Nila Volpi

1.4k total citations
48 papers, 889 citations indexed

About

Nila Volpi is a scholar working on Molecular Biology, Neurology and Epidemiology. According to data from OpenAlex, Nila Volpi has authored 48 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 12 papers in Neurology and 11 papers in Epidemiology. Recurrent topics in Nila Volpi's work include Inflammatory Myopathies and Dermatomyositis (8 papers), Peripheral Neuropathies and Disorders (5 papers) and Systemic Sclerosis and Related Diseases (5 papers). Nila Volpi is often cited by papers focused on Inflammatory Myopathies and Dermatomyositis (8 papers), Peripheral Neuropathies and Disorders (5 papers) and Systemic Sclerosis and Related Diseases (5 papers). Nila Volpi collaborates with scholars based in Italy, United States and South Korea. Nila Volpi's co-authors include Giuseppe Valacchi, Claudia Torricelli, Eva Slabáková, Michela Muscettola, Emanuela Maioli, Karel Souček, Pasquale Annunziata, Símone Rossi, N. Giordano and Alfonso Cerase and has published in prestigious journals such as Nature Genetics, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Nila Volpi

47 papers receiving 878 citations

Peers

Nila Volpi
Qingfang Sun China
Hua Piao China
Ching‐Chi Chiu Taiwan
Yuzhong Wang China
Fengjin Guo China
Qingqing Wang China
Xue Zhang China
David B. Williams United States
Zhaoqi Yan United States
Nobuhiko Omori Japan
Qingfang Sun China
Nila Volpi
Citations per year, relative to Nila Volpi Nila Volpi (= 1×) peers Qingfang Sun

Countries citing papers authored by Nila Volpi

Since Specialization
Citations

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

Fields of papers citing papers by Nila Volpi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nila Volpi

This figure shows the co-authorship network connecting the top 25 collaborators of Nila Volpi. A scholar is included among the top collaborators of Nila Volpi 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 Nila Volpi. Nila Volpi 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.
Lopergolo, Diego, Gian Nicola Gallus, Giuseppe Pieraccini, et al.. (2024). CCDC78: Unveiling the Function of a Novel Gene Associated with Hereditary Myopathy. Cells. 13(17). 1504–1504. 1 indexed citations
2.
Porcelli, Brunetta, Miriana d’Alessandro, Latika Gupta, et al.. (2023). Anti-Cytosolic 5′-Nucleotidase 1A in the Diagnosis of Patients with Suspected Idiopathic Inflammatory Myopathies: An Italian Real-Life, Single-Centre Retrospective Study. Biomedicines. 11(7). 1963–1963. 3 indexed citations
3.
Ginanneschi, Federica, Claudia Vinciguerra, Nila Volpi, et al.. (2023). Chronic inflammatory demyelinating polyneuropathy after SARS-CoV2 vaccination: update of the literature and patient characterization. Immunologic Research. 71(6). 833–838. 4 indexed citations
4.
Guarna, Massimo, et al.. (2022). Elongated styloid process: literature review and morphometric data on a collection of dried skulls. Italian Journal of Anatomy and Embryology. 125(1). 11–17.
5.
Ginanneschi, Federica, Fabio Giannini, Francesco Sicurelli, et al.. (2022). Clinical Features and Outcome of the Guillain–Barre Syndrome: A Single-Center 11-Year Experience. Frontiers in Neurology. 13. 856091–856091. 7 indexed citations
6.
Stefano, Ludovico De, Nila Volpi, Pia De Stefano, et al.. (2020). Sporadic late-onset nemaline myopathy in a patient with silicone breast implants. Clinical Neurology and Neurosurgery. 196. 105999–105999. 4 indexed citations
7.
Scaricamazza, Silvia, I. Salvatori, Giacomo Giacovazzo, et al.. (2020). Skeletal-Muscle Metabolic Reprogramming in ALS-SOD1G93A Mice Predates Disease Onset and Is A Promising Therapeutic Target. iScience. 23(5). 101087–101087. 65 indexed citations
8.
Molinaro, Francesco, Margherita Aglianò, Nila Volpi, et al.. (2020). Clinically Differentiated Abnormalities of the Architecture and Expression of Myosin Isoforms of the Human Cremaster Muscle in Cryptorchidism and Retractile Testis. Urologia Internationalis. 104(11-12). 891–901. 4 indexed citations
9.
Ginanneschi, Federica, Nila Volpi, Fabio Giannini, et al.. (2013). Rhabdomyolysis in an elderly multitreated patient: Multiple drug interactions after statin withdrawal. Journal of the Neurological Sciences. 336(1-2). 284–287. 11 indexed citations
10.
Franchi, Massimo Piergiuseppe, et al.. (2013). Paraneoplastic necrotizing myopathy associated with adenocarcinoma of the lung – a rare entity with atypical onset: a case report. Journal of Medical Case Reports. 7(1). 112–112. 12 indexed citations
11.
Giordano, N., Nila Volpi, Claudio Corallo, et al.. (2012). Expression of RXFP1 in skin of scleroderma patients and control subjects. Scandinavian Journal of Rheumatology. 41(5). 391–395. 15 indexed citations
12.
13.
Cardaioli, Elena, Edoardo Malfatti, Paola Da Pozzo, et al.. (2011). Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene. Journal of the Neurological Sciences. 303(1-2). 142–145. 4 indexed citations
14.
Cantarini, Luca, Nila Volpi, Mauro Galeazzi, et al.. (2010). Colchicine Myopathy and Neuromyopathy. JCR Journal of Clinical Rheumatology. 16(5). 229–232. 13 indexed citations
15.
Giannini, Fabio, Stefania Battistini, Michelangelo Mancuso, et al.. (2010). D90A-SOD1 mutation in ALS: The first report of heterozygous Italian patients and unusual findings. Amyotrophic Lateral Sclerosis. 11(1-2). 216–219. 24 indexed citations
16.
Cantarini, Luca, Nila Volpi, Giuseppe Greco, et al.. (2009). Eosinophilia-associated muscle disorders: an immunohistological study with tissue localisation of major basic protein in distinct clinicopathological forms. Journal of Clinical Pathology. 62(5). 442–447. 9 indexed citations
17.
Annunziata, Pasquale & Nila Volpi. (2009). High levels of C3c in the cerebrospinal fluid from amyotrophic lateral sclerosis patients. Acta Neurologica Scandinavica. 72(1). 61–64. 43 indexed citations
18.
Rossi, Símone, Fabio Giannini, Alfonso Cerase, et al.. (2004). Uncommon findings in idiopathic hypertrophic cranial pachymeningitis. Journal of Neurology. 251(5). 548–555. 32 indexed citations
19.
Meloni, Ilaria, Martine Raynaud, Ilaria Longo, et al.. (2002). FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation. Nature Genetics. 30(4). 436–440. 112 indexed citations
20.
Federico, Antonio, Carla Battisti, Nicola De Stefano, et al.. (1991). Vitamin E Deficiency Secondary to Chronic Intestinal Malabsorption and Effect of Vitamin Supplement: A Case Report. European Neurology. 31(6). 366–371. 4 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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