Claudio Catalli
About
In The Last Decade
Claudio Catalli
10 papers receiving 183 citations
Peers
Comparison fields: 5 of 34
- Cellular and Molecular Neuroscience 148
- Molecular Biology 130
- Neurology 59
- Cardiology and Cardiovascular Medicine 18
- Genetics 16
Countries citing papers authored by Claudio Catalli
This map shows the geographic impact of Claudio Catalli'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 Claudio Catalli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Claudio Catalli more than expected).
Fields of papers citing papers by Claudio Catalli
This network shows the impact of papers produced by Claudio Catalli. 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 Claudio Catalli. The network helps show where Claudio Catalli may publish in the future.
Co-authorship network of co-authors of Claudio Catalli
This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Catalli. A scholar is included among the top collaborators of Claudio Catalli 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 Claudio Catalli. Claudio Catalli 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 | 0 | |
| 3 | 15 | |
| 4 | 4 | |
| 5 | 1 | |
| 6 | 1 | |
| 7 | 1 | |
| 8 | 4 | |
| 9 | 100 | |
| 10 | 18 | |
| 11 | 40 | |
| 12 | Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients. | 1 |
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.