Lyse Ruaud
Impact in
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- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
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- Autism Spectrum Disorder Research
Papers in
- Genetics 9
- Genetics and Neurodevelopmental Disorders 5
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 2
- Connective tissue disorders research 2
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- Mitochondrial Function and Pathology 2
- RNA and protein synthesis mechanisms 1
- Co-authors
- Daniel Amsallem (2 shared papers)Juliette Piard (3 shared papers)Boris Keren (2 shared papers)Delphine Héron (1 shared paper)Alain Verloès (5 shared papers)Julien Thévenon (1 shared paper)Stéphane Père (1 shared paper)Isabelle Maystadt (1 shared paper)
In The Last Decade
Lyse Ruaud
13 papers receiving 111 citations
Peers
Comparison fields: 5 of 35
- Genetics 66
- Cognitive Neuroscience 15
- Molecular Biology 45
- Public Health, Environmental and Occupational Health 17
- Cell Biology 7
Countries citing papers authored by Lyse Ruaud
This map shows the geographic impact of Lyse Ruaud'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 Lyse Ruaud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lyse Ruaud more than expected).
Fields of papers citing papers by Lyse Ruaud
This network shows the impact of papers produced by Lyse Ruaud. 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 Lyse Ruaud. The network helps show where Lyse Ruaud may publish in the future.
Co-authors
The 25 scholars most cited alongside Lyse Ruaud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 33 | |
| 2 | 2015 | 25 | |
| 3 | 2014 | 11 | |
| 4 | 2021 | 10 | |
| 5 | 2018 | 6 | |
| 6 | 2020 | 5 | |
| 7 | 2022 | 5 | |
| 8 | 2021 | 4 | |
| 9 | 2023 | 4 | |
| 10 | 2024 | 4 | |
| 11 | 2019 | 2 | |
| 12 | 2023 | 1 | |
| 13 | 2015 | 1 | |
| 14 | 2023 | 0 |
About Lyse Ruaud
Lyse Ruaud is a scholar working on Genetics, Molecular Biology, Cell Biology, Physiology and Pathology and Forensic Medicine, having authored 14 papers that have together received 111 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Sympathectomy and Hyperhidrosis Treatments (2 papers), Genomics and Rare Diseases (2 papers), Mitochondrial Function and Pathology (2 papers), Connective tissue disorders research (2 papers), RNA and protein synthesis mechanisms (1 paper) and Biomedical Research and Pathophysiology (1 paper). The work is most often cited by research in Genetics (66 citations), Cognitive Neuroscience (15 citations), Molecular Biology (45 citations), Public Health, Environmental and Occupational Health (17 citations) and Cell Biology (7 citations). Lyse Ruaud has collaborated with scholars based in France, Belgium and Germany. Frequent co-authors include Daniel Amsallem, Juliette Piard, Boris Keren, Delphine Héron, Alain Verloès, Julien Thévenon, Stéphane Père, Isabelle Maystadt, Caroline Nava and Agnès Guët. Their work appears in journals such as European Journal of Medical Genetics, Human Mutation, Clinical Genetics, Brain and Birth Defects Research.
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.