F.L. Munier
About
In The Last Decade
F.L. Munier
11 papers receiving 345 citations
Peers
Comparison fields: 5 of 39
- Molecular Biology 297
- Ophthalmology 220
- Radiology, Nuclear Medicine and Imaging 85
- Cell Biology 52
- Cellular and Molecular Neuroscience 42
Countries citing papers authored by F.L. Munier
This map shows the geographic impact of F.L. Munier'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 F.L. Munier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites F.L. Munier more than expected).
Fields of papers citing papers by F.L. Munier
This network shows the impact of papers produced by F.L. Munier. 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 F.L. Munier. The network helps show where F.L. Munier may publish in the future.
Co-authorship network of co-authors of F.L. Munier
This figure shows the co-authorship network connecting the top 25 collaborators of F.L. Munier. A scholar is included among the top collaborators of F.L. Munier 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 F.L. Munier. F.L. Munier is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 16 | |
| 2 | 18 | |
| 3 | Potential Role of Intravitreal Ranibizumab (lucentis®) in the Management of Stage 4 Coats Disease: Report of Two Cases | 0 |
| 4 | 39 | |
| 5 | 9 | |
| 6 | 0 | |
| 7 | Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome. | 26 |
| 8 | 7 | |
| 9 | 11 | |
| 10 | 37 | |
| 11 | Allelic variation in the VMD2 gene in best disease and age-related macular degeneration. | 126 |
| 12 | 5 | |
| 13 | 53 |
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.