Salvatore Rossi

1.2k total citations
25 papers, 201 citations indexed

About

Salvatore Rossi is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Salvatore Rossi has authored 25 papers receiving a total of 201 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Cellular and Molecular Neuroscience, 16 papers in Molecular Biology and 9 papers in Neurology. Recurrent topics in Salvatore Rossi's work include Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (11 papers) and Hereditary Neurological Disorders (6 papers). Salvatore Rossi is often cited by papers focused on Genetic Neurodegenerative Diseases (13 papers), Mitochondrial Function and Pathology (11 papers) and Hereditary Neurological Disorders (6 papers). Salvatore Rossi collaborates with scholars based in Italy, Lebanon and Switzerland. Salvatore Rossi's co-authors include Gabriella Silvestri, Alessia Perna, Vittorio Riso, Tommaso Nicoletti, Giovanna De Michele, Maria Laura Ester Bianchi, Ângela Romano, Melissa Barghigiani, Mario Sabatelli and Filippo M. Santorelli and has published in prestigious journals such as Neurology, International Journal of Molecular Sciences and Journal of Hepatology.

In The Last Decade

Salvatore Rossi

21 papers receiving 201 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Salvatore Rossi Italy 8 144 142 67 24 16 25 201
Melissa Barghigiani Italy 8 147 1.0× 125 0.9× 38 0.6× 34 1.4× 32 2.0× 18 204
Jiaxi Yu China 8 170 1.2× 182 1.3× 99 1.5× 20 0.8× 19 1.2× 20 269
Ullrich Wuellner Germany 6 188 1.3× 212 1.5× 72 1.1× 16 0.7× 6 0.4× 9 289
João Vasconcelos Portugal 12 246 1.7× 209 1.5× 97 1.4× 9 0.4× 12 0.8× 30 293
Lauren R. Moore United States 5 287 2.0× 303 2.1× 91 1.4× 14 0.6× 15 0.9× 6 360
Reyes Claramunt Spain 6 120 0.8× 108 0.8× 29 0.4× 30 1.3× 48 3.0× 11 217
Massimo Plumari Italy 5 76 0.5× 107 0.8× 27 0.4× 16 0.7× 10 0.6× 10 127
Rosanna Trovato Italy 6 79 0.5× 146 1.0× 20 0.3× 22 0.9× 15 0.9× 20 201
Futoshi Aoike Japan 5 185 1.3× 257 1.8× 37 0.6× 13 0.5× 16 1.0× 7 287
Ari Siitonen Finland 8 77 0.5× 130 0.9× 98 1.5× 14 0.6× 33 2.1× 10 224

Countries citing papers authored by Salvatore Rossi

Since Specialization
Citations

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

Fields of papers citing papers by Salvatore Rossi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Salvatore Rossi

This figure shows the co-authorship network connecting the top 25 collaborators of Salvatore Rossi. A scholar is included among the top collaborators of Salvatore Rossi 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 Salvatore Rossi. Salvatore Rossi 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.
Brunetti, Valerio, Salvatore Rossi, Enrico Di Stasio, et al.. (2025). Prevalence and Clinical Correlates of Sleep Disorders in RFC1‐Spectrum Disorders: A Cross‐Sectional Study. Movement Disorders. 40(9). 1990–1995.
2.
Rossi, Salvatore, Tommaso Nicoletti, Ludovico Luca Sicignano, et al.. (2025). Prevalence and Clinical Correlates of Cerebrovascular Alterations in Fabry Disease: A Cross-Sectional Study. Brain Sciences. 15(2). 166–166.
3.
Rossi, Salvatore, Andrea Martinuzzi, Olimpia Musumeci, et al.. (2025). STOP-HSP.net: An Italian formal registry for clinical trial readiness in hereditary spastic paraplegias. Neurological Sciences. 46(6). 2839–2842.
4.
Galatolo, Daniele, Rosanna Trovato, Salvatore Rossi, et al.. (2023). Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice. Neurogenetics. 24(3). 147–160. 3 indexed citations
5.
Rossi, Salvatore, Daniela Orteschi, Paola Concolino, et al.. (2023). Triple Genetic Diagnosis in a Patient with Late-Onset Leukodystrophy and Mild Intellectual Disability. International Journal of Molecular Sciences. 25(1). 495–495. 1 indexed citations
6.
Rossi, Salvatore & Gabriella Silvestri. (2023). Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1). International Journal of Molecular Sciences. 24(3). 2204–2204. 4 indexed citations
7.
Luigetti, Marco, Andrea Di Paolantonio, Valeria Guglielmino, et al.. (2022). Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience. Neurological Sciences. 43(4). 2845–2848. 24 indexed citations
8.
Nicoletti, Tommaso, Salvatore Rossi, Maria Gabriella Vita, et al.. (2022). Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1). Journal of Neurology. 269(9). 5085–5092. 6 indexed citations
9.
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
10.
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
11.
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
12.
Luigetti, Marco, Ângela Romano, Andrea Di Paolantonio, et al.. (2020). Pathological Findings in Chronic Inflammatory Demyelinating Polyradiculoneuropathy: A Single-Center Experience. Brain Sciences. 10(6). 383–383. 7 indexed citations
13.
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
14.
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
15.
Rossi, Salvatore, et al.. (2019). Spectral domain optical coherence tomography findings in myotonic dystrophy. Neuromuscular Disorders. 30(2). 144–150. 8 indexed citations
16.
Rossi, Salvatore, Giacomo Della Marca, Martina Ricci, et al.. (2019). Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study. Journal of the Neurological Sciences. 399. 118–124. 24 indexed citations
17.
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
18.
Rossi, Salvatore, Ângela Romano, Anna Modoni, et al.. (2018). Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2. European Neurology. 79(3-4). 166–170. 1 indexed citations
19.
Santoro, Massimo, Marcella Masciullo, Maria Laura Ester Bianchi, et al.. (2015). Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1). Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852(12). 2645–2652. 25 indexed citations
20.
Bruno, Savino, Andrea Crosignani, Luigi Roffi, et al.. (2014). P465 SVR IS ASSOCIATED WITH NO RISK REDUCTION OF HCC DEVELOPMENT IN PATIENTS WITH HCV-RELATED CIRRHOSIS. A PROSPECTIVE, UP-TO 23 YEARS, COHORT FOLLOW-UP STUDY. Journal of Hepatology. 60(1). S224–S224. 7 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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