Vittorio Riso

629 total citations
15 papers, 393 citations indexed

About

Vittorio Riso is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Vittorio Riso has authored 15 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Vittorio Riso's work include Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (7 papers) and DNA Repair Mechanisms (3 papers). Vittorio Riso is often cited by papers focused on Genetic Neurodegenerative Diseases (10 papers), Mitochondrial Function and Pathology (7 papers) and DNA Repair Mechanisms (3 papers). Vittorio Riso collaborates with scholars based in Italy, United States and Switzerland. Vittorio Riso's co-authors include Andrea Riccio, Marco Giordano, Dina Bellizzi, Giuseppe Passarino, Patrizia D’Aquila, Gabriella Silvestri, Filippo M. Santorelli, Salvatore Rossi, Alessandra Tessa and Raffaele Iorio and has published in prestigious journals such as Journal of Neurology, European Journal of Neurology and Frontiers in Neurology.

In The Last Decade

Vittorio Riso

15 papers receiving 387 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vittorio Riso Italy 9 284 110 80 48 40 15 393
Ichraf Kraoua Tunisia 9 112 0.4× 50 0.5× 111 1.4× 45 0.9× 29 0.7× 64 270
Eduardo López‐Laso Spain 12 224 0.8× 93 0.8× 54 0.7× 141 2.9× 19 0.5× 40 453
Daniele Frattini Italy 13 162 0.6× 168 1.5× 74 0.9× 40 0.8× 110 2.8× 59 464
Mika H. Martikainen Finland 13 205 0.7× 95 0.9× 130 1.6× 135 2.8× 42 1.1× 34 418
I. Desguerre France 12 194 0.7× 41 0.4× 33 0.4× 111 2.3× 40 1.0× 37 400
Ching-Shiang Chi Taiwan 9 173 0.6× 126 1.1× 100 1.3× 30 0.6× 13 0.3× 12 487
Celeste Panteghini Italy 13 133 0.5× 79 0.7× 118 1.5× 65 1.4× 106 2.6× 25 329
Mara Lúcia Schmitz Ferreira Santos Brazil 8 101 0.4× 31 0.3× 70 0.9× 57 1.2× 22 0.6× 37 276
Itxaso Martì Spain 8 125 0.4× 68 0.6× 344 4.3× 24 0.5× 35 0.9× 20 534
Kurt Schlachter Austria 8 77 0.3× 79 0.7× 59 0.7× 68 1.4× 14 0.3× 12 346

Countries citing papers authored by Vittorio Riso

Since Specialization
Citations

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

Fields of papers citing papers by Vittorio Riso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vittorio Riso

This figure shows the co-authorship network connecting the top 25 collaborators of Vittorio Riso. A scholar is included among the top collaborators of Vittorio Riso 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 Vittorio Riso. Vittorio Riso 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.
Riso, Vittorio, Tommaso Nicoletti, Salvatore Rossi, et al.. (2022). Neurological Erdheim–Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature. Brain Sciences. 13(1). 26–26. 2 indexed citations
2.
Damato, Valentina, Gregorio Spagni, Amelia Evoli, et al.. (2021). Clinical features and outcome of patients with autoimmune cerebellar ataxia evaluated with the Scale for the Assessment and Rating of Ataxia. European Journal of Neurology. 29(2). 564–572. 11 indexed citations
3.
Miele, Luca, Alessia Perna, Maria Assunta Zocco, et al.. (2021). Clinical characteristics of metabolic associated fatty liver disease (MAFLD) in subjects with myotonic dystrophy type 1 (DM1). Digestive and Liver Disease. 53(11). 1451–1457. 3 indexed citations
4.
Donato, Ilaria Di, Antonio Gallo, Ivana Ricca, et al.. (2021). POLR3A variants in hereditary spastic paraparesis and ataxia: clinical, genetic, and neuroradiological findings in a cohort of Italian patients. Neurological Sciences. 43(2). 1071–1077. 9 indexed citations
5.
Michele, Giovanna De, Daniele Galatolo, Serena Galosi, et al.. (2021). Episodic ataxia and severe infantile phenotype in spinocerebellar ataxia type 14: expansion of the phenotype and novel mutations. Journal of Neurology. 269(3). 1476–1484. 5 indexed citations
6.
Riso, Vittorio, Daniele Galatolo, Melissa Barghigiani, et al.. (2021). A next generation sequencing‐based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21. European Journal of Neurology. 28(8). 2784–2788. 6 indexed citations
7.
Riso, Vittorio, Salvatore Rossi, Tommaso Nicoletti, et al.. (2021). Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center Experience. Brain Sciences. 11(2). 246–246. 10 indexed citations
8.
Santoro, Massimo, Alessia Perna, Piergiorgio La Rosa, et al.. (2020). Compound heterozygosity for an expanded (GAA) and a (GAAGGA) repeat at FXN locus: from a diagnostic pitfall to potential clues to the pathogenesis of Friedreich ataxia. Neurogenetics. 21(4). 279–287. 3 indexed citations
9.
Luigetti, Marco, Raffaele Iorio, Anna Rita Bentivoglio, et al.. (2020). Assessment of neurological manifestations in hospitalized patients with COVID‐19. European Journal of Neurology. 27(11). 2322–2328. 36 indexed citations
10.
Lupo, Michela, Giusy Olivito, Silvia Clausi, et al.. (2020). Cerebello-Cortical Alterations Linked to Cognitive and Social Problems in Patients With Spastic Paraplegia Type 7: A Preliminary Study. Frontiers in Neurology. 11. 82–82. 21 indexed citations
11.
Perna, Alessia, Daria Maccora, Salvatore Rossi, et al.. (2020). High Prevalence and Gender-Related Differences of Gastrointestinal Manifestations in a Cohort of DM1 Patients: A Perspective, Cross-Sectional Study. Frontiers in Neurology. 11. 394–394. 20 indexed citations
12.
Riso, Vittorio, Salvatore Rossi, Alessia Perna, et al.. (2020). NGS-based detection of a novel mutation in PRKCG (SCA14) in sporadic adult-onset ataxia plus dystonic tremor. Neurological Sciences. 41(10). 2989–2991. 4 indexed citations
13.
Cocozza, Sirio, Giuseppe Pontillo, Giovanna De Michele, et al.. (2020). The “crab sign”: an imaging feature of spinocerebellar ataxia type 48. Neuroradiology. 62(9). 1095–1103. 12 indexed citations
14.
Lieto, Maria, Vittorio Riso, Daniele Galatolo, et al.. (2019). The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families. European Journal of Neurology. 27(3). 498–505. 40 indexed citations
15.
Bellizzi, Dina, Patrizia D’Aquila, Marco Giordano, et al.. (2013). The Control Region of Mitochondrial DNA Shows an Unusual CpG and Non-CpG Methylation Pattern. DNA Research. 20(6). 537–547. 211 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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