Bérénice Herve
- Genetics
- Pediatrics, Perinatology and Child Health
- Molecular Biology
- Public Health, Environmental and Occupational Health
- Immunology
- Co-authors
- François VialardDenise Molina‐GomesDelphine FauvertThibaud QuibelJ. RoumePatrice ClémentGuillaume LegendreD. Subtil
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Prenatal Screening and Diagnostics (4 papers)Chromosomal and Genetic Variations (3 papers)
- Journals
- GeneEuropean Journal of Human GeneticsEuropean Journal of Obstetrics & Gynecology and Reproductive Biology
- Partner nations
- FranceItalyUnited Kingdom
In The Last Decade
Bérénice Herve
14 papers receiving 59 citations
Peers
Comparison fields: 5 of 28
- Genetics 42
- Pediatrics, Perinatology and Child Health 29
- Molecular Biology 19
- Public Health, Environmental and Occupational Health 10
- Immunology 10
Countries citing papers authored by Bérénice Herve
This map shows the geographic impact of Bérénice Herve'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 Bérénice Herve with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bérénice Herve more than expected).
Fields of papers citing papers by Bérénice Herve
This network shows the impact of papers produced by Bérénice Herve. 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 Bérénice Herve. The network helps show where Bérénice Herve may publish in the future.
Co-authorship network of co-authors of Bérénice Herve
This figure shows the co-authorship network connecting the top 25 collaborators of Bérénice Herve. A scholar is included among the top collaborators of Bérénice Herve 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 Bérénice Herve. Bérénice Herve is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 2 | |
| 3 | 1 | |
| 4 | 1 | |
| 5 | 1 | |
| 6 | 6 | |
| 7 | 11 | |
| 8 | 7 | |
| 9 | 4 | |
| 10 | 5 | |
| 11 | 7 | |
| 12 | 17 | |
| 13 | 8 | |
| 14 | 1 |
About Bérénice Herve
Bérénice Herve is a scholar working on Filtration and Separation, Genetics and Pediatrics, Perinatology and Child Health, having authored 14 papers that have together received 72 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (4 papers) and Chromosomal and Genetic Variations (3 papers). The work is most often cited by research in Genetics (42 citations), Pediatrics, Perinatology and Child Health (29 citations) and Obstetrics and Gynecology (4 citations). Bérénice Herve has collaborated with scholars based in France, Italy and United Kingdom. Frequent co-authors include François Vialard, Denise Molina‐Gomes, Delphine Fauvert, Thibaud Quibel, J. Roume, Patrice Clément, Guillaume Legendre, D. Subtil, J. Nizard and Marianne Till. Their work appears in journals such as Gene, European Journal of Human Genetics and European Journal of Obstetrics & Gynecology and Reproductive Biology.
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.