Fiorenza Soli
About
In The Last Decade
Fiorenza Soli
10 papers receiving 71 citations
Peers
Comparison fields: 5 of 27
- Molecular Biology 41
- Genetics 33
- Neurology 10
- Pulmonary and Respiratory Medicine 9
- Epidemiology 9
Countries citing papers authored by Fiorenza Soli
This map shows the geographic impact of Fiorenza Soli'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 Fiorenza Soli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fiorenza Soli more than expected).
Fields of papers citing papers by Fiorenza Soli
This network shows the impact of papers produced by Fiorenza Soli. 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 Fiorenza Soli. The network helps show where Fiorenza Soli may publish in the future.
Co-authorship network of co-authors of Fiorenza Soli
This figure shows the co-authorship network connecting the top 25 collaborators of Fiorenza Soli. A scholar is included among the top collaborators of Fiorenza Soli 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 Fiorenza Soli. Fiorenza Soli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 12 | |
| 2 | 9 | |
| 3 | 3 | |
| 4 | 11 | |
| 5 | 2 | |
| 6 | 3 | |
| 7 | 11 | |
| 8 | 12 | |
| 9 | Survival of Male Patients with Incontinentia Pigmenti Carrying a Lethal Mutation Can Be Explained by Somatic Mosaicism or Klinefelter Syndrome The International IP Consortium | 7 |
| 10 | Autosomal dominant polycystic kidney disease (ADPKD): screening for mutations and polymorphisms in the duplicated region of the PKD1 gene. | 2 |
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.