Marco Spinazzi

3.7k total citations · 1 hit paper
37 papers, 1.7k citations indexed

About

Marco Spinazzi is a scholar working on Molecular Biology, Neurology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Marco Spinazzi has authored 37 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 9 papers in Neurology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Marco Spinazzi's work include Mitochondrial Function and Pathology (14 papers), Muscle Physiology and Disorders (7 papers) and ATP Synthase and ATPases Research (6 papers). Marco Spinazzi is often cited by papers focused on Mitochondrial Function and Pathology (14 papers), Muscle Physiology and Disorders (7 papers) and ATP Synthase and ATPases Research (6 papers). Marco Spinazzi collaborates with scholars based in Italy, France and Belgium. Marco Spinazzi's co-authors include C. Angelini, Leonardo Salviati, Alberto Casarin, Vanessa Pertegato, Bart De Strooper, Luigi Fulizio, B. Tavolato, Enrico Radaelli, Cesare Patrini and Paola Melacini and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and The Journal of Cell Biology.

In The Last Decade

Marco Spinazzi

35 papers receiving 1.7k citations

Hit Papers

Assessment of mitochondrial respiratory chain enzymatic a... 2012 2026 2016 2021 2012 250 500 750

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Marco Spinazzi Italy 18 1.1k 300 219 200 154 37 1.7k
Tanusree Sen United States 24 1.2k 1.1× 427 1.4× 150 0.7× 115 0.6× 156 1.0× 38 2.3k
Matthew B. Cascio United States 11 1.4k 1.4× 500 1.7× 250 1.1× 146 0.7× 107 0.7× 14 2.1k
Alberto Casarin Italy 18 2.1k 1.9× 412 1.4× 209 1.0× 186 0.9× 101 0.7× 28 2.7k
Lorena Perrone Italy 22 742 0.7× 455 1.5× 120 0.5× 115 0.6× 145 0.9× 41 1.5k
Ron J. Bouchard United States 24 1.1k 1.0× 263 0.9× 318 1.5× 192 1.0× 161 1.0× 37 1.9k
Agatha Schlüter Spain 23 1.2k 1.1× 701 2.3× 138 0.6× 111 0.6× 89 0.6× 42 1.8k
Karl Johan Tronstad Norway 28 1.1k 1.0× 342 1.1× 104 0.5× 95 0.5× 109 0.7× 61 1.9k
Rosella Scrima Italy 25 955 0.9× 248 0.8× 126 0.6× 119 0.6× 100 0.6× 49 1.9k
Domenico De Rasmo Italy 30 1.6k 1.5× 392 1.3× 141 0.6× 109 0.5× 134 0.9× 50 2.2k
Soňa Hudecová Slovakia 19 1.1k 1.0× 270 0.9× 167 0.8× 184 0.9× 63 0.4× 46 2.0k

Countries citing papers authored by Marco Spinazzi

Since Specialization
Citations

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

Fields of papers citing papers by Marco Spinazzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marco Spinazzi. 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 Marco Spinazzi. The network helps show where Marco Spinazzi may publish in the future.

