Pierre O. Chappuis
- Oncology top 1%
- Cancer Research top 1%
- Genetics top 1%
- Molecular Biology top 5%
- Pathology and Forensic Medicine top 2%
- Co-authors
- William D. FoulkesLouis R. BéginNora WongChristine BouchardyJean‐Sébastien BrunetElisabetta RapitiNancy HamelGeorges Vlastos
- Topics
- BRCA gene mutations in cancer (52 papers)Genetic factors in colorectal cancer (24 papers)Cancer Genomics and Diagnostics (18 papers)
- Cited by
- Cancer ResearchOncologyGenetics
- Partner nations
- SwitzerlandUnited StatesFrance
In The Last Decade
Pierre O. Chappuis
104 papers receiving 3.5k citations
Peers
Comparison fields: 5 of 112
- Oncology 1.7k
- Cancer Research 1.5k
- Genetics 1.4k
- Molecular Biology 1.3k
- Pathology and Forensic Medicine 702
Countries citing papers authored by Pierre O. Chappuis
This map shows the geographic impact of Pierre O. Chappuis'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 Pierre O. Chappuis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pierre O. Chappuis more than expected).
Fields of papers citing papers by Pierre O. Chappuis
This network shows the impact of papers produced by Pierre O. Chappuis. 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 Pierre O. Chappuis. The network helps show where Pierre O. Chappuis may publish in the future.
Co-authorship network of co-authors of Pierre O. Chappuis
This figure shows the co-authorship network connecting the top 25 collaborators of Pierre O. Chappuis. A scholar is included among the top collaborators of Pierre O. Chappuis based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Pierre O. Chappuis. Pierre O. Chappuis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 72 | |
| 3 | 16 | |
| 4 | 8 | |
| 5 | 6 | |
| 6 | 4 | |
| 7 | 32 | |
| 8 | 5 | |
| 9 | 49 | |
| 10 | 8 | |
| 11 | 63 | |
| 12 | 39 | |
| 13 | 22 | |
| 14 | 84 | |
| 15 | 212 | |
| 16 | 14 | |
| 17 | 43 | |
| 18 | N-acetyltransferase 2 influences cancer prevalence in hMLH1/hMSH2 mutation carriers. | 30 |
| 19 | 30 | |
| 20 | 53 |
About Pierre O. Chappuis
Pierre O. Chappuis is a scholar working on Genetics, Cancer Research and Pathology and Forensic Medicine, having authored 107 papers that have together received 3.6k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (52 papers), Genetic factors in colorectal cancer (24 papers) and Cancer Genomics and Diagnostics (18 papers). The work is most often cited by research in Cancer Research (1.5k citations), Oncology (1.7k citations) and Genetics (1.4k citations). Pierre O. Chappuis has collaborated with scholars based in Switzerland, United States and France. Frequent co-authors include William D. Foulkes, Louis R. Bégin, Nora Wong, Christine Bouchardy, Jean‐Sébastien Brunet, Elisabetta Rapiti, Nancy Hamel, Georges Vlastos, G Fioretta and Helena M. Verkooijen. Their work appears in journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and PLoS ONE.
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.