Fabio Giannini

1.2k total citations
13 papers, 221 citations indexed

About

Fabio Giannini is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Fabio Giannini has authored 13 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Cellular and Molecular Neuroscience and 3 papers in Neurology. Recurrent topics in Fabio Giannini's work include Cardiac, Anesthesia and Surgical Outcomes (2 papers), Sepsis Diagnosis and Treatment (2 papers) and IgG4-Related and Inflammatory Diseases (1 paper). Fabio Giannini is often cited by papers focused on Cardiac, Anesthesia and Surgical Outcomes (2 papers), Sepsis Diagnosis and Treatment (2 papers) and IgG4-Related and Inflammatory Diseases (1 paper). Fabio Giannini collaborates with scholars based in Italy, Brazil and Sweden. Fabio Giannini's co-authors include Antônio Paulo Nassar, Amílcar Oshiro Mocelin, Nila Volpi, Símone Rossi, Paolo Galluzzi, Lucia Pucci, Daniela Galimberti, Alfonso D’Ambrosio, Sabina Bartalini and G Morgese and has published in prestigious journals such as Journal of Neurology, The American Journal of Emergency Medicine and Brain stimulation.

In The Last Decade

Fabio Giannini

12 papers receiving 219 citations

Peers

Fabio Giannini

CMN

NEURO

EPIDE

SURGE

Ethem Göksu Türkiye

Martin Bunge Canada

Vincenzina Lo Re Italy

N. Hirsch United Kingdom

Hisae Mori Japan

Giuseppe Neri Italy

Dilara İçağasıoğlu Türkiye

Huan-Lin Hsu Taiwan

Emmanuel Akano United States

Bong Su Kang South Korea

Ethem Göksu Türkiye

Fabio Giannini

33 ×0.5

75 ×1.3

CMN

156 ×2.8

NEURO

32 ×0.7

EPIDE

76 ×1.7

SURGE

Citations per year, relative to Fabio Giannini Fabio Giannini (= 1×) peers Ethem Göksu

Countries citing papers authored by Fabio Giannini

Since Specialization

Citations

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

Fields of papers citing papers by Fabio Giannini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fabio Giannini

This figure shows the co-authorship network connecting the top 25 collaborators of Fabio Giannini. A scholar is included among the top collaborators of Fabio Giannini 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 Fabio Giannini. Fabio Giannini is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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13 of 13 papers shown

Riolo, Giulia, Claudia Ricci, Carlotta Marzocchi, et al.. (2022). BDNF and Pro-BDNF in Amyotrophic Lateral Sclerosis: A New Perspective for Biomarkers of Neurodegeneration. Brain Sciences. 12(5). 617–617. 22 indexed citations

Russo, Filomena, et al.. (2021). New onset psoriasis in a patient with chronic inflammatory demyelinating polyneuropathy treated with Rituximab. Giornale Italiano di Dermatologia e Venereologia. 155(6). 802–803. 1 indexed citations

Cioncoloni, David, et al.. (2016). Major motor-functional determinants associated with poor self-reported health-related quality of life in myasthenia gravis patients. Neurological Sciences. 37(5). 717–723. 15 indexed citations

Caliandro, Pietro, Luca Padua, Alessandro Rossi, et al.. (2014). Jitter of Corticospinal Neurons During Repetitive Transcranial Magnetic Stimulation. Method and Possible Clinical Implications. Brain stimulation. 7(4). 580–586. 8 indexed citations

Battistini, Stefania, et al.. (2014). Phenotypic variability associated with the R155C VCP gene mutation. 5. 1 indexed citations

Nassar, Antônio Paulo, et al.. (2013). SAPS 3, APACHE IV or GRACE: which score to choose for acute coronary syndrome patients in intensive care units?. Sao Paulo Medical Journal. 131(3). 173–178. 14 indexed citations

Nassar, Antônio Paulo, et al.. (2011). Caution when using prognostic models: A prospective comparison of 3 recent prognostic models. Journal of Critical Care. 27(4). 423.e1–423.e7. 59 indexed citations

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

Bugano, Diogo Diniz Gomes, et al.. (2008). Should naloxone be prescribed in the ED management of patients with cardiac arrest? A case report and review of literature. The American Journal of Emergency Medicine. 26(1). 113.e5–113.e8. 6 indexed citations

10.

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

11.

Zannolli, Raffaella, Sid Gilman, Símone Rossi, et al.. (2002). Hereditary Neuronal Intranuclear Inclusion Disease With Autonomic Failure and Cerebellar Degeneration. Archives of Neurology. 59(8). 1319–1319. 47 indexed citations

12.

Rossi, Símone, Fabio Giannini, Stefano Gonnelli, Riccardo Cioni, & S. Passero. (1992). [Ophthalmoparesis as a presentation form of subacute euthyroid thyroiditis].. PubMed. 61(5). 166–8. 1 indexed citations

13.

Rossi, Alessandro, et al.. (1985). Landouzy-Dejerine disease: a progressive metameric muscular dystrophy of autosomal dominant inheritance with a variable intrafamilial phenotype expression.. PubMed. 7(2). 93–111. 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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