Ferdinando Squitieri
- Neurology top 0.05%
- Neurological disorders and treatments 87
- Parkinson's Disease Mechanisms and Treatments 20
- Neurological diseases and metabolism 6
- Cellular and Molecular Neuroscience top 0.1%
- Genetic Neurodegenerative Diseases 145
- Neurology top 0.5%
- Neurological disorders and treatments 87
- Parkinson's Disease Mechanisms and Treatments 20
- Neurological diseases and metabolism 6
- Molecular Biology top 1%
- Mitochondrial Function and Pathology 70
- DNA Repair Mechanisms 8
- Aging top 5%
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- Fibromyalgia and Chronic Fatigue Syndrome Research 8
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- Advanced Neuroimaging Techniques and Applications 7
- Co-authors
- Milena CannellaPeter HeutinkPatrizia RizzuMichael R. HaydenG. MecoCornelia M. van DuijnBen A. OostraVincenzo Bonifati
- Journals
- Neurological Sciences (12 papers)Journal of Neurology Neurosurgery & Psychiatry (6 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (6 papers)
- Partner nations
- ItalyUnited StatesUnited Kingdom
In The Last Decade
Ferdinando Squitieri
173 papers receiving 10.0k citations
Hit Papers
Peers
Comparison fields: 5 of 149
- Neurology 5.4k
- Cellular and Molecular Neuroscience 6.4k
- Neurology 1.0k
- Molecular Biology 5.7k
- Aging 89
Countries citing papers authored by Ferdinando Squitieri
This map shows the geographic impact of Ferdinando Squitieri'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 Ferdinando Squitieri with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ferdinando Squitieri more than expected).
Fields of papers citing papers by Ferdinando Squitieri
This network shows the impact of papers produced by Ferdinando Squitieri. 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 Ferdinando Squitieri. The network helps show where Ferdinando Squitieri may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Ferdinando Squitieri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2024 | 0 | |
| 2 | 2024 | 1 | |
| 3 | 2024 | 6 | |
| 4 | 2022 | 12 | |
| 5 | 2022 | 2 | |
| 6 | 2022 | 9 | |
| 7 | 2021 | 13 | |
| 8 | 2021 | 2 | |
| 9 | 2021 | 5 | |
| 10 | 2018 | 1 | |
| 11 | 2018 | 16 | |
| 12 | 2018 | 14 | |
| 13 | 2018 | 6 | |
| 14 | 2018 | 3 | |
| 15 | 2017 | 63 | |
| 16 | 2013 | 16 | |
| 17 | 2006 | 155 | |
| 18 | 2003 | 42 | |
| 19 | 2002 | 44 | |
| 20 | 1993 | 32 |
About Ferdinando Squitieri
Ferdinando Squitieri is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 177 papers that have together received 10.2k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (145 papers), Neurological disorders and treatments (87 papers), Mitochondrial Function and Pathology (70 papers), Parkinson's Disease Mechanisms and Treatments (20 papers), Fibromyalgia and Chronic Fatigue Syndrome Research (8 papers), DNA Repair Mechanisms (8 papers), Advanced Neuroimaging Techniques and Applications (7 papers) and Neurological diseases and metabolism (6 papers). The work is most often cited by research in Neurology (5.4k citations), Cellular and Molecular Neuroscience (6.4k citations) and Neurology (1.0k citations). Ferdinando Squitieri has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Milena Cannella, Peter Heutink, Patrizia Rizzu, Michael R. Hayden, G. Meco, Cornelia M. van Duijn, Ben A. Oostra, Vincenzo Bonifati, John C. van Swieten and Elmar Krieger. Their work appears in journals such as Neurological Sciences, Journal of Neurology Neurosurgery & Psychiatry, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Human Molecular Genetics and Value in Health.
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.