Stefania Tranquilli

2.2k total citations
20 papers, 423 citations indexed

About

Stefania Tranquilli is a scholar working on Neurology, Pathology and Forensic Medicine and Epidemiology. According to data from OpenAlex, Stefania Tranquilli has authored 20 papers receiving a total of 423 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Neurology, 6 papers in Pathology and Forensic Medicine and 5 papers in Epidemiology. Recurrent topics in Stefania Tranquilli's work include Multiple Sclerosis Research Studies (5 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Stefania Tranquilli is often cited by papers focused on Multiple Sclerosis Research Studies (5 papers), Amyotrophic Lateral Sclerosis Research (5 papers) and Parkinson's Disease Mechanisms and Treatments (4 papers). Stefania Tranquilli collaborates with scholars based in Italy and Bulgaria. Stefania Tranquilli's co-authors include Maria Giovanna Marrosu, Maria Rita Murru, Eleonora Cocco, Daniela Corongiu, Manuel Mameli, Maria Cristina Mostallino, Jessica Frau, Giovanni Biggio, Paolo Follesa and Saturnino Spiga and has published in prestigious journals such as Journal of Neuroscience, PLoS ONE and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Stefania Tranquilli

19 papers receiving 417 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stefania Tranquilli Italy 12 137 135 122 76 74 20 423
Franca Vulinović Germany 10 92 0.7× 99 0.7× 138 1.1× 16 0.2× 118 1.6× 14 457
Dongxu Zhai Canada 11 114 0.8× 42 0.3× 246 2.0× 49 0.6× 81 1.1× 21 540
Çiğdem Acıoğlu United States 9 62 0.5× 59 0.4× 122 1.0× 25 0.3× 167 2.3× 11 424
Dawei Meng China 11 173 1.3× 146 1.1× 186 1.5× 19 0.3× 59 0.8× 26 429
Oihana Errea Spain 4 47 0.3× 47 0.3× 149 1.2× 22 0.3× 176 2.4× 6 481
Leon Hosang Germany 7 116 0.8× 27 0.2× 171 1.4× 21 0.3× 95 1.3× 9 429
Kyoko Iinuma Japan 11 75 0.5× 104 0.8× 123 1.0× 30 0.4× 65 0.9× 24 374
James A. Windelborn United States 9 45 0.3× 25 0.2× 173 1.4× 44 0.6× 43 0.6× 13 480
Iva Aleksić Serbia 5 102 0.7× 191 1.4× 62 0.5× 28 0.4× 184 2.5× 7 352

Countries citing papers authored by Stefania Tranquilli

Since Specialization
Citations

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

Fields of papers citing papers by Stefania Tranquilli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefania Tranquilli

