Natale Capodicasa
Impact in
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- Viral-associated cancers and disorders
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- Parvovirus B19 Infection Studies
Papers in
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- Trypanosoma species research and implications 1
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- Prion Diseases and Protein Misfolding 1
- Co-authors
- Paola Cattani (3 shared papers)Stefania Ranno (2 shared papers)S. Marchetti (2 shared papers)Guido Fadda (2 shared papers)K. Rivet Amico (2 shared papers)Rosalia Graffeo (2 shared papers)Stefania Zanetti (1 shared paper)Gian Mario Cherchi (1 shared paper)
In The Last Decade
Natale Capodicasa
9 papers receiving 143 citations
Peers
Comparison fields: 5 of 50
- Oncology 61
- Infectious Diseases 32
- Epidemiology 51
- Aging 2
- Public Health, Environmental and Occupational Health 18
Countries citing papers authored by Natale Capodicasa
This map shows the geographic impact of Natale Capodicasa'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 Natale Capodicasa with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natale Capodicasa more than expected).
Fields of papers citing papers by Natale Capodicasa
This network shows the impact of papers produced by Natale Capodicasa. 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 Natale Capodicasa. The network helps show where Natale Capodicasa may publish in the future.
Co-authors
The 25 scholars most cited alongside Natale Capodicasa, 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 | 2003 | 60 | |
| 2 | 2014 | 29 | |
| 3 | Transcriptional activity of human endogenous retrovirus in Albanian children with autism spectrum disorders. | 2016 | 20 |
| 4 | 2020 | 11 | |
| 5 | 2017 | 8 | |
| 6 | Cloning and characterization of human recombinant antibody Fab fragments specific for types 1 and 2 herpes simplex virus. | 1995 | 7 |
| 7 | HHV 8 seroprevalence and transmission within Albanian family groups. | 2003 | 7 |
| 8 | 2015 | 2 | |
| 9 | 2020 | 1 |
About Natale Capodicasa
Natale Capodicasa is a scholar working on Epidemiology, Molecular Biology, Genetics, Public Health, Environmental and Occupational Health and Genetics, having authored 9 papers that have together received 145 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (1 paper), Amyotrophic Lateral Sclerosis Research (1 paper), Trypanosoma species research and implications (1 paper), Genomics and Rare Diseases (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), BRCA gene mutations in cancer (1 paper), Prion Diseases and Protein Misfolding (1 paper) and Chromosomal and Genetic Variations (1 paper). The work is most often cited by research in Oncology (61 citations), Infectious Diseases (32 citations), Epidemiology (51 citations), Aging (2 citations) and Public Health, Environmental and Occupational Health (18 citations). Natale Capodicasa has collaborated with scholars based in Italy, Albania and Türkiye. Frequent co-authors include Paola Cattani, Stefania Ranno, S. Marchetti, Guido Fadda, K. Rivet Amico, Rosalia Graffeo, Stefania Zanetti, Gian Mario Cherchi, Renato Pietro Ricci and Francesca Cerimele. Their work appears in journals such as ChemMedChem, Clinical Microbiology and Infection, Genetics and Molecular Research and PubMed.
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.