Frédéric Baudat
Impact in
- Molecular Biology top 2%
- DNA Repair Mechanisms
- Genomics and Chromatin Dynamics
- CRISPR and Genetic Engineering
- Epigenetics and DNA Methylation
- Aging top 5%
Papers in
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- DNA Repair Mechanisms 31
- Genomics and Chromatin Dynamics 17
- CRISPR and Genetic Engineering 8
- Fungal and yeast genetics research 5
- Epigenetics and DNA Methylation 5
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- Carcinogens and Genotoxicity Assessment 6
- Co-authors
- Bernard de Massy (27 shared papers)Scott Keeney (9 shared papers)Maria Jasin (8 shared papers)Corinne Grey (9 shared papers)Yukiko Imai (4 shared papers)Alain G. Nicolas (4 shared papers)Katia O Manova-Todorova (2 shared papers)Jérôme Buard (3 shared papers)
- Journals
- Nature Genetics (3 papers)PLoS Genetics (3 papers)Chromosoma (3 papers)Proceedings of the National Academy of Sciences (3 papers)Science (3 papers)
- Partner nations
- FranceUnited StatesGermany
In The Last Decade
Frédéric Baudat
39 papers receiving 4.8k citations
Frédéric Baudat's Hit Papers
Peers
Comparison fields: 5 of 85
- Molecular Biology 4.1k
- Aging 82
- Genetics 1.2k
- Reproductive Medicine 306
- Cancer Research 429
Countries citing papers authored by Frédéric Baudat
This map shows the geographic impact of Frédéric Baudat'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 Frédéric Baudat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Frédéric Baudat more than expected).
Fields of papers citing papers by Frédéric Baudat
This network shows the impact of papers produced by Frédéric Baudat. 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 Frédéric Baudat. The network helps show where Frédéric Baudat may publish in the future.
Co-authors
The 25 scholars most cited alongside Frédéric Baudat, 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 40 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice Hit paper breakdown → | 2009 | 748 |
| 2 | 2001 | 722 | |
| 3 | 2000 | 572 | |
| 4 | Meiotic recombination in mammals: localization and regulation Hit paper breakdown → | 2013 | 429 |
| 5 | 1997 | 267 | |
| 6 | 2013 | 203 | |
| 7 | 2011 | 190 | |
| 8 | 2005 | 190 | |
| 9 | 2005 | 177 | |
| 10 | 2007 | 149 | |
| 11 | 2005 | 134 | |
| 12 | 2011 | 123 | |
| 13 | 1999 | 98 | |
| 14 | 2018 | 89 | |
| 15 | 2013 | 84 | |
| 16 | 2018 | 80 | |
| 17 | 2014 | 78 | |
| 18 | 2007 | 67 | |
| 19 | 2009 | 63 | |
| 20 | 1994 | 63 |
About Frédéric Baudat
Frédéric Baudat is a scholar working on Molecular Biology, Cancer Research, Plant Science, Genetics and Cell Biology, having authored 40 papers that have together received 4.9k indexed citations. Recurring topics across this work include DNA Repair Mechanisms (31 papers), Genomics and Chromatin Dynamics (17 papers), Chromosomal and Genetic Variations (11 papers), CRISPR and Genetic Engineering (8 papers), Carcinogens and Genotoxicity Assessment (6 papers), Fungal and yeast genetics research (5 papers), Epigenetics and DNA Methylation (5 papers) and Genetic Mapping and Diversity in Plants and Animals (4 papers). The work is most often cited by research in Molecular Biology (4.1k citations), Aging (82 citations), Genetics (1.2k citations), Reproductive Medicine (306 citations) and Cancer Research (429 citations). Frédéric Baudat has collaborated with scholars based in France, United States and Germany. Frequent co-authors include Bernard de Massy, Scott Keeney, Maria Jasin, Corinne Grey, Yukiko Imai, Alain G. Nicolas, Katia O Manova-Todorova, Jérôme Buard, Paul S. Burgoyne and Adi Fledel-Alon. Their work appears in journals such as Nature Genetics, PLoS Genetics, Chromosoma, Proceedings of the National Academy of Sciences and Science.
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.