WILLARD C. PETERSON
About
In The Last Decade
WILLARD C. PETERSON
16 papers receiving 181 citations
Peers
Comparison fields: 5 of 40
- Genetics 113
- Dermatology 92
- Rheumatology 88
- Molecular Biology 67
- Oncology 59
Countries citing papers authored by WILLARD C. PETERSON
This map shows the geographic impact of WILLARD C. PETERSON'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 WILLARD C. PETERSON with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites WILLARD C. PETERSON more than expected).
Fields of papers citing papers by WILLARD C. PETERSON
This network shows the impact of papers produced by WILLARD C. PETERSON. 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 WILLARD C. PETERSON. The network helps show where WILLARD C. PETERSON may publish in the future.
Co-authorship network of co-authors of WILLARD C. PETERSON
This figure shows the co-authorship network connecting the top 25 collaborators of WILLARD C. PETERSON. A scholar is included among the top collaborators of WILLARD C. PETERSON 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 WILLARD C. PETERSON. WILLARD C. PETERSON is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 29 | |
| 2 | Thioflavine-T reactivity in calcifying epithelioma of Malherbe. | 9 |
| 3 | 2 | |
| 4 | 9 | |
| 5 | Cutaneous findings in Unverricht's syndrome. (Progressive familial myoclonic epilepsy). | 5 |
| 6 | 10 | |
| 7 | Cutaneous aspects of the XXYY genotype. A variant of Klinefelter's syndrome. | 13 |
| 8 | 1 | |
| 9 | 8 | |
| 10 | 48 | |
| 11 | 37 | |
| 12 | 6 | |
| 13 | 28 | |
| 14 | 11 | |
| 15 | 12 | |
| 16 | 15 |
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.