Cédrick Lefol
Impact in
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- Cancer Genomics and Diagnostics
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- Genetic factors in colorectal cancer
Papers in
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- RNA Research and Splicing 4
- CRISPR and Genetic Engineering 2
- DNA Repair Mechanisms 2
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- Genetic factors in colorectal cancer 8
- Co-authors
- Étienne Rouleau (7 shared papers)Rosette Lidereau (6 shared papers)Ivan Bièche (3 shared papers)Sylviane Olschwang (3 shared papers)Hagay Sobol (2 shared papers)Florence Coulet (2 shared papers)Violaine Bourdon (2 shared papers)Florent Soubrier (2 shared papers)
- Journals
- Human Mutation (2 papers)Clinical Genetics (2 papers)Genes Chromosomes and Cancer (2 papers)European Journal of Human Genetics (1 paper)Familial Cancer (1 paper)
- Partner nations
- FranceUnited StatesMonaco
In The Last Decade
Cédrick Lefol
13 papers receiving 197 citations
Peers
Comparison fields: 5 of 39
- Cancer Research 67
- Pathology and Forensic Medicine 62
- Genetics 75
- Molecular Biology 120
- Pulmonary and Respiratory Medicine 36
Countries citing papers authored by Cédrick Lefol
This map shows the geographic impact of Cédrick Lefol'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 Cédrick Lefol with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Cédrick Lefol more than expected).
Fields of papers citing papers by Cédrick Lefol
This network shows the impact of papers produced by Cédrick Lefol. 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 Cédrick Lefol. The network helps show where Cédrick Lefol may publish in the future.
Co-authors
The 25 scholars most cited alongside Cédrick Lefol, 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 | 2009 | 51 | |
| 2 | 2015 | 32 | |
| 3 | 2007 | 27 | |
| 4 | 2020 | 16 | |
| 5 | 2010 | 16 | |
| 6 | 2011 | 15 | |
| 7 | 2012 | 15 | |
| 8 | 2011 | 12 | |
| 9 | 2020 | 8 | |
| 10 | 2023 | 4 | |
| 11 | 2023 | 2 | |
| 12 | 2022 | 1 | |
| 13 | 2024 | 1 |
About Cédrick Lefol
Cédrick Lefol is a scholar working on Molecular Biology, Pathology and Forensic Medicine, Cancer Research, Genetics and Oncology, having authored 13 papers that have together received 200 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (8 papers), Genetic factors in colorectal cancer (8 papers), RNA Research and Splicing (4 papers), BRCA gene mutations in cancer (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Colorectal Cancer Treatments and Studies (2 papers), CRISPR and Genetic Engineering (2 papers) and DNA Repair Mechanisms (2 papers). The work is most often cited by research in Cancer Research (67 citations), Pathology and Forensic Medicine (62 citations), Genetics (75 citations), Molecular Biology (120 citations) and Pulmonary and Respiratory Medicine (36 citations). Cédrick Lefol has collaborated with scholars based in France, United States and Monaco. Frequent co-authors include Étienne Rouleau, Rosette Lidereau, Ivan Bièche, Sylviane Olschwang, Hagay Sobol, Florence Coulet, Violaine Bourdon, Florent Soubrier, Catherine Noguès and Tetsuro Noguchi. Their work appears in journals such as Human Mutation, Clinical Genetics, Genes Chromosomes and Cancer, European Journal of Human Genetics and Familial Cancer.
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.