Cinzia Bertolin

2.8k total citations
21 papers, 317 citations indexed

About

Cinzia Bertolin is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Cinzia Bertolin has authored 21 papers receiving a total of 317 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Cinzia Bertolin's work include Genetic Neurodegenerative Diseases (7 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Amyotrophic Lateral Sclerosis Research (5 papers). Cinzia Bertolin is often cited by papers focused on Genetic Neurodegenerative Diseases (7 papers), Neurogenetic and Muscular Disorders Research (6 papers) and Amyotrophic Lateral Sclerosis Research (5 papers). Cinzia Bertolin collaborates with scholars based in Italy, United Kingdom and France. Cinzia Bertolin's co-authors include Gianni Sorarú, Elena Pegoraro, Ilaria Martinelli, Giorgia Querin, Maria Luisa Mostacciuolo, Luca Bello, Giovanni Vazza, Giulia Perini, Andrea Vettori and Francesca Boaretto and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Scientific Reports.

In The Last Decade

Cinzia Bertolin

21 papers receiving 314 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cinzia Bertolin Italy 10 191 105 105 105 37 21 317
Anna Maija Saukkonen Finland 9 148 0.8× 72 0.7× 53 0.5× 83 0.8× 20 0.5× 12 250
Kimberly Schadt United States 12 360 1.9× 83 0.8× 284 2.7× 120 1.1× 16 0.4× 23 431
Michiel R. Fokkens Netherlands 9 206 1.1× 36 0.3× 176 1.7× 64 0.6× 25 0.7× 11 312
Nicolas Chrestian Canada 10 195 1.0× 34 0.3× 142 1.4× 43 0.4× 26 0.7× 24 272
Elena Sánchez-Ferrero Spain 8 161 0.8× 60 0.6× 164 1.6× 86 0.8× 35 0.9× 10 313
Emanuele Frattini Italy 9 115 0.6× 64 0.6× 44 0.4× 83 0.8× 13 0.4× 14 250
Fabrizia Stregapede Italy 9 83 0.4× 38 0.4× 90 0.9× 43 0.4× 47 1.3× 17 205
Gail Eglon United Kingdom 8 172 0.9× 34 0.3× 190 1.8× 72 0.7× 56 1.5× 10 302
Fatima Jaffer United Kingdom 6 138 0.7× 17 0.2× 86 0.8× 55 0.5× 67 1.8× 12 264
Angela Kokkinis United States 10 283 1.5× 270 2.6× 342 3.3× 162 1.5× 15 0.4× 20 493

Countries citing papers authored by Cinzia Bertolin

Since Specialization
Citations

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

Fields of papers citing papers by Cinzia Bertolin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cinzia Bertolin

This figure shows the co-authorship network connecting the top 25 collaborators of Cinzia Bertolin. A scholar is included among the top collaborators of Cinzia Bertolin 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 Cinzia Bertolin. Cinzia Bertolin 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.
Emmi, Aron, Cinzia Bertolin, Francesco Cavallieri, et al.. (2025). Skin calcium deposits in primary familial brain calcification: A novel potential biomarker. Annals of Clinical and Translational Neurology. 12(4). 737–745. 1 indexed citations
2.
Bonato, Giulia, Angelo Antonini, Marta Campagnolo, et al.. (2024). Genetic mutations in Parkinson’s disease: screening of a selected population from North-Eastern Italy. Neurological Sciences. 46(1). 165–174. 5 indexed citations
3.
Salviati, Leonardo, et al.. (2024). Non-Motor Symptoms in Primary Familial Brain Calcification. Journal of Clinical Medicine. 13(13). 3873–3873. 2 indexed citations
4.
Querin, Giorgia, Ilaria Martinelli, Cinzia Bertolin, et al.. (2023). The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA). Scientific Reports. 13(1). 17311–17311. 6 indexed citations
5.
Salviati, Leonardo, Andrea Bordugo, Marta Camilot, et al.. (2020). Multiple acyl-COA dehydrogenase deficiency in elderly carriers. Journal of Neurology. 267(5). 1414–1419. 22 indexed citations
6.
Caroppo, Francesca, et al.. (2020). A novel KRT1 c.1433A>G p.(Glu478Gly) mutation in a newborn with epidermolytic ichthyosis. SHILAP Revista de lepidopterología. 8(12). 3078–3080. 3 indexed citations
7.
Bello, Luca, Ilaria Martinelli, Cinzia Bertolin, et al.. (2019). Safety and efficacy of edaravone compared to historical controls in patients with amyotrophic lateral sclerosis from North-Eastern Italy. Journal of the Neurological Sciences. 404. 47–51. 15 indexed citations
8.
Spinelli, Edoardo Gioele, Federica Agosta, Pilar M. Ferraro, et al.. (2019). Brain MRI shows white matter sparing in Kennedy's disease and slow‐progressing lower motor neuron disease. Human Brain Mapping. 40(10). 3102–3112. 16 indexed citations
9.
Lombardi, Vittoria, Giorgia Querin, Oliver J. Ziff, et al.. (2019). Muscle and not neuronal biomarkers correlate with severity in spinal and bulbar muscular atrophy. Neurology. 92(11). e1205–e1211. 53 indexed citations
10.
Kleinbub, Johann Roland, Giorgia Querin, Ilaria Martinelli, et al.. (2018). Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study. Scientific Reports. 8(1). 13627–13627. 8 indexed citations
11.
Bertolin, Cinzia, Giorgia Querin, Ilaria Martinelli, et al.. (2018). Insights into the genetic epidemiology of spinal and bulbar muscular atrophy: prevalence estimation and multiple founder haplotypes in the Veneto Italian region. European Journal of Neurology. 26(3). 519–524. 11 indexed citations
12.
Semplicini, Claudio, Cinzia Bertolin, Luca Bello, et al.. (2018). The clinical spectrum of CASQ1 -related myopathy. Neurology. 91(17). e1629–e1641. 17 indexed citations
13.
Querin, Giorgia, Ilaria Martinelli, Luca Bello, et al.. (2016). Validation of the Italian version of the SBMA Functional Rating Scale as outcome measure. Neurological Sciences. 37(11). 1815–1821. 9 indexed citations
14.
Semplicini, Claudio, John Vissing, Julia R. Dahlqvist, et al.. (2015). Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E. Neurology. 84(17). 1772–1781. 45 indexed citations
15.
Bertolin, Cinzia, Carla D’Ascenzo, Giorgia Querin, et al.. (2013). Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. Neurobiology of Aging. 35(5). 1212.e7–1212.e10. 8 indexed citations
16.
Calini, Daniela, Lucia Corrado, Roberto Del Bo, et al.. (2013). Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis. Neurobiology of Aging. 34(11). 2695.e11–2695.e12. 26 indexed citations
17.
Bertolin, Cinzia, Chiara Magri, Sergio Barlati, et al.. (2011). Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder. Journal of Human Genetics. 56(12). 869–872. 16 indexed citations
18.
Bertolin, Cinzia, Francesca Boaretto, Giovanni Barbon, et al.. (2010). Novel mutations in the L1CAM gene support the complexity of L1 syndrome. Journal of the Neurological Sciences. 294(1-2). 124–126. 6 indexed citations
19.
Vazza, Giovanni, Cinzia Bertolin, Andrea Vettori, et al.. (2006). Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26. Molecular Psychiatry. 12(1). 87–93. 38 indexed citations
20.
Vazza, Giovanni, et al.. (2006). A novel 9-bp insertion in the GJB1 gene causing a mild form of X-linked CMT with late onset. Neuromuscular Disorders. 16(12). 878–881. 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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