Nereo Bresolin

27.3k total citations
487 papers, 18.1k citations indexed

About

Nereo Bresolin is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Nereo Bresolin has authored 487 papers receiving a total of 18.1k indexed citations (citations by other indexed papers that have themselves been cited), including 279 papers in Molecular Biology, 101 papers in Genetics and 94 papers in Neurology. Recurrent topics in Nereo Bresolin's work include Mitochondrial Function and Pathology (88 papers), Muscle Physiology and Disorders (72 papers) and Neurogenetic and Muscular Disorders Research (70 papers). Nereo Bresolin is often cited by papers focused on Mitochondrial Function and Pathology (88 papers), Muscle Physiology and Disorders (72 papers) and Neurogenetic and Muscular Disorders Research (70 papers). Nereo Bresolin collaborates with scholars based in Italy, United States and United Kingdom. Nereo Bresolin's co-authors include Giacomo P. Comi, Stefania Corti, G. Scarlato, Manuela Sironi, Roberto Del Bo, Maurizio Moggio, Sabrina Salani, Daniela Galimberti, Elio Scarpini and Monica Nizzardo and has published in prestigious journals such as Science, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Nereo Bresolin

484 papers receiving 17.8k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Nereo Bresolin 10.6k 3.1k 2.8k 2.7k 2.6k 487 18.1k
Giacomo P. Comi 9.0k 0.8× 2.7k 0.9× 2.4k 0.8× 2.8k 1.0× 1.8k 0.7× 570 15.6k
Hannes Vogel 14.1k 1.3× 3.6k 1.2× 2.5k 0.9× 2.3k 0.9× 2.3k 0.9× 352 26.0k
Lewis P. Rowland 8.1k 0.8× 2.8k 0.9× 3.0k 1.1× 7.7k 2.9× 2.0k 0.8× 261 18.2k
Frank Baas 9.4k 0.9× 1.3k 0.4× 3.9k 1.4× 3.2k 1.2× 1.6k 0.6× 361 21.7k
George Karpati 9.9k 0.9× 1.4k 0.5× 2.5k 0.9× 1.3k 0.5× 1.9k 0.7× 255 14.4k
Mahendra S. Rao 18.1k 1.7× 3.5k 1.1× 4.7k 1.7× 922 0.3× 3.3k 1.3× 399 27.1k
Xavier Estivill 10.6k 1.0× 1.1k 0.4× 2.2k 0.8× 1.3k 0.5× 1.4k 0.5× 510 22.2k
Massimo Zeviani 28.0k 2.6× 3.5k 1.1× 3.2k 1.1× 1.6k 0.6× 2.4k 0.9× 411 33.4k
Hannu Kalimo 5.5k 0.5× 1.3k 0.4× 2.5k 0.9× 3.2k 1.2× 2.4k 0.9× 312 15.4k
Filippo M. Santorelli 8.1k 0.8× 972 0.3× 3.2k 1.1× 1.1k 0.4× 1.2k 0.5× 526 12.5k

Countries citing papers authored by Nereo Bresolin

Since Specialization
Citations

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

Fields of papers citing papers by Nereo Bresolin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nereo Bresolin

