E. Menegazzo

793 total citations
15 papers, 570 citations indexed

About

E. Menegazzo is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, E. Menegazzo has authored 15 papers receiving a total of 570 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Cellular and Molecular Neuroscience, 10 papers in Molecular Biology and 8 papers in Neurology. Recurrent topics in E. Menegazzo's work include Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (6 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). E. Menegazzo is often cited by papers focused on Genetic Neurodegenerative Diseases (12 papers), Mitochondrial Function and Pathology (6 papers) and Parkinson's Disease Mechanisms and Treatments (6 papers). E. Menegazzo collaborates with scholars based in Italy, United States and Spain. E. Menegazzo's co-authors include C. Angelini, Massimo Gennarelli, Eric P. Hoffman, Giuseppe Novelli, Bruno Dallapiccola, Jianzhou Wang, Elena Pegoraro, Francesco Mari, Antonio Pizzuti and Maria Luisa Mostacciuolo and has published in prestigious journals such as Journal of the American College of Cardiology, Biological Psychiatry and Human Molecular Genetics.

In The Last Decade

E. Menegazzo

15 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
E. Menegazzo Italy 11 456 432 224 83 33 15 570
Marbella Quiñonez United States 12 182 0.4× 342 0.8× 19 0.1× 141 1.7× 37 1.1× 26 427
G Chauplannaz France 9 142 0.3× 302 0.7× 425 1.9× 29 0.3× 22 0.7× 27 661
Lea Leonardis Slovenia 11 157 0.3× 160 0.4× 196 0.9× 9 0.1× 17 0.5× 27 462
Elisabetta Bucci Italy 12 271 0.6× 174 0.4× 229 1.0× 41 0.5× 18 0.5× 23 404
Michiel R. Fokkens Netherlands 9 176 0.4× 206 0.5× 64 0.3× 30 0.4× 25 0.8× 11 312
Manlio Giacanelli Italy 10 288 0.6× 297 0.7× 142 0.6× 36 0.4× 29 0.9× 14 403
D.E. Wilcox United Kingdom 8 165 0.4× 250 0.6× 60 0.3× 48 0.6× 30 0.9× 10 286
Jihong Qu United States 13 433 0.9× 672 1.6× 33 0.1× 741 8.9× 26 0.8× 17 1.0k
Maria Laura Ester Bianchi Italy 12 248 0.5× 220 0.5× 155 0.7× 27 0.3× 8 0.2× 17 383
Matthew Wicklund United States 12 127 0.3× 223 0.5× 111 0.5× 74 0.9× 29 0.9× 34 412

Countries citing papers authored by E. Menegazzo

Since Specialization
Citations

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

Fields of papers citing papers by E. Menegazzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of E. Menegazzo

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

All Works

15 of 15 papers shown
1.
Gennarelli, Massimo, Paola Amicucci, C. Angelini, et al.. (1999). Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients. Neuromuscular Disorders. 9(4). 215–219. 10 indexed citations
2.
Perini, Giulia, E. Menegazzo, Mario Ermani, et al.. (1999). Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients. Biological Psychiatry. 46(3). 425–431. 56 indexed citations
3.
Marcon, Michela, Chiara Briani, Mario Ermani, et al.. (1998). Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patients. Neurological Sciences. 19(2). 75–80. 13 indexed citations
4.
Angelini, C., Francesco Mari, E. Menegazzo, et al.. (1998). Homozygous ?-sarcoglycan mutation in two siblings: One asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient. Muscle & Nerve. 21(6). 769–775. 51 indexed citations
5.
Guglielmi, M., E. Menegazzo, Michel A. Aegerter, et al.. (1998). Sol-Gel Deposited Sb-Doped Tin Oxide Films. Journal of Sol-Gel Science and Technology. 13(1-3). 679–683. 21 indexed citations
6.
Perini, Giulia, E. Menegazzo, Emilia Ferruzza, et al.. (1997). Cognitive dysfunction and brain imaging (SPET, PET) in genetically defined myotonic dystrophy (DM) patients. Biological Psychiatry. 42(1). 65S–65S. 2 indexed citations
7.
Gennarelli, Massimo, Giuseppe Novelli, Loreto Martorell, et al.. (1996). Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats. American Journal of Medical Genetics. 65(4). 342–347. 64 indexed citations
8.
Mastrogiacomo, I., et al.. (1996). Clinical and hormonal aspects of male hypogonadism in myotonic dystrophy. Neurological Sciences. 17(1). 59–65. 18 indexed citations
9.
Menegazzo, E., et al.. (1996). QUALITY IN MANAGEMENT OF BIOMEDICAL EQUIPMENT. Journal of Clinical Engineering. 21(2). 108–113. 2 indexed citations
10.
Melacini, Paola, C Villanova, E. Menegazzo, et al.. (1995). Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy. Journal of the American College of Cardiology. 25(1). 239–245. 92 indexed citations
11.
Novelli, Giuseppe, Massimo Gennarelli, E. Menegazzo, C. Angelini, & Bruno Dallapiccola. (1995). Discordant clinical outcome in myotonic dystrophy relatives showing (CTG) > 700 repeats. Neuromuscular Disorders. 5(2). 157–159. 19 indexed citations
12.
Wang, Jianzhou, Elena Pegoraro, E. Menegazzo, et al.. (1995). Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation. Human Molecular Genetics. 4(4). 599–606. 148 indexed citations
13.
Mastrogiacomo, I., Giuseppe Novelli, C. Angelini, et al.. (1994). Male Hypogonadism in Myotonic Dystrophy is Related to (Ctg)N Triplet Mutation. Journal of Endocrinological Investigation. 17(5). 381–383. 26 indexed citations
14.
Novelli, Giuseppe, Massimo Gennarelli, E. Menegazzo, et al.. (1993). (CTG)n Triplet Mutation and Phenotype Manifestations in Myotonic Dystrophy Patients. Biochemical Medicine and Metabolic Biology. 50(1). 85–92. 47 indexed citations
15.
Angelini, C., et al.. (1993). Multifactorial study of inflammatory myopathies. Report of 29 cases. Neurological Sciences. 14(1). 69–76. 1 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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