Claudia Cagnoli
- Co-authors
- Alfredo BruscoNicola MigoneCinzia GelleraAlessandro BrussinoStefano Di DonatoCaterina MariottiFranco TaroniPatrizia Pappi
- Topics
- Genetic Neurodegenerative Diseases (11 papers)Mitochondrial Function and Pathology (8 papers)Ubiquitin and proteasome pathways (4 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Claudia Cagnoli
13 papers receiving 541 citations
Peers
Comparison fields: 5 of 42
- Molecular Biology 464
- Cellular and Molecular Neuroscience 394
- Genetics 122
- Neurology 114
- Neurology 56
Countries citing papers authored by Claudia Cagnoli
This map shows the geographic impact of Claudia Cagnoli'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 Claudia Cagnoli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claudia Cagnoli more than expected).
Fields of papers citing papers by Claudia Cagnoli
This network shows the impact of papers produced by Claudia Cagnoli. 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 Claudia Cagnoli. The network helps show where Claudia Cagnoli may publish in the future.
Co-authorship network of co-authors of Claudia Cagnoli
This figure shows the co-authorship network connecting the top 25 collaborators of Claudia Cagnoli. A scholar is included among the top collaborators of Claudia Cagnoli 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 Claudia Cagnoli. Claudia Cagnoli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 15 | |
| 2 | 22 | |
| 3 | 32 | |
| 4 | 53 | |
| 5 | Conventional mutations are associated with a different phenotype than polyglutamine expansions in spinocerebellar ataxias | 5 |
| 6 | 9 | |
| 7 | 36 | |
| 8 | 26 | |
| 9 | 89 | |
| 10 | 88 | |
| 11 | 109 | |
| 12 | 43 | |
| 13 | 23 |
About Claudia Cagnoli
Claudia Cagnoli is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Clinical Biochemistry, having authored 13 papers that have together received 550 indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (11 papers), Mitochondrial Function and Pathology (8 papers) and Ubiquitin and proteasome pathways (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (394 citations), Neurology (114 citations) and Neurology (56 citations). Claudia Cagnoli has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Alfredo Brusco, Nicola Migone, Cinzia Gellera, Alessandro Brussino, Stefano Di Donato, Caterina Mariotti, Franco Taroni, Patrizia Pappi, Daniela Di Bella and Marco Seri. Their work appears in journals such as Brain, Movement Disorders and Human Mutation.
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.