Luca Pradotto

750 total citations
21 papers, 283 citations indexed

About

Luca Pradotto is a scholar working on Neurology, Molecular Biology and Cell Biology. According to data from OpenAlex, Luca Pradotto has authored 21 papers receiving a total of 283 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 8 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in Luca Pradotto's work include Cerebrovascular and genetic disorders (4 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers) and Glioma Diagnosis and Treatment (3 papers). Luca Pradotto is often cited by papers focused on Cerebrovascular and genetic disorders (4 papers), Amyloidosis: Diagnosis, Treatment, Outcomes (4 papers) and Glioma Diagnosis and Treatment (3 papers). Luca Pradotto collaborates with scholars based in Italy, United States and Japan. Luca Pradotto's co-authors include Alessandro Mauro, Isabella Morra, Alessia Di Sapio, Maria Fuciarelli, Anna Di Blasio, Renato Polimanti, Andrea Boghi, Marco Di Girolamo, Monica Mencarelli and Dario Manfellotto and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Neurology Neurosurgery & Psychiatry and Archives of Physical Medicine and Rehabilitation.

In The Last Decade

Luca Pradotto

20 papers receiving 278 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luca Pradotto Italy 11 157 87 42 34 33 21 283
En‐Lin Dong China 10 118 0.8× 33 0.4× 75 1.8× 6 0.2× 57 1.7× 15 324
Hui‐Zhen Su China 8 53 0.3× 29 0.3× 42 1.0× 8 0.2× 53 1.6× 17 269
Maria H. Alanne Finland 9 126 0.8× 66 0.8× 12 0.3× 60 1.8× 43 1.3× 11 324
Laixing Wang China 14 177 1.1× 167 1.9× 27 0.6× 44 1.3× 8 0.2× 34 506
Stefan Nicolau United States 12 196 1.2× 66 0.8× 69 1.6× 16 0.5× 37 1.1× 34 365
Ying‐Qian Lu China 7 90 0.6× 28 0.3× 52 1.2× 5 0.1× 44 1.3× 12 240
Takahisa Fuse Japan 11 99 0.6× 104 1.2× 33 0.8× 68 2.0× 14 0.4× 31 344
H.R. Arvinda India 10 76 0.5× 68 0.8× 59 1.4× 9 0.3× 29 0.9× 19 250
Robea Ballo South Africa 7 137 0.9× 26 0.3× 39 0.9× 31 0.9× 79 2.4× 19 281
Chrysanthi Koutsandrea Greece 12 165 1.1× 85 1.0× 12 0.3× 41 1.2× 96 2.9× 40 660

Countries citing papers authored by Luca Pradotto

Since Specialization
Citations

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

Fields of papers citing papers by Luca Pradotto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luca Pradotto

This figure shows the co-authorship network connecting the top 25 collaborators of Luca Pradotto. A scholar is included among the top collaborators of Luca Pradotto 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 Luca Pradotto. Luca Pradotto 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.
2.
Bodio, Caterina, Paola Adele Lonati, Cecilia Beatrice Chighizola, et al.. (2024). Fibroblasts and Endothelial Cells in Three-Dimensional Models: A New Tool for Addressing the Pathogenesis of Systemic Sclerosis as a Prototype of Fibrotic Vasculopathies. International Journal of Molecular Sciences. 25(5). 2780–2780.
3.
Brugliera, Luigia, Massimo Filippi, Ubaldo Del Carro, et al.. (2020). Nerve Compression Injuries After Prolonged Prone Position Ventilation in Patients With SARS-CoV-2: A Case Series. Archives of Physical Medicine and Rehabilitation. 102(3). 359–362. 32 indexed citations
4.
Vismara, Luca, et al.. (2020). Severe Postoperative Chronic Constipation Related to Anorectal Malformation Managed with Osteopathic Manipulative Treatment. Case Reports in Gastroenterology. 14(1). 220–225. 4 indexed citations
5.
Angelis, Flavio De, Marco Di Girolamo, Marco Luigetti, et al.. (2017). Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis. European Journal of Human Genetics. 25(9). 1055–1060. 25 indexed citations
6.
Angelis, Flavio De, Marco Di Girolamo, Marco Luigetti, et al.. (2017). Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis. BMC Genomics. 18(1). 254–254. 13 indexed citations
7.
Pradotto, Luca, et al.. (2016). Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation. Journal of the Neurological Sciences. 371. 81–84. 17 indexed citations
8.
Scarpina, Federica, et al.. (2016). Utility of Boston Qualitative Scoring System for Rey-Osterrieth Complex Figure: evidence from a Parkinson’s Diseases sample. Neurological Sciences. 37(10). 1603–1611. 9 indexed citations
9.
Pradotto, Luca, Laura Orsi, Monica Mencarelli, et al.. (2016). Recurrent transient global amnesia as presenting symptoms of CADASIL. Clinical Case Reports. 4(11). 1045–1048. 7 indexed citations
10.
Angelis, Flavio De, Marco Di Girolamo, Marco Luigetti, et al.. (2014). Most recent common ancestor ofTTRVal30Met mutation in Italian population and its potential role in genotype-phenotype correlation. Amyloid. 22(2). 73–78. 15 indexed citations
11.
Testi, Silvia, Giovanni Malerba, Moreno Ferrarini, et al.. (2012). Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Journal of the Neurological Sciences. 319(1-2). 37–41. 20 indexed citations
12.
Albani, Giovanni, et al.. (2011). Electrogastrographyc activity in Parkinson's disease patients with and without motor fluctuations. Movement Disorders. 26(9). 1736–1740. 1 indexed citations
13.
Pradotto, Luca, et al.. (2011). A new NOTCH3 mutation presenting as primary intracerebral haemorrhage. Journal of the Neurological Sciences. 315(1-2). 143–145. 12 indexed citations
14.
Priano, Lorenzo, Giorgio Giaccone, Michela Mangieri, et al.. (2009). An atypical case of sporadic fatal insomnia. Journal of Neurology Neurosurgery & Psychiatry. 80(8). 924–927. 5 indexed citations
15.
Brussino, Alessandro, Giovanna Vaula, Cinzia Cagnoli, et al.. (2009). A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. Journal of Neurology Neurosurgery & Psychiatry. 80(2). 237–240. 32 indexed citations
16.
Pradotto, Luca, et al.. (2008). Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene. Journal of the Neurological Sciences. 271(1-2). 207–210. 11 indexed citations
17.
Giordana, Maria Teresa, Elisa Trevisan, Andrea Boghi, et al.. (2002). MDM2 overexpression is associated with short survival in adults withmedulloblastoma. Neuro-Oncology. 4(2). 115–122. 35 indexed citations
18.
Sapio, Alessia Di, et al.. (2002). Molecular Genetic Changes in a Series of Neuroepithelial Tumors of Childhood. Journal of Neuro-Oncology. 59(2). 117–122. 22 indexed citations
19.
Giordana, Maria Teresa, Elisa Trevisan, Andrea Boghi, et al.. (2002). MDM2 overexpression is associated with short survival in adults with medulloblastoma. Neuro-Oncology. 4(2). 115–122. 2 indexed citations
20.
Solaro, Claudio, Angelo Schenone, Alessia Di Sapio, et al.. (2000). An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy. Neuromuscular Disorders. 10(1). 52–55. 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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