Simona Cavalieri
Impact in
- Genetics top 10%
- Virus-based gene therapy research
-
- DNA Repair Mechanisms
- CRISPR and Genetic Engineering
- RNA Interference and Gene Delivery
- Mitochondrial Function and Pathology
Papers in
-
- DNA Repair Mechanisms 8
- CRISPR and Genetic Engineering 5
- Mitochondrial Function and Pathology 3
- Congenital heart defects research 2
- Genetics 9
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 3
- Virus-based gene therapy research 3
- Co-authors
- Luigi Naldini (3 shared papers)Alfredo Brusco (20 shared papers)Massimo Geuna (2 shared papers)Laurie Ailles (2 shared papers)Richard A. Gatti (5 shared papers)Claudio Bordignon (1 shared paper)Elisa Vigna (1 shared paper)Zulma Magnani (1 shared paper)
- Journals
- Molecular Therapy (2 papers)Human Mutation (2 papers)Journal of Neurology (2 papers)Cytogenetic and Genome Research (1 paper)Annals of Human Genetics (1 paper)
- Partner nations
- ItalyUnited StatesRussia
In The Last Decade
Simona Cavalieri
24 papers receiving 748 citations
Peers
Comparison fields: 5 of 62
- Genetics 311
- Molecular Biology 465
- Oncology 150
- Cellular and Molecular Neuroscience 102
- Cancer Research 66
Countries citing papers authored by Simona Cavalieri
This map shows the geographic impact of Simona Cavalieri'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 Simona Cavalieri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simona Cavalieri more than expected).
Fields of papers citing papers by Simona Cavalieri
This network shows the impact of papers produced by Simona Cavalieri. 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 Simona Cavalieri. The network helps show where Simona Cavalieri may publish in the future.
Co-authors
The 25 scholars most cited alongside Simona Cavalieri, 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 129 | |
| 2 | 2002 | 127 | |
| 3 | 2002 | 75 | |
| 4 | 2008 | 59 | |
| 5 | 2011 | 39 | |
| 6 | 2014 | 31 | |
| 7 | 2012 | 31 | |
| 8 | 2015 | 30 | |
| 9 | 2006 | 30 | |
| 10 | 2013 | 25 | |
| 11 | 2007 | 24 | |
| 12 | 2016 | 24 | |
| 13 | 2016 | 23 | |
| 14 | 2012 | 20 | |
| 15 | 2018 | 17 | |
| 16 | 2012 | 17 | |
| 17 | 2007 | 16 | |
| 18 | 2015 | 16 | |
| 19 | 2015 | 12 | |
| 20 | 2016 | 11 |
About Simona Cavalieri
Simona Cavalieri is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Neurology and Oncology, having authored 25 papers that have together received 775 indexed citations. Recurring topics across this work include DNA Repair Mechanisms (8 papers), CRISPR and Genetic Engineering (5 papers), Genetic Neurodegenerative Diseases (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetics and Neurodevelopmental Disorders (3 papers), Mitochondrial Function and Pathology (3 papers), Virus-based gene therapy research (3 papers) and Congenital heart defects research (2 papers). The work is most often cited by research in Genetics (311 citations), Molecular Biology (465 citations), Oncology (150 citations), Cellular and Molecular Neuroscience (102 citations) and Cancer Research (66 citations). Simona Cavalieri has collaborated with scholars based in Italy, United States and Russia. Frequent co-authors include Luigi Naldini, Alfredo Brusco, Massimo Geuna, Laurie Ailles, Richard A. Gatti, Claudio Bordignon, Elisa Vigna, Zulma Magnani, Rainer Loew and Chiara Bonini. Their work appears in journals such as Molecular Therapy, Human Mutation, Journal of Neurology, Cytogenetic and Genome Research and Annals of Human 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.