Patrick Calvas
Impact in
- Ophthalmology top 0.5%
- Retinal Diseases and Treatments
- Glaucoma and retinal disorders
- Genetics top 1%
- Genetics and Neurodevelopmental Disorders
- Ocular Disorders and Treatments
Papers in
-
- Developmental Biology and Gene Regulation 6
- Genetics 38
- Ocular Disorders and Treatments 24
- Congenital Ear and Nasal Anomalies 8
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- François Malecaze (19 shared papers)Nicolas Chassaing (38 shared papers)Weihua Meng (5 shared papers)Jacqueline Butterworth (4 shared papers)Hélène Dollfus (7 shared papers)Jean‐Michel Rozet (10 shared papers)Josseline Kaplan (7 shared papers)S. Gerber (6 shared papers)
- Journals
- Human Mutation (11 papers)Investigative Ophthalmology & Visual Science (8 papers)European Journal of Human Genetics (5 papers)European Journal of Medical Genetics (5 papers)Clinical Genetics (3 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Patrick Calvas
100 papers receiving 4.0k citations
Patrick Calvas's Hit Papers
Peers
Comparison fields: 5 of 109
- Ophthalmology 600
- Genetics 1.3k
- Molecular Biology 2.0k
- Radiology, Nuclear Medicine and Imaging 513
- Sensory Systems 107
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
Showing the 20 most-cited of 105 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | X-Linked Mental Retardation and Autism Are Associated with a Mutation in the NLGN4 Gene, a Member of the Neuroligin Family Hit paper breakdown → | 2004 | 608 |
| 2 | 1996 | 383 | |
| 3 | 2004 | 292 | |
| 4 | 2010 | 179 | |
| 5 | 2011 | 146 | |
| 6 | 1999 | 141 | |
| 7 | 2007 | 119 | |
| 8 | 2002 | 98 | |
| 9 | 2014 | 96 | |
| 10 | 2007 | 87 | |
| 11 | 2009 | 82 | |
| 12 | 2003 | 82 | |
| 13 | 2013 | 78 | |
| 14 | 2006 | 77 | |
| 15 | 2006 | 76 | |
| 16 | 2004 | 68 | |
| 17 | 2019 | 58 | |
| 18 | 2010 | 56 | |
| 19 | 2009 | 54 | |
| 20 | 2011 | 53 |
About Patrick Calvas
Patrick Calvas is a scholar working on Molecular Biology, Genetics, Radiology, Nuclear Medicine and Imaging, Epidemiology and Ophthalmology, having authored 105 papers that have together received 4.2k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (24 papers), Ophthalmology and Visual Impairment Studies (14 papers), Corneal surgery and disorders (9 papers), Congenital Ear and Nasal Anomalies (8 papers), Glaucoma and retinal disorders (7 papers), Developmental Biology and Gene Regulation (6 papers), Metabolism and Genetic Disorders (6 papers) and Genomic variations and chromosomal abnormalities (6 papers). The work is most often cited by research in Ophthalmology (600 citations), Genetics (1.3k citations), Molecular Biology (2.0k citations), Radiology, Nuclear Medicine and Imaging (513 citations) and Sensory Systems (107 citations). Patrick Calvas has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include François Malecaze, Nicolas Chassaing, Weihua Meng, Jacqueline Butterworth, Hélène Dollfus, Jean‐Michel Rozet, Josseline Kaplan, S. Gerber, Isabelle Perrault and Jean‐Louis Dufier. Their work appears in journals such as Human Mutation, Investigative Ophthalmology & Visual Science, European Journal of Human Genetics, European Journal of Medical Genetics and Clinical 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.