Richard A. Lewis

24.7k citations

255 papers · 13.1k indexed · 1 hit paper · h-index 62

Molecular Biology top 0.5%
Ophthalmology top 0.05%
Genetics top 0.2%
Radiology, Nuclear Medicine and Imaging top 0.5%
Cell Biology top 0.5%

Co-authors: James R. Lupski Nicholas Katsanis Vincent M. Riccardi José L. Badano Philip L. Beales Noah F. Shroyer Stephen J. Ansley Robert L. Nussbaum
Topics: Glaucoma and retinal disorders (59 papers)Retinal Development and Disorders (57 papers)Retinal Diseases and Treatments (55 papers)
Cited by: Ophthalmology Genetics Radiology, Nuclear Medicine and Imaging
Journals: Nature Science Proceedings of the National Academy of Sciences
Partner nations: United States United Kingdom Canada

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

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

#	Work	Indexed citations
1	Police ethics committees in England and Wales: Exploratory online and web surveys 2022 ·Policing A Journal of Policy and Practice ·(unknown),(unknown),Richard A. Lewis	0
2	Expansion of the clinical and molecular spectrum of WWOX‐related epileptic encephalopathy 2022 ·American Journal of Medical Genetics Part A ·(unknown),Ye Cao,Eva Fung,Soledad Kleppe,Karen W. Gripp,Jozef Hertecant,Ayman W. El‐Hattab,Jehan Suleiman,Gary Clark,Gretchen Von Allmen,(unknown),Richard A. Lewis,Jill A. Rosenfeld,Jie Dong,(unknown),Xia Wang,Marcus J. Miller,Weimin Bi,Pengfei Liu,Fernando Scaglia	2
3	PRUNE1 c.933G>A synonymous variant induces exon 7 skipping, disrupts the DHHA2 domain, and leads to an atypical NMIHBA syndrome presentation: Case report and review of the literature 2022 ·American Journal of Medical Genetics Part A ·(unknown),David R. Murdock,Lindsay C. Burrage,Hongzheng Dai,Seema R. Lalani,Richard A. Lewis,(unknown),(unknown),Jill A. Rosenfeld,Alyssa A. Tran,James B. Gibson,(unknown),Carlos A. Bacino,Brendan Lee,Hsiao‐Tuan Chao	2
4	A novel de novo intronic variant in ITPR1 causes Gillespie syndrome 2021 ·American Journal of Medical Genetics Part A ·(unknown),Ming‐Ming Jiang,Xiaohui Li,Ronit Marom,Hongzheng Dai,David R. Murdock,Pengfei Liu,Jill V. Hunter,Jason D. Heaney,Laurie Robak,Lisa Emrick,Timothy Lotze,Lauren S. Blieden,(unknown),Richard A. Lewis,Alex V. Levin,Jenina Capasso,William J. Craigen,Jill A. Rosenfeld,Brendan Lee,Lindsay C. Burrage	5
5	Four-Year Outcomes of Two Second-Generation Trabecular Micro-Bypass Stents in Patients with Open-Angle Glaucoma on One Medication 2020 ·Dove Medical Press (Taylor and Francis Group) ·(unknown),(unknown),Richard A. Lewis,John Hovanesian,Lilit Voskanyan	0
6	Evidence for secondary-variant genetic burden and non-random distribution across biological modules in a recessive ciliopathy 2020 ·Nature Genetics ·Maria Kousi,Onuralp Söylemez,(unknown),Niki Mourtzi,Sebastian Akle,Irwin Jungreis,Jean Muller,Christopher A. Cassa,Harrison Brand,Jill A. Rosenfeld,Maxim Y. Wolf,Azita Sadeghpour,(unknown),Richard A. Lewis,Michael E. Talkowski,Hélène Dollfus,Manolis Kellis,Erica E. Davis,Shamil Sunyaev,Nicholas Katsanis	21
7	One Year of Netarsudil and Latanoprost Fixed-Dose Combination for Elevated Intraocular Pressure 2020 ·Ophthalmology Glaucoma ·Jacob W. Brubaker,(unknown),Richard A. Lewis,Dale W. Usner,(unknown),(unknown),Casey Kopczynski,Theresa Heah	20
8	GNAI3: Another Candidate Gene to Screen in Persons with Ocular Albinism 2016 ·PLoS ONE ·(unknown),(unknown),Calvin Pan,(unknown),Jie Zheng,Richard A. Lewis,Debora B. Farber	3
9	Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death 2015 ·Molecular Genetics & Genomic Medicine ·Philip M. Boone,Bo Yuan,Shen Gu,Zhiwei Ma,Tomasz Gambin,Claudia Gonzaga‐Jauregui,Mahim Jain,(unknown),Janson J. White,Shalini N. Jhangiani,Kimberly Walker,Qiaoyan Wang,Donna M. Muzny,Richard A. Gibbs,J. Fielding Hejtmancik,James R. Lupski,Jennifer E. Posey,Richard A. Lewis	25