Co-authorship network of co-authors of Marco Spinazzi

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

All Works

20 of 20 papers shown
1.
Spinazzi, Marco, Marco Savarese, Franck Letournel, et al.. (2025). Myotilin gene duplication causing late‐onset myotilinopathy. European Journal of Neurology. 32(1). e70029–e70029. 1 indexed citations
2.
Romo, Lucía, Emily O’Heir, Juliette Nectoux, et al.. (2025). 490PA recurrent non-coding 3’UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy. Neuromuscular Disorders. 53. 105786–105786.
3.
Vandeputte, Patrick, Christophe Gillet, Christophe Verny, et al.. (2025). Camptocormia as a Phenotypic Variant of FSHD in the Elderly: Clinical, Genetic, and Imaging Features. European Journal of Neurology. 32(10). e70332–e70332.
4.
Fernández‐Eulate, Gorka, Girolamo Alfieri, Marco Spinazzi, et al.. (2024). Phenotype variability and natural history of X-linked myopathy with excessive autophagy. Journal of Neurology. 271(7). 4008–4018. 1 indexed citations
5.
Tard, Céline, Anne‐Frédérique Dessein, Marco Spinazzi, et al.. (2023). Long‐term prognosis of fatty‐acid oxidation disorders in adults: Optimism despite the limited effective therapies available. European Journal of Neurology. 31(2). e16138–e16138. 6 indexed citations
6.
D’Amour, Alexander, Fabrice P. Cordelières, Muriel Faure, et al.. (2023). Anti-SARS-CoV-2 (COVID-19) vaccination efficacy in patients with severe neuromuscular diseases. Revue Neurologique. 179(9). 983–992. 3 indexed citations
7.
Radaelli, Enrico, Charles‐Antoine Assenmacher, Esha Banerjee, et al.. (2023). Mitochondrial defects caused by PARL deficiency lead to arrested spermatogenesis and ferroptosis. eLife. 12. 17 indexed citations
8.
Chanson, Jean‐Baptiste, Françoise Bouhour, Martial Mallaret, et al.. (2023). Myasthenia gravis treatment in the elderly presents with a significant iatrogenic risk: a multicentric retrospective study. Journal of Neurology. 270(12). 5819–5826. 3 indexed citations
9.
Bourg, Nathalie, Jérôme Poupiot, Karine Charton, et al.. (2022). Dlk1-Dio3 cluster miRNAs regulate mitochondrial functions in the dystrophic muscle in Duchenne muscular dystrophy. Life Science Alliance. 6(1). e202201506–e202201506. 9 indexed citations
10.
Spinazzi, Marco, Jérôme Poupiot, Julien Cassereau, et al.. (2021). Late-onset camptocormia caused by a heterozygous in-frame CAPN3 deletion. Neuromuscular Disorders. 31(5). 450–455. 5 indexed citations
11.
Guéguen, Naïg, Olivier R. Baris, Guy Lenaers, Pascal Reynier, & Marco Spinazzi. (2021). Secondary coenzyme Q deficiency in neurological disorders. Free Radical Biology and Medicine. 165. 203–218. 8 indexed citations
12.
Spinazzi, Marco, Enrico Radaelli, Katrien Horré, et al.. (2018). PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome. Proceedings of the National Academy of Sciences. 116(1). 277–286. 69 indexed citations
13.
Malena, Adriana, Marco Spinazzi, María Andrea Desbats, et al.. (2017). Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients. Human Molecular Genetics. 26(6). ddx019–ddx019. 46 indexed citations
14.
Desbats, María Andrea, Annalisa Vetro, Ivan Limongelli, et al.. (2015). Primary coenzyme Q10 deficiency presenting as fatal neonatal multiorgan failure. European Journal of Human Genetics. 23(9). 1254–1258. 39 indexed citations
15.
Spinazzi, Marco, Alberto Casarin, Vanessa Pertegato, et al.. (2011). Optimization of respiratory chain enzymatic assays in muscle for the diagnosis of mitochondrial disorders. Mitochondrion. 11(6). 893–904. 50 indexed citations
16.
Spinazzi, Marco, C. Angelini, & Cesare Patrini. (2010). Subacute sensory ataxia and optic neuropathy with thiamine deficiency. Nature Reviews Neurology. 6(5). 288–293. 30 indexed citations
17.
Vitaliani, Roberta, et al.. (2009). Subacute onset of deafness and vertigo in a patient with leptomeningeal metastasis from ovarian cancer. Neurological Sciences. 30(1). 65–67. 16 indexed citations
18.
Spinazzi, Marco, F. De Lazzari, B. Tavolato, et al.. (2007). Myelo-optico-neuropathy in copper deficiency occurring after partial gastrectomy. Journal of Neurology. 254(8). 1012–1017. 45 indexed citations
19.
Armani, Mario, et al.. (2007). Severe dysphagia in lower cranial nerve involvement as the initial symptom of Wegener's granulomatosis. Journal of the Neurological Sciences. 263(1-2). 187–190. 13 indexed citations
20.
Mari, Francesco, Anna Chiara Nascimbeni, Luigi Fulizio, et al.. (2006). Generalized Lysosome-Associated Membrane Protein-2 Defect Explains Multisystem Clinical Involvement and Allows Leukocyte Diagnostic Screening in Danon Disease. American Journal Of Pathology. 168(4). 1309–1320. 60 indexed citations

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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