Ben R. Roos
About
In The Last Decade
Ben R. Roos
20 papers receiving 503 citations
Peers
Comparison fields: 5 of 42
- Ophthalmology 379
- Molecular Biology 256
- Radiology, Nuclear Medicine and Imaging 158
- Cell Biology 61
- Genetics 41
Countries citing papers authored by Ben R. Roos
This map shows the geographic impact of Ben R. Roos'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 Ben R. Roos with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ben R. Roos more than expected).
Fields of papers citing papers by Ben R. Roos
This network shows the impact of papers produced by Ben R. Roos. 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 Ben R. Roos. The network helps show where Ben R. Roos may publish in the future.
Co-authorship network of co-authors of Ben R. Roos
This figure shows the co-authorship network connecting the top 25 collaborators of Ben R. Roos. A scholar is included among the top collaborators of Ben R. Roos 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 Ben R. Roos. Ben R. Roos 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 | 0 | |
| 4 | 2 | |
| 5 | 16 | |
| 6 | 20 | |
| 7 | 20 | |
| 8 | 1 | |
| 9 | 6 | |
| 10 | Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos. | 22 |
| 11 | 69 | |
| 12 | 6 | |
| 13 | 15 | |
| 14 | 19 | |
| 15 | 20 | |
| 16 | 159 | |
| 17 | Chromosome 7q31 POAG locus: ocular expression of caveolins and lack of association with POAG in a US cohort. | 44 |
| 18 | 17 | |
| 19 | Clinical and genetic characterization of a Danish family with North Carolina macular dystrophy. | 23 |
| 20 | 26 |
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.