Eliot L. Berson

5.7k total citations · 1 hit paper
34 papers, 4.3k citations indexed

About

Eliot L. Berson is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Ophthalmology. According to data from OpenAlex, Eliot L. Berson has authored 34 papers receiving a total of 4.3k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 10 papers in Ophthalmology. Recurrent topics in Eliot L. Berson's work include Retinal Development and Disorders (31 papers), Photoreceptor and optogenetics research (12 papers) and Retinoids in leukemia and cellular processes (7 papers). Eliot L. Berson is often cited by papers focused on Retinal Development and Disorders (31 papers), Photoreceptor and optogenetics research (12 papers) and Retinoids in leukemia and cellular processes (7 papers). Eliot L. Berson collaborates with scholars based in United States and Lebanon. Eliot L. Berson's co-authors include Michael A. Sandberg, Thaddeus P. Dryja, Thaddeus P. Dryja, Lauri B. Hahn, Terri L. McGee, Glenn S. Cowley, Peter Gouras, Elias Reichel, Margaret E. McLaughlin and David W. Yandell and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Eliot L. Berson

34 papers receiving 4.0k citations

Hit Papers

A point mutation of the rhodopsin gene in one form of ret... 1990 2026 2002 2014 1990 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eliot L. Berson United States 27 3.9k 1.7k 1.5k 575 437 34 4.3k
Steven J. Pittler United States 25 2.8k 0.7× 1.1k 0.6× 999 0.7× 369 0.6× 202 0.5× 66 3.1k
Steven Nusinowitz United States 38 4.1k 1.1× 1.3k 0.8× 2.2k 1.5× 393 0.7× 823 1.9× 99 5.2k
Thierry Léveillard France 36 3.4k 0.9× 1.3k 0.7× 1.2k 0.8× 319 0.6× 354 0.8× 113 3.9k
Ronald A. Bush United States 42 4.7k 1.2× 2.0k 1.2× 1.8k 1.2× 495 0.9× 893 2.0× 76 5.4k
Muayyad R. Al‐Ubaidi United States 31 2.8k 0.7× 998 0.6× 823 0.5× 401 0.7× 208 0.5× 92 3.3k
Michael A. Sandberg United States 44 6.1k 1.6× 2.4k 1.4× 2.9k 1.9× 845 1.5× 960 2.2× 113 7.0k
Daniel E. Possin United States 27 2.3k 0.6× 995 0.6× 1.1k 0.7× 286 0.5× 501 1.1× 40 2.8k
Naoyuki Tanimoto Germany 31 2.4k 0.6× 935 0.5× 1.1k 0.7× 329 0.6× 366 0.8× 92 3.1k
Christian Hamel France 28 3.9k 1.0× 751 0.4× 984 0.7× 359 0.6× 246 0.6× 46 4.4k
Ching‐Hwa Sung United States 20 2.9k 0.7× 1.5k 0.9× 488 0.3× 886 1.5× 186 0.4× 28 3.4k

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
1.
Sharon, Dror, et al.. (2001). The mutation spectrum of RPGR-ORF15 in North American patients with X-linked retinitis pigmentosa. 42(4). 642. 6 indexed citations
2.
Zacks, David N., et al.. (2001). Melanoma-associated retinopathy and recurrent exudative retinal detachments in a patient with choroidal melanoma. American Journal of Ophthalmology. 132(4). 578–581. 35 indexed citations
3.
DeAngelis, Margaret M., Terri L. McGee, Bronya J.B. Keats, et al.. (2001). Two families from New England with usher syndrome type IC with distinct haplotypes. American Journal of Ophthalmology. 131(3). 355–358. 3 indexed citations
4.
Rivolta, Carlo, Eliot L. Berson, & Thaddeus P. Dryja. (2001). Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX. Human Mutation. 18(6). 488–498. 77 indexed citations
5.
Sandberg, Michael A., Basil S. Pawlyk, & Eliot L. Berson. (1999). Acuity recovery and cone pigment regeneration after a bleach in patients with retinitis pigmentosa and rhodopsin mutations.. PubMed. 40(10). 2457–61. 20 indexed citations
6.
Yamamoto, Shuji, Kimberly C. Sippel, Eliot L. Berson, & Thaddeus P. Dryja. (1997). Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nature Genetics. 15(2). 175–178. 190 indexed citations
7.
Berson, Eliot L., et al.. (1994). Further Screening of the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa. Genomics. 21(2). 461–463. 68 indexed citations
8.
Sandberg, Michael A., et al.. (1993). Hyperopia and Neovascularization in Age-related Macular Degeneration. Ophthalmology. 100(7). 1009–1013. 43 indexed citations
9.
McLaughlin, Margaret E., Michael A. Sandberg, Eliot L. Berson, & Thaddeus P. Dryja. (1993). Recessive mutations in the gene encoding the β–subunit of rod phosphodiesterase in patients with retinitis pigmentosa. Nature Genetics. 4(2). 130–134. 457 indexed citations
10.
Dryja, Thaddeus P., Eliot L. Berson, Vikram R. Rao, & Daniel D. Oprian. (1993). Heterozygous missense mutation in the rhodopsin gene as a cause of congenital stationary night blindness. Nature Genetics. 4(3). 280–283. 235 indexed citations
11.
Kajiwara, Kazuto, et al.. (1991). Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa. Nature. 354(6353). 480–483. 351 indexed citations
12.
Berson, Eliot L.. (1991). Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His). Archives of Ophthalmology. 109(1). 92–92. 168 indexed citations
13.
Weiner, Asher, et al.. (1991). Hydroxychloroquine Retinopathy. American Journal of Ophthalmology. 112(5). 528–534. 48 indexed citations
14.
Dryja, Thaddeus P., Terri L. McGee, Elias Reichel, et al.. (1990). A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature. 343(6256). 364–366. 806 indexed citations breakdown →
15.
Ringens, Peter J., et al.. (1990). Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA. Experimental Eye Research. 51(1). 15–19. 9 indexed citations
16.
Reichel, Elias, et al.. (1989). An Electroretinographic and Molecular Genetic Study of X-Linked Cone Degeneration. American Journal of Ophthalmology. 108(5). 540–547. 85 indexed citations
17.
Sandberg, Michael A., et al.. (1988). Narrow-Band Filtering for Monitoring Low-Amplitude Cone Electroretinograms in Retinitis Pigmentosa. American Journal of Ophthalmology. 105(5). 500–503. 77 indexed citations
18.
O'Gorman, S, et al.. (1988). Histopathologic Findings in Best's Vitelliform Macular Dystrophy. Archives of Ophthalmology. 106(9). 1261–1268. 128 indexed citations
19.
Berson, Eliot L.. (1987). Electroretinographic findings in retinitis pigmentosa.. PubMed. 31(3). 327–48. 31 indexed citations
20.
Berson, Eliot L., et al.. (1970). Cone and Rod Responses in a Family With Recessively Inherited Retinitis Pigmentosa. Archives of Ophthalmology. 84(3). 288–297. 39 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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