Simona Capponi
Impact in
-
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Neurology top 10%
- Neurological diseases and metabolism
- Botulinum Toxin and Related Neurological Disorders
Papers in
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- Hereditary Neurological Disorders 10
- Genetic Neurodegenerative Diseases 4
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- RNA Research and Splicing 3
- Signaling Pathways in Disease 2
- Genomics and Chromatin Dynamics 2
- Co-authors
- Paola Mandich (11 shared papers)Alessandro Geroldi (10 shared papers)Emilia Bellone (10 shared papers)Fiore Manganelli (5 shared papers)Marina Grandis (6 shared papers)Rossella Gulli (5 shared papers)Paola Fossa (3 shared papers)Chiara Pisciotta (4 shared papers)
- Journals
- Journal of the Peripheral Nervous System (4 papers)Human Mutation (1 paper)Neuropathology (1 paper)Brain Communications (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- ItalyUnited StatesGermany
In The Last Decade
Simona Capponi
16 papers receiving 403 citations
Peers
Comparison fields: 5 of 55
- Cellular and Molecular Neuroscience 222
- Neurology 74
- Neurology 92
- Cell Biology 76
- Molecular Biology 211
Countries citing papers authored by Simona Capponi
This map shows the geographic impact of Simona Capponi'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 Simona Capponi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simona Capponi more than expected).
Fields of papers citing papers by Simona Capponi
This network shows the impact of papers produced by Simona Capponi. 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 Simona Capponi. The network helps show where Simona Capponi may publish in the future.
Co-authors
The 25 scholars most cited alongside Simona Capponi, 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 | 2019 | 70 | |
| 2 | 2014 | 61 | |
| 3 | 2011 | 51 | |
| 4 | 2016 | 39 | |
| 5 | 2013 | 34 | |
| 6 | 2009 | 31 | |
| 7 | 2011 | 21 | |
| 8 | 2015 | 17 | |
| 9 | 2019 | 17 | |
| 10 | 2014 | 15 | |
| 11 | 2018 | 13 | |
| 12 | 2012 | 11 | |
| 13 | 2021 | 10 | |
| 14 | 2015 | 10 | |
| 15 | 2014 | 3 | |
| 16 | 2014 | 2 |
About Simona Capponi
Simona Capponi is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology, Neurology, Cell Biology and Neurology, having authored 16 papers that have together received 405 indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (10 papers), Botulinum Toxin and Related Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers), RNA Research and Splicing (3 papers), Cellular transport and secretion (3 papers), Neurological diseases and metabolism (2 papers), Signaling Pathways in Disease (2 papers) and Genomics and Chromatin Dynamics (2 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (222 citations), Neurology (74 citations), Neurology (92 citations), Cell Biology (76 citations) and Molecular Biology (211 citations). Simona Capponi has collaborated with scholars based in Italy, United States and Germany. Frequent co-authors include Paola Mandich, Alessandro Geroldi, Emilia Bellone, Fiore Manganelli, Marina Grandis, Rossella Gulli, Paola Fossa, Chiara Pisciotta, Paola Ciotti and Angelo Schenone. Their work appears in journals such as Journal of the Peripheral Nervous System, Human Mutation, Neuropathology, Brain Communications 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.