Patrizia Amati
About
In The Last Decade
Patrizia Amati
22 papers receiving 1.0k citations
Peers
Comparison fields: 5 of 65
- Molecular Biology 691
- Clinical Biochemistry 349
- Endocrinology, Diabetes and Metabolism 259
- Genetics 253
- Pathology and Forensic Medicine 109
Countries citing papers authored by Patrizia Amati
This map shows the geographic impact of Patrizia Amati'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 Patrizia Amati with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Patrizia Amati more than expected).
Fields of papers citing papers by Patrizia Amati
This network shows the impact of papers produced by Patrizia Amati. 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 Patrizia Amati. The network helps show where Patrizia Amati may publish in the future.
Co-authorship network of co-authors of Patrizia Amati
This figure shows the co-authorship network connecting the top 25 collaborators of Patrizia Amati. A scholar is included among the top collaborators of Patrizia Amati 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 Patrizia Amati. Patrizia Amati is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 62 | |
| 2 | Les syndromes génétiques avec obésité | 4 |
| 3 | 21 | |
| 4 | 10 | |
| 5 | 17 | |
| 6 | 25 | |
| 7 | 178 | |
| 8 | 1 | |
| 9 | 62 | |
| 10 | 35 | |
| 11 | 8 | |
| 12 | 5 | |
| 13 | An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p. | 83 |
| 14 | 22 | |
| 15 | 65 | |
| 16 | 45 | |
| 17 | 170 | |
| 18 | 11 | |
| 19 | 23 | |
| 20 | Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF). | 108 |
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.