This figure shows the co-authorship network connecting the top 25 collaborators of Nereo Bresolin. A scholar is included among the top collaborators of Nereo Bresolin 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 Nereo Bresolin. Nereo Bresolin 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.
Gagliardi, Delia, Mafalda Rizzuti, Michela Ripolone, et al.. (2022). MicroRNAs as serum biomarkers in Becker muscular dystrophy. Journal of Cellular and Molecular Medicine. 26(17). 4678–4685. 4 indexed citations
2.
Monfrini, Edoardo, Nereo Bresolin, Maria Cristina Saetti, et al.. (2021). Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review. Cells. 10(1). 171–171. 14 indexed citations
3.
Abati, Elena, Stefania Magri, Megi Meneri, et al.. (2021). Charcot–Marie–Tooth disease type 2F associated with biallelic HSPB1 mutations. Annals of Clinical and Translational Neurology. 8(5). 1158–1164. 6 indexed citations
4.
Monfrini, Edoardo, Filippo Cogiamanian, Sabrina Salani, et al.. (2021). A Novel Homozygous VPS11 Variant May Cause Generalized Dystonia. Annals of Neurology. 89(4). 834–839. 18 indexed citations
5.
Nizzardo, Monica, Michela Taiana, Federica Rizzo, et al.. (2020). Synaptotagmin 13 is neuroprotective across motor neuron diseases. Acta Neuropathologica. 139(5). 837–853. 34 indexed citations
6.
Costamagna, Gianluca, Elena Abati, Nereo Bresolin, Giacomo P. Comi, & Stefania Corti. (2020). Management of patients with neuromuscular disorders at the time of the SARS-CoV-2 pandemic. Journal of Neurology. 268(5). 1580–1591. 35 indexed citations
7.
Ronchi, Dario, Edoardo Monfrini, Sara Bonato, et al.. (2020). Dystonia‐ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency. Annals of Clinical and Translational Neurology. 7(5). 839–845. 12 indexed citations
8.
Magri, Francesca, et al.. (2020). Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives. Cellular and Molecular Life Sciences. 77(21). 4299–4313. 16 indexed citations
9.
Monfrini, Edoardo, Dario Ronchi, Giulia Franco, et al.. (2020). Late-onset leukoencephalopathy in a patient with recessive EARS2 mutations. Neurology Genetics. 6(5). e488–e488.
10.
Manini, Arianna, Tommaso Bocci, Edoardo Monfrini, et al.. (2020). A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation. BMC Neurology. 20(1). 408–408. 3 indexed citations
11.
Gioia, Roberta, Federica Rizzo, Elena Abati, et al.. (2020). Neural Stem Cell Transplantation for Neurodegenerative Diseases. International Journal of Molecular Sciences. 21(9). 3103–3103. 177 indexed citations
12.
Gagliardi, Delia, et al.. (2019). Diagnostic and Prognostic Role of Blood and Cerebrospinal Fluid and Blood Neurofilaments in Amyotrophic Lateral Sclerosis: A Review of the Literature. International Journal of Molecular Sciences. 20(17). 4152–4152. 56 indexed citations
13.
Piga, Daniela, Sabrina Salani, Francesca Magri, et al.. (2019). Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies. Therapeutic Advances in Neurological Disorders. 12. 1278055046–1278055046. 25 indexed citations
14.
Nizzardo, Monica, Alessandra Govoni, Michela Taiana, et al.. (2019). Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights. Journal of Cellular and Molecular Medicine. 24(2). 1169–1178. 25 indexed citations
15.
Ronchi, Dario, et al.. (2019). Molecular Approaches for the Treatment of Pompe Disease. Molecular Neurobiology. 57(2). 1259–1280. 17 indexed citations
16.
Abati, Elena, Nereo Bresolin, Giacomo P. Comi, & Stefania Corti. (2019). Advances, Challenges, and Perspectives in Translational Stem Cell Therapy for Amyotrophic Lateral Sclerosis. Molecular Neurobiology. 56(10). 6703–6715. 22 indexed citations
17.
Pascual, Belén, Susanne T. de Bot, Marcondes C. França, et al.. (2019). “Ears of the Lynx” MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia. American Journal of Neuroradiology. 40(1). 199–203. 39 indexed citations
18.
Monfrini, Edoardo, Letizia Straniero, Sara Bonato, et al.. (2019). Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy. Parkinsonism & Related Disorders. 63. 66–72. 18 indexed citations
19.
Brajkovic, Simona, et al.. (2016). Development of Therapeutics for C9ORF72 ALS/FTD-Related Disorders. Molecular Neurobiology. 54(6). 4466–4476. 31 indexed citations
20.
Fumagalli, Matteo, Uberto Pozzoli, Rachele Cagliani, et al.. (2009). Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions. The Journal of Experimental Medicine. 206(6). 1395–1408. 188 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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