Beth Ford
Impact in
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- BRCA gene mutations in cancer
- Genomics and Rare Diseases
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- Genetic factors in colorectal cancer
Papers in
- Genetics 4
- BRCA gene mutations in cancer 4
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- Genetic factors in colorectal cancer 3
- Co-authors
- Kimberly A. Kaphingst (2 shared papers)Elena M. Stoffel (5 shared papers)Sapna Syngal (5 shared papers)Lori A.H. Erby (1 shared paper)Christina Lachance (1 shared paper)Vincent C. Allen (1 shared paper)Peggy Conrad (3 shared papers)Jonathan P. Terdiman (3 shared papers)
- Journals
- Journal of Clinical Oncology (2 papers)Clinical Gastroenterology and Hepatology (1 paper)Genetics in Medicine (1 paper)The American Journal of Gastroenterology (1 paper)Cancer Epidemiology Biomarkers & Prevention (1 paper)
- Partner nations
- United StatesSpain
In The Last Decade
Beth Ford
9 papers receiving 308 citations
Peers
Comparison fields: 5 of 55
- Genetics 166
- Pathology and Forensic Medicine 104
- Oncology 76
- Cancer Research 41
- Public Health, Environmental and Occupational Health 78
Countries citing papers authored by Beth Ford
This map shows the geographic impact of Beth Ford'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 Beth Ford with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beth Ford more than expected).
Fields of papers citing papers by Beth Ford
This network shows the impact of papers produced by Beth Ford. 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 Beth Ford. The network helps show where Beth Ford may publish in the future.
Co-authors
The 21 scholars most cited alongside Beth Ford, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2008 | 92 | |
| 2 | 2010 | 89 | |
| 3 | 2010 | 51 | |
| 4 | 2006 | 35 | |
| 5 | 2009 | 24 | |
| 6 | 2009 | 20 | |
| 7 | Open Wide the Gates of Legal Access | 2015 | 1 |
| 8 | ICD-9-CM expert : for home health services., nursing facilities, and hospices volumes 1, 2, & 3 | 2008 | 1 |
| 9 | 2005 | 1 |
About Beth Ford
Beth Ford is a scholar working on Genetics, Pathology and Forensic Medicine, General Health Professions, Oncology and Public Health, Environmental and Occupational Health, having authored 9 papers that have together received 314 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (4 papers), Genetic factors in colorectal cancer (3 papers), Health Literacy and Information Accessibility (2 papers), Ethics in Clinical Research (2 papers), Colorectal Cancer Screening and Detection (2 papers), Cancer Genomics and Diagnostics (1 paper), Colorectal Cancer Treatments and Studies (1 paper) and Legal Education and Practice Innovations (1 paper). The work is most often cited by research in Genetics (166 citations), Pathology and Forensic Medicine (104 citations), Oncology (76 citations), Cancer Research (41 citations) and Public Health, Environmental and Occupational Health (78 citations). Beth Ford has collaborated with scholars based in United States and Spain. Frequent co-authors include Kimberly A. Kaphingst, Elena M. Stoffel, Sapna Syngal, Lori A.H. Erby, Christina Lachance, Vincent C. Allen, Peggy Conrad, Jonathan P. Terdiman, Rowena Mercado and Daniel C. Chung. Their work appears in journals such as Journal of Clinical Oncology, Clinical Gastroenterology and Hepatology, Genetics in Medicine, The American Journal of Gastroenterology and Cancer Epidemiology Biomarkers & Prevention.
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.