W Feero
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Nutrition, Genetics, and Disease
- Pharmacology top 5%
- Pharmacogenetics and Drug Metabolism
Papers in
- Genetics 33
- BRCA gene mutations in cancer 26
- Genomics and Rare Diseases 14
- Genomic variations and chromosomal abnormalities 3
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- Ethics in Clinical Research 7
- Co-authors
- Muin J. Khoury (7 shared papers)Alan E. Guttmacher (2 shared papers)Francis S. Collins (1 shared paper)David Chambers (1 shared paper)Eric D. Green (1 shared paper)Catherine Wicklund (4 shared papers)David L. Veenstra (3 shared papers)Kristin M. Brinner (1 shared paper)
- Journals
- Genetics in Medicine (7 papers)JAMA (6 papers)Journal of Nursing Scholarship (2 papers)Nursing Outlook (2 papers)American Journal of Obstetrics and Gynecology (2 papers)
- Partner nations
- United StatesCanadaChina
In The Last Decade
W Feero
48 papers receiving 1.6k citations
W Feero's Hit Papers
Peers
Comparison fields: 5 of 127
- Genetics 775
- Pharmacology 101
- Public Health, Environmental and Occupational Health 249
- Pediatrics, Perinatology and Child Health 140
- Issues, ethics and legal aspects 9
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-authors
The 25 scholars most cited alongside W Feero, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 50 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 274 | |
| 2 | Convergence of Implementation Science, Precision Medicine, and the Learning Health Care System Hit paper breakdown → | 2016 | 225 |
| 3 | 2008 | 111 | |
| 4 | 2011 | 96 | |
| 5 | 2008 | 77 | |
| 6 | 2008 | 73 | |
| 7 | 2013 | 71 | |
| 8 | 2010 | 65 | |
| 9 | 2013 | 47 | |
| 10 | 2009 | 39 | |
| 11 | 2018 | 37 | |
| 12 | 2010 | 37 | |
| 13 | Molecular genetic and genetic correlations in sodium channelopathies: lack of founder effect and evidence for a second gene. | 1993 | 37 |
| 14 | 1993 | 35 | |
| 15 | 2010 | 34 | |
| 16 | 2011 | 29 | |
| 17 | 2014 | 29 | |
| 18 | 2016 | 28 | |
| 19 | 2018 | 28 | |
| 20 | 2014 | 27 |
About W Feero
W Feero is a scholar working on Genetics, Public Health, Environmental and Occupational Health, Molecular Biology, Pediatrics, Perinatology and Child Health and General Health Professions, having authored 50 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (26 papers), Genomics and Rare Diseases (14 papers), Ethics in Clinical Research (7 papers), Health Systems, Economic Evaluations, Quality of Life (6 papers), Prenatal Screening and Diagnostics (5 papers), Primary Care and Health Outcomes (4 papers), Cardiac electrophysiology and arrhythmias (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (775 citations), Pharmacology (101 citations), Public Health, Environmental and Occupational Health (249 citations), Pediatrics, Perinatology and Child Health (140 citations) and Issues, ethics and legal aspects (9 citations). W Feero has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Muin J. Khoury, Alan E. Guttmacher, Francis S. Collins, David Chambers, Eric D. Green, Catherine Wicklund, David L. Veenstra, Kristin M. Brinner, Jean Jenkins and Benjamin D. Solomon. Their work appears in journals such as Genetics in Medicine, JAMA, Journal of Nursing Scholarship, Nursing Outlook and American Journal of Obstetrics and Gynecology.
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.