Sara Bonato

1.3k total citations
23 papers, 584 citations indexed

About

Sara Bonato is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Sara Bonato has authored 23 papers receiving a total of 584 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 5 papers in Cellular and Molecular Neuroscience and 5 papers in Neurology. Recurrent topics in Sara Bonato's work include Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Sara Bonato is often cited by papers focused on Mitochondrial Function and Pathology (6 papers), Metabolism and Genetic Disorders (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Sara Bonato collaborates with scholars based in Italy, United Kingdom and Estonia. Sara Bonato's co-authors include Nereo Bresolin, Maria Grazia D’Angelo, Giacomo P. Comi, Dario Ronchi, Stefania Corti, Anna Carla Turconi, Alessio Di Fonzo, Maurizio Moggio, Andreina Bordoni and Luigi Piccinini and has published in prestigious journals such as Brain, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Sara Bonato

23 papers receiving 578 citations

Peers

Sara Bonato

CMN

NEURO

T. E. Bertoríni United States

Tracey Willis United Kingdom

Etsuo Chihara Japan

Claudia Castiglioni Chile

Manoj P. Menezes Australia

Tiziana Mongini Italy

Marek Molčányi Germany

J‐M. Burgunder Switzerland

S. Sinicropi Italy

Z Kamieniecka Denmark

T. E. Bertoríni United States

Sara Bonato

489 ×1.4

158 ×1.3

CMN

139 ×1.8

NEURO

240 ×3.3

38 ×0.6

NEURO

Citations per year, relative to Sara Bonato Sara Bonato (= 1×) peers T. E. Bertoríni

Countries citing papers authored by Sara Bonato

Since Specialization

Citations

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

Fields of papers citing papers by Sara Bonato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sara Bonato

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

All Works

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20 of 20 papers shown

Costamagna, Gianluca, Sara Bonato, Stefania Corti, & Megi Meneri. (2023). Advancing Stroke Research on Cerebral Thrombi with Omic Technologies. International Journal of Molecular Sciences. 24(4). 3419–3419. 4 indexed citations

Schwarz, Ghil, Sara Bonato, Silvia Lanfranconi, et al.. (2023). Intravenous thrombolysis + endovascular thrombectomy versus thrombolysis alone in large vessel occlusion mild stroke: a propensity score matched analysis. European Journal of Neurology. 30(5). 1312–1319. 11 indexed citations

Meneri, Megi, Sara Bonato, Delia Gagliardi, Giacomo P. Comi, & Stefania Corti. (2022). New Insights into Cerebral Vessel Disease Landscapes at Single-Cell Resolution: Pathogenetic and Therapeutic Perspectives. Biomedicines. 10(7). 1693–1693. 6 indexed citations

Carandina, Angelica, Davide Villa, Alessio Di Fonzo, et al.. (2021). Targeting the Autonomic Nervous System for Risk Stratification, Outcome Prediction and Neuromodulation in Ischemic Stroke. International Journal of Molecular Sciences. 22(5). 2357–2357. 28 indexed citations

Cugno, Massimo, Paolo Macor, Mara Giordano, et al.. (2021). Consumption of complement in a 26-year-old woman with severe thrombotic thrombocytopenia after ChAdOx1 nCov-19 vaccination. Journal of Autoimmunity. 124. 102728–102728. 4 indexed citations

Gagliardi, Delia, Irene Faravelli, Manuel Alfredo Podestà, et al.. (2021). Sodium Levels Predict Disability at Discharge in Guillain-Barré Syndrome: A Retrospective Cohort Study. Frontiers in Neurology. 12. 729252–729252. 2 indexed citations

Bonato, Sara, Andrea Artoni, Anna Lecchi, et al.. (2021). Massive cerebral venous thrombosis due to vaccine-induced immune thrombotic thrombocytopenia. Haematologica. 106(11). 3021–3024. 8 indexed citations

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

Villa, Davide, Claudia Cinnante, Silvia Lanfranconi, et al.. (2020). Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG. BMC Neurology. 20(1). 316–316. 7 indexed citations

10.

Lanfranconi, Silvia, et al.. (2020). Safety and efficacy of rt-PA treatment for acute stroke in pseudoxanthoma elasticum: the first report. Journal of Thrombosis and Thrombolysis. 51(1). 176–179. 3 indexed citations

11.

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

12.

Ardolino, Gianluca, Tommaso Bocci, Maurizio Vergari, et al.. (2018). Spinal direct current stimulation (tsDCS) in hereditary spastic paraplegias (HSP): A sham-controlled crossover study. Journal of Spinal Cord Medicine. 44(1). 46–53. 28 indexed citations

13.

Borellini, Linda, Silvia Lanfranconi, Sara Bonato, et al.. (2017). Progressive Encephalomyelitis with Rigidity and Myoclonus Associated With Anti-GlyR Antibodies and Hodgkin’s Lymphoma: A Case Report. Frontiers in Neurology. 8. 401–401. 17 indexed citations

14.

Reyes, Aurelio, Laura Melchionda, Alessia Nasca, et al.. (2015). RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy. The American Journal of Human Genetics. 97(1). 186–193. 80 indexed citations

15.

Bella, Daniela Di, Davide Pareyson, M. Savoiardo, et al.. (2014). Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation. Neurology. 83(13). 1217–1218. 41 indexed citations

16.

Vantaggiato, Chiara, Claudia Crimella, Giovanni Airoldi, et al.. (2013). Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15. Brain. 136(10). 3119–3139. 62 indexed citations

17.

Magri, Francesca, Roberto Del Bo, Maria Grazia D’Angelo, et al.. (2012). Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients. Neuromuscular Disorders. 22(11). 934–943. 47 indexed citations

18.

Ronchi, Dario, Andreina Bordoni, Elisa Fassone, et al.. (2009). Mitochondrial DNA G8363A mutation in the tRNALys gene: Clinical, biochemical and pathological study. Journal of the Neurological Sciences. 281(1-2). 85–92. 36 indexed citations

19.

Airoldi, Giovanni, Andrea Guidarelli, Orazio Cantoni, et al.. (2009). Characterization of two novel SETX mutations in AOA2 patients reveals aspects of the pathophysiological role of senataxin. Neurogenetics. 11(1). 91–100. 23 indexed citations

20.

D’Angelo, Maria Grazia, Luigi Piccinini, M. Romei, et al.. (2008). Gait pattern in Duchenne muscular dystrophy. Gait & Posture. 29(1). 36–41. 88 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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