Daniela Marchetti
Impact in
- Cancer Research top 10%
- MicroRNA in disease regulation
- Protease and Inhibitor Mechanisms
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- Extracellular vesicles in disease
- Congenital heart defects research
- Angiogenesis and VEGF in Cancer
- Circular RNAs in diseases
Papers in
- Genetics 9
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 4
- Genetics and Neurodevelopmental Disorders 3
- Connective tissue disorders research 2
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- Cellular transport and secretion 2
- Co-authors
- Raffaella Giavazzi (2 shared papers)Giulia Taraboletti (2 shared papers)Maria Rosaria Iascone (18 shared papers)Patrizia Borsotti (1 shared paper)Danilo Millimaggi (1 shared paper)Ilaria Giusti (1 shared paper)Vincenza Dolo (1 shared paper)Antonio Pavan (1 shared paper)
- Journals
- Neoplasia (1 paper)Blood (1 paper)Circulation (1 paper)Genes (1 paper)Prenatal Diagnosis (1 paper)
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Daniela Marchetti
19 papers receiving 524 citations
Peers
Comparison fields: 5 of 59
- Cancer Research 146
- Molecular Biology 335
- Immunology and Allergy 26
- Genetics 93
- 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 | 174 | |
| 2 | 2011 | 88 | |
| 3 | 2003 | 73 | |
| 4 | 2019 | 37 | |
| 5 | 2010 | 26 | |
| 6 | 2018 | 24 | |
| 7 | 2022 | 20 | |
| 8 | 2012 | 19 | |
| 9 | 2020 | 10 | |
| 10 | 2017 | 10 | |
| 11 | 2016 | 9 | |
| 12 | 2020 | 8 | |
| 13 | 2018 | 8 | |
| 14 | 2023 | 7 | |
| 15 | Gene symbol: MYH7. | 2007 | 5 |
| 16 | 2022 | 4 | |
| 17 | 2022 | 4 | |
| 18 | 2023 | 3 | |
| 19 | 2023 | 2 | |
| 20 | Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndrome. | 2009 | 1 |
About Daniela Marchetti
Daniela Marchetti is a scholar working on Genetics, Cell Biology, Molecular Biology, Cardiology and Cardiovascular Medicine and Oncology, having authored 21 papers that have together received 532 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Genomics and Rare Diseases (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Pediatric Hepatobiliary Diseases and Treatments (3 papers), Connective tissue disorders research (2 papers), RNA modifications and cancer (2 papers), Congenital heart defects research (2 papers) and Cellular transport and secretion (2 papers). The work is most often cited by research in Cancer Research (146 citations), Molecular Biology (335 citations), Immunology and Allergy (26 citations), Genetics (93 citations) and Cell Biology (41 citations). Daniela Marchetti has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Raffaella Giavazzi, Giulia Taraboletti, Maria Rosaria Iascone, Patrizia Borsotti, Danilo Millimaggi, Ilaria Giusti, Vincenza Dolo, Antonio Pavan, Laura Pezzoli and Veronica Vergani. Their work appears in journals such as Neoplasia, Blood, Circulation, Genes and Prenatal Diagnosis.
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.