Céline Bonnet
Impact in
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
-
- Genetic Neurodegenerative Diseases
Papers in
-
- Mitochondrial Function and Pathology 5
- RNA modifications and cancer 4
- Genetics 25
- Genomic variations and chromosomal abnormalities 13
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
- Co-authors
- Philippe Jonveaux (18 shared papers)Bruno Leheup (18 shared papers)Christophe Philippe (10 shared papers)Julien Engelhardt (1 shared paper)Hugues Loiseau (1 shared paper)Isabelle Baldi (1 shared paper)Luc Bauchet (1 shared paper)A. Grüber (1 shared paper)
- Journals
- European Journal of Medical Genetics (3 papers)Journal of Medical Genetics (2 papers)European Journal of Human Genetics (2 papers)Prenatal Diagnosis (2 papers)Journal of Neurology (2 papers)
- Partner nations
- FranceUnited StatesCanada
In The Last Decade
Céline Bonnet
63 papers receiving 934 citations
Peers
Comparison fields: 5 of 83
- Genetics 342
- Genetics 64
- Cellular and Molecular Neuroscience 115
- Hematology 59
- Pediatrics, Perinatology and Child Health 94
Countries citing papers authored by Céline Bonnet
This map shows the geographic impact of Céline Bonnet'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 Céline Bonnet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Céline Bonnet more than expected).
Fields of papers citing papers by Céline Bonnet
This network shows the impact of papers produced by Céline Bonnet. 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 Céline Bonnet. The network helps show where Céline Bonnet may publish in the future.
Co-authors
The 25 scholars most cited alongside Céline Bonnet, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 68 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2014 | 122 | |
| 2 | 2008 | 90 | |
| 3 | 2008 | 75 | |
| 4 | 2010 | 58 | |
| 5 | 2013 | 57 | |
| 6 | 2006 | 46 | |
| 7 | 2020 | 41 | |
| 8 | 2006 | 36 | |
| 9 | 2009 | 33 | |
| 10 | 2013 | 30 | |
| 11 | 2014 | 30 | |
| 12 | 2006 | 30 | |
| 13 | 2023 | 30 | |
| 14 | 2010 | 26 | |
| 15 | 2020 | 18 | |
| 16 | 2008 | 16 | |
| 17 | 2020 | 14 | |
| 18 | 2017 | 14 | |
| 19 | 2013 | 13 | |
| 20 | 2023 | 12 |
About Céline Bonnet
Céline Bonnet is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Epidemiology and Surgery, having authored 68 papers that have together received 973 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (13 papers), Genetic Neurodegenerative Diseases (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers), Mitochondrial Function and Pathology (5 papers), Congenital Heart Disease Studies (5 papers), Prenatal Screening and Diagnostics (4 papers) and RNA modifications and cancer (4 papers). The work is most often cited by research in Genetics (342 citations), Genetics (64 citations), Cellular and Molecular Neuroscience (115 citations), Hematology (59 citations) and Pediatrics, Perinatology and Child Health (94 citations). Céline Bonnet has collaborated with scholars based in France, United States and Canada. Frequent co-authors include Philippe Jonveaux, Bruno Leheup, Christophe Philippe, Julien Engelhardt, Hugues Loiseau, Isabelle Baldi, Luc Bauchet, A. Grüber, Émilie Berteaud and Mylène Béri. Their work appears in journals such as European Journal of Medical Genetics, Journal of Medical Genetics, European Journal of Human Genetics, Prenatal Diagnosis and Journal of Neurology.
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.