Enrico Alfei
- Genetics
- Molecular Biology
- Physiology
- Pediatrics, Perinatology and Child Health
- Clinical Biochemistry top 10%
- Co-authors
- Chiara PantaleoniStefano D’ArrigoDonatella MilaniOrsetta ZuffardiFrancesca L. SciaccaPierangelo VeggiottiUmberto BalottinSara Bulgheroni
- Topics
- Genomic variations and chromosomal abnormalities (8 papers)Genetics and Neurodevelopmental Disorders (7 papers)Congenital heart defects research (5 papers)
- Partner nations
- ItalyUnited KingdomUnited States
In The Last Decade
Enrico Alfei
24 papers receiving 304 citations
Peers
Comparison fields: 5 of 50
- Genetics 160
- Molecular Biology 140
- Physiology 64
- Pediatrics, Perinatology and Child Health 58
- Clinical Biochemistry 39
Countries citing papers authored by Enrico Alfei
This map shows the geographic impact of Enrico Alfei'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 Enrico Alfei with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Enrico Alfei more than expected).
Fields of papers citing papers by Enrico Alfei
This network shows the impact of papers produced by Enrico Alfei. 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 Enrico Alfei. The network helps show where Enrico Alfei may publish in the future.
Co-authorship network of co-authors of Enrico Alfei
This figure shows the co-authorship network connecting the top 25 collaborators of Enrico Alfei. A scholar is included among the top collaborators of Enrico Alfei 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 Enrico Alfei. Enrico Alfei is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 6 | |
| 3 | 2 | |
| 4 | 4 | |
| 5 | 19 | |
| 6 | 4 | |
| 7 | 7 | |
| 8 | 8 | |
| 9 | 5 | |
| 10 | 9 | |
| 11 | 43 | |
| 12 | 27 | |
| 13 | 20 | |
| 14 | 6 | |
| 15 | 19 | |
| 16 | 9 | |
| 17 | 12 | |
| 18 | 24 | |
| 19 | 30 | |
| 20 | 15 |
About Enrico Alfei
Enrico Alfei is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 25 papers that have together received 333 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Clinical Biochemistry (39 citations), Genetics (160 citations) and Pediatrics, Perinatology and Child Health (58 citations). Enrico Alfei has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Chiara Pantaleoni, Stefano D’Arrigo, Donatella Milani, Orsetta Zuffardi, Francesca L. Sciacca, Pierangelo Veggiotti, Umberto Balottin, Sara Bulgheroni, Silvia Esposito and Claudia Ciaccio. Their work appears in journals such as Journal of Autism and Developmental Disorders, Pharmacological Research and Human Mutation.
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.