W. David Dotson
Impact in
- Genetics top 2%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
- Nutrition, Genetics, and Disease
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
- Genetics 24
- BRCA gene mutations in cancer 20
- Genomics and Rare Diseases 9
- Nutrition, Genetics, and Disease 5
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- Genetics, Bioinformatics, and Biomedical Research 3
- Co-authors
- Muin J. Khoury (21 shared papers)Linda Bradley (3 shared papers)Michael P. Douglas (5 shared papers)Katherine Kolor (14 shared papers)Glenn E. Palomaki (3 shared papers)James E. Haddow (2 shared papers)Steven M. Teutsch (2 shared papers)Ned Calonge (2 shared papers)
- Journals
- Genetics in Medicine (16 papers)PLoS Currents (2 papers)Public Health Genomics (2 papers)Health Affairs (1 paper)Journal of Bacteriology (1 paper)
- Partner nations
- United StatesNetherlandsCanada
In The Last Decade
W. David Dotson
32 papers receiving 1.6k citations
Hit Papers
Peers
Comparison fields: 5 of 123
- Genetics 794
- Cancer Research 362
- Pharmacology 106
- Pathology and Forensic Medicine 218
- Oncology 306
Countries citing papers authored by W. David Dotson
This map shows the geographic impact of W. David Dotson'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. David Dotson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites W. David Dotson more than expected).
Fields of papers citing papers by W. David Dotson
This network shows the impact of papers produced by W. David Dotson. 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. David Dotson. The network helps show where W. David Dotson may publish in the future.
Co-authors
The 25 scholars most cited alongside W. David Dotson, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) initiative: methods of the EGAPP Working Group Hit paper breakdown → | 2009 | 484 |
| 2 | 2018 | 113 | |
| 3 | 2009 | 99 | |
| 4 | 2020 | 98 | |
| 5 | 2017 | 98 | |
| 6 | 2022 | 89 | |
| 7 | 2010 | 68 | |
| 8 | 2001 | 52 | |
| 9 | 2017 | 48 | |
| 10 | 2013 | 46 | |
| 11 | 2019 | 44 | |
| 12 | 2012 | 41 | |
| 13 | 2014 | 39 | |
| 14 | 2011 | 35 | |
| 15 | 2011 | 32 | |
| 16 | 2017 | 31 | |
| 17 | 2017 | 31 | |
| 18 | 2018 | 30 | |
| 19 | 2022 | 24 | |
| 20 | 2014 | 23 |
About W. David Dotson
W. David Dotson is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Economics and Econometrics and Pathology and Forensic Medicine, having authored 34 papers that have together received 1.7k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (20 papers), Genomics and Rare Diseases (9 papers), Health Systems, Economic Evaluations, Quality of Life (6 papers), Ethics in Clinical Research (6 papers), Genetic factors in colorectal cancer (5 papers), Nutrition, Genetics, and Disease (5 papers), Genetics, Bioinformatics, and Biomedical Research (3 papers) and Breast Cancer Treatment Studies (2 papers). The work is most often cited by research in Genetics (794 citations), Cancer Research (362 citations), Pharmacology (106 citations), Pathology and Forensic Medicine (218 citations) and Oncology (306 citations). W. David Dotson has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Muin J. Khoury, Linda Bradley, Michael P. Douglas, Katherine Kolor, Glenn E. Palomaki, James E. Haddow, Steven M. Teutsch, Ned Calonge, Alfred O. Berg and Margaret Piper. Their work appears in journals such as Genetics in Medicine, PLoS Currents, Public Health Genomics, Health Affairs and Journal of Bacteriology.
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.