Francesco Vetrini
Impact in
- Physiology top 0.2%
- Calcium signaling and nucleotide metabolism
- Lysosomal Storage Disorders Research
- Aging top 1%
Papers in
-
- RNA Interference and Gene Delivery 4
- CRISPR and Genetic Engineering 3
- Genetics 18
- Virus-based gene therapy research 8
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic Syndromes and Imprinting 3
- Co-authors
- Andrea Ballabio (6 shared papers)Carmine Settembre (3 shared papers)Tuong Huynh (3 shared papers)Diego L. Medina (2 shared papers)Serkan Erdin (2 shared papers)Marco Sardiello (1 shared paper)Pasqualina Colella (1 shared paper)Chiara Di Malta (1 shared paper)
- Journals
- Molecular Therapy (4 papers)Molecular Case Studies (2 papers)Clinical Genetics (2 papers)Journal of Molecular Diagnostics (2 papers)Human Gene Therapy (1 paper)
- Partner nations
- United StatesItalyCzechia
In The Last Decade
Francesco Vetrini
30 papers receiving 5.3k citations
Francesco Vetrini's Hit Papers
Peers
Comparison fields: 5 of 113
- Physiology 885
- Aging 185
- Epidemiology 3.1k
- Cell Biology 1.1k
- Geriatrics and Gerontology 197
Countries citing papers authored by Francesco Vetrini
This map shows the geographic impact of Francesco Vetrini'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 Francesco Vetrini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Francesco Vetrini more than expected).
Fields of papers citing papers by Francesco Vetrini
This network shows the impact of papers produced by Francesco Vetrini. 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 Francesco Vetrini. The network helps show where Francesco Vetrini may publish in the future.
Co-authors
The 25 scholars most cited alongside Francesco Vetrini, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | TFEB Links Autophagy to Lysosomal Biogenesis Hit paper breakdown → | 2011 | 2496 |
| 2 | A lysosome-to-nucleus signalling mechanism senses and regulates the lysosome via mTOR and TFEB Hit paper breakdown → | 2012 | 1495 |
| 3 | TFEB controls cellular lipid metabolism through a starvation-induced autoregulatory loop Hit paper breakdown → | 2013 | 779 |
| 4 | 2013 | 114 | |
| 5 | 2011 | 66 | |
| 6 | 2004 | 59 | |
| 7 | 2010 | 56 | |
| 8 | 2010 | 42 | |
| 9 | 2013 | 40 | |
| 10 | 2006 | 32 | |
| 11 | Fibroblast growth factor and epidermal growth factor differently affect differentiation of murine retinal stem cells in vitro. | 2007 | 29 |
| 12 | 2011 | 25 | |
| 13 | 2011 | 14 | |
| 14 | 2021 | 11 | |
| 15 | 2021 | 8 | |
| 16 | 2020 | 8 | |
| 17 | 2010 | 7 | |
| 18 | 2013 | 7 | |
| 19 | 2018 | 7 | |
| 20 | 2012 | 6 |
About Francesco Vetrini
Francesco Vetrini is a scholar working on Molecular Biology, Genetics, Epidemiology, Infectious Diseases and Cell Biology, having authored 31 papers that have together received 5.3k indexed citations. Recurring topics across this work include Virus-based gene therapy research (8 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), RNA Interference and Gene Delivery (4 papers), Autophagy in Disease and Therapy (4 papers), CRISPR and Genetic Engineering (3 papers), Viral gastroenteritis research and epidemiology (3 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Physiology (885 citations), Aging (185 citations), Epidemiology (3.1k citations), Cell Biology (1.1k citations) and Geriatrics and Gerontology (197 citations). Francesco Vetrini has collaborated with scholars based in United States, Italy and Czechia. Frequent co-authors include Andrea Ballabio, Carmine Settembre, Tuong Huynh, Diego L. Medina, Serkan Erdin, Marco Sardiello, Pasqualina Colella, Chiara Di Malta, Moisés Garcı́a-Arencibia and David C. Rubinsztein. Their work appears in journals such as Molecular Therapy, Molecular Case Studies, Clinical Genetics, Journal of Molecular Diagnostics and Human Gene Therapy.
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.