Giuliana Galluzzi

2.8k total citations
26 papers, 1.6k citations indexed

About

Giuliana Galluzzi is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Giuliana Galluzzi has authored 26 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Cardiology and Cardiovascular Medicine and 10 papers in Cellular and Molecular Neuroscience. Recurrent topics in Giuliana Galluzzi's work include Muscle Physiology and Disorders (19 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (9 papers). Giuliana Galluzzi is often cited by papers focused on Muscle Physiology and Disorders (19 papers), Cardiomyopathy and Myosin Studies (13 papers) and Genetic Neurodegenerative Diseases (9 papers). Giuliana Galluzzi collaborates with scholars based in Italy, United States and France. Giuliana Galluzzi's co-authors include Enzo Ricci, Pietro Tonali, Massimiliano Mirabella, Giancarlo Deidda, Serenella Servidei, L. Felicetti, Gabriella Silvestri, Luca Colantoni, Giorgio Tasca and S. Cacurri and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Journal of the American College of Cardiology.

In The Last Decade

Giuliana Galluzzi

26 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giuliana Galluzzi Italy 19 1.4k 411 331 306 153 26 1.6k
K. Bushby United Kingdom 20 1.4k 1.0× 371 0.9× 303 0.9× 265 0.9× 170 1.1× 49 1.6k
Luca Bello Italy 21 1.0k 0.7× 249 0.6× 270 0.8× 285 0.9× 136 0.9× 84 1.4k
Sylvie Tuffery‐Giraud France 26 1.2k 0.9× 221 0.5× 432 1.3× 269 0.9× 307 2.0× 72 2.0k
Rita C.M. Pavanello Brazil 18 899 0.6× 254 0.6× 303 0.9× 210 0.7× 154 1.0× 50 1.0k
Barbara C. Byth Canada 9 1.1k 0.8× 167 0.4× 289 0.9× 287 0.9× 190 1.2× 14 1.2k
Anna Fidziańska Poland 25 1.8k 1.3× 802 2.0× 382 1.2× 481 1.6× 104 0.7× 121 2.3k
Karine Nguyen France 19 954 0.7× 243 0.6× 337 1.0× 235 0.8× 178 1.2× 59 1.3k
Joachim Schessl Germany 22 622 0.4× 265 0.6× 386 1.2× 165 0.5× 69 0.5× 43 1.2k
Maria Luisa Mostacciuolo Italy 22 764 0.5× 240 0.6× 521 1.6× 184 0.6× 125 0.8× 48 1.2k
C.S.M. Straathof Netherlands 18 728 0.5× 213 0.5× 154 0.5× 250 0.8× 78 0.5× 35 1.1k

Countries citing papers authored by Giuliana Galluzzi

Since Specialization
Citations

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

Fields of papers citing papers by Giuliana Galluzzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuliana Galluzzi

This figure shows the co-authorship network connecting the top 25 collaborators of Giuliana Galluzzi. A scholar is included among the top collaborators of Giuliana Galluzzi 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 Giuliana Galluzzi. Giuliana Galluzzi 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.
Pellegrino, Marsha, Sabrina Sacconi, Isabella Cascino, et al.. (2017). Estrogens enhance myoblast differentiation in facioscapulohumeral muscular dystrophy by antagonizing DUX4 activity. Journal of Clinical Investigation. 127(4). 1531–1545. 51 indexed citations
2.
Cascino, Isabella, Richard J.L.F. Lemmers, Giuliana Galluzzi, et al.. (2016). Allele-specific DNA hypomethylation characterises FSHD1 and FSHD2. Journal of Medical Genetics. 53(5). 348–355. 48 indexed citations
3.
Tasca, Giorgio, Mauro Monforte, Elisabetta Iannaccone, et al.. (2014). Upper Girdle Imaging in Facioscapulohumeral Muscular Dystrophy. PLoS ONE. 9(6). e100292–e100292. 66 indexed citations
4.
Pastorello, Ebe, Giovanni Vazza, Marta Miorin, et al.. (2009). Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample. Clinical Genetics. 75(6). 550–555. 106 indexed citations
5.
Spitali, Pietro, M. Fabris, Matteo Bovolenta, et al.. (2007). G.P.3.07 Intronic conserved non-coding sequences (CNSs) as a tool to detect non-coding RNAs (ncRNAs) and putative regulatory motifs within the dystrophin gene. Neuromuscular Disorders. 17(9-10). 784–784. 1 indexed citations
6.
Marca, Giacomo Della, Roberto Frusciante, Catello Vollono, et al.. (2007). Sleep quality in Facioscapulohumeral muscular dystrophy. Journal of the Neurological Sciences. 263(1-2). 49–53. 18 indexed citations
7.
Pescatori, Mario, Aldobrando Broccolini, Carlo Minetti, et al.. (2007). Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression. The FASEB Journal. 21(4). 1210–1226. 186 indexed citations
8.
Rossi, Mônica Lanzoni, Enzo Ricci, Luca Colantoni, et al.. (2007). The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure. BMC Medical Genetics. 8(1). 8–8. 23 indexed citations
9.
Trevisan, Carlo P., Ebe Pastorello, Mario Ermani, et al.. (2007). Facioscapulohumeral Muscular Dystrophy: A Multicenter Study on Hearing Function. Audiology and Neurotology. 13(1). 1–6. 33 indexed citations
10.
Trevisan, Carlo P., Ebe Pastorello, Mario Armani, et al.. (2006). Facioscapulohumeral Muscular Dystrophy and Occurrence of Heart Arrhythmia. European Neurology. 56(1). 1–5. 48 indexed citations
11.
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
12.
Giglio, Vincenzo, Vincenzo Pasceri, Fortunato Mangiola, et al.. (2003). Ultrasound tissue characterization detectspreclinical myocardial structural changes inchildren affected by Duchenne muscular dystrophy. Journal of the American College of Cardiology. 42(2). 309–316. 57 indexed citations
13.
Felicetti, L. & Giuliana Galluzzi. (2003). Pulse Field Gel Electrophoresis for the Detection of Facioscapulohumeral Muscular Dystrophy Gene Rearrangements. Neurogenetics. 217. 153–164. 2 indexed citations
14.
Uncini, Antonino, Giuliana Galluzzi, Antonio Di Muzio, et al.. (2002). Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement. Neuromuscular Disorders. 12(9). 874–877. 19 indexed citations
15.
Barletta, Marina Raffaele di, Enzo Ricci, Giuliana Galluzzi, et al.. (2000). Different Mutations in the LMNA Gene Cause Autosomal Dominant and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy. The American Journal of Human Genetics. 66(4). 1407–1412. 299 indexed citations
16.
Ricci, Enzo, Giuliana Galluzzi, Giancarlo Deidda, et al.. (1999). Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype. Annals of Neurology. 45(6). 751–757. 232 indexed citations
17.
18.
Cacurri, S., Giancarlo Deidda, Eliana Vigneti, et al.. (1998). Sequence Homology between 4qter and 10qter Loci Facilitates the Instability of Subtelomeric KpnI Repeat Units Implicated in Facioscapulohumeral Muscular Dystrophy. The American Journal of Human Genetics. 63(1). 181–190. 48 indexed citations
19.
Morrone, Amelia, Enrico Zammarchi, Peter C. Scacheri, et al.. (1997). Asymptomatic dystrophinopathy. American Journal of Medical Genetics. 69(3). 261–267. 30 indexed citations
20.
Cacurri, S., Giancarlo Deidda, Andrea Novelletto, et al.. (1994). Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral musculatur dystrophy (FSHD). Human Genetics. 94(4). 367–374. 12 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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