E. Mancinelli

1.0k total citations
28 papers, 807 citations indexed

About

E. Mancinelli is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, E. Mancinelli has authored 28 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 25 papers in Cellular and Molecular Neuroscience and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in E. Mancinelli's work include Ion channel regulation and function (12 papers), Genetic Neurodegenerative Diseases (12 papers) and Muscle Physiology and Disorders (9 papers). E. Mancinelli is often cited by papers focused on Ion channel regulation and function (12 papers), Genetic Neurodegenerative Diseases (12 papers) and Muscle Physiology and Disorders (9 papers). E. Mancinelli collaborates with scholars based in Italy, United States and France. E. Mancinelli's co-authors include G. Meola, Rosanna Cardani, Valeria Sansone, G Rotondo, Enzo Wanke, A Ferroni, Renata Zippel, Andrea Ciammola, Vincenzo Silani and Jenny Sassone and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and The Journal of Physiology.

In The Last Decade

E. Mancinelli

28 papers receiving 795 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. Mancinelli Italy 17 651 585 131 107 55 28 807
Ruth Rea United Kingdom 8 597 0.9× 444 0.8× 72 0.5× 110 1.0× 100 1.8× 10 730
Marie K. Bondulich United Kingdom 11 582 0.9× 578 1.0× 181 1.4× 31 0.3× 62 1.1× 17 766
Stephan Grueninger Switzerland 10 473 0.7× 479 0.8× 127 1.0× 71 0.7× 29 0.5× 11 600
Seth F. Oliveria United States 8 387 0.6× 287 0.5× 59 0.5× 78 0.7× 35 0.6× 12 553
Chi S. Ho United States 12 395 0.6× 330 0.6× 41 0.3× 88 0.8× 105 1.9× 16 580
John J. Kleiderlein United States 6 565 0.9× 349 0.6× 351 2.7× 49 0.5× 123 2.2× 6 911
Steven K. Harmon United States 9 436 0.7× 427 0.7× 63 0.5× 19 0.2× 38 0.7× 11 625
Johanna Duda Germany 10 276 0.4× 279 0.5× 186 1.4× 34 0.3× 21 0.4× 12 528
Erik Boddeke Netherlands 14 352 0.5× 244 0.4× 62 0.5× 33 0.3× 43 0.8× 15 752
Kathryn Miles United States 14 665 1.0× 383 0.7× 17 0.1× 64 0.6× 74 1.3× 21 890

Countries citing papers authored by E. Mancinelli

Since Specialization
Citations

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

Fields of papers citing papers by E. Mancinelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

