Séverine Audebert‐Bellanger
- Neurology
- Pulmonary and Respiratory Medicine
- Genetics
- Surgery
- Pediatrics, Perinatology and Child Health
- Co-authors
- Claude FérecL. MiseryC. Abasq‐ThomasI. DuguépérouxMartine BlayauE. BrenautP. WolkensteinS. Ferkal
- Topics
- Genomic variations and chromosomal abnormalities (3 papers)Cystic Fibrosis Research Advances (2 papers)Neurofibromatosis and Schwannoma Cases (2 papers)
- Journals
- American Journal of Obstetrics and GynecologyJournal of Medical GeneticsActa Dermato Venereologica
- Partner nations
- FranceUnited KingdomMorocco
In The Last Decade
Séverine Audebert‐Bellanger
10 papers receiving 92 citations
Peers
Comparison fields: 5 of 36
- Neurology 32
- Pulmonary and Respiratory Medicine 28
- Genetics 27
- Surgery 25
- Pediatrics, Perinatology and Child Health 25
Countries citing papers authored by Séverine Audebert‐Bellanger
This map shows the geographic impact of Séverine Audebert‐Bellanger'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 Audebert‐Bellanger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Séverine Audebert‐Bellanger more than expected).
Fields of papers citing papers by Séverine Audebert‐Bellanger
This network shows the impact of papers produced by Séverine Audebert‐Bellanger. 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 Audebert‐Bellanger. The network helps show where Séverine Audebert‐Bellanger may publish in the future.
Co-authorship network of co-authors of Séverine Audebert‐Bellanger
This figure shows the co-authorship network connecting the top 25 collaborators of Séverine Audebert‐Bellanger. A scholar is included among the top collaborators of Séverine Audebert‐Bellanger based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Séverine Audebert‐Bellanger. Séverine Audebert‐Bellanger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 2 | |
| 3 | 15 | |
| 4 | 3 | |
| 5 | 3 | |
| 6 | 3 | |
| 7 | 26 | |
| 8 | 16 | |
| 9 | 1 | |
| 10 | 8 | |
| 11 | 26 |
About Séverine Audebert‐Bellanger
Séverine Audebert‐Bellanger is a scholar working on Neurology, Genetics and Urology, having authored 11 papers that have together received 103 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Cystic Fibrosis Research Advances (2 papers) and Neurofibromatosis and Schwannoma Cases (2 papers). The work is most often cited by research in Neurology (32 citations), Pediatrics, Perinatology and Child Health (25 citations) and Genetics (27 citations). Séverine Audebert‐Bellanger has collaborated with scholars based in France, United Kingdom and Morocco. Frequent co-authors include Claude Férec, L. Misery, C. Abasq‐Thomas, I. Duguépéroux, Martine Blayau, E. Brenaut, P. Wolkenstein, S. Ferkal, Marie‐Pierre Audrézet and Virginie Scotet. Their work appears in journals such as American Journal of Obstetrics and Gynecology, Journal of Medical Genetics and Acta Dermato Venereologica.
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.