Chiara Leoni
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Immunology top 10%
- Galectins and Cancer Biology
Papers in
-
- Protein Tyrosine Phosphatases 42
- RNA modifications and cancer 7
- Congenital heart defects research 7
- Genetics 34
- Connective tissue disorders research 12
- Genetics and Neurodevelopmental Disorders 11
- Genomic variations and chromosomal abnormalities 7
- Co-authors
- Giuseppe Zampino (83 shared papers)Marco Tartaglia (40 shared papers)Roberta Onesimo (58 shared papers)Flavia Valtorta (6 shared papers)Valentina Giorgio (27 shared papers)Paolo Alfieri (10 shared papers)Fabio Benfenati (4 shared papers)Andrea Menegon (4 shared papers)
- Journals
- Genes (11 papers)European Journal of Medical Genetics (5 papers)American Journal of Medical Genetics Part C Seminars in Medical Genetics (4 papers)Orphanet Journal of Rare Diseases (3 papers)European Journal of Pediatrics (3 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Chiara Leoni
120 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 123
- Genetics 372
- Immunology 244
- Molecular Biology 776
- Gastroenterology 57
- Biological Psychiatry 19
Countries citing papers authored by Chiara Leoni
This map shows the geographic impact of Chiara Leoni'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 Chiara Leoni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chiara Leoni more than expected).
Fields of papers citing papers by Chiara Leoni
This network shows the impact of papers produced by Chiara Leoni. 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 Chiara Leoni. The network helps show where Chiara Leoni may publish in the future.
Co-authors
The 25 scholars most cited alongside Chiara Leoni, 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 130 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1985 | 78 | |
| 2 | 2009 | 73 | |
| 3 | 2010 | 70 | |
| 4 | 2014 | 64 | |
| 5 | 2012 | 51 | |
| 6 | 2009 | 45 | |
| 7 | 1999 | 42 | |
| 8 | 2013 | 40 | |
| 9 | 2002 | 36 | |
| 10 | 2019 | 33 | |
| 11 | 2016 | 33 | |
| 12 | 2017 | 33 | |
| 13 | 2021 | 29 | |
| 14 | 2022 | 28 | |
| 15 | 1997 | 27 | |
| 16 | 2010 | 26 | |
| 17 | 1999 | 24 | |
| 18 | 2016 | 23 | |
| 19 | 2011 | 23 | |
| 20 | 2021 | 22 |
About Chiara Leoni
Chiara Leoni is a scholar working on Molecular Biology, Genetics, Surgery, Pulmonary and Respiratory Medicine and Immunology, having authored 130 papers that have together received 1.4k indexed citations. Recurring topics across this work include Protein Tyrosine Phosphatases (42 papers), Connective tissue disorders research (12 papers), Genetics and Neurodevelopmental Disorders (11 papers), Galectins and Cancer Biology (9 papers), Tracheal and airway disorders (7 papers), RNA modifications and cancer (7 papers), Congenital heart defects research (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). The work is most often cited by research in Genetics (372 citations), Immunology (244 citations), Molecular Biology (776 citations), Gastroenterology (57 citations) and Biological Psychiatry (19 citations). Chiara Leoni has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Giuseppe Zampino, Marco Tartaglia, Roberta Onesimo, Flavia Valtorta, Valentina Giorgio, Paolo Alfieri, Fabio Benfenati, Andrea Menegon, Eugenio Mercuri and Laura Cesarini. Their work appears in journals such as Genes, European Journal of Medical Genetics, American Journal of Medical Genetics Part C Seminars in Medical Genetics, Orphanet Journal of Rare Diseases and European Journal of Pediatrics.
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.