Elide Mantuano

1.8k total citations
48 papers, 1.3k citations indexed

About

Elide Mantuano is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Elide Mantuano has authored 48 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 21 papers in Cellular and Molecular Neuroscience and 9 papers in Neurology. Recurrent topics in Elide Mantuano's work include Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (9 papers) and Neurological disorders and treatments (7 papers). Elide Mantuano is often cited by papers focused on Genetic Neurodegenerative Diseases (18 papers), Mitochondrial Function and Pathology (9 papers) and Neurological disorders and treatments (7 papers). Elide Mantuano collaborates with scholars based in Italy, United Kingdom and United States. Elide Mantuano's co-authors include Liana Veneziano, Marina Frontali, Carla Jodice, Rosa Maria Corbo, Flavia Trettel, Anna Villa, Dario Strina, Paolo Macchi, M. Spadaro and Luigi D. Notarangelo and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Scientific Reports.

In The Last Decade

Elide Mantuano

47 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elide Mantuano Italy 18 644 534 193 175 161 48 1.3k
Leon Kohen Germany 28 1.1k 1.7× 293 0.5× 56 0.3× 53 0.3× 127 0.8× 73 1.9k
Xiaoping Wu United States 21 644 1.0× 244 0.5× 66 0.3× 44 0.3× 142 0.9× 41 1.2k
Makoto Hamanoue Japan 19 543 0.8× 472 0.9× 76 0.4× 46 0.3× 202 1.3× 34 1.4k
Vı́ctor Volpini Spain 23 605 0.9× 532 1.0× 395 2.0× 44 0.3× 35 0.2× 45 1.2k
Astrid Speer Germany 17 633 1.0× 149 0.3× 132 0.7× 40 0.2× 127 0.8× 24 1.1k
Marta Segarra Germany 19 495 0.8× 211 0.4× 62 0.3× 47 0.3× 165 1.0× 24 1.1k
Pearl S. Rosenbaum United States 18 740 1.1× 196 0.4× 90 0.5× 239 1.4× 89 0.6× 34 1.4k
Bettina Brunner Germany 8 537 0.8× 225 0.4× 430 2.2× 102 0.6× 204 1.3× 13 1.4k
Pamela G. Galloway United States 14 349 0.5× 189 0.4× 294 1.5× 46 0.3× 103 0.6× 29 1.0k
Shuji Wakatsuki Japan 18 728 1.1× 496 0.9× 105 0.5× 38 0.2× 72 0.4× 39 1.4k

Countries citing papers authored by Elide Mantuano

Since Specialization
Citations

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

Fields of papers citing papers by Elide Mantuano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elide Mantuano

