Antonella Fabretto
- Co-authors
- Paolo GaspariniVanna PecileDanilo LicastroFlavio FaletraDiego VozziEmmanouil AthanasakisAldo SkabarPio D’Adamo
- Topics
- Genomic variations and chromosomal abnormalities (6 papers)Genomics and Rare Diseases (5 papers)Genetics and Neurodevelopmental Disorders (4 papers)
- Cited by
- Sensory SystemsGeneticsNeurology
- Partner nations
- ItalyNetherlandsGermany
In The Last Decade
Antonella Fabretto
20 papers receiving 190 citations
Peers
Comparison fields: 5 of 56
- Molecular Biology 99
- Genetics 84
- Sensory Systems 38
- Immunology 25
- Surgery 17
Countries citing papers authored by Antonella Fabretto
This map shows the geographic impact of Antonella Fabretto'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 Antonella Fabretto with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Antonella Fabretto more than expected).
Fields of papers citing papers by Antonella Fabretto
This network shows the impact of papers produced by Antonella Fabretto. 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 Antonella Fabretto. The network helps show where Antonella Fabretto may publish in the future.
Co-authorship network of co-authors of Antonella Fabretto
This figure shows the co-authorship network connecting the top 25 collaborators of Antonella Fabretto. A scholar is included among the top collaborators of Antonella Fabretto based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Antonella Fabretto. Antonella Fabretto is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 3 | |
| 2 | 6 | |
| 3 | 2 | |
| 4 | 6 | |
| 5 | 20 | |
| 6 | 1 | |
| 7 | 21 | |
| 8 | 31 | |
| 9 | 4 | |
| 10 | 2 | |
| 11 | 24 | |
| 12 | 4 | |
| 13 | 5 | |
| 14 | 3 | |
| 15 | Molecular epidemiology of Usher syndrome in Italy. | 28 |
| 16 | 3 | |
| 17 | 6 | |
| 18 | 6 | |
| 19 | 2 | |
| 20 | 17 |
About Antonella Fabretto
Antonella Fabretto is a scholar working on Sensory Systems, Genetics and Genetics, having authored 20 papers that have together received 194 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). The work is most often cited by research in Sensory Systems (38 citations), Genetics (84 citations) and Neurology (14 citations). Antonella Fabretto has collaborated with scholars based in Italy, Netherlands and Germany. Frequent co-authors include Paolo Gasparini, Vanna Pecile, Danilo Licastro, Flavio Faletra, Diego Vozzi, Emmanouil Athanasakis, Aldo Skabar, Pio D’Adamo, Anna Morgan and Carmela Ziviello. Their work appears in journals such as PLoS ONE, Radiology and Gene.
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.