Eyal Banin
About
In The Last Decade
Eyal Banin
176 papers receiving 6.3k citations
Peers
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
Countries citing papers authored by Eyal Banin
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
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
| # | 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.