Séverine Bacrot
Impact in
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- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
Papers in
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- RNA modifications and cancer 3
- Cancer-related gene regulation 1
- Genetics 3
- Connective tissue disorders research 2
- Co-authors
- Céline Huber (2 shared papers)Mathilde Doyard (2 shared papers)Arnold Münnich (2 shared papers)Valérie Cormier‐Daire (3 shared papers)Olivier Alibeu (2 shared papers)Patrick Nitschké (2 shared papers)J. Leroux (1 shared paper)Samia A. Temtamy (1 shared paper)
In The Last Decade
Séverine Bacrot
7 papers receiving 126 citations
Peers
Comparison fields: 5 of 30
- Genetics 73
- Developmental Neuroscience 10
- Rheumatology 26
- Genetics 14
- Molecular Biology 67
Countries citing papers authored by Séverine Bacrot
This map shows the geographic impact of Séverine Bacrot'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 Bacrot with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Séverine Bacrot more than expected).
Fields of papers citing papers by Séverine Bacrot
This network shows the impact of papers produced by Séverine Bacrot. 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 Bacrot. The network helps show where Séverine Bacrot may publish in the future.
Co-authors
The 25 scholars most cited alongside Séverine Bacrot, 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 | 2018 | 53 | |
| 2 | 2014 | 36 | |
| 3 | 2014 | 16 | |
| 4 | 2018 | 11 | |
| 5 | 2020 | 5 | |
| 6 | 2021 | 4 | |
| 7 | 2019 | 1 |
About Séverine Bacrot
Séverine Bacrot is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Cancer Research and Pathology and Forensic Medicine, having authored 7 papers that have together received 126 indexed citations. Recurring topics across this work include RNA modifications and cancer (3 papers), Connective tissue disorders research (2 papers), Cancer-related molecular mechanisms research (2 papers), Williams Syndrome Research (1 paper), Neonatal Health and Biochemistry (1 paper), Selenium in Biological Systems (1 paper), Fetal and Pediatric Neurological Disorders (1 paper) and Cancer-related gene regulation (1 paper). The work is most often cited by research in Genetics (73 citations), Developmental Neuroscience (10 citations), Rheumatology (26 citations), Genetics (14 citations) and Molecular Biology (67 citations). Séverine Bacrot has collaborated with scholars based in France, Italy and Australia. Frequent co-authors include Céline Huber, Mathilde Doyard, Arnold Münnich, Valérie Cormier‐Daire, Olivier Alibeu, Patrick Nitschké, J. Leroux, Samia A. Temtamy, Caroline Michot and Sophie Monnot. Their work appears in journals such as Human Mutation, Journal of Medical Genetics, Molecular Genetics and Metabolism, Birth Defects Research and American Journal of Medical Genetics Part A.
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.