Caroline Benjamin
Impact in
- Cancer Research top 2%
- Cancer, Hypoxia, and Metabolism
- Genetics top 5%
- BRCA gene mutations in cancer
- Genomics and Rare Diseases
Papers in
- Genetics 27
- BRCA gene mutations in cancer 25
- Genomics and Rare Diseases 7
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- Ethics and Legal Issues in Pediatric Healthcare 5
- Co-authors
- R Harris (13 shared papers)John R.W. Yates (3 shared papers)M.A. Ferguson‐Smith (3 shared papers)Eamonn R. Maher (3 shared papers)Anthony T. Moore (1 shared paper)A. Prysor Williams (1 shared paper)Newton E. Morton (1 shared paper)Julian R. Sampson (1 shared paper)
- Journals
- European Journal of Human Genetics (5 papers)Journal of Nursing Scholarship (3 papers)Genetics in Medicine (3 papers)Lara D. Veeken (2 papers)Public Health Genomics (2 papers)
- Partner nations
- United KingdomFranceUnited States
In The Last Decade
Caroline Benjamin
43 papers receiving 2.1k citations
Caroline Benjamin's Hit Papers
Peers
Comparison fields: 5 of 107
- Cancer Research 831
- Genetics 633
- Neurology 293
- Ophthalmology 149
- Pulmonary and Respiratory Medicine 272
Countries citing papers authored by Caroline Benjamin
This map shows the geographic impact of Caroline Benjamin'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 Caroline Benjamin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Caroline Benjamin more than expected).
Fields of papers citing papers by Caroline Benjamin
This network shows the impact of papers produced by Caroline Benjamin. 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 Caroline Benjamin. The network helps show where Caroline Benjamin may publish in the future.
Co-authors
The 25 scholars most cited alongside Caroline Benjamin, 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 45 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Clinical Features and Natural History of von Hippel-Lindau Disease Hit paper breakdown → | 1990 | 743 |
| 2 | 1991 | 450 | |
| 3 | Proceed with care: direct predictive testing for Huntington disease. | 1994 | 90 |
| 4 | 1993 | 80 | |
| 5 | 2018 | 79 | |
| 6 | 2010 | 75 | |
| 7 | 1995 | 70 | |
| 8 | 2018 | 62 | |
| 9 | 2014 | 60 | |
| 10 | 1992 | 48 | |
| 11 | 2020 | 41 | |
| 12 | 2018 | 37 | |
| 13 | 2005 | 36 | |
| 14 | 1990 | 36 | |
| 15 | 2018 | 30 | |
| 16 | 2008 | 29 | |
| 17 | 1990 | 28 | |
| 18 | 2008 | 25 | |
| 19 | 2020 | 23 | |
| 20 | 2014 | 23 |
About Caroline Benjamin
Caroline Benjamin is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, General Health Professions, Public Health, Environmental and Occupational Health and Molecular Biology, having authored 45 papers that have together received 2.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (25 papers), Genomics and Rare Diseases (7 papers), Ethics and Legal Issues in Pediatric Healthcare (5 papers), Ethics in medical practice (3 papers), Genetic Neurodegenerative Diseases (3 papers), Ethics in Clinical Research (3 papers), Cancer, Hypoxia, and Metabolism (3 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Cancer Research (831 citations), Genetics (633 citations), Neurology (293 citations), Ophthalmology (149 citations) and Pulmonary and Respiratory Medicine (272 citations). Caroline Benjamin has collaborated with scholars based in United Kingdom, France and United States. Frequent co-authors include R Harris, John R.W. Yates, M.A. Ferguson‐Smith, Eamonn R. Maher, Anthony T. Moore, A. Prysor Williams, Newton E. Morton, Julian R. Sampson, L Iselius and Anna Middleton. Their work appears in journals such as European Journal of Human Genetics, Journal of Nursing Scholarship, Genetics in Medicine, Lara D. Veeken and Public Health Genomics.
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.