Michele Callea
About
In The Last Decade
Michele Callea
57 papers receiving 400 citations
Peers
Comparison fields: 5 of 83
- Molecular Biology 229
- Genetics 91
- Oral Surgery 88
- Emergency Medical Services 43
- Urology 41
Countries citing papers authored by Michele Callea
This map shows the geographic impact of Michele Callea'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 Michele Callea with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michele Callea more than expected).
Fields of papers citing papers by Michele Callea
This network shows the impact of papers produced by Michele Callea. 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 Michele Callea. The network helps show where Michele Callea may publish in the future.
Co-authorship network of co-authors of Michele Callea
This figure shows the co-authorship network connecting the top 25 collaborators of Michele Callea. A scholar is included among the top collaborators of Michele Callea 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 Michele Callea. Michele Callea 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 | 4 | |
| 3 | 8 | |
| 4 | 3 | |
| 5 | 4 | |
| 6 | 1 | |
| 7 | 1 | |
| 8 | 10 | |
| 9 | 32 | |
| 10 | 4 | |
| 11 | 3 | |
| 12 | 4 | |
| 13 | 0 | |
| 14 | A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype. | 1 |
| 15 | 2 | |
| 16 | Síndrome de Williams-Beuren. Enfoque diagnóstico a través del fenotipo | 2 |
| 17 | A case of cleidocranial dysplasia with peculiar dental features: pathogenetic role of the RUNX2 mutation and long term follow-up. | 7 |
| 18 | Alagille Syndrome: A review | 1 |
| 19 | Bifid Uvula and Submucous Cleft Palate in Cornelia De Lange Syndrome | 4 |
| 20 | DENTAL PHENOTYPE IN A PATIENT WITH HYPOIDROTIC ECTODERMAL DYSPLASIA AND SEVERE IMMUNODEFICIENCY | 0 |
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.