Catherine Vovan
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
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- Muscle Physiology and Disorders
- Epigenetics and DNA Methylation
- Genomics and Chromatin Dynamics
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 6
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- Muscle Physiology and Disorders 11
- Epigenetics and DNA Methylation 2
- Co-authors
- Rafaëlle Bernard (10 shared papers)Shahram Attarian (8 shared papers)Karine Nguyen (8 shared papers)Nicolas Lévy (8 shared papers)Charlène Chaix (8 shared papers)Frédérique Magdinier (6 shared papers)Marie-Cécile Gaillard (5 shared papers)Marc Bartoli (5 shared papers)
In The Last Decade
Catherine Vovan
11 papers receiving 286 citations
Peers
Comparison fields: 5 of 22
- Genetics 119
- Molecular Biology 249
- Genetics 7
- Pediatrics, Perinatology and Child Health 10
- Immunology and Allergy 3
Countries citing papers authored by Catherine Vovan
This map shows the geographic impact of Catherine Vovan'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 Catherine Vovan with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Catherine Vovan more than expected).
Fields of papers citing papers by Catherine Vovan
This network shows the impact of papers produced by Catherine Vovan. 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 Catherine Vovan. The network helps show where Catherine Vovan may publish in the future.
Co-authors
The 25 scholars most cited alongside Catherine Vovan, 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 | 2014 | 73 | |
| 2 | 2011 | 46 | |
| 3 | 2017 | 46 | |
| 4 | 2015 | 33 | |
| 5 | 2019 | 30 | |
| 6 | 2019 | 20 | |
| 7 | 2009 | 12 | |
| 8 | 2016 | 12 | |
| 9 | 2023 | 10 | |
| 10 | 2018 | 7 | |
| 11 | 2010 | 1 |
About Catherine Vovan
Catherine Vovan is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Cell Biology and Nuclear Energy and Engineering, having authored 11 papers that have together received 290 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (11 papers), Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (6 papers), Epigenetics and DNA Methylation (2 papers), Calpain Protease Function and Regulation (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (119 citations), Molecular Biology (249 citations), Genetics (7 citations), Pediatrics, Perinatology and Child Health (10 citations) and Immunology and Allergy (3 citations). Catherine Vovan has collaborated with scholars based in France, Japan and Italy. Frequent co-authors include Rafaëlle Bernard, Shahram Attarian, Karine Nguyen, Nicolas Lévy, Charlène Chaix, Frédérique Magdinier, Marie-Cécile Gaillard, Marc Bartoli, Francesca Puppo and Emmanuelle Salort‐Campana. Their work appears in journals such as Neurology Genetics, Human Mutation, Neurology, Neuromuscular Disorders and European Journal of Human Genetics.
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.