Simona Cavani
Impact in
- Hematology top 5%
- Acute Myeloid Leukemia Research
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 22
- Genomic variations and chromosomal abnormalities 18
- Genetics and Neurodevelopmental Disorders 7
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- Congenital heart defects research 7
- Epigenetics and DNA Methylation 3
- Sexual Differentiation and Disorders 2
- Co-authors
- Michela Malacarne (17 shared papers)Mauro Pierluigi (14 shared papers)M. Pierluigi (5 shared papers)Maria Piccione (9 shared papers)Chiara Perfumo (4 shared papers)Federico Zara (2 shared papers)Dean Nižetić (4 shared papers)Finbarr E. Cotter (3 shared papers)
- Journals
- European Journal of Medical Genetics (2 papers)European Journal of Human Genetics (2 papers)British Journal of Haematology (2 papers)Prenatal Diagnosis (1 paper)Clinical Genetics (1 paper)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Simona Cavani
30 papers receiving 646 citations
Peers
Comparison fields: 5 of 70
- Hematology 138
- Genetics 346
- Genetics 72
- Pediatrics, Perinatology and Child Health 124
- Molecular Biology 262
Countries citing papers authored by Simona Cavani
This map shows the geographic impact of Simona Cavani'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 Cavani with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simona Cavani more than expected).
Fields of papers citing papers by Simona Cavani
This network shows the impact of papers produced by Simona Cavani. 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 Cavani. The network helps show where Simona Cavani may publish in the future.
Co-authors
The 25 scholars most cited alongside Simona Cavani, 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 | 2001 | 129 | |
| 2 | 2003 | 109 | |
| 3 | 2004 | 48 | |
| 4 | 2013 | 40 | |
| 5 | 2006 | 34 | |
| 6 | 2007 | 33 | |
| 7 | 2012 | 31 | |
| 8 | 2012 | 29 | |
| 9 | 2000 | 29 | |
| 10 | 2017 | 24 | |
| 11 | 2017 | 24 | |
| 12 | 1998 | 18 | |
| 13 | 2010 | 17 | |
| 14 | 2002 | 16 | |
| 15 | 2011 | 16 | |
| 16 | 2011 | 15 | |
| 17 | 2003 | 10 | |
| 18 | 2019 | 8 | |
| 19 | 2010 | 8 | |
| 20 | A common European framework for quality assessment for constitutional, acquired and molecular cytogenetic investigations. E.C.A. Permanent Working Group for Cytogenetics and Society | 2012 | 8 |
About Simona Cavani
Simona Cavani is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Pulmonary and Respiratory Medicine, having authored 31 papers that have together received 694 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Prenatal Screening and Diagnostics (8 papers), Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (7 papers), Chromosomal and Genetic Variations (5 papers), Epigenetics and DNA Methylation (3 papers), Sperm and Testicular Function (2 papers) and Sexual Differentiation and Disorders (2 papers). The work is most often cited by research in Hematology (138 citations), Genetics (346 citations), Genetics (72 citations), Pediatrics, Perinatology and Child Health (124 citations) and Molecular Biology (262 citations). Simona Cavani has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Michela Malacarne, Mauro Pierluigi, M. Pierluigi, Maria Piccione, Chiara Perfumo, Federico Zara, Dean Nižetić, Finbarr E. Cotter, Franca Dagna‐Bricarelli and Joan Overhauser. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, British Journal of Haematology, Prenatal Diagnosis and Clinical 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.