Séverine Drunat
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cell Biology top 10%
- Microtubule and mitosis dynamics
Papers in
- Genetics 30
- Genetics and Neurodevelopmental Disorders 13
- Genomic variations and chromosomal abnormalities 12
- Neurogenetic and Muscular Disorders Research 8
- Genomics and Rare Diseases 5
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- RNA modifications and cancer 10
- Congenital heart defects research 5
- Co-authors
- Alain Verloès (22 shared papers)Sandrine Passemard (13 shared papers)Hélène Cavé (4 shared papers)Pierre Gressèns (8 shared papers)Gilles Grateau (2 shared papers)N. Moatti (4 shared papers)Sophie Valleix (2 shared papers)Marc Delpech (2 shared papers)
- Journals
- European Journal of Medical Genetics (6 papers)European Journal of Human Genetics (3 papers)Neurology Genetics (3 papers)British Journal of Haematology (2 papers)The American Journal of Human Genetics (2 papers)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Séverine Drunat
53 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 84
- Genetics 443
- Cell Biology 160
- Molecular Biology 581
- Pediatrics, Perinatology and Child Health 144
- Genetics 77
Countries citing papers authored by Séverine Drunat
This map shows the geographic impact of Séverine Drunat'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 Séverine Drunat with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Séverine Drunat more than expected).
Fields of papers citing papers by Séverine Drunat
This network shows the impact of papers produced by Séverine Drunat. 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 Séverine Drunat. The network helps show where Séverine Drunat may publish in the future.
Co-authors
The 25 scholars most cited alongside Séverine Drunat, 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 57 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 104 | |
| 2 | 2000 | 68 | |
| 3 | 2013 | 67 | |
| 4 | 2012 | 52 | |
| 5 | 2015 | 50 | |
| 6 | 2016 | 47 | |
| 7 | 2000 | 44 | |
| 8 | 2017 | 43 | |
| 9 | 2009 | 41 | |
| 10 | 2012 | 37 | |
| 11 | 2010 | 34 | |
| 12 | 2001 | 33 | |
| 13 | 2008 | 32 | |
| 14 | 2013 | 30 | |
| 15 | 2019 | 30 | |
| 16 | 2015 | 28 | |
| 17 | 2012 | 27 | |
| 18 | Primary Autosomal Recessive Microcephalies and Seckel Syndrome Spectrum Disorders | 2013 | 26 |
| 19 | 2009 | 24 | |
| 20 | 2014 | 23 |
About Séverine Drunat
Séverine Drunat is a scholar working on Genetics, Molecular Biology, Cell Biology, Genetics and Surgery, having authored 57 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (13 papers), Genomic variations and chromosomal abnormalities (12 papers), RNA modifications and cancer (10 papers), Neurogenetic and Muscular Disorders Research (8 papers), Microtubule and mitosis dynamics (7 papers), Congenital heart defects research (5 papers), Prenatal Screening and Diagnostics (5 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Genetics (443 citations), Cell Biology (160 citations), Molecular Biology (581 citations), Pediatrics, Perinatology and Child Health (144 citations) and Genetics (77 citations). Séverine Drunat has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Alain Verloès, Sandrine Passemard, Hélène Cavé, Pierre Gressèns, Gilles Grateau, N. Moatti, Sophie Valleix, Marc Delpech, Karine Demuth and Michel Polak. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Neurology Genetics, British Journal of Haematology and The American 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.