Pamela Magini
- Genetics top 5%
- Molecular Biology
- Cancer Research
- Neurology
- Pediatrics, Perinatology and Child Health
- Co-authors
- Marco SeriTommaso PippucciG. Cara RomeoClaudio GrazianoAlberto MagiMatteo BenelliGian Franco GensiniBetti Giusti
- Topics
- Genomic variations and chromosomal abnormalities (17 papers)Genomics and Rare Diseases (10 papers)Genetics and Neurodevelopmental Disorders (10 papers)
- Partner nations
- ItalyUnited KingdomRussia
In The Last Decade
Pamela Magini
37 papers receiving 697 citations
Peers
Comparison fields: 5 of 77
- Genetics 349
- Molecular Biology 347
- Cancer Research 119
- Neurology 58
- Pediatrics, Perinatology and Child Health 53
Countries citing papers authored by Pamela Magini
This map shows the geographic impact of Pamela Magini'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 Pamela Magini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Pamela Magini more than expected).
Fields of papers citing papers by Pamela Magini
This network shows the impact of papers produced by Pamela Magini. 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 Pamela Magini. The network helps show where Pamela Magini may publish in the future.
Co-authorship network of co-authors of Pamela Magini
This figure shows the co-authorship network connecting the top 25 collaborators of Pamela Magini. A scholar is included among the top collaborators of Pamela Magini 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 Pamela Magini. Pamela Magini is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 17 | |
| 2 | 0 | |
| 3 | 1 | |
| 4 | 11 | |
| 5 | 6 | |
| 6 | 1 | |
| 7 | 4 | |
| 8 | 33 | |
| 9 | 8 | |
| 10 | 15 | |
| 11 | 25 | |
| 12 | 41 | |
| 13 | 12 | |
| 14 | 4 | |
| 15 | 43 | |
| 16 | 33 | |
| 17 | 32 | |
| 18 | 13 | |
| 19 | 9 | |
| 20 | 23 |
About Pamela Magini
Pamela Magini is a scholar working on Genetics, Genetics and Developmental Biology, having authored 38 papers that have together received 717 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genomics and Rare Diseases (10 papers) and Genetics and Neurodevelopmental Disorders (10 papers). The work is most often cited by research in Genetics (349 citations), Developmental Biology (23 citations) and Cancer Research (119 citations). Pamela Magini has collaborated with scholars based in Italy, United Kingdom and Russia. Frequent co-authors include Marco Seri, Tommaso Pippucci, G. Cara Romeo, Claudio Graziano, Alberto Magi, Matteo Benelli, Gian Franco Gensini, Betti Giusti, Eleonora Mangano and Romina D’Aurizio. Their work appears in journals such as Blood, International Journal of Molecular Sciences and Genome Research.
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.