Paolo Broda

1.9k total citations
17 papers, 1.2k citations indexed

About

Paolo Broda is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Paolo Broda has authored 17 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 7 papers in Cardiology and Cardiovascular Medicine and 6 papers in Cell Biology. Recurrent topics in Paolo Broda's work include Muscle Physiology and Disorders (8 papers), Cardiomyopathy and Myosin Studies (6 papers) and Metabolism, Diabetes, and Cancer (5 papers). Paolo Broda is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Cardiomyopathy and Myosin Studies (6 papers) and Metabolism, Diabetes, and Cancer (5 papers). Paolo Broda collaborates with scholars based in Italy, United States and Ireland. Paolo Broda's co-authors include Carlo Minetti, Michael P. Lisanti, Federica Sotgia, M. Bado, G Cordone, Claudio Bruno, Federico Zara, F. Dagna Bricarelli, Ferruccio Galbiati and Daniela Volonté and has published in prestigious journals such as Nature Genetics, Neurology and Biochemical and Biophysical Research Communications.

In The Last Decade

Paolo Broda

17 papers receiving 1.2k citations

Peers

Countries citing papers authored by Paolo Broda

Since Specialization

Citations

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

Fields of papers citing papers by Paolo Broda

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paolo Broda

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

All Works

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17 of 17 papers shown

#	Work	Indexed citations
1	The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic Outcome 2021 ·Frontiers in Neurology ·(unknown), Chiara Fiorillo, Paolo Broda, (unknown), Monica Traverso, Alice Donati, Salvatore Savasta, Raffaele Falsaperla, Maria Margherita Mancardi, Marina Pedemonte, Chiara Panicucci, Gianluca Piatelli, Mattia Pacetti, Andrea Moscatelli, Luca A. Ramenghi, Lino Nobili, Carlo Minetti, Claudio Bruno	2
2	Novel TRIM32 mutation in sarcotubular myopathy. 2019 ·PubMed ·Chiara Panicucci, Monica Traverso, (unknown), (unknown), Michele Iacomino, Chiara Gemelli, Alberto Tagliafico, Paolo Broda, Federico Zara, Claudio Bruno, Carlo Minetti, Chiara Fiorillo	14
3	Clinical and molecular consequences of exon 78 deletion in DMD gene 2018 ·Journal of Human Genetics ·Monica Traverso, Stefania Assereto, (unknown), Michele Iacomino, Marina Pedemonte, (unknown), (unknown), Paolo Broda, Carlo Minetti, Elisabetta Gazzerro, Francesca Madia, Claudio Bruno, Federico Zara, Chiara Fiorillo	7
4	Expanding the histopathological spectrum of CFL2‐related myopathies 2018 ·Clinical Genetics ·Fabiana Fattori, Chiara Fiorillo, Carmelo Rodolico, Giorgio Tasca, Margherita Verardo, Emanuele Bellacchio, Simone Pizzi, Andrea Ciolfi, Gigliola Fagiolari, (unknown), Paolo Broda, Marina Pedemonte, Maurizio Moggio, Claudio Bruno, Marco Tartaglia, Enrico Bertini, Adele D’Amico	8
5	Spinal motor neuron involvement in a patient with homozygous PRUNE mutation 2017 ·European Journal of Paediatric Neurology ·Michele Iacomino, Chiara Fiorillo, Annalaura Torella, Mariasavina Severino, Paolo Broda, Cátia Romano, Raffaele Falsaperla, (unknown), Carlo Minetti, Pasquale Striano, Vincenzo Nigro, Federico Zara	9
