Anna Masato

675 total citations · 1 hit paper
16 papers, 435 citations indexed

About

Anna Masato is a scholar working on Neurology, Cell Biology and Molecular Biology. According to data from OpenAlex, Anna Masato has authored 16 papers receiving a total of 435 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 5 papers in Cell Biology and 4 papers in Molecular Biology. Recurrent topics in Anna Masato's work include Parkinson's Disease Mechanisms and Treatments (10 papers), Autophagy in Disease and Therapy (4 papers) and Cellular transport and secretion (4 papers). Anna Masato is often cited by papers focused on Parkinson's Disease Mechanisms and Treatments (10 papers), Autophagy in Disease and Therapy (4 papers) and Cellular transport and secretion (4 papers). Anna Masato collaborates with scholars based in Italy, United Kingdom and United States. Anna Masato's co-authors include Luigi Bubacco, Nicoletta Plotegher, Daniela Boassa, Marco Bisaglia, Michele Sandre, Elisa Greggio, Giorgio Arrigoni, Elena Giusto, Anna Erlandsson and Isabella Tessari and has published in prestigious journals such as Angewandte Chemie International Edition, Nature Communications and International Journal of Molecular Sciences.

In The Last Decade

Anna Masato

16 papers receiving 426 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Impaired dopamine metabolism in Parkinson’s disease pathogenesis

2019 227 citations Anna Masato, Nicoletta Plotegher et al. Molecular Neurodegeneration profile →

Peers

Anna Masato

NEURO

CMN

PHYSI

NEURO

Xin Yuan China

Sergio Cárdenas Chile

Carolina Perez-Pastene Chile

Sandro Huenchuguala Chile

Giuseppina Natale Italy

Jeswinder Sian‐Hülsmann Germany

Fatemeh Nouri Emamzadeh United Kingdom

Richard M. Meade United Kingdom

Neeraj Pandey United States

Alessandro Mechelli Italy

Xin Yuan China

Anna Masato

184 ×0.8

NEURO

113 ×0.8

81 ×0.6

CMN

102 ×1.3

PHYSI

79 ×1.2

NEURO

Citations per year, relative to Anna Masato Anna Masato (= 1×) peers Xin Yuan

Countries citing papers authored by Anna Masato

Since Specialization

Citations

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

Fields of papers citing papers by Anna Masato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Masato

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Masato. A scholar is included among the top collaborators of Anna Masato 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 Anna Masato. Anna Masato is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

16 of 16 papers shown

Masato, Anna, Annapaola Andolfo, Edoardo Bellini, et al.. (2024). Sequestosome-1 (SQSTM1/p62) as a target in dopamine catabolite-mediated cellular dyshomeostasis. Cell Death and Disease. 15(6). 424–424. 1 indexed citations

Masato, Anna & Luigi Bubacco. (2024). The αSynuclein half-life conundrum. Neurobiology of Disease. 196. 106524–106524. 1 indexed citations

Giamogante, Flavia, Lucia Barazzuol, Alessandra Esposito, et al.. (2024). A SPLICS reporter reveals $${{{{{\boldsymbol{\alpha }}}}}}$$-synuclein regulation of lysosome-mitochondria contacts which affects TFEB nuclear translocation. Nature Communications. 15(1). 1516–1516. 8 indexed citations

Masato, Anna, Nicoletta Plotegher, Michele Sandre, et al.. (2023). DOPAL initiates αSynuclein-dependent impaired proteostasis and degeneration of neuronal projections in Parkinson’s disease. npj Parkinson s Disease. 9(1). 42–42. 28 indexed citations

Carmosino, Monica, Andrea Gerbino, Anna Masato, et al.. (2023). Neuroprotective Effect of Antiapoptotic URG7 Protein on Human Neuroblastoma Cell Line SH-SY5Y. International Journal of Molecular Sciences. 25(1). 481–481. 1 indexed citations

Sandre, Michele, et al.. (2023). Scavenging neurotoxic aldehydes using lysine carbon dots. Nanoscale Advances. 5(5). 1356–1367. 4 indexed citations

Masato, Anna, Michele Sandre, Francesca Moret, et al.. (2023). SARS-CoV-2-Mimicking Pseudoviral Particles Accelerate α-Synuclein Aggregation In Vitro. ACS Chemical Neuroscience. 15(2). 215–221. 6 indexed citations

Faustini, Gaia, Francesca Longhena, Anna Masato, et al.. (2022). Synapsin III gene silencing redeems alpha-synuclein transgenic mice from Parkinson's disease-like phenotype. Molecular Therapy. 30(4). 1465–1483. 14 indexed citations

Sandre, Michele, Isabella Tessari, Nicoletta Plotegher, et al.. (2021). Parkinson’s Disease–Associated LRRK2 Interferes with Astrocyte-Mediated Alpha-Synuclein Clearance. Molecular Neurobiology. 58(7). 3119–3140. 61 indexed citations

10.

Masato, Anna, et al.. (2021). Metformin Repurposing for Parkinson Disease Therapy: Opportunities and Challenges. International Journal of Molecular Sciences. 23(1). 398–398. 54 indexed citations

11.

Masato, Anna, Michele Sandre, Angelo Antonini, & Luigi Bubacco. (2021). Patients Stratification Strategies to Optimize the Effectiveness of Scavenging Biogenic Aldehydes: Towards a Neuroprotective Approach for Parkinson's Disease. Current Neuropharmacology. 19(10). 1618–1639. 12 indexed citations

12.

Crisma, Marco, et al.. (2020). Photoresponsive Prion‐Mimic Foldamer to Induce Controlled Protein Aggregation. Angewandte Chemie. 133(10). 5233–5238. 1 indexed citations

13.

Crisma, Marco, et al.. (2020). Photoresponsive Prion‐Mimic Foldamer to Induce Controlled Protein Aggregation. Angewandte Chemie International Edition. 60(10). 5173–5178. 11 indexed citations

14.

Masato, Anna, Nicoletta Plotegher, Daniela Boassa, & Luigi Bubacco. (2019). Impaired dopamine metabolism in Parkinson’s disease pathogenesis. Molecular Neurodegeneration. 14(1). 35–35. 227 indexed citations breakdown →

15.

Biosa, Alice, Anna Masato, Roberta Filograna, et al.. (2019). Superoxide Dismutases SOD1 and SOD2 Rescue the Toxic Effect of Dopamine-Derived Products in Human SH-SY5Y Neuroblastoma Cells. Neurotoxicity Research. 36(4). 746–755. 5 indexed citations

16.

Shimada, Hitoshi, et al.. (2007). 1.017 Brain acetylcholinesterase changes in Dementia with Lewy Bodies and Parkinson's disease with Dementia demonstrated by PET. Parkinsonism & Related Disorders. 13. S31–S32. 1 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.

Explore authors with similar magnitude of impact