This figure shows the co-authorship network connecting the top 25 collaborators of Elide Mantuano. A scholar is included among the top collaborators of Elide Mantuano 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 Elide Mantuano. Elide Mantuano 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.
Scarabino, Daniela, Liana Veneziano, Suran Nethisinghe, et al.. (2024). Unusual Age‐Dependent Behavior of Leukocytes Telomere Length in Friedreich's Ataxia. Movement Disorders. 39(11). 2058–2066. 2 indexed citations
2.
Mangano, Giuseppe Donato, Elide Mantuano, Liana Veneziano, et al.. (2023). Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow‐up study. Headache The Journal of Head and Face Pain. 63(7). 889–898. 4 indexed citations
3.
Scarabino, Daniela, Liana Veneziano, Alessia Fiore, et al.. (2022). Leukocyte Telomere Length Variability as a Potential Biomarker in Patients with PolyQ Diseases. Antioxidants. 11(8). 1436–1436. 4 indexed citations
4.
Thust, Stefanie, Liana Veneziano, Michael Parkinson, et al.. (2022). Altered pituitary morphology as a sign of benign hereditary chorea caused by TITF1/NKX2.1 mutations. Neurogenetics. 23(2). 91–102. 4 indexed citations
5.
Giunti, Paola, Elide Mantuano, & Marina Frontali. (2020). Episodic Ataxias: Faux or Real?. International Journal of Molecular Sciences. 21(18). 6472–6472. 8 indexed citations
6.
Soligo, Marzia, et al.. (2020). Construction and preliminary characterization of human recombinant proNGF-A variant. Neurochemistry International. 140. 104812–104812. 2 indexed citations
7.
Scarabino, Daniela, Elisabetta Broggio, Giuseppe Gambina, et al.. (2020). Relationship between proinflammatory cytokines (Il-1beta, Il-18) and leukocyte telomere length in mild cognitive impairment and Alzheimer's disease. Experimental Gerontology. 136. 110945–110945. 41 indexed citations
8.
Giunti, Paola, Elide Mantuano, Marina Frontali, & Liana Veneziano. (2015). Molecular mechanism of Spinocerebellar Ataxia type 6: glutamine repeat disorder, channelopathy and transcriptional dysregulation. The multifaceted aspects of a single mutation. Frontiers in Cellular Neuroscience. 9. 36–36. 24 indexed citations
9.
Provenzano, Claudia, Liana Veneziano, Elide Mantuano, et al.. (2015). Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea. Journal of the Neurological Sciences. 360. 78–83. 7 indexed citations
10.
Panichi, Vincenzo, Alberto Rosati, Roberto Bigazzi, et al.. (2011). Anaemia and resistance to erythropoiesis-stimulating agents as prognostic factors in haemodialysis patients: results from the RISCAVID study. Nephrology Dialysis Transplantation. 26(8). 2641–2648. 110 indexed citations
11.
Panichi, Vincenzo, Giovanni Manca Rizza, Daniele Taccola, et al.. (2005). C-reactive protein in patients on chronic hemodialysis with different techniques and different membranes. Biomedicine & Pharmacotherapy. 60(1). 14–17. 11 indexed citations
12.
Mantuano, Elide, Liana Veneziano, Carla Jodice, & Marina Frontali. (2003). Spinocerebellar ataxia type 6 and episodic ataxia type 2: differences and similarities between two allelic disorders. Cytogenetic and Genome Research. 100(1-4). 147–153. 33 indexed citations
13.
Wengler, Georg S., Maurilia Fiorini, Patrizia Mella, et al.. (1998). Mutation analysis by a non‐radioactive single‐strand conformation polymorphism assay in nine families with X‐linked severe combined immunodeficiency (SCIDX1). British Journal of Haematology. 101(3). 582–587. 9 indexed citations
14.
Scacchi, R., Laura Bernardini, Elide Mantuano, et al.. (1998). DNA Polymorphisms of Apolipoprotein B and Angiotensin I-Converting Enzyme Genes and Relationships with Lipid Levels in Italian Patients with Vascular Dementia or Alzheimer’s Disease. Dementia and Geriatric Cognitive Disorders. 9(4). 186–190. 59 indexed citations
15.
16.
Villa, Anna, Luigi D. Notarangelo, Paolo Macchi, et al.. (1995). X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene. Nature Genetics. 9(4). 414–417. 203 indexed citations
17.
Mantuano, Elide, Fabio Candotti, Silvia Giliani, et al.. (1993). Analysis of X-chromosome inactivation in bone marrow precursors from carriers of Wiskott-Aldrich syndrome and X-linked severe combined immunodeficiency: evidence that the Wiskott-Aldrich gene is expressed prior to granulocyte-macrophage colony-forming-unit.. PubMed. 4(1-4). 271–6. 9 indexed citations
18.
Notarangelo, L. D., Fabio Candotti, Ornella Parolini, et al.. (1993). Application of Molecular Analysis to Genetic Counseling in the Wiskott–Aldrich Syndrome (WAS). DNA and Cell Biology. 12(7). 645–649. 3 indexed citations
19.
Palmarino, R., Elide Mantuano, & P. Lucarelli. (1988). Genetic Variations of Insulin-Like Growth Factor I in Italy. Human Heredity. 38(3). 186–188. 2 indexed citations
20.
Lucarelli, P., et al.. (1988). Evidence for linkage equilibrium between two RFLPs associated with the human SST locus. Human Genetics. 78(3). 291–292. 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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