Claudio Bruno

1.9k total citations
30 papers, 1.3k citations indexed

About

Claudio Bruno is a scholar working on Molecular Biology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, Claudio Bruno has authored 30 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Rheumatology and 6 papers in Clinical Biochemistry. Recurrent topics in Claudio Bruno's work include Glycogen Storage Diseases and Myoclonus (12 papers), Mitochondrial Function and Pathology (6 papers) and Metabolism and Genetic Disorders (6 papers). Claudio Bruno is often cited by papers focused on Glycogen Storage Diseases and Myoclonus (12 papers), Mitochondrial Function and Pathology (6 papers) and Metabolism and Genetic Disorders (6 papers). Claudio Bruno collaborates with scholars based in Italy, United States and Netherlands. Claudio Bruno's co-authors include Carlo Minetti, Michael P. Lisanti, Federica Sotgia, Antoni L. Andreu, Salvatore DiMauro, Elisabetta Gazzerro, Sara Shanske, Eduardo Bonilla, M. Bado and Filippo M. Santorelli and has published in prestigious journals such as New England Journal of Medicine, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Claudio Bruno

30 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Claudio Bruno Italy 20 833 320 314 246 203 30 1.3k
Denise Cassandrini Italy 23 735 0.9× 185 0.6× 228 0.7× 315 1.3× 176 0.9× 62 1.3k
Edoardo Malfatti France 19 867 1.0× 94 0.3× 170 0.5× 149 0.6× 158 0.8× 89 1.1k
G Cordone Italy 16 907 1.1× 534 1.7× 57 0.2× 69 0.3× 64 0.3× 38 1.2k
Mariko Yagi Japan 21 1.1k 1.3× 85 0.3× 64 0.2× 60 0.2× 226 1.1× 66 1.5k
Carlo P. Trevisan Italy 21 853 1.0× 159 0.5× 74 0.2× 37 0.2× 54 0.3× 38 1.2k
Gunter Scharer United States 17 616 0.7× 44 0.1× 583 1.9× 217 0.9× 232 1.1× 29 1.1k
Tomàs Pinós Spain 17 347 0.4× 89 0.3× 67 0.2× 348 1.4× 232 1.1× 58 810
Tania Tiepolo Italy 7 840 1.0× 158 0.5× 57 0.2× 31 0.1× 60 0.3× 9 1.1k
J. Colomer Spain 17 479 0.6× 160 0.5× 50 0.2× 39 0.2× 84 0.4× 42 934
Caterina Garone Italy 21 1.3k 1.6× 42 0.1× 641 2.0× 126 0.5× 182 0.9× 45 1.7k

Countries citing papers authored by Claudio Bruno

Since Specialization
Citations

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

Fields of papers citing papers by Claudio Bruno

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Claudio Bruno

This figure shows the co-authorship network connecting the top 25 collaborators of Claudio Bruno. A scholar is included among the top collaborators of Claudio Bruno 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 Claudio Bruno. Claudio Bruno 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.
Savarese, Marco, Giuseppina Di Fruscio, Margherita Mutarelli, et al.. (2014). MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples. Acta Neuropathologica Communications. 2(1). 100–100. 48 indexed citations
2.
Grandis, Marina, Rossella Gulli, Denise Cassandrini, et al.. (2010). The spectrum of GNE mutations: allelic heterogeneity for a common phenotype. Neurological Sciences. 31(3). 377–380. 14 indexed citations
3.
Gazzerro, Elisabetta, Federica Sotgia, Claudio Bruno, Michael P. Lisanti, & Carlo Minetti. (2009). Caveolinopathies: from the biology of caveolin-3 to human diseases. European Journal of Human Genetics. 18(2). 137–145. 151 indexed citations
4.
Assereto, Stefania, Silvia Stringara, Elisabetta Gazzerro, et al.. (2008). Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies. Cell Cycle. 7(14). 2199–2207. 16 indexed citations
5.
Schubert, William, Federica Sotgia, Alex W. Cohen, et al.. (2007). Caveolin-1(−/−)- and Caveolin-2(−/−)-Deficient Mice Both Display Numerous Skeletal Muscle Abnormalities, with Tubular Aggregate Formation. American Journal Of Pathology. 170(1). 316–333. 52 indexed citations
6.
Bruno, Claudio, Denise Cassandrini, Stefania Assereto, et al.. (2007). Neuromuscular forms of glycogen branching enzyme deficiency.. PubMed. 26(1). 75–8. 22 indexed citations
7.
Bruno, Claudio, Denise Cassandrini, Andrea Martinuzzi, et al.. (2006). McArdle disease: the mutation spectrum ofPYGMin a large Italian cohort. Human Mutation. 27(7). 718–718. 52 indexed citations
8.
Bruno, Claudio & Carlo Minetti. (2004). Congenital myopathies. Current Neurology and Neuroscience Reports. 4(1). 68–73. 11 indexed citations
9.
Bruno, Claudio, Filippo M. Santorelli, Stefania Assereto, et al.. (2003). Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene. Muscle & Nerve. 28(4). 508–511. 40 indexed citations
10.
Minetti, Carlo, M. Bado, Paolo Broda, et al.. (2002). Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency. American Journal Of Pathology. 160(1). 265–270. 92 indexed citations
11.
Bruno, Claudio, et al.. (2002). Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease. Neuromuscular Disorders. 12(5). 498–500. 7 indexed citations
12.
Bruno, Claudio, Roberta Biancheri, Barbara Garavaglia, et al.. (2002). A Novel Mutation in the SURF1 Gene in a Child With Leigh Disease, Peripheral Neuropathy, and Cytochrome-c Oxidase Deficiency. Journal of Child Neurology. 17(3). 233–236. 25 indexed citations
13.
Tessa, Alessandra, Ilma Floriana Carbone, Maria Cristina Matteoli, et al.. (2001). Identification of novel WFS1 mutations in Italian children with Wolfram syndrome. Human Mutation. 17(4). 348–349. 47 indexed citations
14.
Bruno, Claudio, Mervi Löfberg, Heidi Jänkälä, et al.. (1999). Molecular characterization of McArdle’s disease in two large Finnish families. Journal of the Neurological Sciences. 165(2). 121–125. 16 indexed citations
15.
Bruno, Claudio, M. DiRocco, M. Bado, et al.. (1999). A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy. Neuromuscular Disorders. 9(6-7). 403–407. 22 indexed citations
16.
Andreu, Antoni L., Michael G. Hanna, Heinz Reichmann, et al.. (1999). Exercise Intolerance Due to Mutations in the CytochromebGene of Mitochondrial DNA. New England Journal of Medicine. 341(14). 1037–1044. 322 indexed citations
17.
Bruno, Claudio, Noriko Kawashima, Antoni L. Andreu, et al.. (1999). A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease. Neuromuscular Disorders. 9(1). 34–37. 23 indexed citations
18.
Minetti, Carlo, Barbara Garavaglia, M. Bado, et al.. (1998). Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria. Neuromuscular Disorders. 8(1). 3–6. 20 indexed citations
19.
Bruno, Claudio, Carlo Minetti, Yingying Tang, et al.. (1998). Primary adrenal insufficiency in a child with a mitochondrial DNA deletion. Journal of Inherited Metabolic Disease. 21(2). 155–161. 16 indexed citations
20.
Bruno, Claudio, Giovanni Manfredi, Antoni L. Andreu, et al.. (1998). A Splice Junction Mutation in the αMGene of Phosphorylase Kinase in a Patient with Myopathy. Biochemical and Biophysical Research Communications. 249(3). 648–651. 36 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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