Patrick Calvas
Impact in
-
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
- Neurology top 10%
- Neurological diseases and metabolism
- Neurological disorders and treatments
Papers in
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- Genetic Neurodegenerative Diseases 6
- Hereditary Neurological Disorders 2
- Genetics 5
- Genomics and Rare Diseases 3
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Jean‐Louis Mandel (1 shared paper)Valérie Biancalana (1 shared paper)Alexis Brice (2 shared papers)Alexandra Dürr (2 shared papers)Qiuping Yuan (1 shared paper)Olivier Rascol (1 shared paper)Martin Schalling (1 shared paper)Giovanni Stévanin (1 shared paper)
- Journals
- European Journal of Human Genetics (2 papers)Movement Disorders (2 papers)Journal of Neurology (2 papers)Human Mutation (2 papers)Otology & Neurotology (1 paper)
- Partner nations
- FranceUnited StatesBelgium
In The Last Decade
Patrick Calvas
18 papers receiving 689 citations
Peers
Comparison fields: 5 of 55
- Cellular and Molecular Neuroscience 372
- Neurology 71
- Clinical Biochemistry 51
- Neurology 99
- Molecular Biology 424
Countries citing papers authored by Patrick Calvas
This map shows the geographic impact of Patrick Calvas'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 Patrick Calvas with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrick Calvas more than expected).
Fields of papers citing papers by Patrick Calvas
This network shows the impact of papers produced by Patrick Calvas. 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 Patrick Calvas. The network helps show where Patrick Calvas may publish in the future.
Co-authors
The 25 scholars most cited alongside Patrick Calvas, 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 | 2000 | 131 | |
| 2 | 2018 | 100 | |
| 3 | 2001 | 91 | |
| 4 | 2015 | 81 | |
| 5 | 2015 | 55 | |
| 6 | 2016 | 49 | |
| 7 | 2012 | 39 | |
| 8 | 2016 | 32 | |
| 9 | 2019 | 31 | |
| 10 | 2001 | 21 | |
| 11 | 2019 | 21 | |
| 12 | 2021 | 21 | |
| 13 | 2016 | 17 | |
| 14 | 2019 | 9 | |
| 15 | 2011 | 8 | |
| 16 | 2022 | 6 | |
| 17 | 2024 | 1 | |
| 18 | 2020 | 1 | |
| 19 | 2008 | 0 | |
| 20 | 2008 | 0 |
About Patrick Calvas
Patrick Calvas is a scholar working on Cellular and Molecular Neuroscience, Genetics, Molecular Biology, Neurology and Cell Biology, having authored 20 papers that have together received 714 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (6 papers), Mitochondrial Function and Pathology (5 papers), Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (2 papers), DNA Repair Mechanisms (2 papers), Hereditary Neurological Disorders (2 papers), Healthcare Systems and Practices (1 paper) and Ear Surgery and Otitis Media (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (372 citations), Neurology (71 citations), Clinical Biochemistry (51 citations), Neurology (99 citations) and Molecular Biology (424 citations). Patrick Calvas has collaborated with scholars based in France, United States and Belgium. Frequent co-authors include Jean‐Louis Mandel, Valérie Biancalana, Alexis Brice, Alexandra Dürr, Qiuping Yuan, Olivier Rascol, Martin Schalling, Giovanni Stévanin, David Brassat and Agnès Camuzat. Their work appears in journals such as European Journal of Human Genetics, Movement Disorders, Journal of Neurology, Human Mutation and Otology & Neurotology.
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.