P. Copet
Impact in
- Genetics top 10%
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Autism Spectrum Disorder Research
Papers in
- Genetics 9
- Genetic Syndromes and Imprinting 9
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 2
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- Autism Spectrum Disorder Research 3
- Co-authors
- Denise Thuilleaux (7 shared papers)Virginie Laurier (8 shared papers)M. Tauber (4 shared papers)Catherine Molinas (3 shared papers)Catherine Arnaud (2 shared papers)Virginie Ehlinger (2 shared papers)Silvia González-Martínez (1 shared paper)Óscar Vegas (1 shared paper)
In The Last Decade
P. Copet
9 papers receiving 328 citations
Peers
Comparison fields: 5 of 41
- Genetics 276
- Cognitive Neuroscience 98
- Endocrine and Autonomic Systems 24
- Pharmacy 17
- Developmental Neuroscience 12
Countries citing papers authored by P. Copet
This map shows the geographic impact of P. Copet'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 P. Copet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. Copet more than expected).
Fields of papers citing papers by P. Copet
This network shows the impact of papers produced by P. Copet. 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 P. Copet. The network helps show where P. Copet may publish in the future.
Co-authors
The 20 scholars most cited alongside P. Copet, 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 | 2011 | 82 | |
| 2 | 2007 | 63 | |
| 3 | 2010 | 53 | |
| 4 | 2014 | 49 | |
| 5 | 2013 | 29 | |
| 6 | 2015 | 22 | |
| 7 | 2017 | 22 | |
| 8 | 2013 | 17 | |
| 9 | 2018 | 7 |
About P. Copet
P. Copet is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Social Psychology and Neurology, having authored 9 papers that have together received 344 indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (9 papers), Genetics and Neurodevelopmental Disorders (7 papers), Autism Spectrum Disorder Research (3 papers), Genomic variations and chromosomal abnormalities (2 papers), Epigenetics and DNA Methylation (1 paper), Prenatal Screening and Diagnostics (1 paper), Neurological disorders and treatments (1 paper) and Neuroendocrine regulation and behavior (1 paper). The work is most often cited by research in Genetics (276 citations), Cognitive Neuroscience (98 citations), Endocrine and Autonomic Systems (24 citations), Pharmacy (17 citations) and Developmental Neuroscience (12 citations). P. Copet has collaborated with scholars based in France and Spain. Frequent co-authors include Denise Thuilleaux, Virginie Laurier, M. Tauber, Catherine Molinas, Catherine Arnaud, Virginie Ehlinger, Silvia González-Martínez, Óscar Vegas, Francisco Alén and Carlos F. Arias. Their work appears in journals such as Journal of Intellectual Disability Research, Journal of Neurodevelopmental Disorders, Orphanet Journal of Rare Diseases, Journal of Applied Research in Intellectual Disabilities and American Journal on Intellectual and Developmental Disabilities.
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.