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 24
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 12
- Genomic variations and chromosomal abnormalities 7
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- RNA modifications and cancer 5
- Co-authors
- Gaëtan Lesca (28 shared papers)Damien Sanlaville (24 shared papers)Audrey Labalme (16 shared papers)Vincent des Portes (6 shared papers)Dorothée Ville (5 shared papers)Christine Vinciguerra (6 shared papers)Patrick Edery (8 shared papers)Mathilde Frétigny (6 shared papers)
- Journals
- European Journal of Medical Genetics (7 papers)European Journal of Human Genetics (6 papers)Journal of Thrombosis and Haemostasis (5 papers)European Journal of Paediatric Neurology (3 papers)Epilepsia (2 papers)
- Partner nations
- FranceUnited StatesItaly
In The Last Decade
Nicolas Chatron
39 papers receiving 280 citations
Peers
Comparison fields: 5 of 45
- Genetics 101
- Hematology 30
- Cellular and Molecular Neuroscience 36
- Sensory Systems 9
- Psychiatry and Mental health 25
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 46 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 29 | |
| 2 | 2019 | 18 | |
| 3 | 2019 | 17 | |
| 4 | 2019 | 15 | |
| 5 | 2019 | 12 | |
| 6 | 2020 | 11 | |
| 7 | 2021 | 11 | |
| 8 | 2020 | 10 | |
| 9 | 2018 | 10 | |
| 10 | 2016 | 10 | |
| 11 | 2021 | 10 | |
| 12 | 2018 | 9 | |
| 13 | 2017 | 9 | |
| 14 | 2023 | 8 | |
| 15 | 2020 | 8 | |
| 16 | 2022 | 7 | |
| 17 | 2023 | 7 | |
| 18 | 2023 | 7 | |
| 19 | 2018 | 6 | |
| 20 | 2019 | 6 |
About Nicolas Chatron
Nicolas Chatron is a scholar working on Genetics, Molecular Biology, Hematology, Psychiatry and Mental health and Pediatrics, Perinatology and Child Health, having authored 46 papers that have together received 281 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (12 papers), Genomic variations and chromosomal abnormalities (7 papers), Hemophilia Treatment and Research (6 papers), Epilepsy research and treatment (6 papers), Prenatal Screening and Diagnostics (5 papers), RNA modifications and cancer (5 papers) and Metabolism and Genetic Disorders (4 papers). The work is most often cited by research in Genetics (101 citations), Hematology (30 citations), Cellular and Molecular Neuroscience (36 citations), Sensory Systems (9 citations) and Psychiatry and Mental health (25 citations). Nicolas Chatron has collaborated with scholars based in France, United States and Italy. Frequent co-authors include Gaëtan Lesca, Damien Sanlaville, Audrey Labalme, Vincent des Portes, Dorothée Ville, Christine Vinciguerra, Patrick Edery, Mathilde Frétigny, Audrey Putoux and Sara Cabet. 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 Epilepsia.
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.