Flavia Cerrato
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- Prenatal Screening and Diagnostics 28
- Genetics top 2%
- Genetic Syndromes and Imprinting 41
- Genomics and Rare Diseases 1
- Molecular Biology top 5%
- Epigenetics and DNA Methylation 37
- RNA modifications and cancer 2
- Renal and related cancers 2
- Cancer-related gene regulation 2
- Kruppel-like factors research 2
- Co-authors
- Andrea RiccioAngela SparagoMargherita SilengoGiovanni Battista FerreroMaria VernucciAgostina De CrescenzoMaria Vittoria CubellisGaetano Verde
- Journals
- Proceedings of the National Academy of Sciences (1 paper)Nucleic Acids Research (1 paper)Nature Genetics (2 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Flavia Cerrato
41 papers receiving 1.5k citations
Peers
Comparison fields: 5 of 76
- Pediatrics, Perinatology and Child Health 815
- Genetics 1.2k
- Molecular Biology 1.3k
- Cancer Research 135
- Pathology and Forensic Medicine 60
Countries citing papers authored by Flavia Cerrato
This map shows the geographic impact of Flavia Cerrato'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 Flavia Cerrato with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Flavia Cerrato more than expected).
Fields of papers citing papers by Flavia Cerrato
This network shows the impact of papers produced by Flavia Cerrato. 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 Flavia Cerrato. The network helps show where Flavia Cerrato may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Flavia Cerrato, 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 | 0 | |
| 2 | 2024 | 12 | |
| 3 | 2023 | 3 | |
| 4 | 2023 | 2 | |
| 5 | 2023 | 0 | |
| 6 | 2021 | 5 | |
| 7 | 2021 | 3 | |
| 8 | 2020 | 7 | |
| 9 | 2019 | 32 | |
| 10 | 2019 | 24 | |
| 11 | 2019 | 25 | |
| 12 | 2018 | 24 | |
| 13 | 2018 | 12 | |
| 14 | 2015 | 6 | |
| 15 | 2012 | 33 | |
| 16 | 2011 | 98 | |
| 17 | 2008 | 66 | |
| 18 | 2008 | 57 | |
| 19 | 2005 | 38 | |
| 20 | 2003 | 15 |
About Flavia Cerrato
Flavia Cerrato is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology, having authored 44 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (41 papers), Epigenetics and DNA Methylation (37 papers), Prenatal Screening and Diagnostics (28 papers), RNA modifications and cancer (2 papers), Renal and related cancers (2 papers), Cancer-related gene regulation (2 papers), Kruppel-like factors research (2 papers) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (815 citations), Genetics (1.2k citations) and Molecular Biology (1.3k citations). Flavia Cerrato has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Andrea Riccio, Angela Sparago, Margherita Silengo, Giovanni Battista Ferrero, Maria Vernucci, Agostina De Crescenzo, Maria Vittoria Cubellis, Gaetano Verde, Silvia Russo and Orazio Palumbo. Their work appears in journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Nature Genetics.
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.