Patrick Calvas
Impact in
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- Ocular Disorders and Treatments
- Genomic variations and chromosomal abnormalities
- Congenital Ear and Nasal Anomalies
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- Congenital heart defects research
- Retinal Development and Disorders
- Developmental Biology and Gene Regulation
- Connexins and lens biology
Papers in
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- Mitochondrial Function and Pathology 1
- Co-authors
- G. Bourrouillou (3 shared papers)Florian Heitz (1 shared paper)Emilienne Kühlein (1 shared paper)M. Rolland (1 shared paper)Nicolas Chassaing (3 shared papers)Adeline Vigouroux (1 shared paper)François Malecaze (1 shared paper)Marlène Rio (1 shared paper)
- Journals
- European Journal of Medical Genetics (1 paper)Investigative Ophthalmology & Visual Science (1 paper)Clinical Genetics (1 paper)Dermatology (1 paper)European Neurology (1 paper)
- Partner nations
- FranceNetherlandsSwitzerland
In The Last Decade
Patrick Calvas
8 papers receiving 93 citations
Peers
Comparison fields: 5 of 28
- Genetics 51
- Genetics 9
- Molecular Biology 59
- Epidemiology 20
- Radiology, Nuclear Medicine and Imaging 11
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 | 22q11 deletion in DGS/VCFS monozygotic twins with discordant phenotypes. | 1999 | 42 |
| 2 | 2008 | 35 | |
| 3 | 2009 | 7 | |
| 4 | 2008 | 5 | |
| 5 | 2022 | 3 | |
| 6 | 2012 | 2 | |
| 7 | [Detection of triple X syndrome during a familial inquiry for hemophilia A]. | 1989 | 1 |
| 8 | Length polymorphism of a microsatellite in human and non human primates. | 1994 | 1 |
| 9 | 2025 | 1 |
About Patrick Calvas
Patrick Calvas is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Physiology, Genetics and Surgery, having authored 9 papers that have together received 97 indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (2 papers), Congenital Ear and Nasal Anomalies (1 paper), Congenital Heart Disease Studies (1 paper), Hemophilia Treatment and Research (1 paper), Corneal Surgery and Treatments (1 paper), Toxin Mechanisms and Immunotoxins (1 paper), Mitochondrial Function and Pathology (1 paper) and Ocular Surface and Contact Lens (1 paper). The work is most often cited by research in Genetics (51 citations), Genetics (9 citations), Molecular Biology (59 citations), Epidemiology (20 citations) and Radiology, Nuclear Medicine and Imaging (11 citations). Patrick Calvas has collaborated with scholars based in France, Netherlands and Switzerland. Frequent co-authors include G. Bourrouillou, Florian Heitz, Emilienne Kühlein, M. Rolland, Nicolas Chassaing, Adeline Vigouroux, François Malecaze, Marlène Rio, Heather Etchevers and Matthias Titeux. Their work appears in journals such as European Journal of Medical Genetics, Investigative Ophthalmology & Visual Science, Clinical Genetics, Dermatology and European Neurology.
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.