M. Cicilano
About
In The Last Decade
M. Cicilano
10 papers receiving 431 citations
Peers
Comparison fields: 5 of 40
- Hematology 334
- Nutrition and Dietetics 312
- Genetics 268
- Molecular Biology 37
- Obstetrics and Gynecology 37
Countries citing papers authored by M. Cicilano
This map shows the geographic impact of M. Cicilano'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 M. Cicilano with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites M. Cicilano more than expected).
Fields of papers citing papers by M. Cicilano
This network shows the impact of papers produced by M. Cicilano. 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 M. Cicilano. The network helps show where M. Cicilano may publish in the future.
Co-authorship network of co-authors of M. Cicilano
This figure shows the co-authorship network connecting the top 25 collaborators of M. Cicilano. A scholar is included among the top collaborators of M. Cicilano 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 M. Cicilano. M. Cicilano is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 38 | |
| 2 | Prostate cancer gene 3 urine assay cutoff in diagnosis of prostate cancer: a validation study on an Italian patient population undergoing first and repeat biopsy. | 20 |
| 3 | 30 | |
| 4 | Screening of the C282Y mutation in the HFE gene in Italy by Taqman technology. | 2 |
| 5 | 180 | |
| 6 | Recurrent mutations in the iron regulatory element of L-ferritin in hereditary hyperferritinemia-cataract syndrome. | 39 |
| 7 | 2 | |
| 8 | Juvenile and adult hemochromatosis are distinct genetic disorders. | 68 |
| 9 | 2 | |
| 10 | 64 |
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.