Patrizia Ciscato

2.1k total citations
47 papers, 1.1k citations indexed

About

Patrizia Ciscato is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Patrizia Ciscato has authored 47 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 42 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Patrizia Ciscato's work include Muscle Physiology and Disorders (29 papers), Genetic Neurodegenerative Diseases (12 papers) and Cardiomyopathy and Myosin Studies (10 papers). Patrizia Ciscato is often cited by papers focused on Muscle Physiology and Disorders (29 papers), Genetic Neurodegenerative Diseases (12 papers) and Cardiomyopathy and Myosin Studies (10 papers). Patrizia Ciscato collaborates with scholars based in Italy, United States and Greece. Patrizia Ciscato's co-authors include A. Prelle, Maurizio Moggio, Giacomo P. Comi, Nereo Bresolin, G. Scarlato, Francesco Fortunato, Monica Sciacco, Andreina Bordoni, Chiara Zecca and Stefania Corti and has published in prestigious journals such as Nature, PLoS ONE and Brain.

In The Last Decade

Patrizia Ciscato

45 papers receiving 1.0k citations

Peers

Patrizia Ciscato

CCM

GENET

CMN

Martin Krahn France

Simona Zanotti Italy

Yasushi Oya Japan

Akanchha Kesari United States

Emma Clement United Kingdom

Andoni Urtizberea France

Karine Nguyen France

Judy U. Earley United States

L. Feng United Kingdom

Michele Hadhazy United States

Martin Krahn France

Patrizia Ciscato

1.1k ×1.3

245 ×1.2

CCM

218 ×1.2

GENET

289 ×1.6

CMN

175 ×1.3

Citations per year, relative to Patrizia Ciscato Patrizia Ciscato (= 1×) peers Martin Krahn

Countries citing papers authored by Patrizia Ciscato

Since Specialization

Citations

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

Fields of papers citing papers by Patrizia Ciscato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrizia Ciscato

This figure shows the co-authorship network connecting the top 25 collaborators of Patrizia Ciscato. A scholar is included among the top collaborators of Patrizia Ciscato 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 Patrizia Ciscato. Patrizia Ciscato 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

Piga, Daniela, Simona Zanotti, Michela Ripolone, et al.. (2024). Association between ZASP/LDB3 Pro26Ser and Inclusion Body Myopathy. International Journal of Molecular Sciences. 25(12). 6547–6547. 1 indexed citations

Piga, Daniela, M. Rimoldi, Francesca Magri, et al.. (2024). Case report: A novel ACTA1 variant in a patient with nemaline rods and increased glycogen deposition. Frontiers in Neurology. 15. 1340693–1340693. 1 indexed citations

Rimoldi, M., Daniele Velardo, Megi Meneri, et al.. (2023). Lafora Disease: A Case Report and Evolving Treatment Advancements. Brain Sciences. 13(12). 1679–1679. 2 indexed citations

Magri, Francesca, Laura Napoli, Michela Ripolone, et al.. (2023). The Profiling of 179 miRNA Expression in Serum from Limb Girdle Muscular Dystrophy Patients and Healthy Controls. International Journal of Molecular Sciences. 24(24). 17402–17402.

Rimoldi, M., Francesca Magri, Michela Ripolone, et al.. (2023). Prominent muscle involvement in a familial form of mitochondrial disease due to a COA8 variant. Frontiers in Genetics. 14. 1278572–1278572. 3 indexed citations

Ripolone, Michela, Simona Zanotti, Laura Napoli, et al.. (2023). MERRF Mutation A8344G in a Four-Generation Family without Central Nervous System Involvement: Clinical and Molecular Characterization. Journal of Personalized Medicine. 13(1). 147–147. 4 indexed citations

Magri, Francesca, Simona Zanotti, Sabrina Salani, et al.. (2022). Antisense Morpholino-Based In Vitro Correction of a Pseudoexon-Generating Variant in the SGCB Gene. International Journal of Molecular Sciences. 23(17). 9817–9817. 1 indexed citations

Zanotti, Simona, Francesca Magri, Michela Ripolone, et al.. (2022). Immunofluorescence signal intensity measurements as a semi-quantitative tool to assess sarcoglycan complex expression in muscle biopsy. European Journal of Histochemistry. 66(3). 5 indexed citations

Pagliarani, Serena, Patrizia Ciscato, Gigliola Fagiolari, et al.. (2020). MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form. Molecular Genetics & Genomic Medicine. 8(9). e1320–e1320. 11 indexed citations

10.

Ronchi, Dario, Edoardo Monfrini, Sara Bonato, et al.. (2020). Dystonia‐ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency. Annals of Clinical and Translational Neurology. 7(5). 839–845. 12 indexed citations

11.

Protti, Alessandro, Francesco Fortunato, Maria Luisa Caspani, et al.. (2014). Mitochondrial Changes in Platelets Are Not Related to Those in Skeletal Muscle during Human Septic Shock. PLoS ONE. 9(5). e96205–e96205. 23 indexed citations

12.

Magri, Francesca, Roberto Del Bo, Maria Grazia D’Angelo, et al.. (2012). Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients. Neuromuscular Disorders. 22(11). 934–943. 47 indexed citations

13.

Magri, Francesca, Roberto Del Bo, Maria Grazia D’Angelo, et al.. (2011). Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing. BMC Medical Genetics. 12(1). 37–37. 28 indexed citations

14.

Beffy, Pascale, Cristina Barsanti, R. Del Carratore, et al.. (2005). Expression and localization of myotonic dystrophy protein kinase in human skeletal muscle cells determined with a novel antibody: Possible role of the protein in cytoskeleton rearrangements during differentiation. Cell Biology International. 29(9). 742–753. 5 indexed citations

15.

Gabellini, Davide, Giuseppe D’Antona, Maurizio Moggio, et al.. (2005). Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1. Nature. 439(7079). 973–977. 170 indexed citations

16.

Zanotti, Simona, Tiziana Negri, Cristina Cappelletti, et al.. (2005). Decorin and biglycan expression is differentially altered in several muscular dystrophies. Brain. 128(11). 2546–2555. 71 indexed citations

17.

Cagliani, Rachele, Francesca Magri, Antonio Toscano, et al.. (2005). Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies. Human Mutation. 26(3). 283–283. 59 indexed citations

18.

Prelle, A., Lucia Tancredi, Monica Sciacco, et al.. (2002). Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels. Journal of Neurology. 249(3). 305–311. 82 indexed citations

19.

Prelle, A., Patrizia Ciscato, Maurizio Moggio, et al.. (1995). Utrophin expression during human fetal development. International Journal of Developmental Neuroscience. 13(6). 585–593. 13 indexed citations

20.

Moggio, Maurizio, A. Prelle, Gigliola Fagiolari, et al.. (1994). Anionic phospholipids calcium binding sites in Duchenne and murine X‐linked muscular dystrophy. Muscle & Nerve. 17(5). 485–488. 1 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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