Patrick Calvas
Impact in
- Genetics top 1%
- Ocular Disorders and Treatments
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
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- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Papers in
- Genetics 95
- Ocular Disorders and Treatments 54
- Genomics and Rare Diseases 19
- Genomic variations and chromosomal abnormalities 12
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- Genetic Neurodegenerative Diseases 11
- Hereditary Neurological Disorders 8
- Co-authors
- Nicolas Chassaing (49 shared papers)François Malecaze (25 shared papers)Alain Hovnanian (8 shared papers)Weihua Meng (6 shared papers)Marie‐Claire Vincent (8 shared papers)Jacqueline A. Butterworth (5 shared papers)Hélène Dollfus (7 shared papers)Olivier Rascol (5 shared papers)
- Journals
- Human Mutation (12 papers)Journal of Medical Genetics (10 papers)Investigative Ophthalmology & Visual Science (9 papers)European Journal of Human Genetics (9 papers)The American Journal of Human Genetics (9 papers)
- Partner nations
- FranceUnited KingdomUnited States
In The Last Decade
Patrick Calvas
169 papers receiving 7.4k citations
Patrick Calvas's Hit Papers
Peers
Comparison fields: 5 of 114
- Genetics 2.6k
- Cellular and Molecular Neuroscience 936
- Molecular Biology 2.3k
- Ophthalmology 322
- Clinical Biochemistry 143
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 178 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 | 636 |
| 2 | 2004 | 431 | |
| 3 | 1996 | 390 | |
| 4 | 2004 | 299 | |
| 5 | 2005 | 229 | |
| 6 | 2010 | 188 | |
| 7 | 2011 | 155 | |
| 8 | 1999 | 146 | |
| 9 | 2004 | 137 | |
| 10 | 2004 | 137 | |
| 11 | 2002 | 136 | |
| 12 | 2000 | 131 | |
| 13 | 2007 | 128 | |
| 14 | 2012 | 126 | |
| 15 | 2016 | 117 | |
| 16 | 2014 | 104 | |
| 17 | 2018 | 101 | |
| 18 | 2002 | 100 | |
| 19 | 2001 | 92 | |
| 20 | 2013 | 92 |
About Patrick Calvas
Patrick Calvas is a scholar working on Genetics, Cellular and Molecular Neuroscience, Molecular Biology, Epidemiology and Clinical Biochemistry, having authored 178 papers that have together received 7.6k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (54 papers), Genomics and Rare Diseases (19 papers), Ophthalmology and Visual Impairment Studies (14 papers), Retinal Development and Disorders (13 papers), Genomic variations and chromosomal abnormalities (12 papers), Genetic Neurodegenerative Diseases (11 papers), Hereditary Neurological Disorders (8 papers) and dental development and anomalies (7 papers). The work is most often cited by research in Genetics (2.6k citations), Cellular and Molecular Neuroscience (936 citations), Molecular Biology (2.3k citations), Ophthalmology (322 citations) and Clinical Biochemistry (143 citations). Patrick Calvas has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Nicolas Chassaing, François Malecaze, Alain Hovnanian, Weihua Meng, Marie‐Claire Vincent, Jacqueline A. Butterworth, Hélène Dollfus, Olivier Rascol, Ludovic Martin and Josseline Kaplan. Their work appears in journals such as Human Mutation, Journal of Medical Genetics, Investigative Ophthalmology & Visual Science, European Journal of Human Genetics and The American 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.