Silvia Masnada

1.6k total citations
24 papers, 257 citations indexed

About

Silvia Masnada is a scholar working on Molecular Biology, Psychiatry and Mental health and Clinical Biochemistry. According to data from OpenAlex, Silvia Masnada has authored 24 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Psychiatry and Mental health and 6 papers in Clinical Biochemistry. Recurrent topics in Silvia Masnada's work include Epilepsy research and treatment (7 papers), interferon and immune responses (5 papers) and Metabolism and Genetic Disorders (5 papers). Silvia Masnada is often cited by papers focused on Epilepsy research and treatment (7 papers), interferon and immune responses (5 papers) and Metabolism and Genetic Disorders (5 papers). Silvia Masnada collaborates with scholars based in Italy, United Kingdom and United States. Silvia Masnada's co-authors include Pierangelo Veggiotti, Valentina De Giorgis, Davide Tonduti, Ludovica Pasca, Anna Tagliabue, Costanza Varesio, Cinzia Ferraris, M. Filippini, Marialuisa Valente and Luisa Chiapparini and has published in prestigious journals such as International Journal of Molecular Sciences, Frontiers in Immunology and Nutrients.

In The Last Decade

Silvia Masnada

22 papers receiving 254 citations

Peers

Silvia Masnada
Anaïs Thouin United Kingdom
Åse Elfving Sweden
Enrico Alfei Italy
Sabine Grønborg Denmark
Mara Lúcia Schmitz Ferreira Santos Brazil
Maura Ruzhnikov United States
Anna Marcé‐Grau Spain
Danijela Petković Ramadža Croatia
Clara DM van Karnebeek Canada
Marjan E. Steenweg Netherlands
Anaïs Thouin United Kingdom
Silvia Masnada
Citations per year, relative to Silvia Masnada Silvia Masnada (= 1×) peers Anaïs Thouin

Countries citing papers authored by Silvia Masnada

Since Specialization
Citations

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

Fields of papers citing papers by Silvia Masnada

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Masnada

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Masnada. A scholar is included among the top collaborators of Silvia Masnada 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 Silvia Masnada. Silvia Masnada 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
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Spagnoli, Carlotta, Stefano Giuseppe Caraffi, A Cavalli, et al.. (2024). Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International Journal of Molecular Sciences. 25(2). 1248–1248. 9 indexed citations
3.
Spagnoli, Carlotta, et al.. (2024). Educational needs and career development of young epileptologists in Italy. Epilepsia Open. 9(2). 613–625. 2 indexed citations
4.
Furia, Francesca, Katrine M. Johannesen, Ángel Aledo‐Serrano, et al.. (2024). Sleep disturbances in SCN8A‐related disorders. Epilepsia Open. 9(6). 2186–2197. 3 indexed citations
5.
Masnada, Silvia, Paola Anna Erba, Anna Camporesi, et al.. (2023). FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. Neurological Sciences. 44(9). 3037–3043. 4 indexed citations
6.
7.
Spagnoli, Carlotta, Silvia Masnada, Simona Balestrini, et al.. (2023). Impact of gender inequality on the educational and career development of young epileptologists in Italy: A survey of the Young Epilepsy Section – Italian chapter. Epilepsy & Behavior. 145. 109328–109328. 3 indexed citations
8.
Alfei, Enrico, et al.. (2023). Paradigm shift in the treatment of tuberous sclerosis: Effectiveness of everolimus. Pharmacological Research. 195. 106884–106884. 6 indexed citations
9.
Nicita, Francesco, Silvia Masnada, Roberta Battini, et al.. (2021). Alexander disease evolution over time: data from an Italian cohort of pediatric-onset patients. Molecular Genetics and Metabolism. 134(4). 353–358. 6 indexed citations
10.
Masnada, Silvia, Catherine Sarret, Clara E. Antonello, et al.. (2021). Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome. Molecular Genetics and Metabolism. 135(1). 109–113. 20 indexed citations
11.
Masnada, Silvia, Clara E. Antonello, Cecilia Parazzini, et al.. (2021). Ruxolitinib in Aicardi-Goutières syndrome. Metabolic Brain Disease. 36(5). 859–863. 17 indexed citations
12.
Tonduti, Davide, Silvia Masnada, Enrico Bertini, et al.. (2021). Spinal cord involvement and paroxysmal events in “Infantile Onset Transient Hypomyelination” due to TMEM63A mutation. Journal of Human Genetics. 66(10). 1035–1037. 18 indexed citations
13.
Gavazzi, Francesco, Holly Dubbs, Valentina De Giorgis, et al.. (2020). Late-Onset Aicardi-Goutières Syndrome: A Characterization of Presenting Clinical Features. Pediatric Neurology. 115. 1–6. 17 indexed citations
14.
Giorgis, Valentina De, Costanza Varesio, Maurizio Viri, et al.. (2020). The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings. Seizure. 86. 197–209. 3 indexed citations
15.
Masnada, Silvia, Cecilia Parazzini, P Bini, et al.. (2020). Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency. European Journal of Paediatric Neurology. 28. 151–158. 20 indexed citations
16.
Masnada, Silvia, Daniele Gibelli, Claudia Dolci, et al.. (2020). 3D facial morphometry in Italian patients affected by Aicardi syndrome. American Journal of Medical Genetics Part A. 182(10). 2325–2332. 6 indexed citations
17.
Bertoli, Simona, Silvia Masnada, Ramona De Amicis, et al.. (2020). Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis. European Journal of Clinical Nutrition. 74(9). 1290–1298. 8 indexed citations
18.
Masnada, Silvia, Veronica Saletti, Luisa Chiapparini, et al.. (2019). Novel mutations in SLC16A2 associated with a less severe phenotype of MCT8 deficiency. Metabolic Brain Disease. 34(6). 1565–1575. 15 indexed citations
19.
Pasca, Ludovica, Roberto Caraballo, Valentina De Giorgis, et al.. (2018). Ketogenic diet use in children with intractable epilepsy secondary to malformations of cortical development: A two- centre experience. Seizure. 57. 34–37. 17 indexed citations
20.

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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