Filippo M. Santorelli

22.4k citations
526 papers · 12.5k indexed · h-index 57
Topics
Mitochondrial Function and Pathology (203 papers)Genetic Neurodegenerative Diseases (108 papers)Hereditary Neurological Disorders (102 papers)

In The Last Decade

Filippo M. Santorelli

494 papers receiving 12.2k citations

Peers

Filippo M. Santorelli
Comparison fields: 5 of 144
  • Molecular Biology 8.1k
  • Cellular and Molecular Neuroscience 3.2k
  • Clinical Biochemistry 3.0k
  • Neurology 1.5k
  • Cell Biology 1.3k
Replace Giovanni Manfredi with:
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Ikuya Nonaka Japan
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Filippo M. Santorelli relative to Giovanni Manfredi United States Giovanni Manfredi's profile →
Citations per field
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Giovanni Manfredi · 1×
Citations per year

Countries citing papers authored by Filippo M. Santorelli

Since Specialization
Citations

This map shows the geographic impact of Filippo M. Santorelli'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 Filippo M. Santorelli with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Filippo M. Santorelli more than expected).

Fields of papers citing papers by Filippo M. Santorelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Filippo M. Santorelli. 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 Filippo M. Santorelli. The network helps show where Filippo M. Santorelli may publish in the future.

Co-authorship network of co-authors of Filippo M. Santorelli

This figure shows the co-authorship network connecting the top 25 collaborators of Filippo M. Santorelli. A scholar is included among the top collaborators of Filippo M. Santorelli 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 Filippo M. Santorelli. Filippo M. Santorelli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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The mitochondrial A3243G mutation in maternally inherited migraine without aura.
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About Filippo M. Santorelli

Filippo M. Santorelli is a scholar working on Clinical Biochemistry, Cellular and Molecular Neuroscience and Neurology, having authored 526 papers that have together received 12.5k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (203 papers), Genetic Neurodegenerative Diseases (108 papers) and Hereditary Neurological Disorders (102 papers). The work is most often cited by research in Clinical Biochemistry (3.0k citations), Cellular and Molecular Neuroscience (3.2k citations) and Neurology (1.5k citations). Filippo M. Santorelli has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Enrico Bertini, S. DiMauro, Alessandra Tessa, Sara Shanske, Rosalba Carrozzo, Carlo Dionisi‐Vici, Carlo Casali, Fiorella Piemonte, Hermann Schägger and Laura Vilarinho. Their work appears in journals such as Journal of Biological Chemistry, Journal of the American College of Cardiology and PLoS ONE.

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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