Fábio Passetti
Impact in
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- MicroRNA in disease regulation
- Cancer-related molecular mechanisms research
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- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- RNA Research and Splicing
- Protein Tyrosine Phosphatases
- Circular RNAs in diseases
Papers in
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- RNA modifications and cancer 10
- RNA Research and Splicing 8
- RNA and protein synthesis mechanisms 8
- Genomics and Phylogenetic Studies 3
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- MicroRNA in disease regulation 6
- Cancer-related molecular mechanisms research 6
- Cancer Genomics and Diagnostics 2
- Co-authors
- Carlos Gil Ferreira (11 shared papers)Fabrício F. Costa (2 shared papers)Gabriel Wajnberg (8 shared papers)Ernesto R. Caffarena (2 shared papers)Chong Ae Kim (1 shared paper)José Eduardo Krieger (1 shared paper)Bruce D. Gelb (1 shared paper)Débora Romeo Bertola (1 shared paper)
- Journals
- International Journal of Molecular Sciences (3 papers)Frontiers in Genetics (2 papers)PLoS ONE (2 papers)Scientific Reports (1 paper)Leukemia Research (1 paper)
- Partner nations
- BrazilUnited StatesIndia
In The Last Decade
Fábio Passetti
33 papers receiving 468 citations
Peers
Comparison fields: 5 of 81
- Cancer Research 99
- Molecular Biology 309
- Immunology 47
- Neurology 33
- Hematology 18
Countries citing papers authored by Fábio Passetti
This map shows the geographic impact of Fábio Passetti'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 Fábio Passetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fábio Passetti more than expected).
Fields of papers citing papers by Fábio Passetti
This network shows the impact of papers produced by Fábio Passetti. 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 Fábio Passetti. The network helps show where Fábio Passetti may publish in the future.
Co-authors
The 25 scholars most cited alongside Fábio Passetti, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 61 | |
| 2 | 2009 | 48 | |
| 3 | 2016 | 47 | |
| 4 | 2015 | 39 | |
| 5 | 2018 | 26 | |
| 6 | 2017 | 21 | |
| 7 | 2009 | 18 | |
| 8 | 2019 | 18 | |
| 9 | 2014 | 15 | |
| 10 | 2013 | 14 | |
| 11 | 2017 | 13 | |
| 12 | 2011 | 13 | |
| 13 | 2021 | 12 | |
| 14 | 2012 | 11 | |
| 15 | 2021 | 11 | |
| 16 | 2003 | 11 | |
| 17 | 2014 | 10 | |
| 18 | 2016 | 10 | |
| 19 | 2018 | 9 | |
| 20 | 2019 | 9 |
About Fábio Passetti
Fábio Passetti is a scholar working on Molecular Biology, Cancer Research, Cellular and Molecular Neuroscience, Epidemiology and Public Health, Environmental and Occupational Health, having authored 34 papers that have together received 476 indexed citations. Recurring topics across this work include RNA modifications and cancer (10 papers), RNA Research and Splicing (8 papers), RNA and protein synthesis mechanisms (8 papers), MicroRNA in disease regulation (6 papers), Cancer-related molecular mechanisms research (6 papers), Genomics and Phylogenetic Studies (3 papers), Alzheimer's disease research and treatments (2 papers) and Cancer Genomics and Diagnostics (2 papers). The work is most often cited by research in Cancer Research (99 citations), Molecular Biology (309 citations), Immunology (47 citations), Neurology (33 citations) and Hematology (18 citations). Fábio Passetti has collaborated with scholars based in Brazil, United States and India. Frequent co-authors include Carlos Gil Ferreira, Fabrício F. Costa, Gabriel Wajnberg, Ernesto R. Caffarena, Chong Ae Kim, José Eduardo Krieger, Bruce D. Gelb, Débora Romeo Bertola, Alexandre C. Pereira and Ludwine Messiaen. Their work appears in journals such as International Journal of Molecular Sciences, Frontiers in Genetics, PLoS ONE, Scientific Reports and Leukemia Research.
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.