Scott C. Wildenberg
About
In The Last Decade
Scott C. Wildenberg
9 papers receiving 901 citations
Peers
Comparison fields: 5 of 67
- Epidemiology 415
- Radiology, Nuclear Medicine and Imaging 413
- Cell Biology 336
- Ophthalmology 328
- Molecular Biology 232
Countries citing papers authored by Scott C. Wildenberg
This map shows the geographic impact of Scott C. Wildenberg'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 Scott C. Wildenberg with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Scott C. Wildenberg more than expected).
Fields of papers citing papers by Scott C. Wildenberg
This network shows the impact of papers produced by Scott C. Wildenberg. 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 Scott C. Wildenberg. The network helps show where Scott C. Wildenberg may publish in the future.
Co-authorship network of co-authors of Scott C. Wildenberg
This figure shows the co-authorship network connecting the top 25 collaborators of Scott C. Wildenberg. A scholar is included among the top collaborators of Scott C. Wildenberg 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 Scott C. Wildenberg. Scott C. Wildenberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 150 | |
| 2 | 200 | |
| 3 | 9 | |
| 4 | 179 | |
| 5 | 53 | |
| 6 | 115 | |
| 7 | Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3". | 149 |
| 8 | 1 | |
| 9 | A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2. | 66 |
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.