W Feero
- Genetics top 2%
- Public Health, Environmental and Occupational Health top 5%
- Molecular Biology
- General Health Professions top 5%
- Pediatrics, Perinatology and Child Health top 5%
- Co-authors
- Alan E. GuttmacherMuin J. KhouryFrancis S. CollinsDavid ChambersEric D. GreenCatherine WicklundKristin M. BrinnerDavid L. Veenstra
- Topics
- BRCA gene mutations in cancer (27 papers)Genomics and Rare Diseases (15 papers)Ethics in Clinical Research (7 papers)
- Partner nations
- United StatesCanadaChina
In The Last Decade
W Feero
48 papers receiving 1.6k citations
Peers
Comparison fields: 5 of 135
- Genetics 853
- Public Health, Environmental and Occupational Health 381
- Molecular Biology 380
- General Health Professions 225
- Pediatrics, Perinatology and Child Health 205
Countries citing papers authored by W Feero
This map shows the geographic impact of W Feero'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 W Feero with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W Feero more than expected).
Fields of papers citing papers by W Feero
This network shows the impact of papers produced by W Feero. 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 W Feero. The network helps show where W Feero may publish in the future.
Co-authorship network of co-authors of W Feero
This figure shows the co-authorship network connecting the top 25 collaborators of W Feero. A scholar is included among the top collaborators of W Feero 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 W Feero. W Feero 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 | 4 | |
| 3 | 37 | |
| 4 | 28 | |
| 5 | 10 | |
| 6 | 7 | |
| 7 | 46 | |
| 8 | 20 | |
| 9 | 28 | |
| 10 | 94 | |
| 11 | 34 | |
| 12 | 37 | |
| 13 | 1 | |
| 14 | 77 | |
| 15 | 14 | |
| 16 | 19 | |
| 17 | 110 | |
| 18 | 9 | |
| 19 | 3 | |
| 20 | 15 |
About W Feero
W Feero is a scholar working on Genetics, Issues, ethics and legal aspects and Health Informatics, having authored 50 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (27 papers), Genomics and Rare Diseases (15 papers) and Ethics in Clinical Research (7 papers). The work is most often cited by research in Genetics (853 citations), Public Health, Environmental and Occupational Health (381 citations) and Pharmacology (108 citations). W Feero has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Alan E. Guttmacher, Muin J. Khoury, Francis S. Collins, David Chambers, Eric D. Green, Catherine Wicklund, Kristin M. Brinner, David L. Veenstra, Jean Jenkins and Brian W. Jack. Their work appears in journals such as New England Journal of Medicine, JAMA and Nature Genetics.
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.