Mariarosaria Calvello
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- BRCA gene mutations in cancer 12
- Genomic variations and chromosomal abnormalities 5
- Genetic Syndromes and Imprinting 3
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- DNA Repair Mechanisms 3
- Epigenetics and DNA Methylation 3
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- Genetic factors in colorectal cancer 5
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- Cancer Genomics and Diagnostics 4
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- Colorectal Cancer Screening and Detection 3
- Co-authors
- Monica MiozzoBernardo BonanniSilvia TabanoFaustina LalattaSilvia Maria SirchiaJacopo AzzolliniMaria Francesca BedeschiPatrizia Colapietro
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Mariarosaria Calvello
23 papers receiving 228 citations
Peers
Comparison fields: 5 of 51
- Genetics 134
- Reproductive Medicine 18
- Molecular Biology 124
- Pediatrics, Perinatology and Child Health 35
- Neurology 26
Countries citing papers authored by Mariarosaria Calvello
This map shows the geographic impact of Mariarosaria Calvello'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 Mariarosaria Calvello with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mariarosaria Calvello more than expected).
Fields of papers citing papers by Mariarosaria Calvello
This network shows the impact of papers produced by Mariarosaria Calvello. 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 Mariarosaria Calvello. The network helps show where Mariarosaria Calvello may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Mariarosaria Calvello, 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 | 2025 | 1 | |
| 2 | 2025 | 1 | |
| 3 | 2025 | 0 | |
| 4 | 2023 | 8 | |
| 5 | 2023 | 5 | |
| 6 | 2022 | 2 | |
| 7 | 2022 | 3 | |
| 8 | 2022 | 6 | |
| 9 | 2021 | 9 | |
| 10 | 2020 | 1 | |
| 11 | 2019 | 24 | |
| 12 | 2018 | 24 | |
| 13 | 2017 | 19 | |
| 14 | 2017 | 14 | |
| 15 | 2017 | 7 | |
| 16 | 2017 | 3 | |
| 17 | 2016 | 18 | |
| 18 | 2013 | 31 | |
| 19 | 2013 | 7 | |
| 20 | 2012 | 12 |
About Mariarosaria Calvello
Mariarosaria Calvello is a scholar working on Genetics, Pathology and Forensic Medicine and Cancer Research, having authored 25 papers that have together received 231 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (12 papers), Genetic factors in colorectal cancer (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (4 papers), Genetic Syndromes and Imprinting (3 papers), DNA Repair Mechanisms (3 papers), Epigenetics and DNA Methylation (3 papers) and Colorectal Cancer Screening and Detection (3 papers). The work is most often cited by research in Genetics (134 citations), Reproductive Medicine (18 citations) and Molecular Biology (124 citations). Mariarosaria Calvello has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Monica Miozzo, Bernardo Bonanni, Silvia Tabano, Faustina Lalatta, Silvia Maria Sirchia, Jacopo Azzollini, Maria Francesca Bedeschi, Patrizia Colapietro, Silvia Maitz and Angelo Selicorni. Their work appears in journals such as Cancers, European Journal of Cancer, Genes, Epigenetics and PLoS ONE.
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.