Nicolas Chatron
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
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- Hemophilia Treatment and Research
Papers in
- Genetics 26
- Genetics and Neurodevelopmental Disorders 15
- Genomics and Rare Diseases 11
- Genomic variations and chromosomal abnormalities 9
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- Cancer-related gene regulation 4
- Co-authors
- Damien Sanlaville (24 shared papers)Gaëtan Lesca (27 shared papers)Audrey Labalme (16 shared papers)Patrick Edery (7 shared papers)Vincent des Portes (5 shared papers)Christine Vinciguerra (6 shared papers)Dorothée Ville (5 shared papers)Audrey Putoux (6 shared papers)
- Journals
- European Journal of Medical Genetics (7 papers)European Journal of Human Genetics (5 papers)Journal of Thrombosis and Haemostasis (5 papers)European Journal of Paediatric Neurology (3 papers)Prenatal Diagnosis (2 papers)
- Partner nations
- FranceItalyUnited States
In The Last Decade
Nicolas Chatron
38 papers receiving 262 citations
Peers
Comparison fields: 5 of 48
- Genetics 123
- Hematology 29
- Cellular and Molecular Neuroscience 37
- Molecular Biology 129
- Psychiatry and Mental health 27
Countries citing papers authored by Nicolas Chatron
This map shows the geographic impact of Nicolas Chatron'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 Nicolas Chatron with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Nicolas Chatron more than expected).
Fields of papers citing papers by Nicolas Chatron
This network shows the impact of papers produced by Nicolas Chatron. 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 Nicolas Chatron. The network helps show where Nicolas Chatron may publish in the future.
Co-authors
The 25 scholars most cited alongside Nicolas Chatron, 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 44 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 28 | |
| 2 | 2019 | 18 | |
| 3 | 2019 | 16 | |
| 4 | 2019 | 14 | |
| 5 | 2019 | 11 | |
| 6 | 2020 | 10 | |
| 7 | 2020 | 10 | |
| 8 | 2018 | 10 | |
| 9 | 2018 | 9 | |
| 10 | 2016 | 9 | |
| 11 | 2021 | 9 | |
| 12 | 2017 | 9 | |
| 13 | 2021 | 9 | |
| 14 | 2020 | 8 | |
| 15 | 2023 | 7 | |
| 16 | 2023 | 7 | |
| 17 | 2019 | 6 | |
| 18 | 2018 | 6 | |
| 19 | 2022 | 6 | |
| 20 | 2023 | 5 |
About Nicolas Chatron
Nicolas Chatron is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Hematology, having authored 44 papers that have together received 263 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (15 papers), Genomics and Rare Diseases (11 papers), Genomic variations and chromosomal abnormalities (9 papers), Epilepsy research and treatment (7 papers), Hemophilia Treatment and Research (6 papers), Prenatal Screening and Diagnostics (6 papers), Cancer-related gene regulation (4 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Genetics (123 citations), Hematology (29 citations), Cellular and Molecular Neuroscience (37 citations), Molecular Biology (129 citations) and Psychiatry and Mental health (27 citations). Nicolas Chatron has collaborated with scholars based in France, Italy and United States. Frequent co-authors include Damien Sanlaville, Gaëtan Lesca, Audrey Labalme, Patrick Edery, Vincent des Portes, Christine Vinciguerra, Dorothée Ville, Audrey Putoux, Massimiliano Rossi and Caroline Schluth‐Bolard. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Journal of Thrombosis and Haemostasis, European Journal of Paediatric Neurology and Prenatal Diagnosis.
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.