Stefania Aurino

979 total citations
23 papers, 707 citations indexed

About

Stefania Aurino is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Stefania Aurino has authored 23 papers receiving a total of 707 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Cellular and Molecular Neuroscience and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Stefania Aurino's work include Muscle Physiology and Disorders (15 papers), Genetic Neurodegenerative Diseases (7 papers) and Cardiomyopathy and Myosin Studies (6 papers). Stefania Aurino is often cited by papers focused on Muscle Physiology and Disorders (15 papers), Genetic Neurodegenerative Diseases (7 papers) and Cardiomyopathy and Myosin Studies (6 papers). Stefania Aurino collaborates with scholars based in Italy, United States and Türkiye. Stefania Aurino's co-authors include Vincenzo Nigro, Giulio Piluso, C. Angelini, Dirk Fischer, Rolf Schröder, Paolo Montuori, Mafalda Cacciottolo, Maria Triassi, Daniele Naviglio and Horst Urbach and has published in prestigious journals such as Neurology, Analytical Biochemistry and Annals of Neurology.

In The Last Decade

Stefania Aurino

23 papers receiving 694 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefania Aurino Italy 14 568 218 218 116 101 23 707
Lars Klinge Germany 17 643 1.1× 132 0.6× 160 0.7× 113 1.0× 120 1.2× 21 948
Rachel E. Thomson United States 12 704 1.2× 88 0.4× 56 0.3× 92 0.8× 138 1.4× 16 902
Mingxuan Xu United States 11 156 0.3× 112 0.5× 45 0.2× 99 0.9× 45 0.4× 24 555
M.P. Freda Italy 10 559 1.0× 157 0.7× 280 1.3× 87 0.8× 77 0.8× 11 616
Lidia González‐Quereda Spain 13 476 0.8× 119 0.5× 156 0.7× 109 0.9× 58 0.6× 35 540
Jesse M. Flynn United States 9 620 1.1× 77 0.4× 52 0.2× 81 0.7× 82 0.8× 9 734
R. Mein United Kingdom 12 617 1.1× 99 0.5× 171 0.8× 152 1.3× 75 0.7× 23 703
H Jedrzejowska Poland 12 172 0.3× 127 0.6× 65 0.3× 60 0.5× 42 0.4× 27 372
C. Scotton Italy 14 443 0.8× 84 0.4× 89 0.4× 65 0.6× 60 0.6× 20 541
Meriel McEntagart United Kingdom 14 273 0.5× 157 0.7× 101 0.5× 66 0.6× 41 0.4× 24 576

Countries citing papers authored by Stefania Aurino

Since Specialization
Citations

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

Fields of papers citing papers by Stefania Aurino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Aurino

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Aurino. A scholar is included among the top collaborators of Stefania Aurino 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 Stefania Aurino. Stefania Aurino 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.
Guglielmi, Valeria, Vincenzo Nigro, Manuela Malatesta, et al.. (2023). A novel in‐frame deletion in MYOT causes an early adult onset distal myopathy. Clinical Genetics. 104(6). 705–710. 4 indexed citations
2.
Tasca, Giorgio, Zagaa Odgerel, Mauro Monforte, et al.. (2012). Novel FLNC mutation in a patient with myofibrillar myopathy in combination with late‐onset cerebellar ataxia. Muscle & Nerve. 46(2). 275–282. 22 indexed citations
3.
Montuori, Paolo, et al.. (2012). Metals loads into the Mediterranean Sea: estimate of Sarno River inputs and ecological risk. Ecotoxicology. 22(2). 295–307. 52 indexed citations
4.
Piluso, Giulio, Francesca Del Vecchio Blanco, Annalaura Torella, et al.. (2011). Motor Chip: A Comparative Genomic Hybridization Microarray for Copy-Number Mutations in 245 Neuromuscular Disorders. Clinical Chemistry. 57(11). 1584–1596. 35 indexed citations
5.
Cacciottolo, Mafalda, Stefania Aurino, Francesco Mari, et al.. (2011). Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations. European Journal of Human Genetics. 19(9). 974–980. 65 indexed citations
6.
Roncarati, Roberta, Michael V.G. Latronico, Beatrice Musumeci, et al.. (2011). Unexpectedly low mutation rates in beta‐myosin heavy chain and cardiac myosin binding protein genes in italian patients with hypertrophic cardiomyopathy. Journal of Cellular Physiology. 226(11). 2894–2900. 13 indexed citations
7.
Kobayashi, Yvonne M., Luca D’Orsi, Stefania Aurino, et al.. (2011). Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex. Human Molecular Genetics. 20(23). 4644–4654. 29 indexed citations
8.
Nigro, Vincenzo, Stefania Aurino, & Giulio Piluso. (2011). Limb girdle muscular dystrophies. Current Opinion in Neurology. 24(5). 429–436. 59 indexed citations
9.
Bonnal, Raoul J.P., Marco Severgnini, Alessandra Castaldi, et al.. (2010). Reliable resequencing of the human dystrophin locus by universal long polymerase chain reaction and massive pyrosequencing. Analytical Biochemistry. 406(2). 176–184. 13 indexed citations
10.
Tammaro, Angela, Adele Bracco, Santolo Cozzolino, et al.. (2010). Novel missense mutations and unexpected multiple changes of RYR1 gene in 75 malignant hyperthermia families. Clinical Genetics. 79(5). 438–447. 29 indexed citations
11.
Santoro, Lucio, Maria Nolano, Chiara Fiorillo, et al.. (2010). Perioral skin biopsy to study skeletal muscle protein expression. Muscle & Nerve. 41(3). 392–398. 9 indexed citations
12.
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
13.
Piluso, Giulio, Valentina Saccone, Ettore Bismuto, et al.. (2009). A Missense Mutation in CASK Causes FG Syndrome in an Italian Family. The American Journal of Human Genetics. 84(2). 162–177. 71 indexed citations
14.
Aurino, Stefania, Göknur Haliloğlu, Beril Talim, et al.. (2006). Calpain-3 mutations in Turkey. European Journal of Pediatrics. 165(5). 293–298. 31 indexed citations
15.
Lanzillo, Roberta, Stefania Aurino, Francesco Vitale, et al.. (2006). Early onset calpainopathy with normal non-functional calpain 3 level. Developmental Medicine & Child Neurology. 48(4). 304–306. 10 indexed citations
16.
Aurino, Stefania & Vincenzo Nigro. (2006). Readthrough strategies for stop codons in Duchenne muscular dystrophy.. PubMed. 25(1). 5–12. 26 indexed citations
17.
Fischer, Dirk, Maggie C. Walter, K Kesper, et al.. (2005). Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs. Journal of Neurology. 252(5). 538–547. 103 indexed citations
18.
Balci, B., Ekkehard Wilichowski, Göknur Haliloğlu, et al.. (2004). Beta-sarcoglycan gene mutations in Turkey.. PubMed. 23(3). 154–8. 5 indexed citations
19.
Fischer, Dirk, Stefania Aurino, Vincenzo Nigro, & Rolf Schröder. (2003). On symptomatic heterozygous alpha‐sarcoglycan gene mutation carriers. Annals of Neurology. 54(5). 674–678. 8 indexed citations
20.
Tammaro, Angela, Adele Bracco, Santolo Cozzolino, et al.. (2003). Scanning for Mutations of the Ryanodine Receptor (RYR1) Gene by Denaturing HPLC: Detection of Three Novel Malignant Hyperthermia Alleles. Clinical Chemistry. 49(5). 761–768. 33 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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