Fabio Corsolini

1.5k total citations
54 papers, 1.0k citations indexed

About

Fabio Corsolini is a scholar working on Molecular Biology, Physiology and Cell Biology. According to data from OpenAlex, Fabio Corsolini has authored 54 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Molecular Biology, 29 papers in Physiology and 13 papers in Cell Biology. Recurrent topics in Fabio Corsolini's work include Lysosomal Storage Disorders Research (28 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Cellular transport and secretion (10 papers). Fabio Corsolini is often cited by papers focused on Lysosomal Storage Disorders Research (28 papers), Carbohydrate Chemistry and Synthesis (10 papers) and Cellular transport and secretion (10 papers). Fabio Corsolini collaborates with scholars based in Italy, United Kingdom and United States. Fabio Corsolini's co-authors include Mirella Filocamo, Stefano Regis, Marina Stroppiano, Barbara Tappino, Rosanna Gatti, Maja Di Rocco, Roberta Biancheri, Susanna Lualdi, Gloria Bonuccelli and Serena Grossi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and PLoS ONE.

In The Last Decade

Fabio Corsolini

54 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabio Corsolini Italy 21 545 507 245 227 155 54 1.0k
Maria Francisca Coutinho Portugal 13 437 0.8× 333 0.7× 201 0.8× 255 1.1× 67 0.4× 43 846
Stefano Regis Italy 22 521 1.0× 1.2k 2.3× 244 1.0× 317 1.4× 169 1.1× 57 1.9k
Elena L. Aronovich United States 19 388 0.7× 618 1.2× 222 0.9× 119 0.5× 389 2.5× 38 1.0k
Susanna Lualdi Italy 19 371 0.7× 376 0.7× 153 0.6× 106 0.5× 90 0.6× 25 690
Winnie Xin United States 18 348 0.6× 493 1.0× 121 0.5× 235 1.0× 146 0.9× 29 1.2k
Teresa Occhiodoro Australia 12 260 0.5× 577 1.1× 113 0.5× 130 0.6× 146 0.9× 14 937
Michie Shimmoto Japan 15 582 1.1× 407 0.8× 231 0.9× 292 1.3× 83 0.5× 44 918
Dominick Amato Canada 16 352 0.6× 341 0.7× 91 0.4× 262 1.2× 128 0.8× 42 1.1k
Hiroyuki Sonoda Japan 13 325 0.6× 305 0.6× 123 0.5× 109 0.5× 54 0.3× 37 723
Dao Pan United States 16 366 0.7× 437 0.9× 143 0.6× 127 0.6× 300 1.9× 40 871

Countries citing papers authored by Fabio Corsolini

Since Specialization
Citations

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

Fields of papers citing papers by Fabio Corsolini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabio Corsolini

