Nicoletta Checcarelli

1.4k total citations
23 papers, 731 citations indexed

About

Nicoletta Checcarelli is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Nicoletta Checcarelli has authored 23 papers receiving a total of 731 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 8 papers in Clinical Biochemistry and 3 papers in Surgery. Recurrent topics in Nicoletta Checcarelli's work include Mitochondrial Function and Pathology (13 papers), ATP Synthase and ATPases Research (8 papers) and Metabolism and Genetic Disorders (8 papers). Nicoletta Checcarelli is often cited by papers focused on Mitochondrial Function and Pathology (13 papers), ATP Synthase and ATPases Research (8 papers) and Metabolism and Genetic Disorders (8 papers). Nicoletta Checcarelli collaborates with scholars based in Italy, United States and Greece. Nicoletta Checcarelli's co-authors include Salvatore DiMauro, Antoni L. Andreu, Sara Shanske, So Iwata, A. Prelle, Carolyn M. Sue, Maurizio Moggio, Darryl C. De Vivo, G. Scarlato and A. Gallanti and has published in prestigious journals such as Neurology, Annals of Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Nicoletta Checcarelli

22 papers receiving 713 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nicoletta Checcarelli Italy 14 531 187 96 90 88 23 731
Karine Lascelles United Kingdom 16 295 0.6× 102 0.5× 183 1.9× 143 1.6× 123 1.4× 25 858
D Fontan France 14 271 0.5× 68 0.4× 152 1.6× 87 1.0× 67 0.8× 43 719
Marion Gérard France 14 436 0.8× 94 0.5× 386 4.0× 55 0.6× 85 1.0× 29 837
Sara Bonato Italy 13 362 0.7× 73 0.4× 31 0.3× 79 0.9× 64 0.7× 23 584
C. Ortez Spain 15 422 0.8× 35 0.2× 118 1.2× 92 1.0× 154 1.8× 76 691
Nina Barišić Croatia 17 396 0.7× 57 0.3× 106 1.1× 161 1.8× 45 0.5× 61 860
Robyn Labrum United Kingdom 14 488 0.9× 54 0.3× 84 0.9× 175 1.9× 145 1.6× 21 772
Claudia Castiglioni Chile 15 320 0.6× 33 0.2× 125 1.3× 61 0.7× 99 1.1× 47 566
Hanna Mierzewska Poland 15 444 0.8× 126 0.7× 127 1.3× 98 1.1× 8 0.1× 57 728
Guja Astrea Italy 15 393 0.7× 25 0.1× 88 0.9× 42 0.5× 105 1.2× 53 655

Countries citing papers authored by Nicoletta Checcarelli

Since Specialization
Citations

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

Fields of papers citing papers by Nicoletta Checcarelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nicoletta Checcarelli

