Déborah Bourc’his
Impact in
- Genetics top 0.2%
- Genetic Syndromes and Imprinting
- Molecular Biology top 0.5%
- Epigenetics and DNA Methylation
- RNA modifications and cancer
- CRISPR and Genetic Engineering
- Cancer-related gene regulation
- Genomics and Chromatin Dynamics
Papers in
-
- Epigenetics and DNA Methylation 52
- CRISPR and Genetic Engineering 11
- Pluripotent Stem Cells Research 7
- RNA modifications and cancer 7
- Genetics 42
- Genetic Syndromes and Imprinting 32
- Genetics and Neurodevelopmental Disorders 12
- Co-authors
- Timothy H. Bestor (18 shared papers)Max Greenberg (8 shared papers)Guoliang Xu (2 shared papers)Gregory J. Hannon (2 shared papers)Chyuan‐Sheng Lin (2 shared papers)E. Viégas-Pèquignot (8 shared papers)Aurélie Teissandier (14 shared papers)Dirk G. de Rooij (2 shared papers)
- Journals
- Human Reproduction (5 papers)Genes & Development (4 papers)eLife (4 papers)Science (4 papers)Nature (3 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Déborah Bourc’his
73 papers receiving 10.7k citations
Déborah Bourc’his's Hit Papers
Peers
Comparison fields: 5 of 134
- Genetics 3.7k
- Molecular Biology 9.1k
- Pediatrics, Perinatology and Child Health 1.7k
- Plant Science 2.4k
- Cancer Research 821
Countries citing papers authored by Déborah Bourc’his
This map shows the geographic impact of Déborah Bourc’his'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 Déborah Bourc’his with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Déborah Bourc’his more than expected).
Fields of papers citing papers by Déborah Bourc’his
This network shows the impact of papers produced by Déborah Bourc’his. 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 Déborah Bourc’his. The network helps show where Déborah Bourc’his may publish in the future.
Co-authors
The 25 scholars most cited alongside Déborah Bourc’his, 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 76 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | The diverse roles of DNA methylation in mammalian development and disease Hit paper breakdown → | 2019 | 1426 |
| 2 | Dnmt3L and the Establishment of Maternal Genomic Imprints Hit paper breakdown → | 2001 | 1115 |
| 3 | Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene Hit paper breakdown → | 1999 | 955 |
| 4 | A piRNA Pathway Primed by Individual Transposons Is Linked to De Novo DNA Methylation in Mice Hit paper breakdown → | 2008 | 953 |
| 5 | Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L Hit paper breakdown → | 2004 | 949 |
| 6 | MIWI2 Is Essential for Spermatogenesis and Repression of Transposons in the Mouse Male Germline Hit paper breakdown → | 2007 | 940 |
| 7 | Genomic Imprinting and Physiological Processes in Mammals Hit paper breakdown → | 2019 | 377 |
| 8 | 1998 | 357 | |
| 9 | 2001 | 331 | |
| 10 | 2016 | 279 | |
| 11 | 2016 | 215 | |
| 12 | m6A RNA methylation regulates the fate of endogenous retroviruses Hit paper breakdown → | 2021 | 212 |
| 13 | 2008 | 151 | |
| 14 | 2007 | 150 | |
| 15 | 2010 | 143 | |
| 16 | 2015 | 139 | |
| 17 | 2010 | 130 | |
| 18 | 2008 | 125 | |
| 19 | 2012 | 111 | |
| 20 | 2004 | 98 |
About Déborah Bourc’his
Déborah Bourc’his is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Plant Science and Public Health, Environmental and Occupational Health, having authored 76 papers that have together received 10.9k indexed citations. Recurring topics across this work include Epigenetics and DNA Methylation (52 papers), Genetic Syndromes and Imprinting (32 papers), Prenatal Screening and Diagnostics (20 papers), Chromosomal and Genetic Variations (13 papers), Genetics and Neurodevelopmental Disorders (12 papers), CRISPR and Genetic Engineering (11 papers), Pluripotent Stem Cells Research (7 papers) and RNA modifications and cancer (7 papers). The work is most often cited by research in Genetics (3.7k citations), Molecular Biology (9.1k citations), Pediatrics, Perinatology and Child Health (1.7k citations), Plant Science (2.4k citations) and Cancer Research (821 citations). Déborah Bourc’his has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Timothy H. Bestor, Max Greenberg, Guoliang Xu, Gregory J. Hannon, Chyuan‐Sheng Lin, E. Viégas-Pèquignot, Aurélie Teissandier, Dirk G. de Rooij, Christopher Schaefer and H. J. G. van de Kant. Their work appears in journals such as Human Reproduction, Genes & Development, eLife, Science and Nature.
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.