10	Early onset and severe clinical course associated with the m.5540G>A mutation in MT-TW 2014 ·Molecular Genetics and Metabolism Reports ·Jorge L. Granadillo,(unknown),Richard A. Lewis,(unknown),(unknown),Jing Wang,Lee-Jun Wong,Fernando Scaglia	3
11	Missense mutations in FBN1 exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome 2013 ·American Journal of Medical Genetics Part A ·Alana C. Cecchi,Naomi Ogawa,Hugo R. Martinez,(unknown),Yuxin Fan,Daniel J. Penny,Dongchuan Guo,Steven Eisenberg,Hazim J. Safi,Anthony L. Estrera,Richard A. Lewis,Deborah E. Meyers,Dianna M. Milewicz	33
12	Canaloplasty: Three-year results of circumferential viscodilation and tensioning of Schlemm canal using a microcatheter to treat open-angle glaucoma 2011 ·Journal of Cataract & Refractive Surgery ·Richard A. Lewis,(unknown),Manfred Tetz,Norbert Koerber,John R. Kearney,Bradford J. Shingleton,Thomas W. Samuelson	132
13	The Severe Forms of Retinal Dystrophies Are Frequently Caused by a New Class of Mutations Affecting ABCA4 Localization 2005 ·Investigative Ophthalmology & Visual Science ·Wojciech Wiszniewski,(unknown),Alexander N. Yatsenko,Milan Jamrich,Theodore G. Wensel,Richard A. Lewis,James R. Lupski	1
14	ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies 2005 ·Human Molecular Genetics ·Wojciech Wiszniewski,(unknown),Alexander N. Yatsenko,Milan Jamrich,Theodore G. Wensel,Richard A. Lewis,James R. Lupski	89
15	Diagnostic DNA Testing for X-Linked Ocular Albinism ( OA1 ) with a Hierarchical Mutation Screening Protocol 2002 ·Genetic Testing ·Madhuri Hegde,Richard A. Lewis,C. Sue Richards	7
16	Triallelic Inheritance in Bardet-Biedl Syndrome, a Mendelian Recessive Disorder 2001 ·Science ·Nicholas Katsanis,Stephen J. Ansley,José L. Badano,Erica R. Eichers,Richard A. Lewis,Bethan E. Hoskins,Peter Scambler,William S. Davidson,Philip L. Beales,James R. Lupski	438
17	Randomized, Controlled Study of the Safety and Efficacy of Intravenous Cidofovir for the Treatment of Relapsing Cytomegalovirus Retinitis in Patients With AIDS 1998 ·Journal of Acquired Immune Deficiency Syndromes & Human Retrovirology ·Jacob Lalezari,Gary N. Holland,Françoise Kramer,George McKinley,Carol A. Kemper,(unknown),Robert G. Nelson,W. D. Hardy,Baruch D. Kuppermann,Donald W. Northfelt,M Youle,Margaret Johnson,Richard A. Lewis,David V. Weinberg,Gary L. Simon,Richard A. Wolitz,(unknown),Robert Stagg,Howard S. Jaffe	72
18	The use of directly fluoresceinated chromosome-specific DNA probes for uni- and multicolour identification of human chromosomes by in situ hybridization 1994 ·Analytical Cellular Pathology ·Yuri B. Yurov,Svetlana G. Vorsanova,Gérard Roizès,Richard A. Lewis	1
19	Linkage studies of usher syndrome type 1: Exclusion results from the usher syndrome consortium 1992 ·Genomics ·Bronya J.B. Keats,(unknown),Larry D. Atwood,Mary Z. Pelias,J. Fielding Hejtmancik,William J. Kimberling,Mark Leppert,Richard A. Lewis,Richard J. Smith	4
20	EPIDEMIC ASTHMA IN NEW ORLEANS: A SUMMARY OF KNOWLEDGE TO DATE. 1963 ·PubMed ·Richard A. Lewis	5

About Richard A. Lewis

Richard A. Lewis is a scholar working on Ophthalmology, Genetics and Cell Biology, having authored 255 papers that have together received 13.1k indexed citations. Recurring topics across this work include Glaucoma and retinal disorders (59 papers), Retinal Development and Disorders (57 papers) and Retinal Diseases and Treatments (55 papers). The work is most often cited by research in Ophthalmology (4.9k citations), Genetics (3.9k citations) and Radiology, Nuclear Medicine and Imaging (2.4k citations). Richard A. Lewis has collaborated with scholars based in United States, United Kingdom and Canada. Frequent 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. Their work appears in journals such as Nature, Science and Proceedings of the National Academy of Sciences.

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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