Carlo Minetti

15.8k total citations
190 papers, 7.5k citations indexed

About

Carlo Minetti is a scholar working on Molecular Biology, Cell Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Carlo Minetti has authored 190 papers receiving a total of 7.5k indexed citations (citations by other indexed papers that have themselves been cited), including 129 papers in Molecular Biology, 37 papers in Cell Biology and 28 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Carlo Minetti's work include Muscle Physiology and Disorders (46 papers), Caveolin-1 and cellular processes (26 papers) and Cardiomyopathy and Myosin Studies (24 papers). Carlo Minetti is often cited by papers focused on Muscle Physiology and Disorders (46 papers), Caveolin-1 and cellular processes (26 papers) and Cardiomyopathy and Myosin Studies (24 papers). Carlo Minetti collaborates with scholars based in Italy, United States and United Kingdom. Carlo Minetti's co-authors include Michael P. Lisanti, Federica Sotgia, Federico Zara, Ferruccio Galbiati, Daniela Volonté, Claudio Bruno, Elisabetta Gazzerro, Marina Pedemonte, M. Bado and Pasquale Striano and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and Nature Genetics.

In The Last Decade

Carlo Minetti

185 papers receiving 7.3k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Carlo Minetti 5.4k 2.4k 1.0k 1.0k 805 190 7.5k
Norma B. Romero 6.1k 1.1× 1.7k 0.7× 655 0.6× 2.3k 2.2× 1.6k 2.0× 193 7.6k
Matthias Vorgerd 3.1k 0.6× 1.2k 0.5× 684 0.7× 1.0k 1.0× 1.4k 1.7× 183 5.1k
Zohar Argov 3.5k 0.6× 796 0.3× 890 0.9× 1.1k 1.0× 1.1k 1.4× 180 6.3k
Lucía Morandi 3.7k 0.7× 613 0.3× 744 0.7× 786 0.8× 754 0.9× 143 5.2k
B. Eymard 4.4k 0.8× 849 0.4× 776 0.7× 1.5k 1.4× 2.3k 2.9× 240 8.2k
Zarife Sahenk 4.6k 0.8× 784 0.3× 1.4k 1.3× 778 0.7× 1.9k 2.3× 145 7.7k
Pascal Laforêt 3.8k 0.7× 715 0.3× 2.0k 1.9× 1.3k 1.2× 1.4k 1.8× 270 7.4k
Francesco Muntoni 6.6k 1.2× 947 0.4× 730 0.7× 1.9k 1.9× 1.2k 1.4× 158 7.7k
Benedikt Schoser 4.1k 0.8× 814 0.3× 2.3k 2.2× 1.1k 1.1× 2.0k 2.5× 337 8.2k
Claudio Bruno 3.3k 0.6× 697 0.3× 588 0.6× 482 0.5× 483 0.6× 146 4.6k