This figure shows the co-authorship network connecting the top 25 collaborators of Fabio Corsolini. A scholar is included among the top collaborators of Fabio Corsolini 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 Fabio Corsolini. Fabio Corsolini 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.
Regis, Stefano, Silvia Bruno, Andrea Nicola Mazzarello, et al.. (2023). Effects of Deacetylase Inhibition on the Activation of the Antioxidant Response and Aerobic Metabolism in Cellular Models of Fanconi Anemia. Antioxidants. 12(5). 1100–1100. 6 indexed citations
2.
Bruno, Silvia, Cristina Capanni, Marta Columbaro, et al.. (2023). Altered Mitochondrial Dynamic in Lymphoblasts and Fibroblasts Mutated for FANCA-A Gene: The Central Role of DRP1. International Journal of Molecular Sciences. 24(7). 6557–6557. 3 indexed citations
3.
Fioredda, Francesca, Enrico Cappelli, Elena Palmisani, et al.. (2019). Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil. Blood Advances. 3(21). 3432–3435. 5 indexed citations
4.
Grossi, Serena, et al.. (2016). MLPA-based approach for initial and simultaneous detection of GBA deletions and recombinant alleles in patients affected by Gaucher Disease. Molecular Genetics and Metabolism. 119(4). 329–337. 4 indexed citations
5.
Ravera, Silvia, Carlo Dufour, Simone Cesaro, et al.. (2016). Evaluation of energy metabolism and calcium homeostasis in cells affected by Shwachman-Diamond syndrome. Scientific Reports. 6(1). 25441–25441. 38 indexed citations
6.
Regis, Stefano, Fabio Corsolini, Serena Grossi, et al.. (2013). Restoration of the Normal Splicing Pattern of the PLP1 Gene by Means of an Antisense Oligonucleotide Directed against an Exonic Mutation. PLoS ONE. 8(9). e73633–e73633. 12 indexed citations
7.
Grossi, Serena, Stefano Regis, Roberta Biancheri, et al.. (2011). Molecular Genetic Analysis of the PLP1 Gene in 38 Families with PLP1-related disorders: Identification and Functional Characterization of 11 Novel PLP1 Mutations. Orphanet Journal of Rare Diseases. 6(1). 40–40. 32 indexed citations
8.
Tappino, Barbara, Roberta Biancheri, Matthew Mort, et al.. (2010). Identification and characterization of 15 novel GALC gene mutations causing Krabbe disease. Human Mutation. 31(12). E1894–E1914. 90 indexed citations
9.
Regis, Stefano, Serena Grossi, Fabio Corsolini, Roberta Biancheri, & Mirella Filocamo. (2009). PLP1 gene duplication causes overexpression and alteration of the PLP/DM20 splicing balance in fibroblasts from Pelizaeus–Merzbacher disease patients. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1792(6). 548–554. 23 indexed citations
10.
Dardis, Andrea, Camillo Rosano, Patrizia Tarugi, et al.. (2009). Molecular analysis of NPC1 and NPC2 gene in 34 Niemann–Pick C Italian Patients: identification and structural modeling of novel mutations. Neurogenetics. 10(3). 229–239. 32 indexed citations
11.
Caroli, Francesco, Roberta Biancheri, Marco Seri, et al.. (2007). GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease. Clinical Genetics. 72(5). 427–433. 24 indexed citations
12.
Bicocchi, Maria Patrizia, Barbara R. Migeon, Mirella Pasino, et al.. (2005). Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A. European Journal of Human Genetics. 13(5). 635–640. 34 indexed citations
13.
Stroppiano, Marina, Fabio Corsolini, Maja Di Rocco, et al.. (2004). Screening of 25 Italian patients with Niemann-Pick a reveals fourteen new mutations, one common and thirteen private, inSMPD1. Human Mutation. 24(1). 105–105. 25 indexed citations
14.
Filocamo, Mirella, Stefano Regis, Fabio Corsolini, et al.. (2003). Expression studies of two novel in CIS‐mutations identified in an intermediate case of Hunter syndrome. American Journal of Medical Genetics Part A. 120A(1). 84–87. 13 indexed citations
15.
Regis, Stefano, et al.. (2003). An unusual arylsulfatase A pseudodeficiency allele carrying a splice site mutation in a metachromatic leukodystrophy patient. European Journal of Human Genetics. 12(2). 150–154. 9 indexed citations
16.
Filocamo, Mirella, Marina Stroppiano, Marco Seri, et al.. (2002). Analysis of the glucocerebrosidase gene and mutation profile in 144 Italian gaucher patients. Human Mutation. 20(3). 234–235. 50 indexed citations
17.
Bonuccelli, Gloria, Paola Di Natale, Fabio Corsolini, et al.. (2001). The effect of four mutations on the expression of iduronate-2-sulfatase in mucopolysaccharidosis type II. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1537(3). 233–238. 16 indexed citations
18.
Regis, Stefano, Mirella Filocamo, Roberto Cusano, et al.. (2001). Prenatal diagnosis of Pelizaeus‐Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR. Prenatal Diagnosis. 21(8). 668–671. 13 indexed citations
19.
Carrozzo, Romeo, Rossana Tonlorenzi, Fabio Corsolini, & Rosanna Gatti. (1996). Two New Nonsense mutations (Q80X; Q389X) in patients with severe hunter syndrome ( mucopolysaccharidosis type II). Human Mutation. 7(2). 184–185. 6 indexed citations
20.

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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