This figure shows the co-authorship network connecting the top 25 collaborators of Nicoletta Checcarelli. A scholar is included among the top collaborators of Nicoletta Checcarelli 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 Nicoletta Checcarelli. Nicoletta Checcarelli 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.
Molteni, Franco, et al.. (2019). Efficiency in stroke management from acute care to rehabilitation: bedside versus telemedicine consultation. European Journal of Physical and Rehabilitation Medicine. 55(2). 141–147. 3 indexed citations
2.
Zangari, Rosalia, Elisa R. Zanier, Giuseppe Torgano, et al.. (2016). Early ficolin-1 is a sensitive prognostic marker for functional outcome in ischemic stroke. Journal of Neuroinflammation. 13(1). 16–16. 53 indexed citations
3.
Corrado, Giovanni, et al.. (2013). An Unusual Cause of Ischemic Stroke with Successful Thrombolysis. Journal of Stroke and Cerebrovascular Diseases. 22(8). e691–e692. 5 indexed citations
4.
Corrado, Giovanni, Nicoletta Checcarelli, Mauro Santarone, Claudia Stöllberger, & Josef Finsterer. (2006). Left Ventricular Hypertrabeculation/Noncompaction with PMP22 Duplication-Based Charcot-Marie-Tooth Disease Type 1A. Cardiology. 105(3). 142–145. 23 indexed citations
5.
Checcarelli, Nicoletta, et al.. (2006). Measurement of ATP production in mitochondrial disorders. Journal of Inherited Metabolic Disease. 29(1). 86–91. 26 indexed citations
6.
Pons, Roser, Antoni L. Andreu, Nicoletta Checcarelli, et al.. (2004). Mitochondrial DNA abnormalities and autistic spectrum disorders. The Journal of Pediatrics. 144(1). 81–85. 102 indexed citations
7.
Giordano, Carla, Francesco Pallotti, Winsome F. Walker, et al.. (2002). Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. Biochemical and Biophysical Research Communications. 293(1). 521–529. 30 indexed citations
8.
Manfredi, Giovanni, Antonella Spinazzola, Nicoletta Checcarelli, & Ali Naini. (2001). Assay of mitochondrial ATP synthesis in animal cells. Methods in cell biology. 65. 133–145. 30 indexed citations
9.
Andreu, Antoni L., Nicoletta Checcarelli, So Iwata, Sara Shanske, & Salvatore DiMauro. (2000). A Missense Mutation in the Mitochondrial Cytochrome b Gene in a Revisited Case with Histiocytoid Cardiomyopathy. Pediatric Research. 48(3). 311–314. 116 indexed citations
10.
Moggio, Maurizio, A. Prelle, Monica Sciacco, et al.. (1999). Critically ill patients: immunological evidence of inflammation in muscle biopsy.. PubMed. 18(1). 23–30. 13 indexed citations
11.
Moggio, Maurizio, A. Prelle, Gigliola Fagiolari, et al.. (1994). Anionic phospholipids calcium binding sites in Duchenne and murine X‐linked muscular dystrophy. Muscle & Nerve. 17(5). 485–488. 1 indexed citations
12.
Checcarelli, Nicoletta, A. Prelle, Maurizio Moggio, et al.. (1994). Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy. Journal of the Neurological Sciences. 123(1-2). 74–79. 24 indexed citations
13.
Moggio, Maurizio, Giacomo P. Comi, Claudio Mariani, et al.. (1994). Multiple sclerosis and mitochondrial myopathy: An unusual combination of diseases. Journal of Neurology. 241(8). 511–516. 12 indexed citations
14.
Prelle, A., Gigliola Fagiolari, Nicoletta Checcarelli, et al.. (1994). Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level. Acta Neuropathologica. 87(4). 371–376.
15.
Prelle, A., Gigliola Fagiolari, Nicoletta Checcarelli, et al.. (1994). Mitochondrial myopathy: correlation between oxidative defect and mitochondrial DNA deletions at single fiber level. Acta Neuropathologica. 87(4). 371–376. 18 indexed citations
16.
Prelle, A., Maurizio Moggio, Nicoletta Checcarelli, et al.. (1993). Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis. Journal of the Neurological Sciences. 117(1-2). 24–27. 12 indexed citations
17.
Vita, Giuseppe, António Toscano, A. Prelle, et al.. (1993). Muscle Mitochondria Investigation in Myotonic Dystrophy. European Neurology. 33(6). 423–427. 8 indexed citations
18.
Prelle, A., Maurizio Moggio, Giacomo P. Comi, et al.. (1992). Congenital myopathy associated with abnormal accumulation of desmin and dystrophin. Neuromuscular Disorders. 2(3). 169–175. 35 indexed citations
19.
Gallanti, A., A. Prelle, Maurizio Moggio, et al.. (1992). Desmin and Vimentin as markers of regeneration in muscle diseases. Acta Neuropathologica. 85(1). 88–92. 73 indexed citations
20.
Prelle, A., Maurizio Moggio, A. Gallanti, et al.. (1991). Appearance and localization of dystrophin in normal human fetal muscle. International Journal of Developmental Neuroscience. 9(6). 607–612. 11 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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