Andrea Accogli
- Molecular Biology
- Genetics top 10%
- Surgery
- Pediatrics, Perinatology and Child Health top 10%
- Cellular and Molecular Neuroscience
- Co-authors
- Valeria CapraMyriam SrourMarco PavanelloMariasavina SeverinoArmando CamaMarcello ScalaGianluca PiatelliMarco Gattorno
- Topics
- Genetics and Neurodevelopmental Disorders (12 papers)Genomic variations and chromosomal abnormalities (11 papers)Genomics and Rare Diseases (9 papers)
- Partner nations
- ItalyCanadaUnited States
In The Last Decade
Andrea Accogli
62 papers receiving 749 citations
Peers
Comparison fields: 5 of 85
- Molecular Biology 322
- Genetics 217
- Surgery 116
- Pediatrics, Perinatology and Child Health 115
- Cellular and Molecular Neuroscience 85
Countries citing papers authored by Andrea Accogli
This map shows the geographic impact of Andrea Accogli'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 Andrea Accogli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Andrea Accogli more than expected).
Fields of papers citing papers by Andrea Accogli
This network shows the impact of papers produced by Andrea Accogli. 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 Andrea Accogli. The network helps show where Andrea Accogli may publish in the future.
Co-authorship network of co-authors of Andrea Accogli
This figure shows the co-authorship network connecting the top 25 collaborators of Andrea Accogli. A scholar is included among the top collaborators of Andrea Accogli 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 Andrea Accogli. Andrea Accogli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 8 | |
| 3 | 5 | |
| 4 | 3 | |
| 5 | 25 | |
| 6 | 4 | |
| 7 | 3 | |
| 8 | 5 | |
| 9 | 5 | |
| 10 | 9 | |
| 11 | 13 | |
| 12 | 36 | |
| 13 | 16 | |
| 14 | 22 | |
| 15 | 8 | |
| 16 | 22 | |
| 17 | 11 | |
| 18 | 15 | |
| 19 | 11 | |
| 20 | 101 |
About Andrea Accogli
Andrea Accogli is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 65 papers that have together received 771 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Genomics and Rare Diseases (9 papers). The work is most often cited by research in Genetics (217 citations), Developmental Neuroscience (27 citations) and Pediatrics, Perinatology and Child Health (115 citations). Andrea Accogli has collaborated with scholars based in Italy, Canada and United States. Frequent co-authors include Valeria Capra, Myriam Srour, Marco Pavanello, Mariasavina Severino, Armando Cama, Marcello Scala, Gianluca Piatelli, Marco Gattorno, Elisabetta Traggiai and Silvia Federici. Their work appears in journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Neurology.
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.