Roberto Ciccone
Impact in
- Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 41
- Genomic variations and chromosomal abnormalities 31
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 6
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- Congenital heart defects research 8
- Genomics and Chromatin Dynamics 5
- Co-authors
- Orsetta Zuffardi (43 shared papers)Roberto Giorda (17 shared papers)María Clara Bonaglia (9 shared papers)Annalisa Vetro (7 shared papers)Erika Della Mina (9 shared papers)Francesca Novara (9 shared papers)Elena Rossi (5 shared papers)Tiziano Pramparo (7 shared papers)
- Journals
- European Journal of Medical Genetics (10 papers)European Journal of Human Genetics (9 papers)Human Genetics (4 papers)Clinical Genetics (3 papers)Journal of Medical Genetics (2 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Roberto Ciccone
53 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 83
- Genetics 950
- Pediatrics, Perinatology and Child Health 270
- Developmental Neuroscience 36
- Molecular Biology 622
- Plant Science 249
Countries citing papers authored by Roberto Ciccone
This map shows the geographic impact of Roberto Ciccone'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 Roberto Ciccone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Roberto Ciccone more than expected).
Fields of papers citing papers by Roberto Ciccone
This network shows the impact of papers produced by Roberto Ciccone. 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 Roberto Ciccone. The network helps show where Roberto Ciccone may publish in the future.
Co-authors
The 25 scholars most cited alongside Roberto Ciccone, 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 55 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2007 | 123 | |
| 2 | 2007 | 98 | |
| 3 | 2008 | 96 | |
| 4 | 2009 | 87 | |
| 5 | 2011 | 86 | |
| 6 | 2008 | 86 | |
| 7 | 2011 | 75 | |
| 8 | 2008 | 67 | |
| 9 | 2008 | 63 | |
| 10 | 2014 | 46 | |
| 11 | 2005 | 40 | |
| 12 | 2007 | 36 | |
| 13 | 2012 | 34 | |
| 14 | 2007 | 33 | |
| 15 | 2009 | 33 | |
| 16 | 2009 | 33 | |
| 17 | 2022 | 31 | |
| 18 | 2012 | 31 | |
| 19 | 2008 | 31 | |
| 20 | 2014 | 30 |
About Roberto Ciccone
Roberto Ciccone is a scholar working on Genetics, Molecular Biology, Plant Science, Pediatrics, Perinatology and Child Health and Genetics, having authored 55 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (31 papers), Chromosomal and Genetic Variations (11 papers), Genetics and Neurodevelopmental Disorders (10 papers), Congenital heart defects research (8 papers), Genomics and Rare Diseases (6 papers), Genomics and Chromatin Dynamics (5 papers), Prenatal Screening and Diagnostics (5 papers) and Management, Economics, and Public Policy (3 papers). The work is most often cited by research in Genetics (950 citations), Pediatrics, Perinatology and Child Health (270 citations), Developmental Neuroscience (36 citations), Molecular Biology (622 citations) and Plant Science (249 citations). Roberto Ciccone has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Orsetta Zuffardi, Roberto Giorda, María Clara Bonaglia, Annalisa Vetro, Erika Della Mina, Francesca Novara, Elena Rossi, Tiziano Pramparo, Maria Grazia Patricelli and Stefania Gimelli. Their work appears in journals such as European Journal of Medical Genetics, European Journal of Human Genetics, Human Genetics, Clinical Genetics and Journal of Medical 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.