Beatrice Tiosano
About
In The Last Decade
Beatrice Tiosano
24 papers receiving 435 citations
Peers
Comparison fields: 5 of 56
- Radiology, Nuclear Medicine and Imaging 287
- Public Health, Environmental and Occupational Health 212
- Molecular Biology 117
- Ophthalmology 64
- Genetics 33
Countries citing papers authored by Beatrice Tiosano
This map shows the geographic impact of Beatrice Tiosano'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 Beatrice Tiosano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beatrice Tiosano more than expected).
Fields of papers citing papers by Beatrice Tiosano
This network shows the impact of papers produced by Beatrice Tiosano. 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 Beatrice Tiosano. The network helps show where Beatrice Tiosano may publish in the future.
Co-authorship network of co-authors of Beatrice Tiosano
This figure shows the co-authorship network connecting the top 25 collaborators of Beatrice Tiosano. A scholar is included among the top collaborators of Beatrice Tiosano 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 Beatrice Tiosano. Beatrice Tiosano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 2 | |
| 3 | 1 | |
| 4 | 99 | |
| 5 | 1 | |
| 6 | 10 | |
| 7 | 6 | |
| 8 | 2 | |
| 9 | A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews. | 14 |
| 10 | [MINIMALLY INVASIVE GLAUCOMA SURGERIES]. | 0 |
| 11 | 83 | |
| 12 | 2 | |
| 13 | 6 | |
| 14 | A combination of oculopharyngeal muscular dystrophy and a variant of enhanced S-cone syndrome in Bukharan Jews due to linked mutations in PABPN1 and NRL | 1 |
| 15 | 23 | |
| 16 | 13 | |
| 17 | 101 | |
| 18 | 6 | |
| 19 | 8 | |
| 20 | 5 |
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.