Daniela Marchetti
Impact in
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- MicroRNA in disease regulation
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- Extracellular vesicles in disease
- Congenital heart defects research
- Angiogenesis and VEGF in Cancer
Papers in
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- RNA modifications and cancer 4
- Protein Tyrosine Phosphatases 2
- Hedgehog Signaling Pathway Studies 2
- Genetics 11
- Genomics and Rare Diseases 5
- Genomic variations and chromosomal abnormalities 5
- Genetics and Neurodevelopmental Disorders 3
- Connective tissue disorders research 2
- Co-authors
- Giulia Taraboletti (2 shared papers)Raffaella Giavazzi (2 shared papers)Maria Iascone (18 shared papers)Antonio Pavan (1 shared paper)Patrizia Borsotti (1 shared paper)Vincenza Dolo (1 shared paper)Danilo Millimaggi (1 shared paper)Ilaria Giusti (1 shared paper)
- Journals
- The Journal of Pediatrics (1 paper)Neoplasia (1 paper)Bioinformatics (1 paper)Circulation (1 paper)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (1 paper)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Daniela Marchetti
19 papers receiving 488 citations
Peers
Comparison fields: 5 of 62
- Cancer Research 145
- Molecular Biology 351
- Immunology and Allergy 25
- Genetics 113
- Cell Biology 41
Countries citing papers authored by Daniela Marchetti
This map shows the geographic impact of Daniela Marchetti'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 Daniela Marchetti with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniela Marchetti more than expected).
Fields of papers citing papers by Daniela Marchetti
This network shows the impact of papers produced by Daniela Marchetti. 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 Daniela Marchetti. The network helps show where Daniela Marchetti may publish in the future.
Co-authors
The 25 scholars most cited alongside Daniela Marchetti, 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 21 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 165 | |
| 2 | 2011 | 81 | |
| 3 | 2003 | 72 | |
| 4 | 2019 | 34 | |
| 5 | 2010 | 25 | |
| 6 | 2018 | 24 | |
| 7 | 2022 | 17 | |
| 8 | 2012 | 17 | |
| 9 | 2017 | 9 | |
| 10 | 2018 | 9 | |
| 11 | 2020 | 8 | |
| 12 | 2020 | 8 | |
| 13 | 2016 | 8 | |
| 14 | 2023 | 4 | |
| 15 | Gene symbol: MYH7. | 2007 | 4 |
| 16 | 2023 | 3 | |
| 17 | 2022 | 3 | |
| 18 | 2023 | 2 | |
| 19 | 2022 | 2 | |
| 20 | 2023 | 0 |
About Daniela Marchetti
Daniela Marchetti is a scholar working on Molecular Biology, Genetics, Oncology, Surgery and Cardiology and Cardiovascular Medicine, having authored 21 papers that have together received 495 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers), RNA modifications and cancer (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Connective tissue disorders research (2 papers), Protein Tyrosine Phosphatases (2 papers), Hedgehog Signaling Pathway Studies (2 papers) and Cardiomyopathy and Myosin Studies (2 papers). The work is most often cited by research in Cancer Research (145 citations), Molecular Biology (351 citations), Immunology and Allergy (25 citations), Genetics (113 citations) and Cell Biology (41 citations). Daniela Marchetti has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Giulia Taraboletti, Raffaella Giavazzi, Maria Iascone, Antonio Pavan, Patrizia Borsotti, Vincenza Dolo, Danilo Millimaggi, Ilaria Giusti, Laura Pezzoli and Marco Rusnati. Their work appears in journals such as The Journal of Pediatrics, Neoplasia, Bioinformatics, Circulation and American Journal of Medical Genetics Part B Neuropsychiatric 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.