Mylène Béri‐Dexheimer
- Co-authors
- Jean‐Louis GuéantCéline BonnetPhilippe JonveauxChristophe PhilippeBruno LeheupVéronique Latger‐CannardPascal ChambonMarie‐José Gregoire
- Topics
- Genomic variations and chromosomal abnormalities (3 papers)Genetics and Neurodevelopmental Disorders (2 papers)Chromosomal and Genetic Variations (2 papers)
- Cited by
- HematologyGenetics
In The Last Decade
Mylène Béri‐Dexheimer
8 papers receiving 159 citations
Peers
Comparison fields: 5 of 41
- Genetics 54
- Hematology 54
- Molecular Biology 45
- Genetics 34
- Pharmacology 29
Countries citing papers authored by Mylène Béri‐Dexheimer
This map shows the geographic impact of Mylène Béri‐Dexheimer'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 Mylène Béri‐Dexheimer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mylène Béri‐Dexheimer more than expected).
Fields of papers citing papers by Mylène Béri‐Dexheimer
This network shows the impact of papers produced by Mylène Béri‐Dexheimer. 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 Mylène Béri‐Dexheimer. The network helps show where Mylène Béri‐Dexheimer may publish in the future.
Co-authorship network of co-authors of Mylène Béri‐Dexheimer
This figure shows the co-authorship network connecting the top 25 collaborators of Mylène Béri‐Dexheimer. A scholar is included among the top collaborators of Mylène Béri‐Dexheimer 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 Mylène Béri‐Dexheimer. Mylène Béri‐Dexheimer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 4 | |
| 2 | 11 | |
| 3 | 5 | |
| 4 | 9 | |
| 5 | 72 | |
| 6 | 22 | |
| 7 | 2 | |
| 8 | 34 |
About Mylène Béri‐Dexheimer
Mylène Béri‐Dexheimer is a scholar working on Genetics, Genetics and Immunology and Allergy, having authored 8 papers that have together received 159 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). The work is most often cited by research in Hematology (54 citations), Genetics (34 citations) and Genetics (54 citations). Mylène Béri‐Dexheimer has collaborated with scholars based in France and Italy. Frequent co-authors include Jean‐Louis Guéant, Céline Bonnet, Philippe Jonveaux, Christophe Philippe, Bruno Leheup, Véronique Latger‐Cannard, Pascal Chambon, Marie‐José Gregoire, Thomas Lecompte and Pierre Bordigoni. Their work appears in journals such as Frontiers in Immunology, Journal of Medical Genetics and European 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.