This figure shows the co-authorship network connecting the top 25 collaborators of Stefania Tranquilli. A scholar is included among the top collaborators of Stefania Tranquilli 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 Stefania Tranquilli. Stefania Tranquilli 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.
Littera, Roberto, Stefania Tranquilli, Aldesia Provenzano, et al.. (2022). A Protective HLA Extended Haplotype Outweighs the Major COVID-19 Risk Factor Inherited From Neanderthals in the Sardinian Population. Frontiers in Immunology. 13. 891147–891147. 3 indexed citations
2.
Lorefice, Lorena, Federica Murgia, Giuseppe Fenu, et al.. (2019). Assessing the Metabolomic Profile of Multiple Sclerosis Patients Treated with Interferon Beta 1a by 1H-NMR Spectroscopy. Neurotherapeutics. 16(3). 797–807. 19 indexed citations
3.
Lorefice, Lorena, Maria Rita Murru, Giancarlo Coghe, et al.. (2017). Charcot–Marie–Tooth disease: genetic subtypes in the Sardinian population. Neurological Sciences. 38(6). 1019–1025. 9 indexed citations
4.
5.
Stefano, Francesca Di, Antonino Cannas, Giuseppe Borghero, et al.. (2016). Progressive apraxia of speech in a patient with a C9orf72 mutation. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(7-8). 608–609.
6.
Lorefice, Lorena, Giuseppe Fenu, Daniela Corongiu, et al.. (2015). A genetic association study of two genes linked to neurodegeneration in a Sardinian multiple sclerosis population: The TARDBP Ala382Thr mutation and C9orf72 expansion. Journal of the Neurological Sciences. 357(1-2). 229–234. 4 indexed citations
7.
Frau, Jessica, Davide Cossu, Giancarlo Coghe, et al.. (2015). Role of interferon-beta in Mycobacterium avium subspecies paratuberculosis antibody response in Sardinian MS patients. Journal of the Neurological Sciences. 349(1-2). 249–250. 11 indexed citations
8.
Floris, Gianluca, Giuseppe Borghero, Francesca Di Stefano, et al.. (2015). Phenotypic variability related to C9orf72 mutation in a large Sardinian kindred. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 17(3-4). 245–248. 5 indexed citations
9.
Floris, Gianluca, Giuseppe Borghero, Antonino Cannas, et al.. (2014). Constructional apraxia in frontotemporal dementia associated with the C9orf72 mutation: Broadening the clinical and neuropsychological phenotype. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 16(1-2). 8–15. 10 indexed citations
10.
Floris, Gianluca, Giuseppe Borghero, Antonino Cannas, et al.. (2014). Clinical phenotypes and radiological findings in frontotemporal dementia related to TARDBP mutations. Journal of Neurology. 262(2). 375–384. 45 indexed citations
11.
Cossu, Davide, Speranza Masala, Eleonora Cocco, et al.. (2013). Association of Mycobacterium avium subsp. paratuberculosis and SLC11A1 polymorphisms in Sardinian multiple sclerosis patients. The Journal of Infection in Developing Countries. 7(3). 203–207. 21 indexed citations
12.
Frau, Jessica, Davide Cossu, Giancarlo Coghe, et al.. (2013). Mycobacterium avium subsp. paratuberculosis and multiple sclerosis in Sardinian patients: epidemiology and clinical features. Multiple Sclerosis Journal. 19(11). 1437–1442. 31 indexed citations
13.
Cocco, Eleonora, Alessandra Meloni, Maria Rita Murru, et al.. (2012). Vitamin D Responsive Elements within the HLA-DRB1 Promoter Region in Sardinian Multiple Sclerosis Associated Alleles. PLoS ONE. 7(7). e41678–e41678. 29 indexed citations
14.
Cocco, Eleonora, Claudia Sardu, E. Pieroni, et al.. (2012). HLA-DRB1-DQB1 Haplotypes Confer Susceptibility and Resistance to Multiple Sclerosis in Sardinia. PLoS ONE. 7(4). e33972–e33972. 30 indexed citations
15.
Solla, Paolo, Alessandra Bolino, Maria Giovanna Marrosu, et al.. (2010). Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy. Journal of Neurology Neurosurgery & Psychiatry. 81(9). 958–962. 30 indexed citations
16.
Solla, Paolo, Antonino Cannas, Gianluca Floris, et al.. (2010). ParkinExon Rearrangements and Sequence Variants inLRRK2Mutations Carriers: Analysis on a Possible Modifier Effect onLRRK2Penetrance. Parkinson s Disease. 2010. 1–5. 4 indexed citations
17.
Carboni, Nicola, Maurizio Porcu, Marco Mura, et al.. (2009). Evolution of the phenotype in a family with an LMNA gene mutation presenting with isolated cardiac involvement. Muscle & Nerve. 41(1). 85–91. 16 indexed citations
18.
Floris, Gianluca, Antonino Cannas, Paolo Solla, et al.. (2008). Genetic analysis for five LRRK2 mutations in a Sardinian parkinsonian population: Importance of G2019S and R1441C mutations in sporadic Parkinson's disease patients. Parkinsonism & Related Disorders. 15(4). 277–280. 23 indexed citations
19.
Murru, Maria Rita, Maria Giovanna Marrosu, Eleonora Cocco, et al.. (2006). A novel Cx32 mutation causes X-linked Charcot-Marie-Tooth disease with brainstem involvement and brain magnetic resonance spectroscopy abnormalities. Neurological Sciences. 27(1). 18–23. 17 indexed citations
20.
Sanna, Enrico, Maria Cristina Mostallino, Fabio Busonero, et al.. (2003). Changes in GABAAReceptor Gene Expression Associated with Selective Alterations in Receptor Function and Pharmacology after Ethanol Withdrawal. Journal of Neuroscience. 23(37). 11711–11724. 110 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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