Fabrizia Franchi
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- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 1
- Mesenchymal stem cell research 1
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- Prenatal Screening and Diagnostics 2
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- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 1
- Mesenchymal stem cell research 1
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- Chromosomal and Genetic Variations 4
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- Tissue Engineering and Regenerative Medicine 2
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- Pluripotent Stem Cells Research 1
- Extracellular vesicles in disease 1
- Co-authors
- Gianfranco CrociGiovanni Battista La SalaOrsetta ZuffardiFrancesca BerettiManuela ZavattiGiuseppina ComitiniTullia MaraldiFrancesca Casciaro
- Partner nations
- ItalyUnited StatesSwitzerland
In The Last Decade
Fabrizia Franchi
8 papers receiving 211 citations
Peers
Comparison fields: 5 of 43
- Genetics 131
- Pediatrics, Perinatology and Child Health 61
- Genetics 27
- Plant Science 74
- Cancer Research 28
Countries citing papers authored by Fabrizia Franchi
This map shows the geographic impact of Fabrizia Franchi'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 Fabrizia Franchi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fabrizia Franchi more than expected).
Fields of papers citing papers by Fabrizia Franchi
This network shows the impact of papers produced by Fabrizia Franchi. 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 Fabrizia Franchi. The network helps show where Fabrizia Franchi may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Fabrizia Franchi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 54 | |
| 2 | 2017 | 10 | |
| 3 | 2016 | 3 | |
| 4 | 2013 | 13 | |
| 5 | 2012 | 22 | |
| 6 | 2005 | 16 | |
| 7 | The same molecular mechanism at the maternal meiosis I produces mono- and dicentric 8p duplications. | 1996 | 95 |
| 8 | 1987 | 3 |
About Fabrizia Franchi
Fabrizia Franchi is a scholar working on Genetics, Genetics and Dermatology, having authored 8 papers that have together received 216 indexed citations. Recurring topics across this work include Chromosomal and Genetic Variations (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Tissue Engineering and Regenerative Medicine (2 papers), Prenatal Screening and Diagnostics (2 papers), Genomics and Rare Diseases (1 paper), Pluripotent Stem Cells Research (1 paper), Extracellular vesicles in disease (1 paper) and Mesenchymal stem cell research (1 paper). The work is most often cited by research in Genetics (131 citations), Pediatrics, Perinatology and Child Health (61 citations) and Genetics (27 citations). Fabrizia Franchi has collaborated with scholars based in Italy, United States and Switzerland. Frequent co-authors include Gianfranco Croci, Giovanni Battista La Sala, Orsetta Zuffardi, Francesca Beretti, Manuela Zavatti, Giuseppina Comitini, Tullia Maraldi, Francesca Casciaro, Elena Rossi and Stephen Wood. Their work appears in journals such as BioFactors, Cytotherapy and Genetics Selection Evolution.
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.