Sara Carrideo
- Neurology top 5%
- Cellular and Molecular Neuroscience top 5%
- Molecular Biology
- Psychiatry and Mental health top 10%
- Genetics
- Co-authors
- Aldo QuattroneGrazia AnnesiFerdinanda AnnesiDonatella CivitelliAntonio GambardellaElvira Valeria De MarcoGiuseppe NicolettiPatrizia Tarantino
- Topics
- Parkinson's Disease Mechanisms and Treatments (8 papers)Nuclear Receptors and Signaling (4 papers)Autism Spectrum Disorder Research (4 papers)
- Partner nations
- ItalyUnited States
In The Last Decade
Sara Carrideo
16 papers receiving 626 citations
Peers
Comparison fields: 5 of 65
- Neurology 317
- Cellular and Molecular Neuroscience 293
- Molecular Biology 201
- Psychiatry and Mental health 185
- Genetics 104
Countries citing papers authored by Sara Carrideo
This map shows the geographic impact of Sara Carrideo'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 Sara Carrideo with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Carrideo more than expected).
Fields of papers citing papers by Sara Carrideo
This network shows the impact of papers produced by Sara Carrideo. 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 Sara Carrideo. The network helps show where Sara Carrideo may publish in the future.
Co-authorship network of co-authors of Sara Carrideo
This figure shows the co-authorship network connecting the top 25 collaborators of Sara Carrideo. A scholar is included among the top collaborators of Sara Carrideo 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 Sara Carrideo. Sara Carrideo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 14 | |
| 2 | 34 | |
| 3 | 68 | |
| 4 | 15 | |
| 5 | 20 | |
| 6 | Novel human pathological mutations. Gene symbol: MEN1. Disease: MEN1, Multiple endocrine neoplasia, type 1. | 2 |
| 7 | 154 | |
| 8 | 161 | |
| 9 | 13 | |
| 10 | Sex Differences in Clinical and Genetic Determinants of Levodopa Peak-Dose Dyskinesias in Parkinson Disease | 9 |
| 11 | 13 | |
| 12 | 26 | |
| 13 | 43 | |
| 14 | 38 | |
| 15 | 13 | |
| 16 | 17 |
About Sara Carrideo
Sara Carrideo is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 16 papers that have together received 640 indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (8 papers), Nuclear Receptors and Signaling (4 papers) and Autism Spectrum Disorder Research (4 papers). The work is most often cited by research in Neurology (317 citations), Cellular and Molecular Neuroscience (293 citations) and Psychiatry and Mental health (185 citations). Sara Carrideo has collaborated with scholars based in Italy and United States. Frequent co-authors include Aldo Quattrone, Grazia Annesi, Ferdinanda Annesi, Donatella Civitelli, Antonio Gambardella, Elvira Valeria De Marco, Giuseppe Nicoletti, Patrizia Tarantino, Patrizia Spadafora and Mario Zappia. Their work appears in journals such as Proceedings of the National Academy of Sciences, Neurology and Epilepsia.
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.