Dror Sharon
About
In The Last Decade
Dror Sharon
130 papers receiving 3.6k citations
Peers
Comparison fields: 5 of 105
- Molecular Biology 2.9k
- Ophthalmology 1.4k
- Genetics 786
- Cellular and Molecular Neuroscience 627
- Cell Biology 494
Countries citing papers authored by Dror Sharon
This map shows the geographic impact of Dror Sharon'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 Dror Sharon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dror Sharon more than expected).
Fields of papers citing papers by Dror Sharon
This network shows the impact of papers produced by Dror Sharon. 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 Dror Sharon. The network helps show where Dror Sharon may publish in the future.
Co-authorship network of co-authors of Dror Sharon
This figure shows the co-authorship network connecting the top 25 collaborators of Dror Sharon. A scholar is included among the top collaborators of Dror Sharon 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 Dror Sharon. Dror Sharon 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 | 0 | |
| 3 | 4 | |
| 4 | 5 | |
| 5 | 2 | |
| 6 | 7 | |
| 7 | Retinal Degeneration Associated with Mutations in the KIZ Gene | 0 |
| 8 | 11 | |
| 9 | 22 | |
| 10 | Whole exome sequencing reveals a homozygous splicing mutation in CEP78 as the cause of atypical Usher syndrome in Eastern Jewish patients | 1 |
| 11 | 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 |
| 12 | 52 | |
| 13 | Clinical evaluation of two consanguineous families with homozygous mutations in BEST1. | 24 |
| 14 | 93 | |
| 15 | Evaluating the Photoreceptor Mosaic in Blue Cone Monochromacy (BCM) | 3 |
| 16 | 21 | |
| 17 | Identification of Novel Retinal Degeneration Loci in Consanguineous Israeli and Palestinian Families With Retinal Disease | 1 |
| 18 | Shared Mutations in NR2E3 In Enhanced S-cone Syndrome, Goldmann-Favre Syndrome, and Clumped Pigmentary Retinal Degeneration | 2 |
| 19 | The mutation spectrum of RPGR-ORF15 in North American patients with X-linked retinitis pigmentosa | 6 |
| 20 | 12 |
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.