Eyal Banin

10.0k total citations
183 papers, 6.4k citations indexed

About

Eyal Banin is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Eyal Banin has authored 183 papers receiving a total of 6.4k indexed citations (citations by other indexed papers that have themselves been cited), including 149 papers in Molecular Biology, 85 papers in Ophthalmology and 36 papers in Genetics. Recurrent topics in Eyal Banin's work include Retinal Development and Disorders (131 papers), Retinal Diseases and Treatments (72 papers) and Photoreceptor and optogenetics research (18 papers). Eyal Banin is often cited by papers focused on Retinal Development and Disorders (131 papers), Retinal Diseases and Treatments (72 papers) and Photoreceptor and optogenetics research (18 papers). Eyal Banin collaborates with scholars based in Israel, United States and Netherlands. Eyal Banin's co-authors include Dror Sharon, Alexey Obolensky, Martin Friedlander, Michael I. Dorrell, Samuel G. Jacobson, Artur V. Cideciyan, Stacey K. Moreno, Ann H. Milam, Edith Aguilar and John R. Heckenlively and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Neuron.

In The Last Decade

Eyal Banin

176 papers receiving 6.3k citations

Peers

Eyal Banin
Comparison fields: 5 of 135
  • Molecular Biology 4.9k
  • Ophthalmology 2.4k
  • Genetics 1.3k
  • Cellular and Molecular Neuroscience 1.1k
  • Radiology, Nuclear Medicine and Imaging 1.0k
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Citations per field, relative to Eyal Banin
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Citations per year, relative to Eyal Banin
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Countries citing papers authored by Eyal Banin

Since Specialization
Citations

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

Fields of papers citing papers by Eyal Banin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eyal Banin. 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 Eyal Banin. The network helps show where Eyal Banin may publish in the future.

Co-authorship network of co-authors of Eyal Banin

This figure shows the co-authorship network connecting the top 25 collaborators of Eyal Banin. A scholar is included among the top collaborators of Eyal Banin 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 Eyal Banin. Eyal Banin 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 0
2 1
3 0
4 4
5 4
6 7
7
Retinal Degeneration Associated with Mutations in the KIZ Gene
0
8 9
9 30
10 23
11
Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients
1
12
Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia – Long Term Follow-up
1
13
GENE THERAPY IN A SHEEP MODEL OF CNGA3 ACHROMATOPSIA
1
14
RECOVERY OF VISUAL FUNCTION FOLLOWING GENE THERAPY IN A LARGE ANIMAL MODEL OF CNGA3 ACHROMATOPSIA
1
15
Phase I Gene Therapy Trial in Israeli Patients with Leber Congenital Amaurosis Caused by a Founder RPE65 Mutation: Safety and Efficacy Update with Up to Two Years of Follow-up
1
16
Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM)
3
17
Cone Dysfunction and Congenital Day Blindness in Awassi Sheep Is Caused by a Mutation in the CNGA3 Gene
1
18 210
19 21
20
Identification of Novel Retinal Degeneration Loci in Consanguineous Israeli and Palestinian Families With Retinal Disease
1

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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