis, Richard A., Manfred Tetz, Norbert Koerber, et al.. (2011). Canaloplasty: Three-year results of circumferential viscodilation and tensioning of Schlemm canal using a microcatheter to treat open-angle glaucoma. Journal of Cataract & Refractive Surgery. 37(4). 682–690. 132 indexed citations

10.

Abd‐El‐Barr, Muhammad M., Erica R. Eichers, Zhuo Yang, et al.. (2006). Cone–Rod Dystrophy, Mislocalization of Visual Pigments, and Inner Retinal Changes in a Mouse Model of Bardet–Biedl Syndrome. Investigative Ophthalmology & Visual Science. 47(13). 2971–2971. 1 indexed citations

11.

Wiszniewski, Wojciech, Alexander N. Yatsenko, Milan Jamrich, et al.. (2005). ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies. Human Molecular Genetics. 14(19). 2769–2778. 89 indexed citations

12.

Blazo, Maria, et al.. (2004). Outcomes of systematic screening for optic pathway tumors in children with Neurofibromatosis Type 1. American Journal of Medical Genetics Part A. 127A(3). 224–229. 84 indexed citations

13.

Hegde, Madhuri, Richard A. Lewis, & C. Sue Richards. (2002). Diagnostic DNA Testing for X-Linked Ocular Albinism ( OA1 ) with a Hierarchical Mutation Screening Protocol. Genetic Testing. 6(1). 7–14. 7 indexed citations

14.

Katsanis, Nicholas, Stephen J. Ansley, José L. Badano, et al.. (2001). Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder. Science. 293(5538). 2256–2259. 438 indexed citations

15.

Stoilov, Ivaylo, Nurten Akarsu, Magda Barsoum‐Homsy, et al.. (1998). Sequence Analysis and Homology Modeling Suggest That Primary Congenital Glaucoma on 2p21 Results from Mutations Disrupting Either the Hinge Region or the Conserved Core Structures of Cytochrome P4501B1. The American Journal of Human Genetics. 62(3). 573–584. 288 indexed citations

16.

Lalezari, Jacob, Gary N. Holland, Françoise Kramer, et al.. (1998). Randomized, Controlled Study of the Safety and Efficacy of Intravenous Cidofovir for the Treatment of Relapsing Cytomegalovirus Retinitis in Patients With AIDS. Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology. 17(4). 339–344. 72 indexed citations

17.

Robin, Alan L., R David, Howard Barnebey, et al.. (1995). Effect of brimonidine 0.5% on intraocular pressure spikes following 360° argon laser trabeculoplasty. 26(5). 404–409. 18 indexed citations

18.

Keats, Bronya J.B., Larry D. Atwood, Mary Z. Pelias, et al.. (1992). Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium. Genomics. 14(3). 707–714. 4 indexed citations

19.

Johnson, Chris A., Anthony J. Adams, Craig W. Adams, & Richard A. Lewis. (1988). Evidence for a Neural Basis of Age-Related Visual Field Changes. TuC3–TuC3. 1 indexed citations

20.

Lewis, Richard A., et al.. (1987). Mapping the Lowe oculocerebrorenal syndrome to Xq24-q26 by use of restriction fragment length polymorphisms.. Journal of Clinical Investigation. 79(1). 282–285. 65 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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