6	Congenital myopathy with protein aggregates and nemaline bodies related to CFL2 mutations 2017 ·Neuromuscular Disorders ·Fabiana Fattori, Chiara Fiorillo, Carmelo Rodolico, Giorgio Tasca, Margherita Verardo, Emanuele Bellacchio, Gigliola Fagiolari, (unknown), Paolo Broda, Maurizio Moggio, Claudio Bruno, Marco Tartaglia, Enrico Bertini, Adele D’Amico	2
7	Genetic and Early Clinical Manifestations of Females Heterozygous for Duchenne/Becker Muscular Dystrophy 2015 ·Pediatric Neurology ·Riccardo Papa, Francesca Madia, (unknown), Federica Trucco, Marina Pedemonte, Monica Traverso, Paolo Broda, Claudio Bruno, Federico Zara, Carlo Minetti, Chiara Fiorillo	32
8	Hyperactivation of oxidative mitochondrial metabolism in epithelial cancer cells in situ 2011 ·Cell Cycle ·Diana Whitaker‐Menezes, Ubaldo Martinez‐Outschoorn, Neal Flomenberg, Ruth Birbe, Agnieszka K. Witkiewicz, Anthony Howell, Stephanos Pavlides, Aristotelis Tsirigos, Adam Ertel, Richard G. Pestell, Paolo Broda, Carlo Minetti, Michael P. Lisanti, Federica Sotgia	237
9	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
10	POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes 2007 ·Biochemical and Biophysical Research Communications ·Roberta Biancheri, Antonio Falace, Alessandra Tessa, Marina Pedemonte, Sara Scapolan, Denise Cassandrini, Chiara Aiello, Andrea Rossi, Paolo Broda, Federico Zara, Filippo M. Santorelli, Carlo Minetti, Claudio Bruno	58
11	POMGnT1 Mutations in Congenital Muscular Dystrophy 2006 ·Archives of Neurology ·Roberta Biancheri, Enrico Bertini, Antonio Falace, Marina Pedemonte, Andrea Rossi, Adele D’Amico, Sara Scapolan, (unknown), Stefania Petrini, Denise Cassandrini, Paolo Broda, M. Manfredi, Federico Zara, Filippo M. Santorelli, Carlo Minetti, Claudio Bruno	27
12	Phenotypic Heterogeneity in Two Unrelated Danon Patients Associated with the SameLAMP‐2Gene Mutation 2005 ·Neuropediatrics ·Enrico Bertini, Maria Alice Donati, Paolo Broda, Denise Cassandrini, Stefania Petrini, Carlo Dionisi‐Vici, Luigi Ballerini, Renata Boldrini, Adele D’Amico, Elisabetta Pasquini, Carlo Minetti, Filippo M. Santorelli, Claudio Bruno	21
13	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
14	Mutation in the CAV3 gene causes partial caveolin-3 deficiency and persistent elevated levels of serum creatine kinase 2000 ·Neurology ·Ilma Floriana Carbone, Claudio Bruno, Federica Sotgia, M. Bado, Paolo Broda, (unknown), (unknown), Federico Zara, F. Dagna Bricarelli, G Cordone, Michael P. Lisanti, Carlo Minetti	113
15	Increased Number of Caveolae and Caveolin-3 Overexpression in Duchenne Muscular Dystrophy 1999 ·Biochemical and Biophysical Research Communications ·Silvia Repetto, M. Bado, Paolo Broda, Giuseppe Lucania, (unknown), Federica Sotgia, Ilaria Carbone, Antonio Pavan, Eduardo Bonilla, G Cordone, Michael P. Lisanti, Carlo Minetti	84
16	Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy 1998 ·Nature Genetics ·Carlo Minetti, Federica Sotgia, Claudio Bruno, Paolo Scartezzini, Paolo Broda, M. Bado, (unknown), Michela Mazzocco, Aliana Egeo, Maria Alice Donati, Daniela Volonté, Ferruccio Galbiati, G Cordone, F. Dagna Bricarelli, Michael P. Lisanti, Federico Zara	456
17	[Muscle phosphorylase deficiency in childhood. A case report]. 1994 ·PubMed ·Claudio Bruno, (unknown), M. Bado, Giuseppe Morreale, Paolo Broda, Carlo Minetti, (unknown), G Cordone	3

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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