Virginie Moncoutier
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- Cancer Genomics and Diagnostics 3
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- BRCA gene mutations in cancer 3
- Genomic variations and chromosomal abnormalities 2
- Genomics and Rare Diseases 1
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- CRISPR and Genetic Engineering 3
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- Genetic factors in colorectal cancer 2
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- Testicular diseases and treatments 1
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- Ovarian cancer diagnosis and treatment 1
Virginie Moncoutier
7 papers receiving 87 citations
Peers
Comparison fields: 5 of 29
- Cancer Research 31
- Genetics 54
- Molecular Biology 51
- Pathology and Forensic Medicine 10
- Oncology 12
Countries citing papers authored by Virginie Moncoutier
This map shows the geographic impact of Virginie Moncoutier'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 Virginie Moncoutier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Virginie Moncoutier more than expected).
Fields of papers citing papers by Virginie Moncoutier
This network shows the impact of papers produced by Virginie Moncoutier. 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 Virginie Moncoutier. The network helps show where Virginie Moncoutier may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Virginie Moncoutier, 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 | 2023 | 2 | |
| 2 | 2023 | 4 | |
| 3 | 2022 | 1 | |
| 4 | 2017 | 6 | |
| 5 | 2013 | 46 | |
| 6 | 2010 | 11 | |
| 7 | 2003 | 18 |
About Virginie Moncoutier
Virginie Moncoutier is a scholar working on Cancer Research, Genetics and Reproductive Medicine, having authored 7 papers that have together received 88 indexed citations. Recurring topics across this work include Cancer Genomics and Diagnostics (3 papers), CRISPR and Genetic Engineering (3 papers), BRCA gene mutations in cancer (3 papers), Genetic factors in colorectal cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genomics and Rare Diseases (1 paper), Testicular diseases and treatments (1 paper) and Ovarian cancer diagnosis and treatment (1 paper). The work is most often cited by research in Cancer Research (31 citations), Genetics (54 citations) and Molecular Biology (51 citations). Virginie Moncoutier has collaborated with scholars based in France and Spain. Frequent co-authors include Dominique Stoppa‐Lyonnet, Lisa Golmard, Bruno Zeitouni, Thomas Rio Frio, Emmanuel Barillot, Marc‐Henri Stern, Patricia Legoix-Né, Claude Houdayer, Séverine Lair and Henrique Tenreiro. Their work appears in journals such as Journal of Medical Genetics, Human Mutation and European Journal of Human 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.