Arianna Manini

788 total citations
24 papers, 299 citations indexed

About

Arianna Manini is a scholar working on Neurology, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Arianna Manini has authored 24 papers receiving a total of 299 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Neurology, 11 papers in Molecular Biology and 6 papers in Cellular and Molecular Neuroscience. Recurrent topics in Arianna Manini's work include Amyotrophic Lateral Sclerosis Research (7 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Arianna Manini is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (7 papers), Neurogenetic and Muscular Disorders Research (5 papers) and Genetic Neurodegenerative Diseases (5 papers). Arianna Manini collaborates with scholars based in Italy, United Kingdom and United States. Arianna Manini's co-authors include Leonardo Pantoni, Stefania Corti, Giacomo P. Comi, Elena Abati, Dario Ronchi, Simone Pomati, Michela Brambilla, Laura Maggiore, Claudia Morelli and Federico Verde and has published in prestigious journals such as Neurology, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Arianna Manini

23 papers receiving 291 citations

Author Peers

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

Author Last Decade Papers Cites
Arianna Manini 136 110 45 41 41 24 299
Koji Abe 121 0.9× 114 1.0× 47 1.0× 54 1.3× 47 1.1× 24 321
Matt Parton 201 1.5× 62 0.6× 31 0.7× 60 1.5× 27 0.7× 15 331
Stephan Neudecker 170 1.3× 106 1.0× 27 0.6× 59 1.4× 29 0.7× 14 333
Michelle M. Mezei 165 1.2× 158 1.4× 25 0.6× 76 1.9× 35 0.9× 19 326
Etienne Léveillé 62 0.5× 82 0.7× 48 1.1× 37 0.9× 40 1.0× 26 246
Andrzej Potemkowski 98 0.7× 85 0.8× 42 0.9× 13 0.3× 32 0.8× 38 448
Tjalf Ziemssen 66 0.5× 53 0.5× 33 0.7× 32 0.8× 28 0.7× 26 237
Matteo Tagliapietra 80 0.6× 99 0.9× 41 0.9× 18 0.4× 21 0.5× 19 245
Laura Adobbati 140 1.0× 70 0.6× 28 0.6× 20 0.5× 21 0.5× 13 253
Maria del Mar Amador 133 1.0× 231 2.1× 33 0.7× 96 2.3× 92 2.2× 25 482

Countries citing papers authored by Arianna Manini

Since Specialization
Citations

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

Fields of papers citing papers by Arianna Manini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arianna Manini

This figure shows the co-authorship network connecting the top 25 collaborators of Arianna Manini. A scholar is included among the top collaborators of Arianna Manini 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 Arianna Manini. Arianna Manini 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.
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
2.
Facchini, Stefano, Natalia Dominik, Arianna Manini, et al.. (2023). Optical Genome Mapping Enables Detection and Accurate Sizing of RFC1 Repeat Expansions. Biomolecules. 13(10). 1546–1546. 11 indexed citations
3.
Manini, Arianna, Alessio Maranzano, Francesco Gentile, et al.. (2023). Association of the risk factor UNC13A with survival and upper motor neuron involvement in amyotrophic lateral sclerosis. Frontiers in Aging Neuroscience. 15. 1067954–1067954. 9 indexed citations
4.
Manini, Arianna, Delia Gagliardi, Megi Meneri, et al.. (2023). NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients. Scientific Reports. 13(1). 3187–3187. 2 indexed citations
5.
Verde, Federico, Eleonora Colombo, Alessio Maranzano, et al.. (2023). Phenotypic correlates of serum neurofilament light chain levels in amyotrophic lateral sclerosis. Frontiers in Aging Neuroscience. 15. 1132808–1132808. 12 indexed citations
6.
Manini, Arianna, Antonia Ratti, Alessio Maranzano, et al.. (2022). TMEM106B Acts as a Modifier of Cognitive and Motor Functions in Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences. 23(16). 9276–9276. 5 indexed citations
7.
Manini, Arianna, Delia Gagliardi, Megi Meneri, et al.. (2022). Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis. Annals of Clinical and Translational Neurology. 9(11). 1820–1825. 4 indexed citations
8.
Manini, Arianna, Elena Abati, Giacomo P. Comi, Stefania Corti, & Dario Ronchi. (2022). Mitochondrial DNA homeostasis impairment and dopaminergic dysfunction: A trembling balance. Ageing Research Reviews. 76. 101578–101578. 21 indexed citations
9.
10.
Manini, Arianna, Megi Meneri, Carmelo Rodolico, et al.. (2022). Case Report: Thymidine Kinase 2 (TK2) Deficiency: A Novel Mutation Associated With Childhood-Onset Mitochondrial Myopathy and Atypical Progression. Frontiers in Neurology. 13. 857279–857279.
11.
Manini, Arianna, Leonardo Caporali, Megi Meneri, et al.. (2022). Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions. Frontiers in Genetics. 13. 906667–906667. 5 indexed citations
12.
Scopelliti, Giuseppe, Arianna Manini, Marco Schiavone, et al.. (2022). Etiologic reclassification of cryptogenic stroke after implantable cardiac monitoring and computed tomography angiography re-assessment. Journal of Neurology. 270(1). 377–385. 3 indexed citations
13.
Abati, Elena, Arianna Manini, Daniele Velardo, et al.. (2022). Clinical and genetic features of a cohort of patients with MFN2-related neuropathy. Scientific Reports. 12(1). 6181–6181. 18 indexed citations
14.
Manini, Arianna, et al.. (2022). Adeno-Associated Virus (AAV)-Mediated Gene Therapy for Duchenne Muscular Dystrophy: The Issue of Transgene Persistence. Frontiers in Neurology. 12. 814174–814174. 38 indexed citations
15.
Abati, Elena, Arianna Manini, Giacomo P. Comi, & Stefania Corti. (2022). Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases. Cellular and Molecular Life Sciences. 79(7). 374–374. 46 indexed citations
16.
Fumagalli, Monica, Dario Ronchi, Maria Francesca Bedeschi, et al.. (2022). A novel RRM2B mutation associated with mitochondrial DNA depletion syndrome. Molecular Genetics and Metabolism Reports. 32. 100887–100887. 5 indexed citations
17.
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
18.
Manini, Arianna, Michela Brambilla, Laura Maggiore, Simone Pomati, & Leonardo Pantoni. (2021). The impact of lockdown during SARS-CoV-2 outbreak on behavioral and psychological symptoms of dementia. Neurological Sciences. 42(3). 825–833. 27 indexed citations
19.
Manini, Arianna & Leonardo Pantoni. (2021). CADASIL from Bench to Bedside: Disease Models and Novel Therapeutic Approaches. Molecular Neurobiology. 58(6). 2558–2573. 33 indexed citations
20.
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

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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