Edoardo Monfrini

1.1k total citations
46 papers, 393 citations indexed

About

Edoardo Monfrini is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Edoardo Monfrini has authored 46 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Neurology, 17 papers in Cellular and Molecular Neuroscience and 14 papers in Molecular Biology. Recurrent topics in Edoardo Monfrini's work include Parkinson's Disease Mechanisms and Treatments (13 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurological disorders and treatments (8 papers). Edoardo Monfrini is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (13 papers), Genetic Neurodegenerative Diseases (13 papers) and Neurological disorders and treatments (8 papers). Edoardo Monfrini collaborates with scholars based in Italy, United States and France. Edoardo Monfrini's co-authors include Alessio Di Fonzo, Giacomo P. Comi, Nereo Bresolin, Giulietta Riboldi, Stefania Corti, Stefano Duga, Letizia Straniero, Roberto Erro, Paola Rinchetti and Michael Zech and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

Edoardo Monfrini

40 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Edoardo Monfrini Italy 13 196 141 90 88 77 46 393
Jennifer Müller vom Hagen Germany 12 150 0.8× 169 1.2× 152 1.7× 117 1.3× 62 0.8× 15 440
Daita Kaneda Japan 10 110 0.6× 183 1.3× 101 1.1× 79 0.9× 47 0.6× 39 402
Eleni Zamba‐Papanicolaou Cyprus 14 160 0.8× 290 2.1× 78 0.9× 230 2.6× 57 0.7× 45 597
Susen Schaake Germany 11 234 1.2× 115 0.8× 53 0.6× 137 1.6× 25 0.3× 22 407
Eugénie Mutez France 12 283 1.4× 171 1.2× 74 0.8× 160 1.8× 46 0.6× 28 427
Lourdes Ispierto Spain 12 161 0.8× 205 1.5× 83 0.9× 101 1.1× 20 0.3× 26 430
Yunlan Du China 11 154 0.8× 168 1.2× 123 1.4× 128 1.5× 48 0.6× 13 460
Lumine Matsumoto Japan 5 152 0.8× 206 1.5× 36 0.4× 130 1.5× 30 0.4× 6 373
Janel O. Johnson United States 10 163 0.8× 153 1.1× 34 0.4× 94 1.1× 38 0.5× 11 364
Chiara Reale Italy 11 157 0.8× 121 0.9× 40 0.4× 113 1.3× 23 0.3× 19 320

Countries citing papers authored by Edoardo Monfrini

Since Specialization
Citations

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

Fields of papers citing papers by Edoardo Monfrini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Edoardo Monfrini

This figure shows the co-authorship network connecting the top 25 collaborators of Edoardo Monfrini. A scholar is included among the top collaborators of Edoardo Monfrini 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 Edoardo Monfrini. Edoardo Monfrini 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.
Monfrini, Edoardo, et al.. (2024). Dystonic Tremor as Main Clinical Manifestation of SCA21. Movement Disorders Clinical Practice. 11(11). 1445–1450.
2.
Abati, Elena, Delia Gagliardi, Arianna Manini, et al.. (2024). Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort. Brain Communications. 6(5). fcae312–fcae312. 1 indexed citations
3.
Monfrini, Edoardo, Dario Ronchi, Megi Meneri, et al.. (2024). Unleashing the potential of mRNA therapeutics for inherited neurological diseases. Brain. 147(9). 2934–2945. 4 indexed citations
4.
Lucchi, Chiara, S. Grisanti, Edoardo Monfrini, et al.. (2024). Neurosteroid Levels in GBA Mutated and Non-Mutated Parkinson’s Disease: A Possible Factor Influencing Clinical Phenotype?. Biomolecules. 14(8). 1022–1022. 1 indexed citations
5.
Cavallieri, Francesco, Edoardo Monfrini, Alessandro Fraternali, et al.. (2024). A Case of 18p Chromosomal Deletion Encompassing GNAL in a Patient With Dystonia-Parkinsonism. Journal of Movement Disorders. 17(2). 236–238. 2 indexed citations
6.
Monfrini, Edoardo, Linda Borellini, Eleonora Mauri, et al.. (2023). GABRB1‐related early onset developmental and epileptic encephalopathy: Clinical trajectory and novel de novo mutation. Epileptic Disorders. 25(6). 867–873. 5 indexed citations
7.
Fonzo, Alessio Di, et al.. (2023). Genetic Evidence for Endolysosomal Dysfunction in Parkinson’s Disease: A Critical Overview. International Journal of Molecular Sciences. 24(7). 6338–6338. 10 indexed citations
8.
Monfrini, Edoardo, Sara Pelucchi, Maija Hollmén, et al.. (2023). A form of inherited hyperferritinemia associated with bi-allelic pathogenic variants of STAB1. The American Journal of Human Genetics. 110(8). 1436–1443. 1 indexed citations
9.
Monfrini, Edoardo, Cláudia Ferreira da Rosa Sobreira, Valentina Emmanuele, et al.. (2023). Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency. Neurology Genetics. 9(2). e200058–e200058. 3 indexed citations
10.
Monfrini, Edoardo, Alessio Di Fonzo, & Francesca Morgante. (2023). Chorea‐Acanthocytosis Presenting with Parkinsonism‐Dystonia without Chorea. Movement Disorders Clinical Practice. 10(S3). S32–S34. 4 indexed citations
11.
Cavallieri, Francesco, Rubens Gisbert Cury, Valentina Fioravanti, et al.. (2023). Recent Advances in the Treatment of Genetic Forms of Parkinson’s Disease: Hype or Hope?. Cells. 12(5). 764–764. 7 indexed citations
12.
Manini, Arianna, Letizia Straniero, Edoardo Monfrini, et al.. (2021). Screening of LRP10 mutations in Parkinson's disease patients from Italy. Parkinsonism & Related Disorders. 89. 17–21. 6 indexed citations
13.
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
14.
Monfrini, Edoardo, Michael Zech, Dora Steel, et al.. (2021). HOPS-associated neurological disorders (HOPSANDs): linking endolysosomal dysfunction to the pathogenesis of dystonia. Brain. 144(9). 2610–2615. 24 indexed citations
15.
Monfrini, Edoardo, Francesca Spagnolo, Margherita Canesi, et al.. (2021). VPS13C-associated Parkinson's disease: Two novel cases and review of the literature. Parkinsonism & Related Disorders. 94. 37–39. 13 indexed citations
16.
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
17.
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.
18.
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
19.
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
20.
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

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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