D. Scalabrini

938 total citations
27 papers, 687 citations indexed

About

D. Scalabrini is a scholar working on Neurology, Molecular Biology and Physiology. According to data from OpenAlex, D. Scalabrini has authored 27 papers receiving a total of 687 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Neurology, 9 papers in Molecular Biology and 9 papers in Physiology. Recurrent topics in D. Scalabrini's work include Multiple Sclerosis Research Studies (8 papers), Alzheimer's disease research and treatments (7 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). D. Scalabrini is often cited by papers focused on Multiple Sclerosis Research Studies (8 papers), Alzheimer's disease research and treatments (7 papers) and Amyotrophic Lateral Sclerosis Research (7 papers). D. Scalabrini collaborates with scholars based in Italy, United States and Germany. D. Scalabrini's co-authors include Elio Scarpini, Daniela Galimberti, Nereo Bresolin, Chiara Fenoglio, E. Venturelli, Claudio Mariani, Ilaria Guidi, Francesca Clerici, Francesca Cortini and Carlo Lovati and has published in prestigious journals such as Brain Research, Neurobiology of Aging and Journal of the Neurological Sciences.

In The Last Decade

D. Scalabrini

27 papers receiving 678 citations

Peers

D. Scalabrini
Anthousa Tsoutsou Greece
Vineela Gandham United States
Janet Cady United States
Jonathan Hasselmann United States
Parham Nejad United States
Gabriele Tosadori Italy
Jibin Yao United States
Xiangmin Peng United States
Trinh Pham United States
Tommaso Carlucci Italy
Anthousa Tsoutsou Greece
D. Scalabrini
Citations per year, relative to D. Scalabrini D. Scalabrini (= 1×) peers Anthousa Tsoutsou

Countries citing papers authored by D. Scalabrini

Since Specialization
Citations

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

Fields of papers citing papers by D. Scalabrini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D. Scalabrini

This figure shows the co-authorship network connecting the top 25 collaborators of D. Scalabrini. A scholar is included among the top collaborators of D. Scalabrini 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 D. Scalabrini. D. Scalabrini 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.
Galimberti, Daniela, James P. MacMurray, D. Scalabrini, et al.. (2011). GSK3β genetic variability in patients with Multiple Sclerosis. Neuroscience Letters. 497(1). 46–48. 19 indexed citations
2.
Venturelli, E., Chiara Villa, Chiara Fenoglio, et al.. (2010). Is KIF24 a genetic risk factor for Frontotemporal Lobar Degeneration?. Neuroscience Letters. 482(3). 240–244. 8 indexed citations
3.
Boneschi, Filippo Martinelli, Federica Esposito, D. Scalabrini, et al.. (2010). Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort. European Journal of Neurology. 17(5). 740–745. 10 indexed citations
4.
Riz, Milena De, Daniela Galimberti, Chiara Fenoglio, et al.. (2009). Cerebrospinal fluid progranulin levels in patients with different multiple sclerosis subtypes. Neuroscience Letters. 469(2). 234–236. 18 indexed citations
5.
Villa, Chiara, E. Venturelli, Chiara Fenoglio, et al.. (2009). DCUN1D1is a risk factor for frontotemporal lobar degeneration. European Journal of Neurology. 16(7). 870–873. 15 indexed citations
6.
Villa, Chiara, E. Venturelli, Chiara Fenoglio, et al.. (2009). Candidate gene analysis of semaphorins in patients with Alzheimer’s disease. Neurological Sciences. 31(2). 169–173. 11 indexed citations
7.
Fenoglio, Chiara, Daniela Galimberti, Francesca Cortini, et al.. (2009). Rs5848 Variant Influences GRN mRNA Levels in Brain and Peripheral Mononuclear Cells in Patients with Alzheimer's Disease. Journal of Alzheimer s Disease. 18(3). 603–612. 53 indexed citations
8.
Cortini, Francesca, Chiara Fenoglio, Ilaria Guidi, et al.. (2008). Novel exon 1 progranulin gene variant in Alzheimer’s disease. European Journal of Neurology. 15(10). 1111–1117. 44 indexed citations
9.
Galimberti, Daniela, E. Venturelli, Chiara Fenoglio, et al.. (2008). Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration. Journal of Neurology. 255(4). 539–544. 72 indexed citations
10.
Scalabrini, D., Chiara Fenoglio, Elio Scarpini, et al.. (2007). Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis. Neuroscience Letters. 425(3). 173–176. 6 indexed citations
11.
Galimberti, Daniela, Elio Scarpini, E. Venturelli, et al.. (2007). Association of a NOS1 promoter repeat with Alzheimer's disease. Neurobiology of Aging. 29(9). 1359–1365. 27 indexed citations
12.
Venturelli, E., Chiara Villa, Elio Scarpini, et al.. (2007). Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration. European Journal of Neurology. 15(1). 77–81. 21 indexed citations
13.
Galimberti, Daniela, D. Scalabrini, Chiara Fenoglio, et al.. (2007). Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis. Journal of the Neurological Sciences. 267(1-2). 86–90. 22 indexed citations
14.
Galimberti, Daniela, D. Scalabrini, Chiara Fenoglio, et al.. (2006). CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical course. European Journal of Neurology. 14(2). 162–167. 18 indexed citations
15.
Venturelli, E., Daniela Galimberti, Chiara Fenoglio, et al.. (2006). Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease. Neuroscience Letters. 404(1-2). 217–221. 12 indexed citations
16.
Galimberti, Daniela, Chiara Fenoglio, Carlo Lovati, et al.. (2005). Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease. Neurobiology of Aging. 27(12). 1763–1768. 177 indexed citations
17.
Fenoglio, Chiara, Daniela Galimberti, Maria Ban, et al.. (2005). SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis. Neuroscience Letters. 394(2). 92–96. 11 indexed citations
18.
Scalabrini, D., Daniela Galimberti, Chiara Fenoglio, et al.. (2005). P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis. Neuroscience Letters. 388(3). 149–152. 12 indexed citations
19.
Venturelli, E., Daniela Galimberti, Carlo Lovati, et al.. (2005). The T-786C NOS3 polymorphism in Alzheimer's disease: Association and influence on gene expression. Neuroscience Letters. 382(3). 300–303. 19 indexed citations
20.
Scalabrini, D., et al.. (2004). Radiation hybrid mapping of two members of the Toll‐like receptor gene family in pigs. Animal Genetics. 35(3). 251–252. 6 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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