Sara Benedetti

2.5k total citations
54 papers, 1.5k citations indexed

About

Sara Benedetti is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Sara Benedetti has authored 54 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 19 papers in Cardiology and Cardiovascular Medicine and 10 papers in Genetics. Recurrent topics in Sara Benedetti's work include Cardiac electrophysiology and arrhythmias (14 papers), Ion channel regulation and function (13 papers) and Nuclear Structure and Function (12 papers). Sara Benedetti is often cited by papers focused on Cardiac electrophysiology and arrhythmias (14 papers), Ion channel regulation and function (13 papers) and Nuclear Structure and Function (12 papers). Sara Benedetti collaborates with scholars based in Italy, United States and France. Sara Benedetti's co-authors include Gaetano Finocchiaro, Bianca Pollo, Maria Grazia Bruzzone, Lorenzo Magrassi, Elena Cattaneo, Angelo L. Vescovi, Maurizio Ferrari, Francesco Di Meco, Chiara Di Resta and Silvia Selleri and has published in prestigious journals such as Nature Medicine, SHILAP Revista de lepidopterología and Radiology.

In The Last Decade

Sara Benedetti

52 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sara Benedetti Italy	21	912	340	321	244	241	54	1.5k
Constanze Kaiser United States	10	827 0.9×	108 0.3×	76 0.2×	143 0.6×	403 1.7×	12	1.3k
Marie Vandromme France	28	1.8k 1.9×	279 0.8×	107 0.3×	135 0.6×	216 0.9×	33	2.0k
Dominique Daegelen France	25	1.5k 1.6×	363 1.1×	253 0.8×	97 0.4×	68 0.3×	51	1.9k
Stefano Regis Italy	22	1.2k 1.3×	169 0.5×	114 0.4×	90 0.4×	185 0.8×	57	1.9k
Vishram Kedar United States	12	1.1k 1.3×	71 0.2×	313 1.0×	46 0.2×	139 0.6×	16	1.4k
Ignacio Sancho-Martinez United States	18	1.8k 1.9×	154 0.5×	71 0.2×	67 0.3×	133 0.6×	31	2.0k
Tomoyuki Sumi Japan	16	1.1k 1.2×	111 0.3×	95 0.3×	43 0.2×	118 0.5×	21	1.5k
Virginia Haurigot Spain	24	1.3k 1.4×	989 2.9×	123 0.4×	158 0.6×	239 1.0×	35	2.0k
William E. Tidyman United States	15	1.4k 1.5×	233 0.7×	87 0.3×	47 0.2×	322 1.3×	24	1.7k
William C. Skarnes United Kingdom	10	983 1.1×	119 0.3×	76 0.2×	27 0.1×	78 0.3×	12	1.2k

Countries citing papers authored by Sara Benedetti

Since Specialization

Citations

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

Fields of papers citing papers by Sara Benedetti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Benedetti

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

Sambo, Margherita, et al.. (2024). Meropenem-vaborbactam as intrathecal-sparing therapy for the treatment of carbapenem-resistant K. pneumoniae shunt-related ventriculitis: two case reports and review of the literature. European Journal of Clinical Microbiology & Infectious Diseases. 44(1). 193–196. 3 indexed citations

Berardo, Clarissa, Sara Benedetti, Federica Rey, et al.. (2024). Towards genomic-Newborn Screening: Technical feasibility of Exome Sequencing starting from dried blood spots. Molecular Genetics and Metabolism Reports. 39. 101074–101074.

Fois, Marco, Andrea De Vito, Elena Ricci, et al.. (2024). Efficacy and Safety of Ceftazidime–Avibactam Alone versus Ceftazidime–Avibactam Plus Fosfomycin for the Treatment of Hospital-Acquired Pneumonia and Ventilator-Associated Pneumonia: A Multicentric Retrospective Study from the SUSANA Cohort. Antibiotics. 13(7). 616–616. 3 indexed citations

Salvarani, Nicolò, Giovanni Peretto, Silvia Crasto, et al.. (2023). Functional Characterisation of the Rare SCN5A p.E1225K Variant, Segregating in a Brugada Syndrome Familial Case, in Human Cardiomyocytes from Pluripotent Stem Cells. International Journal of Molecular Sciences. 24(11). 9548–9548. 2 indexed citations

