Claudio Bruno

1.9k citations

30 papers · 1.3k indexed · h-index 20

Co-authors: Carlo Minetti Michael P. Lisanti Federica Sotgia Antoni L. Andreu Salvatore DiMauro Elisabetta Gazzerro Sara Shanske Eduardo Bonilla
Topics: Glycogen Storage Diseases and Myoclonus (12 papers)Mitochondrial Function and Pathology (6 papers)Metabolism and Genetic Disorders (6 papers)
Cited by: Clinical Biochemistry Cell Biology Rheumatology
Journals: New England Journal of Medicine Neurology Biochemical and Biophysical Research Communications
Partner nations: Italy United States Netherlands

In The Last Decade

Claudio Bruno

30 papers receiving 1.2k citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	MotorPlex provides accurate variant detection across large muscle genes both in single myopathic patients and in pools of DNA samples 2014 ·Acta Neuropathologica Communications ·Marco Savarese,Giuseppina Di Fruscio,Margherita Mutarelli,Annalaura Torella,Francesca Magri,Filippo M. Santorelli,Giacomo P. Comi,Claudio Bruno,Vincenzo Nigro	48
2	The spectrum of GNE mutations: allelic heterogeneity for a common phenotype 2010 ·Neurological Sciences ·Marina Grandis,Rossella Gulli,Denise Cassandrini,Elisabetta Gazzerro,Luana Benedetti,(unknown),Lucilla Nobbio,Claudio Bruno,Carlo Minetti,Emilia Bellone,Lizia Reni,Gianluigi Mancardi,Paola Mandich,Angelo Schenone	14
3	Caveolinopathies: from the biology of caveolin-3 to human diseases 2009 ·European Journal of Human Genetics ·Elisabetta Gazzerro,Federica Sotgia,Claudio Bruno,Michael P. Lisanti,Carlo Minetti	151
4	Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathies 2008 ·Cell Cycle ·Stefania Assereto,(unknown),Silvia Stringara,Elisabetta Gazzerro,Paolo Broda,Grazia Paola Nicchia,Maria Svelto,Claudio Bruno,Vincenzo Nigro,Michael P. Lisanti,Antonio Frigeri,Carlo Minetti	16
5	Caveolin-1(−/−)- and Caveolin-2(−/−)-Deficient Mice Both Display Numerous Skeletal Muscle Abnormalities, with Tubular Aggregate Formation 2007 ·American Journal Of Pathology ·William Schubert,Federica Sotgia,Alex W. Cohen,Franco Capozza,Gloria Bonuccelli,Claudio Bruno,Carlo Minetti,Eduardo Bonilla,Salvatore DiMauro,Michael P. Lisanti	52
6	Neuromuscular forms of glycogen branching enzyme deficiency. 2007 ·PubMed ·Claudio Bruno,Denise Cassandrini,Stefania Assereto,Hasan O. Akman,Carlo Minetti,S. Di Mauro	22
7	McArdle disease: the mutation spectrum ofPYGMin a large Italian cohort 2006 ·Human Mutation ·Claudio Bruno,Denise Cassandrini,Andrea Martinuzzi,António Toscano,Maurizio Moggio,Lucía Morandi,Serenella Servidei,Tiziana Mongini,C. Angelini,Olimpia Musumeci,Giacomo P. Comi,Costanza Lamperti,Massimiliano Filosto,Federico Zara,Carlo Minetti	52
8	Congenital myopathies 2004 ·Current Neurology and Neuroscience Reports ·Claudio Bruno,Carlo Minetti	11
9	Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene 2003 ·Muscle & Nerve ·Claudio Bruno,Filippo M. Santorelli,Stefania Assereto,E. Tonoli,Alessandra Tessa,Monica Traverso,Sara Scapolan,M. Bado,Silvana Tedeschi,Carlo Minetti	40
10	Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency 2002 ·American Journal Of Pathology ·Carlo Minetti,M. Bado,Paolo Broda,Federica Sotgia,Claudio Bruno,Ferruccio Galbiati,Daniela Volonté,Giuseppe Lucania,Antonio Pavan,Eduardo Bonilla,Michael P. Lisanti,G Cordone	92
11	Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease 2002 ·Neuromuscular Disorders ·Claudio Bruno,Roberta Lanzillo,(unknown),(unknown),Carlo Minetti,Lucio Santoro	7
