Eliot L. Berson

21.6k total citations · 3 hit papers
222 papers, 16.0k citations indexed

About

Eliot L. Berson is a scholar working on Molecular Biology, Ophthalmology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Eliot L. Berson has authored 222 papers receiving a total of 16.0k indexed citations (citations by other indexed papers that have themselves been cited), including 181 papers in Molecular Biology, 75 papers in Ophthalmology and 61 papers in Cellular and Molecular Neuroscience. Recurrent topics in Eliot L. Berson's work include Retinal Development and Disorders (160 papers), Photoreceptor and optogenetics research (54 papers) and Retinal Diseases and Treatments (50 papers). Eliot L. Berson is often cited by papers focused on Retinal Development and Disorders (160 papers), Photoreceptor and optogenetics research (54 papers) and Retinal Diseases and Treatments (50 papers). Eliot L. Berson collaborates with scholars based in United States, Switzerland and Canada. Eliot L. Berson's co-authors include Thaddeus P. Dryja, Michael A. Sandberg, Dyonne T. Hartong, Terri L. McGee, Bernard Rosner, Kazuto Kajiwara, Carol Weigel-DiFranco, Carlo Rivolta, Susan Y. Schmidt and Basil S. Pawlyk and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Eliot L. Berson

221 papers receiving 15.4k citations

Hit Papers

Retinitis pigmentosa 1993 2026 2004 2015 2006 1994 1993 500 1000 1.5k 2.0k

Peers

Eliot L. Berson
Comparison fields: 5 of 140
  • Molecular Biology 13.8k
  • Ophthalmology 6.2k
  • Cellular and Molecular Neuroscience 4.6k
  • Cell Biology 2.0k
  • Genetics 2.0k
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Citations per field, relative to Eliot L. Berson
Eliot L. Berson · 1×
Citations per year, relative to Eliot L. Berson
Eliot L. Berson · 1×

Countries citing papers authored by Eliot L. Berson

Since Specialization
Citations

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

Fields of papers citing papers by Eliot L. Berson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eliot L. Berson. 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 Eliot L. Berson. The network helps show where Eliot L. Berson may publish in the future.

Co-authorship network of co-authors of Eliot L. Berson

This figure shows the co-authorship network connecting the top 25 collaborators of Eliot L. Berson. A scholar is included among the top collaborators of Eliot L. Berson 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 Eliot L. Berson. Eliot L. Berson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
# Work Indexed citations
1 2
2
FAM161A Mutations In Patients With Early-onset Retinitis Pigmentosa In The United States
1
3 90
4
A Single-Base Substitution Within an Intronic Repetitive Element in PRPF31 Causes Dominant Retinitis Pigmentosa With Reduced Penetrance
6
5 127
6
Macular Pseudoholes in Retinitis Pigmentosa
0
7
Disease Progression in Patients with X–Linked Retinitis Pigmentosa Due to RPGR Gene Mutations
1
8
Search for Recessive Retinitis Pigmentosa Genes Using Microarray Analysis of RNA Expression Levels in Lymphoblasts
3
9
Recessive Mutations in the CYP4V2 Gene in East Asian and Middle Eastern Patients With Bietti Crytalline Corneoretinal Dystrophy
1
10
Screening of 51 Newly Identified USH2A Exons Among Patients With Usher Syndrome Type II and Non–Syndromic Recessive Retinitis Pigmentosa
2
11
Rod and Cone Opsin Mislocalization in an Autopsy Eye From a Female Carrier of X–linked RP With a Gly436Asp Mutation in the RPGR Gene
2
12
USH3A mutations in patients with a prior diagnosis of Usher syndrome type I, Usher syndrome type II, and nonsyndromic recessive retinitis pigmentosa
3
13
Defects in RGS9 or its anchor protein R9AP in patients with bradyopsia, a novel form of retinal dysfunction
2
14
All-Exon Screen of the Ush2a Gene in Recessive Nonsyndromic Retinitis Pigmentosa and Usher Syndrome Type II
1
15 109
16
Absence of photoreceptor rescue with D-cis-diltiazem in the rd mouse.
62
17 81
18
Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosa.
30
19
Identification of proteins in retinas and IPM from eyes with retinitis pigmentosa.
13
20
Sex-linked retinitis pigmentosa: ultrastructure of photoreceptors and pigment epithelium.
121

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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