Ferraro, Simona, Sara Benedetti, Savina Mannarino, et al.. (2023). Prediction of atherosclerotic cardiovascular risk in early childhood. Clinica Chimica Acta. 552. 117684–117684. 4 indexed citations

Resta, Chiara Di, Jan van den Berg, Andrea Villatore, et al.. (2022). Concealed Substrates in Brugada Syndrome: Isolated Channelopathy or Associated Cardiomyopathy?. Genes. 13(10). 1755–1755. 6 indexed citations

Micaglio, Emanuele, Michelle M. Monasky, Giuseppe Ciconte, et al.. (2019). Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype. Frontiers in Genetics. 10. 547–547. 10 indexed citations

Micaglio, Emanuele, Michelle M. Monasky, Giuseppe Ciconte, et al.. (2019). SCN5A Nonsense Mutation and NF1 Frameshift Mutation in a Family With Brugada Syndrome and Neurofibromatosis. Frontiers in Genetics. 10. 50–50. 13 indexed citations

Resta, Chiara Di, Alessandro Pietrelli, Simone Sala, et al.. (2015). High-throughput genetic characterization of a cohort of Brugada syndrome patients. Human Molecular Genetics. 24(20). 5828–5835. 31 indexed citations

10.

Agosta, Federica, Marina Scarlato, Edoardo Gioele Spinelli, et al.. (2015). Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage. Radiology. 276(1). 207–218. 28 indexed citations

11.

Resta, Chiara Di, Martina Manzoni, Massimo Zoni Berisso, et al.. (2014). Evaluation of damaging effects of splicing mutations: Validation of an in vitro method for diagnostic laboratories. Clinica Chimica Acta. 436. 276–282. 6 indexed citations

12.

Magagnotti, Cinzia, Angela Bachi, Gianpaolo Zerbini, et al.. (2012). Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(6). 970–979. 14 indexed citations

13.

Crimella, Claudia, Cinzia Baschirotto, Alessia Arnoldi, et al.. (2011). Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot–Marie–Tooth type 2. Clinical Genetics. 82(2). 157–164. 110 indexed citations

14.

Solla, Paolo, Alessandra Bolino, Maria Giovanna Marrosu, et al.. (2010). Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy. Journal of Neurology Neurosurgery & Psychiatry. 81(9). 958–962. 30 indexed citations

15.

Pegoraro, Elena, Bruno F. Gavassini, Sara Benedetti, et al.. (2005). Co-segregation of LMNA and PMP22 gene mutations in the same family. Neuromuscular Disorders. 15(12). 858–862. 7 indexed citations

16.

Benedetti, Sara & Luciano Merlini. (2004). Laminopathies: from the heart of the cell to the clinics. Current Opinion in Neurology. 17(5). 553–560. 22 indexed citations

17.

Vytopil, Michal, Sara Benedetti, Enzo Ricci, et al.. (2003). Mutation analysis of the lamin A/C gene (LMNA) among patients with different cardiomuscular phenotypes. Journal of Medical Genetics. 40(12). e132–e132. 87 indexed citations

18.

Sacco, Maria Grazia, Sara Benedetti, M. Caniatti, et al.. (1999). Retrovirus-mediated IL-4 gene therapy in spontaneous adenocarcinomas from MMTV-neu transgenic mice. Gene Therapy. 6(11). 1893–1897. 11 indexed citations

19.

Cirenei, N., B. Colombo, Marc Mesnil, et al.. (1998). In vitro and in vivo effects of retrovirus-mediated transfer of the connexin 43 gene in malignant gliomas: consequences for HSVtk/GCV anticancer gene therapy. Gene Therapy. 5(9). 1221–1226. 26 indexed citations

20.

Benedetti, Sara, Francesco DiMeco, Bianca Pollo, et al.. (1997). Limited Efficacy of the HSV-TK/GCV System for Gene Therapy of Malignant Gliomas and Perspectives for the Combined Transduction of the Interleukin-4 Gene. Human Gene Therapy. 8(11). 1345–1353. 57 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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