Séverine Drunat
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Cell Biology top 10%
- Microtubule and mitosis dynamics
Papers in
-
- RNA modifications and cancer 9
- Congenital heart defects research 4
- Genetics 26
- Genetics and Neurodevelopmental Disorders 10
- Genomic variations and chromosomal abnormalities 10
- Neurogenetic and Muscular Disorders Research 8
- Co-authors
- Alain Verloès (23 shared papers)Sandrine Passemard (16 shared papers)Hélène Cavé (4 shared papers)Pierre Gressèns (9 shared papers)Sophie Valleix (2 shared papers)Gilles Grateau (2 shared papers)Marc Delpech (2 shared papers)N. Moatti (4 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)Clinical Genetics (2 papers)
- Partner nations
- FranceGermanyUnited Kingdom
In The Last Decade
Séverine Drunat
54 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 83
- Genetics 415
- Cell Biology 155
- Molecular Biology 540
- Genetics 75
- Pediatrics, Perinatology and Child Health 127
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 60 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2002 | 110 | |
| 2 | 2013 | 74 | |
| 3 | 2000 | 69 | |
| 4 | 2012 | 52 | |
| 5 | 2015 | 52 | |
| 6 | 2016 | 47 | |
| 7 | 2009 | 46 | |
| 8 | 2000 | 46 | |
| 9 | 2017 | 43 | |
| 10 | 2010 | 39 | |
| 11 | 2012 | 38 | |
| 12 | 2001 | 34 | |
| 13 | 2008 | 32 | |
| 14 | 2013 | 31 | |
| 15 | 2019 | 30 | |
| 16 | Primary Autosomal Recessive Microcephalies and Seckel Syndrome Spectrum Disorders | 2013 | 29 |
| 17 | 2015 | 28 | |
| 18 | 2014 | 27 | |
| 19 | 2012 | 27 | |
| 20 | 2009 | 26 |
About Séverine Drunat
Séverine Drunat is a scholar working on Molecular Biology, Genetics, Cell Biology, Genetics and Surgery, having authored 60 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (10 papers), Genomic variations and chromosomal abnormalities (10 papers), RNA modifications and cancer (9 papers), Neurogenetic and Muscular Disorders Research (8 papers), Microtubule and mitosis dynamics (7 papers), Congenital heart defects research (4 papers), Prenatal Screening and Diagnostics (4 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Genetics (415 citations), Cell Biology (155 citations), Molecular Biology (540 citations), Genetics (75 citations) and Pediatrics, Perinatology and Child Health (127 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, Sophie Valleix, Gilles Grateau, Marc Delpech, N. Moatti, 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 Clinical 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.