Caterina Garone

3.7k total citations
45 papers, 1.7k citations indexed

About

Caterina Garone is a scholar working on Molecular Biology, Clinical Biochemistry and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Caterina Garone has authored 45 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 17 papers in Clinical Biochemistry and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Caterina Garone's work include Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (17 papers) and RNA modifications and cancer (10 papers). Caterina Garone is often cited by papers focused on Mitochondrial Function and Pathology (20 papers), Metabolism and Genetic Disorders (17 papers) and RNA modifications and cancer (10 papers). Caterina Garone collaborates with scholars based in Italy, United States and United Kingdom. Caterina Garone's co-authors include Michio Hirano, Saba Tadesse, Salvatore DiMauro, Sarah E. Calvo, Vamsi K. Mootha, Catarina M. Quinzii, Emilio Franzonı, Beatriz García-Díaz, Carlo Viscomi and Alison G. Compton and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Caterina Garone

44 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Caterina Garone Italy 21 1.3k 641 182 148 138 45 1.7k
Angela Abicht Germany 27 1.2k 0.9× 341 0.5× 269 1.5× 156 1.1× 86 0.6× 124 2.1k
Christine Barnérias France 20 704 0.5× 236 0.4× 283 1.6× 193 1.3× 140 1.0× 73 1.4k
Bernhard Weschke Germany 13 547 0.4× 298 0.5× 152 0.8× 29 0.2× 133 1.0× 23 985
Ángeles García‐Cazorla Spain 16 550 0.4× 616 1.0× 204 1.1× 34 0.2× 132 1.0× 37 1.1k
Denise Cassandrini Italy 23 735 0.6× 228 0.4× 176 1.0× 132 0.9× 57 0.4× 62 1.3k
Ivo Kremensky Bulgaria 18 753 0.6× 127 0.2× 295 1.6× 118 0.8× 84 0.6× 75 1.4k
Birgit Uhlenberg Germany 10 529 0.4× 273 0.4× 175 1.0× 21 0.1× 160 1.2× 16 981
Reeval Segel Israel 18 649 0.5× 174 0.3× 249 1.4× 102 0.7× 211 1.5× 40 1.1k
Gunter Scharer United States 17 616 0.5× 583 0.9× 232 1.3× 25 0.2× 191 1.4× 29 1.1k
Chandree L. Beaulieu Canada 20 645 0.5× 107 0.2× 459 2.5× 89 0.6× 64 0.5× 33 1.1k

Countries citing papers authored by Caterina Garone

Since Specialization
Citations

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

Fields of papers citing papers by Caterina Garone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caterina Garone

This figure shows the co-authorship network connecting the top 25 collaborators of Caterina Garone. A scholar is included among the top collaborators of Caterina Garone 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 Caterina Garone. Caterina Garone 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.
Bonetti, Silvia, et al.. (2025). Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures. Neurology. 104(7). e213373–e213373.
2.
Palombo, Flavia, Melania Giannotta, Monica Maffei, et al.. (2023). Expanding the Clinical Spectrum of UBTF -Related Neurodevelopmental Disorder. Neurology Genetics. 9(6). e200098–e200098. 2 indexed citations
3.
Haute, Lindsey Van, Song-Yi Lee, Christopher A. Powell, et al.. (2019). NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs. Nucleic Acids Research. 47(16). 8720–8733. 116 indexed citations
4.
Levene, Michelle, et al.. (2018). Mitochondrial Neurogastrointestinal Encephalomyopathy: Into the Fourth Decade, What We Have Learned So Far. Frontiers in Genetics. 9. 669–669. 45 indexed citations
5.
Lopez‐Gómez, Carlos, Rebecca Levy, Maria J. Sanchez‐Quintero, et al.. (2017). Oral deoxynucleoside for the treatment of thymidine kinase 2 deficiency (P3.195). Neurology. 88(16_supplement). 1 indexed citations
6.
Lopez‐Gómez, Carlos, Rebecca J. Levy, Maria J. Sanchez‐Quintero, et al.. (2017). Deoxycytidine and Deoxythymidine Treatment for Thymidine Kinase 2 Deficiency. Annals of Neurology. 81(5). 641–652. 70 indexed citations
7.
Emmanuele, Valentina, Akatsuki Kubota, Beatriz García-Díaz, et al.. (2014). Fhl1 W122S causes loss of protein function and late-onset mild myopathy. Human Molecular Genetics. 24(3). 714–726. 7 indexed citations
8.
García-Díaz, Beatriz, Caterina Garone, Emanuele Barca, et al.. (2014). Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathy. Brain. 137(5). 1337–1349. 15 indexed citations
9.
Garone, Caterina, Maria Alice Donati, Michele Sacchini, et al.. (2013). Mitochondrial Encephalomyopathy Due to a Novel Mutation inACAD9. JAMA Neurology. 70(9). 1177–1177. 34 indexed citations
10.
Ronchi, Dario, Caterina Garone, Andrea Bordoni, et al.. (2012). Next-generation sequencing reveals DGUOK mutations in adult patients with mitochondrial DNA multiple deletions. Brain. 135(11). 3404–3415. 73 indexed citations
11.
DiMauro, S. & Caterina Garone. (2011). Metabolic disorders of fetal life: Glycogenoses and mitochondrial defects of the mitochondrial respiratory chain. Seminars in Fetal and Neonatal Medicine. 16(4). 181–189. 24 indexed citations
12.
Garone, Caterina, Saba Tadesse, & Michio Hirano. (2011). Clinical and genetic spectrum of mitochondrial neurogastrointestinal encephalomyopathy. Brain. 134(11). 3326–3332. 149 indexed citations
13.
Franzonı, Emilio, Caterina Garone, Valentina Marchiani, et al.. (2010). A new case of idiopathic hemiplegia hemiconvulsion syndrome. Neurological Sciences. 31(6). 799–805. 4 indexed citations
14.
DiMauro, Salvatore & Caterina Garone. (2010). Historical perspective on mitochondrial medicine. PubMed. 16(2). 106–113. 24 indexed citations
15.
Cordelli, Duccio Maria, Caterina Garone, Valentina Marchiani, et al.. (2010). Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). Neuromuscular Disorders. 20(5). 343–345. 2 indexed citations
16.
Ramesh, Venkateswaran, Bruno De Bernardi, Caterina Garone, et al.. (2010). Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis. Developmental Medicine & Child Neurology. 52(8). 725–732. 73 indexed citations
17.
DiMauro, Salvatore, Caterina Garone, & Ali Naini. (2010). Metabolic Myopathies. Current Rheumatology Reports. 12(5). 386–393. 24 indexed citations
18.
Franzonı, Emilio, Valentina Marchiani, I Cecconi, et al.. (2006). Preliminary report on effects of oxcarbazepine‐treatment on serum lipid levels in children. European Journal of Neurology. 13(12). 1389–1391. 15 indexed citations
19.
Coppola, Giangennaro, Emilio Franzonı, Alberto Verrotti, et al.. (2006). Levetiracetam or oxcarbazepine as monotherapy in newly diagnosed benign epilepsy of childhood with centrotemporal spikes (BECTS): An open-label, parallel group trial. Brain and Development. 29(5). 281–284. 67 indexed citations
20.
Franzonı, Emilio, Caterina Garone, Stefano Gualandi, et al.. (2006). Open prospective study on oxcarbazepine in epilepsy in children: A preliminary report. Seizure. 15(5). 292–298. 7 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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