Ferdinando Squitieri

15.6k citations
180 papers · 10.3k · 2 hit papers · h-index 49

Impact in

    • Genetic Neurodegenerative Diseases
    • Nuclear Receptors and Signaling
  • Neurology top 0.05%
    • Neurological disorders and treatments
    • Parkinson's Disease Mechanisms and Treatments
    • Neurological diseases and metabolism

Papers in

    • Genetic Neurodegenerative Diseases 145
    • Neurological disorders and treatments 58
    • Parkinson's Disease Mechanisms and Treatments 11
    • Neurological diseases and metabolism 6
    • Intracerebral and Subarachnoid Hemorrhage Research 6

Ferdinando Squitieri

175 papers receiving 10.1k citations

Ferdinando Squitieri's Hit Papers

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism 2003 · 2.2k citations
2.2k0+11+22Years since publication50010001.5k2.0k

Peers

Ferdinando Squitieri
Comparison fields: 5 of 149
  • Cellular and Molecular Neuroscience 6.4k
  • Neurology 4.7k
  • Neurology 909
  • Molecular Biology 5.1k
  • Aging 88
Replace Olaf Rieß with:
Olaf Rieß Germany
Albert R. La Spada United States
Rejko Krüger Germany
Laura Mangiarini United Kingdom
Lüdger Schöls Germany
Georg Auburger Germany
Edward S. Stenroos United States
Susan Ide United States
Thomas D. Bird United States
Giuseppe Di Iorio Italy
Ferdinando Squitieri relative to Olaf Rieß Germany Olaf Rieß's profile →
Citations per field
00.5×1.5×
Olaf Rieß · 1×
Citations per year

Countries citing papers authored by Ferdinando Squitieri

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authors

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.

Border = papers with Ferdinando Squitieri Line = papers co-authored together Ferdinando Squitieri links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 180 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism
Hit paper breakdown →
20032175
2
The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease
Hit paper breakdown →
1993818
3 1994431
4 2003315
5 2017276
6 2003262
7
Brain white-matter volume loss and glucose hypometabolism precede the clinical symptoms of Huntington's disease.
2006229
8 2009195
9 1993183
10 2006154
11 1994148
12 2003139
13 2007135
14 2011133
15 2019130
16 2019126
17 2004103
18 201898
19 201297
20 199393

About Ferdinando Squitieri

Ferdinando Squitieri is a scholar working on Cellular and Molecular Neuroscience, Neurology, Molecular Biology, Neurology and Psychiatry and Mental health, having authored 180 papers that have together received 10.3k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (145 papers), Neurological disorders and treatments (58 papers), Mitochondrial Function and Pathology (54 papers), Parkinson's Disease Mechanisms and Treatments (11 papers), DNA Repair Mechanisms (8 papers), Fibromyalgia and Chronic Fatigue Syndrome Research (7 papers), Neurological diseases and metabolism (6 papers) and Intracerebral and Subarachnoid Hemorrhage Research (6 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (6.4k citations), Neurology (4.7k citations), Neurology (909 citations), Molecular Biology (5.1k citations) and Aging (88 citations). Ferdinando Squitieri has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Milena Cannella, Patrizia Rizzu, Peter Heutink, Michael R. Hayden, Cornelia M. van Duijn, Vincenzo Bonifati, G. Meco, Ben A. Oostra, John C. van Swieten and Elmar Krieger. Their work appears in journals such as Neurological Sciences, Journal of Neurology Neurosurgery & Psychiatry, Value in Health, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Human Molecular Genetics.

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.

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