This figure shows the co-authorship network connecting the top 25 collaborators of E. Mancinelli. A scholar is included among the top collaborators of E. Mancinelli 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. Mancinelli. E. Mancinelli 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.
Rusconi, Francesco, E. Mancinelli, Graziano Colombo, et al.. (2010). Proteome profile in Myotonic Dystrophy type 2 myotubes reveals dysfunction in protein processing and mitochondrial pathways. Neurobiology of Disease. 38(2). 273–280. 16 indexed citations
2.
Meola, G., Valeria Sansone, G Rotondo, & E. Mancinelli. (2009). Muscle biopsy and cell cultures: potential diagnostic tools in hereditary skeletal muscle channelopathies. European Journal of Histochemistry. 47(1). 17–17. 4 indexed citations
3.
Cardani, Rosanna, E. Mancinelli, Marzia Giagnacovo, Valeria Sansone, & G. Meola. (2009). Ribonuclear inclusions as biomarker of myotonic dystrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies. European Journal of Histochemistry. 53(2). 13–13. 14 indexed citations
4.
Cardani, Rosanna, Annalisa Botta, Fabrizio Rinaldi, et al.. (2009). Ribonuclear inclusions and MBNL1 nuclear sequestration do not affect myoblast differentiation but alter gene splicing in myotonic dystrophy type 2. Neuromuscular Disorders. 19(5). 335–343. 26 indexed citations
5.
Cardani, Rosanna, E. Mancinelli, Valeria Sansone, G Rotondo, & G. Meola. (2009). Biomolecular identification of (CCTG)n mutation in myotonic dystrophy type 2 (DM2) by FISH on muscle biopsy. European Journal of Histochemistry. 48(4). 437–437. 45 indexed citations
6.
Perdoni, Federica, Manuela Malatesta, Rosanna Cardani, et al.. (2009). RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study. European Journal of Histochemistry. 53(3). 18–18. 31 indexed citations
7.
Lucchiari, Sabrina, Serena Pagliarani, Stefania Corti, et al.. (2008). Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion. Journal of the Neurological Sciences. 275(1-2). 159–163. 9 indexed citations
8.
Tricarico, Domenico, Antonietta Mele, G Rotondo, et al.. (2008). Acetazolamide prevents vacuolar myopathy in skeletal muscle of K+‐depleted rats. British Journal of Pharmacology. 154(1). 183–190. 26 indexed citations
9.
Cardani, Rosanna, E. Mancinelli, Greta Saino, Luigi Bonavina, & G. Meola. (2008). A putative role of ribonuclear inclusions and MBNL1 in the impairment of gallbladder smooth muscle contractility with cholelithiasis in myotonic dystrophy type 1. Neuromuscular Disorders. 18(8). 641–645. 16 indexed citations
10.
Sassone, Jenny, Andrea Ciammola, Cinzia Tiloca, et al.. (2007). Apoptosis induced by proteasome inhibition in human myoblast cultures.. SHILAP Revista de lepidopterología. 50(2). 109–18. 4 indexed citations
11.
Ciammola, Andrea, Jenny Sassone, Luisella Alberti, et al.. (2006). Increased apoptosis, huntingtin inclusions and altered differentiation in muscle cell cultures from Huntington's disease subjects. Cell Death and Differentiation. 13(12). 2068–2078. 75 indexed citations
12.
Botta, Annalisa, Fabrizio Rinaldi, E. Bonifazi, et al.. (2006). Gene Expression Analysis in Myotonic Dystrophy: Indications for a Common Molecular Pathogenic Pathway in DM1 and DM2. Gene Expression. 13(6). 339–351. 38 indexed citations
13.
Vihola, Anna, Guillaume Bassez, G. Meola, et al.. (2003). Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology. 60(11). 1854–1857. 125 indexed citations
14.
Tonini, Raffaella, Silvana Franceschetti, Daniela Parolaro, et al.. (2001). Involvement of CDC25Mm/Ras-GRF1-Dependent Signaling in the Control of Neuronal Excitability. Molecular and Cellular Neuroscience. 18(6). 691–701. 22 indexed citations
15.
Tonini, Raffaella, E. Mancinelli, Michele Mazzanti, et al.. (1999). Expression of Ras‐GRF in the SK‐N‐BE neuroblastoma accelerates retinoic‐acid‐induced neuronal differentiation and increases the functional expression of the IRK1 potassium channel. European Journal of Neuroscience. 11(3). 959–966. 24 indexed citations
16.
Wanke, Enzo, Laura Bianchi, Massimo Mantegazza, et al.. (1994). Muscarinic Regulation of Ca2+ Currents in Rat Sensory Neurons: Channel and Receptor Types, Dose ‐ response Relationships and Cross‐talk Pathways. European Journal of Neuroscience. 6(3). 381–391. 35 indexed citations
17.
Meola, G., et al.. (1991). Increased acetylcholine sensitivity in Duchenne muscular dystrophy myotubes. Neurological Sciences. 12(2). 181–185. 2 indexed citations
18.
Mancinelli, E., Alessandro Sardini, G. Meola, et al.. (1989). Properties of acetylcholine-receptor activation in human Duchenne muscular dystrophy myotubes. Proceedings of the Royal Society of London. Series B, Biological sciences. 237(1287). 247–257. 6 indexed citations
19.
Ferroni, A, et al.. (1989). Two high voltage-activated calcium currents are present in isolation in adult rat spinal neurons. Biochemical and Biophysical Research Communications. 159(2). 379–384. 10 indexed citations
20.
Mancinelli, E., et al.. (1986). Duchenne muscular dystrophy (DMD): Altered acetylcholine (ACh) sensitivity in human myotubes in culture. Cell Biology International Reports. 10(3). 208–208. 2 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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