Francesca Ferrante
Impact in
-
- Genomics and Chromatin Dynamics
- Epigenetics and DNA Methylation
- Angiogenesis and VEGF in Cancer
- Developmental Biology and Gene Regulation
- RNA modifications and cancer
- Cancer-related gene regulation
- Histone Deacetylase Inhibitors Research
- RNA Research and Splicing
Papers in
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- Genomics and Chromatin Dynamics 8
- Epigenetics and DNA Methylation 6
- Developmental Biology and Gene Regulation 6
- Cancer-related gene regulation 5
- CRISPR and Genetic Engineering 4
- RNA Research and Splicing 3
- RNA modifications and cancer 3
- Ubiquitin and proteasome pathways 3
- Co-authors
- Tilman Borggrefe (16 shared papers)Benedetto Daniele Giaimo (14 shared papers)Sandra B. Hake (1 shared paper)Ralf H. Adams (2 shared papers)Daniel Biljes (1 shared paper)Urs H. Langen (1 shared paper)Frank Berkenfeld (1 shared paper)Hongryeol Park (1 shared paper)
- Journals
- Nucleic Acids Research (6 papers)Blood (4 papers)Nature Communications (2 papers)American Journal of Clinical Pathology (2 papers)Epigenetics & Chromatin (2 papers)
- Partner nations
- GermanyUnited StatesUnited Kingdom
In The Last Decade
Francesca Ferrante
23 papers receiving 838 citations
Peers
Comparison fields: 5 of 85
- Molecular Biology 647
- Cancer Research 109
- Neurology 37
- Cell Biology 66
- Immunology and Allergy 20
Countries citing papers authored by Francesca Ferrante
This map shows the geographic impact of Francesca Ferrante'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 Francesca Ferrante with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesca Ferrante more than expected).
Fields of papers citing papers by Francesca Ferrante
This network shows the impact of papers produced by Francesca Ferrante. 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 Francesca Ferrante. The network helps show where Francesca Ferrante may publish in the future.
Co-authors
The 25 scholars most cited alongside Francesca Ferrante, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 286 | |
| 2 | 2019 | 203 | |
| 3 | 2015 | 71 | |
| 4 | 2016 | 59 | |
| 5 | 2019 | 53 | |
| 6 | 2018 | 43 | |
| 7 | 2020 | 32 | |
| 8 | 2022 | 18 | |
| 9 | 2020 | 12 | |
| 10 | 2017 | 12 | |
| 11 | 2022 | 11 | |
| 12 | 2005 | 8 | |
| 13 | 2012 | 7 | |
| 14 | 2005 | 6 | |
| 15 | 2023 | 6 | |
| 16 | 2022 | 5 | |
| 17 | 2025 | 4 | |
| 18 | 2024 | 2 | |
| 19 | 2024 | 1 | |
| 20 | 2021 | 1 |
About Francesca Ferrante
Francesca Ferrante is a scholar working on Molecular Biology, Neurology, Rheumatology, Hematology and Physiology, having authored 26 papers that have together received 843 indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (8 papers), Epigenetics and DNA Methylation (6 papers), Developmental Biology and Gene Regulation (6 papers), Cancer-related gene regulation (5 papers), CRISPR and Genetic Engineering (4 papers), RNA Research and Splicing (3 papers), RNA modifications and cancer (3 papers) and Ubiquitin and proteasome pathways (3 papers). The work is most often cited by research in Molecular Biology (647 citations), Cancer Research (109 citations), Neurology (37 citations), Cell Biology (66 citations) and Immunology and Allergy (20 citations). Francesca Ferrante has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Tilman Borggrefe, Benedetto Daniele Giaimo, Sandra B. Hake, Ralf H. Adams, Daniel Biljes, Urs H. Langen, Frank Berkenfeld, Hongryeol Park, Martin Stehling and Takashi Nagasawa. Their work appears in journals such as Nucleic Acids Research, Blood, Nature Communications, American Journal of Clinical Pathology and Epigenetics & Chromatin.
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.