Countries citing papers authored by Carlo Minetti

Since Specialization
Citations

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

Fields of papers citing papers by Carlo Minetti

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carlo Minetti

This figure shows the co-authorship network connecting the top 25 collaborators of Carlo Minetti. A scholar is included among the top collaborators of Carlo Minetti 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 Carlo Minetti. Carlo Minetti 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.
Piccolo, Gianluca, et al.. (2024). Dermatologic Effects of Selumetinib in Pediatric Patients with Neurofibromatosis Type 1: Clinical Challenges and Therapeutic Management. Journal of Clinical Medicine. 13(6). 1792–1792. 5 indexed citations
2.
Brolatti, Noemi, Federica Trucco, Paola Tacchetti, et al.. (2023). Structured Light Plethysmography for Non-Invasive Assessment of Respiratory Pattern in Spinal Muscular Atrophy Type 1. Journal of Clinical Medicine. 12(24). 7553–7553.
3.
Riva, Antonella, Michele Iacomino, Chiara Piccardo, et al.. (2023). Exome sequencing data screening to identify undiagnosed Aromatic l-amino acid decarboxylase deficiency in neurodevelopmental disorders. Biochemical and Biophysical Research Communications. 673. 131–136. 5 indexed citations
4.
Raffaghello, Lizzia, Elisa Principi, Chiara Panicucci, et al.. (2022). P2X7 Receptor Antagonist Reduces Fibrosis and Inflammation in a Mouse Model of Alpha-Sarcoglycan Muscular Dystrophy. Pharmaceuticals. 15(1). 89–89. 15 indexed citations
5.
Panicucci, Chiara, Lizzia Raffaghello, Santina Bruzzone, et al.. (2020). eATP/P2X7R Axis: An Orchestrated Pathway Triggering Inflammasome Activation in Muscle Diseases. International Journal of Molecular Sciences. 21(17). 5963–5963. 15 indexed citations
6.
Torre, Michele, Noemi Brolatti, Gianluca Piccolo, et al.. (2020). Anterior chest wall deformities in children with neurofibromatosis type 1. Acta Paediatrica. 110(2). 594–595. 2 indexed citations
7.
Marchese, Francesca, Maria Stella Vari, Ganna Balagura, et al.. (2020). An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy. Cannabis and Cannabinoid Research. 7(2). 199–206. 11 indexed citations
8.
Scala, Marcello, Giorgia Brigati, Chiara Fiorillo, et al.. (2019). Novel homozygous TSFM pathogenic variant associated with encephalocardiomyopathy with sensorineural hearing loss and peculiar neuroradiologic findings. Neurogenetics. 20(3). 165–172. 7 indexed citations
9.
Gazzerro, Elisabetta, Stefania Assereto, Sımona Baldassari, et al.. (2018). The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan–Deficient Muscular Dystrophy. American Journal Of Pathology. 189(2). 354–369. 10 indexed citations
10.
Fiorillo, Chiara, Maria Rosaria D’Apice, Federica Trucco, et al.. (2018). Characterization of MDPL Fibroblasts Carrying the Recurrent p.Ser605del Mutation in POLD1 Gene. DNA and Cell Biology. 37(12). 1061–1067. 19 indexed citations
11.
Assereto, Stefania, Rosanna Piccirillo, Paolo Scudieri, et al.. (2016). The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophy. Laboratory Investigation. 96(8). 862–871. 16 indexed citations
12.
Wedderburn, Lucy R., Hemlata Varsani, Brenda Banwell, et al.. (2010). VALIDATION OF A HISTOPATHOLOGICAL SCORE TOOL FOR THE MEASUREMENT OF SEVERITY IN MUSCLE BIOPSIES FROM PATIENTS WITH JUVENILE DERMATOMYOSITIS. UCL Discovery (University College London). 1 indexed citations
13.
Pezzella, Marianna, Pierangelo Veggiotti, Alberto Bettinelli, et al.. (2010). Galloway–Mowat syndrome: An early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment. Two novel cases and review of literature. Seizure. 19(2). 132–135. 17 indexed citations
14.
Falace, Antonio, Fabia Filipello, Veronica La Padula, et al.. (2010). TBC1D24, an ARF6-Interacting Protein, Is Mutated in Familial Infantile Myoclonic Epilepsy. The American Journal of Human Genetics. 87(3). 365–370. 114 indexed citations
15.
Mercier, Isabelle Le, Jean-François Jasmin, Stephanos Pavlides, et al.. (2009). Clinical and translational implications of the caveolin gene family: lessons from mouse models and human genetic disorders. Laboratory Investigation. 89(6). 614–623. 65 indexed citations
16.
Torella, Annalaura, Francesca Del Vecchio Blanco, Anna Cuomo, et al.. (2009). One Hundred Twenty-One Dystrophin Point Mutations Detected from Stored DNA Samples by Combinatorial Denaturing High-Performance Liquid Chromatography. Journal of Molecular Diagnostics. 12(1). 65–73. 15 indexed citations
17.
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
18.
Sotgia, Federica, Terence M. Williams, William Schubert, et al.. (2006). Caveolin-1 Deficiency (−/−) Conveys Premalignant Alterations in Mammary Epithelia, with Abnormal Lumen Formation, Growth Factor Independence, and Cell Invasiveness. American Journal Of Pathology. 168(1). 292–309. 59 indexed citations
19.
Bonuccelli, Gloria, Federica Sotgia, William Schubert, et al.. (2003). Proteasome Inhibitor (MG-132) Treatment of mdx Mice Rescues the Expression and Membrane Localization of Dystrophin and Dystrophin-Associated Proteins. American Journal Of Pathology. 163(4). 1663–1675. 110 indexed citations
20.
Oliveira, Acary Souza Bullé, et al.. (1992). Carrier detection of duchenne and becker muscular dystrophy using muscle dystrophin immunohistochemistry. Arquivos de Neuro-Psiquiatria. 50(4). 478–485. 4 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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