Patrick R. Benusiglio
Impact in
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- Genetic factors in colorectal cancer
- Cancer Research top 5%
- Cancer Genomics and Diagnostics
Papers in
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- Genetic factors in colorectal cancer 16
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- Cancer Genomics and Diagnostics 6
- Co-authors
- Laure Dossus (1 shared paper)Olivier Caron (10 shared papers)Brigitte Bressac–de Paillerets (5 shared papers)Laurence Brugières (4 shared papers)Thierry Frébourg (2 shared papers)Émilie Consolino (2 shared papers)Camille Charbonnier (1 shared paper)Gaëlle Bougeard (1 shared paper)
- Journals
- Journal of Medical Genetics (8 papers)European Journal of Human Genetics (3 papers)Familial Cancer (3 papers)Genetics in Medicine (3 papers)European Journal of Medical Genetics (3 papers)
- Partner nations
- FranceUnited KingdomNetherlands
In The Last Decade
Patrick R. Benusiglio
69 papers receiving 2.6k citations
Patrick R. Benusiglio's Hit Papers
Peers
Comparison fields: 5 of 87
- Pathology and Forensic Medicine 614
- Cancer Research 443
- Oncology 657
- Pulmonary and Respiratory Medicine 691
- Genetics 576
Countries citing papers authored by Patrick R. Benusiglio
This map shows the geographic impact of Patrick R. Benusiglio'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 Patrick R. Benusiglio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick R. Benusiglio more than expected).
Fields of papers citing papers by Patrick R. Benusiglio
This network shows the impact of papers produced by Patrick R. Benusiglio. 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 Patrick R. Benusiglio. The network helps show where Patrick R. Benusiglio may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick R. Benusiglio, 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 73 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Revisiting Li-Fraumeni Syndrome From TP53 Mutation Carriers Hit paper breakdown → | 2015 | 567 |
| 2 | Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers Hit paper breakdown → | 2015 | 424 |
| 3 | Hereditary diffuse gastric cancer: updated clinical practice guidelines Hit paper breakdown → | 2020 | 314 |
| 4 | 2015 | 150 | |
| 5 | 2013 | 126 | |
| 6 | 2017 | 109 | |
| 7 | 2018 | 83 | |
| 8 | 2014 | 81 | |
| 9 | 2021 | 68 | |
| 10 | 2005 | 53 | |
| 11 | 2023 | 41 | |
| 12 | 2015 | 40 | |
| 13 | 2021 | 37 | |
| 14 | 2022 | 36 | |
| 15 | 2006 | 35 | |
| 16 | 2017 | 34 | |
| 17 | 2018 | 34 | |
| 18 | 2014 | 33 | |
| 19 | 2021 | 31 | |
| 20 | 2022 | 29 |
About Patrick R. Benusiglio
Patrick R. Benusiglio is a scholar working on Pathology and Forensic Medicine, Cancer Research, Genetics, Molecular Biology and Oncology, having authored 73 papers that have together received 2.7k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (16 papers), BRCA gene mutations in cancer (11 papers), Cancer-related gene regulation (8 papers), Renal cell carcinoma treatment (7 papers), Cancer Genomics and Diagnostics (6 papers), Cancer-related Molecular Pathways (6 papers), RNA modifications and cancer (5 papers) and DNA Repair Mechanisms (5 papers). The work is most often cited by research in Pathology and Forensic Medicine (614 citations), Cancer Research (443 citations), Oncology (657 citations), Pulmonary and Respiratory Medicine (691 citations) and Genetics (576 citations). Patrick R. Benusiglio has collaborated with scholars based in France, United Kingdom and Netherlands. Frequent co-authors include Laure Dossus, Olivier Caron, Brigitte Bressac–de Paillerets, Laurence Brugières, Thierry Frébourg, Émilie Consolino, Camille Charbonnier, Gaëlle Bougeard, Mariette Renaux‐Petel and Muriel Belotti. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Familial Cancer, Genetics in Medicine and European Journal of Medical 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.