Concetta Simona Perrotta
- Genetics top 10%
- Molecular Biology
- Pediatrics, Perinatology and Child Health
- Plant Science
- Cognitive Neuroscience
- Co-authors
- Teresa MattinaPaul GrossfeldClaudio CastellanPeter HammondAlessandra BaumerFrancesca FaravelliElena RossiMariluce Riegel
- Topics
- Genomic variations and chromosomal abnormalities (4 papers)Genetics and Neurodevelopmental Disorders (3 papers)Genetic Syndromes and Imprinting (2 papers)
- Journals
- Journal of Medical GeneticsInternational Journal of Geriatric PsychiatryEuropean Journal of Human Genetics
- Partner nations
- ItalyUnited KingdomBelgium
In The Last Decade
Concetta Simona Perrotta
9 papers receiving 316 citations
Peers
Comparison fields: 5 of 58
- Genetics 212
- Molecular Biology 139
- Pediatrics, Perinatology and Child Health 59
- Plant Science 59
- Cognitive Neuroscience 53
Countries citing papers authored by Concetta Simona Perrotta
This map shows the geographic impact of Concetta Simona Perrotta'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 Concetta Simona Perrotta with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Concetta Simona Perrotta more than expected).
Fields of papers citing papers by Concetta Simona Perrotta
This network shows the impact of papers produced by Concetta Simona Perrotta. 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 Concetta Simona Perrotta. The network helps show where Concetta Simona Perrotta may publish in the future.
Co-authorship network of co-authors of Concetta Simona Perrotta
This figure shows the co-authorship network connecting the top 25 collaborators of Concetta Simona Perrotta. A scholar is included among the top collaborators of Concetta Simona Perrotta based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Concetta Simona Perrotta. Concetta Simona Perrotta is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 2 | |
| 3 | 12 | |
| 4 | 8 | |
| 5 | 32 | |
| 6 | 21 | |
| 7 | 132 | |
| 8 | 83 | |
| 9 | 40 |
About Concetta Simona Perrotta
Concetta Simona Perrotta is a scholar working on Genetics, Cognitive Neuroscience and Molecular Biology, having authored 9 papers that have together received 331 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genetic Syndromes and Imprinting (2 papers). The work is most often cited by research in Genetics (212 citations), Pediatrics, Perinatology and Child Health (59 citations) and Cognitive Neuroscience (53 citations). Concetta Simona Perrotta has collaborated with scholars based in Italy, United Kingdom and Belgium. Frequent co-authors include Teresa Mattina, Paul Grossfeld, Claudio Castellan, Peter Hammond, Alessandra Baumer, Francesca Faravelli, Elena Rossi, Mariluce Riegel, Orsetta Zuffardi and Roberto Ciccone. Their work appears in journals such as Journal of Medical Genetics, International Journal of Geriatric Psychiatry and European 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.