Sara Scapolan

540 total citations
11 papers, 348 citations indexed

About

Sara Scapolan is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Sara Scapolan has authored 11 papers receiving a total of 348 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Sara Scapolan's work include Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Sara Scapolan is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Cardiomyopathy and Myosin Studies (3 papers) and Genetic Neurodegenerative Diseases (3 papers). Sara Scapolan collaborates with scholars based in Italy, United States and Switzerland. Sara Scapolan's co-authors include Claudio Bruno, Carlo Minetti, Marina Pedemonte, Filippo M. Santorelli, Roberta Biancheri, Denise Cassandrini, Federico Zara, Alessandra Tessa, Andrea Rossi and Gabriele Siciliano and has published in prestigious journals such as Annals of Neurology, Biochemical and Biophysical Research Communications and Muscle & Nerve.

In The Last Decade

Sara Scapolan

11 papers receiving 335 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sara Scapolan Italy	10	271	70	57	49	45	11	348
Daniela Piga Italy	9	289 1.1×	79 1.1×	19 0.3×	14 0.3×	42 0.9×	21	401
Leigh B. Waddell Australia	9	314 1.2×	68 1.0×	71 1.2×	45 0.9×	47 1.0×	16	371
C R Müller Germany	12	262 1.0×	132 1.9×	44 0.8×	70 1.4×	27 0.6×	17	387
Tomoko Lee Japan	14	317 1.2×	61 0.9×	74 1.3×	51 1.0×	15 0.3×	43	400
Masatoshi Murata Japan	12	159 0.6×	48 0.7×	28 0.5×	19 0.4×	50 1.1×	18	371
Yo Okizuka Japan	10	307 1.1×	28 0.4×	69 1.2×	66 1.3×	13 0.3×	18	363
Elena Perli Italy	11	411 1.5×	117 1.7×	77 1.4×	24 0.5×	10 0.2×	14	529
Lisa Worgan Australia	9	281 1.0×	189 2.7×	17 0.3×	65 1.3×	25 0.6×	14	376
I‐Fen Cheng Germany	6	262 1.0×	61 0.9×	75 1.3×	11 0.2×	16 0.4×	10	364

Countries citing papers authored by Sara Scapolan

Since Specialization

Citations

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

Fields of papers citing papers by Sara Scapolan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Scapolan

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

All Works

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11 of 11 papers shown

Fiorillo, Chiara, Francesca Moro, Guja Astrea, et al.. (2013). Novel mutations in the fukutin gene in a boy with asymptomatic hyperCKemia. Neuromuscular Disorders. 23(12). 1010–1015. 4 indexed citations

Fiorillo, Chiara, Giacomo Brisca, Denise Cassandrini, et al.. (2012). Subclinical myopathy in a child with neutral lipid storage disease and mutations in the PNPLA2 gene. Biochemical and Biophysical Research Communications. 430(1). 241–244. 24 indexed citations

Cassandrini, Denise, Chiara Fiorillo, Sara Scapolan, et al.. (2011). Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT‐II deficiency. Clinical Genetics. 82(3). 232–239. 34 indexed citations

Giunta, Cecilia, Céline Chambaz, Marina Pedemonte, Sara Scapolan, & Beat Steinmann. (2008). The arthrochalasia type of Ehlers–Danlos syndrome (EDS VIIA and VIIB): The diagnostic value of collagen fibril ultrastructure. American Journal of Medical Genetics Part A. 146A(10). 1341–1346. 24 indexed citations

Traverso, Monica, Elisabetta Gazzerro, Stefania Assereto, et al.. (2008). Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitro. Laboratory Investigation. 88(3). 275–283. 32 indexed citations

Trevisan, Carlo P., Ebe Pastorello, Giuliano Tomelleri, et al.. (2008). Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions. European Journal of Neurology. 15(12). 1353–1358. 39 indexed citations

Biancheri, Roberta, Antonio Falace, Alessandra Tessa, et al.. (2007). POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. Biochemical and Biophysical Research Communications. 363(4). 1033–1037. 58 indexed citations

Biancheri, Roberta, Federico Zara, Claudio Bruno, et al.. (2007). Phenotypic characterization of hypomyelination and congenital cataract. Annals of Neurology. 62(2). 121–127. 33 indexed citations

Biancheri, Roberta, Enrico Bertini, Antonio Falace, et al.. (2006). POMGnT1 Mutations in Congenital Muscular Dystrophy. Archives of Neurology. 63(10). 1491–1491. 27 indexed citations

10.

Manno, G., Mario Cruciani, Luca Romano, et al.. (2005). Antimicrobial use and Pseudomonas aeruginosa susceptibility profile in a cystic fibrosis centre. International Journal of Antimicrobial Agents. 25(3). 193–197. 33 indexed citations

11.

Bruno, Claudio, Filippo M. Santorelli, Stefania Assereto, et al.. (2003). Progressive exercise intolerance associated with a new muscle‐restricted nonsense mutation (G142X) in the mitochondrial cytochrome b gene. Muscle & Nerve. 28(4). 508–511. 40 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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