Viola Alesi
Impact in
- Genetics top 10%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
Papers in
- Genetics 38
- Genomic variations and chromosomal abnormalities 20
- Genetics and Neurodevelopmental Disorders 11
- Genomics and Rare Diseases 10
- Glioma Diagnosis and Treatment 7
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- Congenital heart defects research 11
- RNA modifications and cancer 6
- Co-authors
- Antonio Novelli (46 shared papers)Sara Loddo (19 shared papers)Bruno Dallapiccola (27 shared papers)M. Cristina Digilio (20 shared papers)Marco Tartaglia (4 shared papers)Silvia Genovese (21 shared papers)Maria Lisa Dentici (19 shared papers)Deny Menghini (2 shared papers)
- Journals
- International Journal of Molecular Sciences (4 papers)European Journal of Human Genetics (2 papers)Journal of Cardiovascular Development and Disease (2 papers)Cytogenetic and Genome Research (2 papers)Clinical Genetics (2 papers)
- Partner nations
- ItalyUnited StatesFrance
In The Last Decade
Viola Alesi
59 papers receiving 532 citations
Peers
Comparison fields: 5 of 68
- Genetics 309
- Genetics 72
- Developmental Neuroscience 17
- Molecular Biology 263
- Neurology 29
Countries citing papers authored by Viola Alesi
This map shows the geographic impact of Viola Alesi'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 Viola Alesi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Viola Alesi more than expected).
Fields of papers citing papers by Viola Alesi
This network shows the impact of papers produced by Viola Alesi. 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 Viola Alesi. The network helps show where Viola Alesi may publish in the future.
Co-authors
The 25 scholars most cited alongside Viola Alesi, 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 59 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2019 | 47 | |
| 2 | 2009 | 44 | |
| 3 | 2018 | 43 | |
| 4 | 2017 | 33 | |
| 5 | 2018 | 32 | |
| 6 | 2022 | 29 | |
| 7 | 2020 | 24 | |
| 8 | 2019 | 23 | |
| 9 | 2017 | 20 | |
| 10 | 2013 | 16 | |
| 11 | 2018 | 15 | |
| 12 | 2020 | 15 | |
| 13 | 2014 | 13 | |
| 14 | 2022 | 12 | |
| 15 | 2012 | 11 | |
| 16 | 2017 | 9 | |
| 17 | 2020 | 9 | |
| 18 | 2018 | 9 | |
| 19 | 2018 | 9 | |
| 20 | 2021 | 8 |
About Viola Alesi
Viola Alesi is a scholar working on Genetics, Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health and Neurology, having authored 59 papers that have together received 558 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (20 papers), Congenital heart defects research (11 papers), Genetics and Neurodevelopmental Disorders (11 papers), Genomics and Rare Diseases (10 papers), Glioma Diagnosis and Treatment (7 papers), RNA modifications and cancer (6 papers), Prenatal Screening and Diagnostics (6 papers) and Chromosomal and Genetic Variations (6 papers). The work is most often cited by research in Genetics (309 citations), Genetics (72 citations), Developmental Neuroscience (17 citations), Molecular Biology (263 citations) and Neurology (29 citations). Viola Alesi has collaborated with scholars based in Italy, United States and France. Frequent co-authors include Antonio Novelli, Sara Loddo, Bruno Dallapiccola, M. Cristina Digilio, Marco Tartaglia, Silvia Genovese, Maria Lisa Dentici, Deny Menghini, Eleonora Napoli and Stefano Vicari. Their work appears in journals such as International Journal of Molecular Sciences, European Journal of Human Genetics, Journal of Cardiovascular Development and Disease, Cytogenetic and Genome Research 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.