Eleonora Di Gregorio
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- Genetic Neurodegenerative Diseases 10
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- Genomic variations and chromosomal abnormalities 7
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
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- Mitochondrial Function and Pathology 11
- RNA regulation and disease 5
- Nuclear Structure and Function 4
- RNA Research and Splicing 4
- Co-authors
- Alfredo BruscoAlessandro BrussinoGiovanna VaulaElisa GiorgioCecilia ManciniSimona CavalieriLaura OrsiElga Fabia Belligni
- Journals
- SHILAP Revista de lepidopterología (1 paper)Annals of Neurology (1 paper)Scientific Reports (1 paper)
- Partner nations
- ItalyUnited StatesRussia
In The Last Decade
Eleonora Di Gregorio
32 papers receiving 544 citations
Peers
Comparison fields: 5 of 56
- Cellular and Molecular Neuroscience 134
- Genetics 170
- Molecular Biology 389
- Neurology 40
- Neurology 51
Countries citing papers authored by Eleonora Di Gregorio
This map shows the geographic impact of Eleonora Di Gregorio'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 Eleonora Di Gregorio with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eleonora Di Gregorio more than expected).
Fields of papers citing papers by Eleonora Di Gregorio
This network shows the impact of papers produced by Eleonora Di Gregorio. 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 Eleonora Di Gregorio. The network helps show where Eleonora Di Gregorio may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Eleonora Di Gregorio, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2021 | 7 | |
| 2 | 2020 | 2 | |
| 3 | 2019 | 16 | |
| 4 | 2019 | 1 | |
| 5 | 2018 | 15 | |
| 6 | 2017 | 24 | |
| 7 | 2017 | 24 | |
| 8 | 2016 | 11 | |
| 9 | 2015 | 2 | |
| 10 | 2015 | 25 | |
| 11 | 2015 | 2 | |
| 12 | 2015 | 16 | |
| 13 | 2014 | 30 | |
| 14 | 2012 | 19 | |
| 15 | 2012 | 19 | |
| 16 | 2011 | 16 | |
| 17 | 2010 | 32 | |
| 18 | 2009 | 31 | |
| 19 | 2009 | 3 | |
| 20 | 2009 | 32 |
About Eleonora Di Gregorio
Eleonora Di Gregorio is a scholar working on Developmental Biology, Cellular and Molecular Neuroscience and Genetics, having authored 32 papers that have together received 569 indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (11 papers), Genetic Neurodegenerative Diseases (10 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (6 papers), RNA regulation and disease (5 papers), Genomics and Rare Diseases (4 papers), Nuclear Structure and Function (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (134 citations), Genetics (170 citations) and Molecular Biology (389 citations). Eleonora Di Gregorio has collaborated with scholars based in Italy, United States and Russia. Frequent co-authors include Alfredo Brusco, Alessandro Brussino, Giovanna Vaula, Elisa Giorgio, Cecilia Mancini, Simona Cavalieri, Laura Orsi, Elga Fabia Belligni, Margherita Silengo and Giovanni Battista Ferrero. Their work appears in journals such as SHILAP Revista de lepidopterología, Annals of Neurology and Scientific Reports.
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.