Séverine Bacrot
Impact in
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- Connective tissue disorders research
- Neurogenetic and Muscular Disorders Research
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
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- Williams Syndrome Research
Papers in
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- RNA modifications and cancer 2
- Congenital heart defects research 1
- Genetics 3
- Connective tissue disorders research 2
- Ocular Disorders and Treatments 1
- Co-authors
- Céline Huber (2 shared papers)Arnold Münnich (2 shared papers)Mathilde Doyard (2 shared papers)Valérie Cormier‐Daire (3 shared papers)Caroline Michot (3 shared papers)Olivier Alibeu (2 shared papers)Patrick Nitschké (2 shared papers)Mona Aglan (1 shared paper)
In The Last Decade
Séverine Bacrot
7 papers receiving 130 citations
Peers
Comparison fields: 5 of 27
- Genetics 66
- Developmental Neuroscience 9
- Rheumatology 20
- Genetics 14
- Molecular Biology 57
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 | 55 | |
| 2 | 2014 | 38 | |
| 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, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience, having authored 7 papers that have together received 130 indexed citations. Recurring topics across this work include Connective tissue disorders research (2 papers), RNA modifications and cancer (2 papers), Fetal and Pediatric Neurological Disorders (1 paper), Biomedical Research and Pathophysiology (1 paper), Aortic aneurysm repair treatments (1 paper), Congenital heart defects research (1 paper), Ocular Disorders and Treatments (1 paper) and Williams Syndrome Research (1 paper). The work is most often cited by research in Genetics (66 citations), Developmental Neuroscience (9 citations), Rheumatology (20 citations), Genetics (14 citations) and Molecular Biology (57 citations). Séverine Bacrot has collaborated with scholars based in France, Italy and Australia. Frequent co-authors include Céline Huber, Arnold Münnich, Mathilde Doyard, Valérie Cormier‐Daire, Caroline Michot, Olivier Alibeu, Patrick Nitschké, Mona Aglan, Jean‐Paul Bonnefont and Sophie Monnot. Their work appears in journals such as Molecular Genetics and Metabolism, Birth Defects Research, Journal of Medical Genetics, Human Mutation 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.