12	A Novel Mutation in the SURF1 Gene in a Child With Leigh Disease, Peripheral Neuropathy, and Cytochrome-c Oxidase Deficiency 2002 ·Journal of Child Neurology ·Claudio Bruno,Roberta Biancheri,Barbara Garavaglia,(unknown),Andrea Rossi,(unknown),M. Bado,M. Gréco,Massimo Zeviani,Carlo Minetti	25
13	Identification of novel WFS1 mutations in Italian children with Wolfram syndrome 2001 ·Human Mutation ·Alessandra Tessa,Ilma Floriana Carbone,Maria Cristina Matteoli,Claudio Bruno,Carlo Patrono,Ippolita Patrizia Patera,F. De Luca,Renata Lorini,Filippo M. Santorelli	47
14	Molecular characterization of McArdle’s disease in two large Finnish families 1999 ·Journal of the Neurological Sciences ·Claudio Bruno,Mervi Löfberg,(unknown),Heidi Jänkälä,George Hadjigeorgiou,Antoni L. Andreu,Sara Shanske,Hannu Somer,Salvatore DiMauro	16
15	A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy 1999 ·Neuromuscular Disorders ·Claudio Bruno,M. DiRocco,(unknown),M. Bado,C Marino,Seiichi Tsujino,Sara Shanske,Giulia Maria Stella,Carlo Minetti,O. P. van Diggelen,S. DiMauro	22
16	Exercise Intolerance Due to Mutations in the CytochromebGene of Mitochondrial DNA 1999 ·New England Journal of Medicine ·Antoni L. Andreu,Michael G. Hanna,Heinz Reichmann,Claudio Bruno,Audrey S. Penn,Kurenai Tanji,Francesco Pallotti,So Iwata,Eduardo Bonilla,Bolesław Lach,J A Morgan-Hughes,Sara Shanske,Carolyn M. Sue,Teeratorn Pulkes,Asra Tus Saleha Siddiqui,John B. Clark,John M. Land,Momi Iwata,Jochen Schaefer,Salvatore DiMauro	322
17	A nonsense mutation in the myophosphorylase gene in a Japanese family with McArdle's disease 1999 ·Neuromuscular Disorders ·Claudio Bruno,(unknown),Noriko Kawashima,Antoni L. Andreu,Sara Shanske,George Hadjigeorgiou,(unknown),Salvatore DiMauro	23
18	Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria 1998 ·Neuromuscular Disorders ·Carlo Minetti,Barbara Garavaglia,M. Bado,Federica Invernizzi,Claudio Bruno,M. Rimoldi,Roser Pons,Franco Taroni,G Cordone	20
19	Primary adrenal insufficiency in a child with a mitochondrial DNA deletion 1998 ·Journal of Inherited Metabolic Disease ·Claudio Bruno,Carlo Minetti,Yingying Tang,Paulo Magalhães,Filippo M. Santorelli,Sara Shanske,M. Bado,G Cordone,R. Gatti,S. DiMauro	16
20	A Splice Junction Mutation in the αMGene of Phosphorylase Kinase in a Patient with Myopathy 1998 ·Biochemical and Biophysical Research Communications ·Claudio Bruno,Giovanni Manfredi,Antoni L. Andreu,Sara Shanske,Sindu Krishna,(unknown),Salvatore DiMauro	36

About Claudio Bruno

Claudio Bruno is a scholar working on Clinical Biochemistry, Rheumatology and Cell Biology, having authored 30 papers that have together received 1.3k indexed citations. Recurring topics across this work include Glycogen Storage Diseases and Myoclonus (12 papers), Mitochondrial Function and Pathology (6 papers) and Metabolism and Genetic Disorders (6 papers). The work is most often cited by research in Clinical Biochemistry (314 citations), Cell Biology (320 citations) and Rheumatology (246 citations). Claudio Bruno has collaborated with scholars based in Italy, United States and Netherlands. Frequent 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. Their work appears in journals such as New England Journal of Medicine, Neurology and Biochemical and Biophysical Research Communications.

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