Roberta Solazzi

401 total citations
20 papers, 162 citations indexed

About

Roberta Solazzi is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Roberta Solazzi has authored 20 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Psychiatry and Mental health. Recurrent topics in Roberta Solazzi's work include Genetics and Neurodevelopmental Disorders (9 papers), Epilepsy research and treatment (7 papers) and Genomics and Rare Diseases (6 papers). Roberta Solazzi is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Epilepsy research and treatment (7 papers) and Genomics and Rare Diseases (6 papers). Roberta Solazzi collaborates with scholars based in Italy, United Kingdom and France. Roberta Solazzi's co-authors include Elena Freri, Tiziana Granata, Laura Canafoglia, Cinzia Gellera, Barbara Castellotti, Francesca Ragona, Jacopo C. DiFrancesco, Nardo Nardocci, Francesca Darra and Silvana Franceschetti and has published in prestigious journals such as Cerebral Cortex, Epilepsia and Clinical Neurophysiology.

In The Last Decade

Roberta Solazzi

20 papers receiving 162 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roberta Solazzi Italy 8 91 67 55 31 22 20 162
Maura Ruzhnikov United States 9 73 0.8× 48 0.7× 96 1.7× 23 0.7× 37 1.7× 21 213
Raffaella Minardi Italy 7 80 0.9× 55 0.8× 45 0.8× 25 0.8× 10 0.5× 21 134
Cheuk Wing Fung China 9 54 0.6× 31 0.5× 67 1.2× 21 0.7× 23 1.0× 18 177
Ahmed Abdelmoity United States 11 95 1.0× 91 1.4× 55 1.0× 33 1.1× 52 2.4× 25 264
Giacomo Garone Italy 10 117 1.3× 47 0.7× 106 1.9× 57 1.8× 12 0.5× 26 270
Emmanuelle Lagrue France 8 79 0.9× 23 0.3× 110 2.0× 64 2.1× 15 0.7× 20 229
Yasuhiro Suzuki Japan 8 58 0.6× 98 1.5× 122 2.2× 42 1.4× 26 1.2× 16 259
Livia Pisciotta Italy 9 47 0.5× 30 0.4× 102 1.9× 24 0.8× 8 0.4× 22 166
Vandana Shashi United States 4 77 0.8× 90 1.3× 76 1.4× 45 1.5× 7 0.3× 4 170

Countries citing papers authored by Roberta Solazzi

Since Specialization
Citations

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

Fields of papers citing papers by Roberta Solazzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roberta Solazzi

This figure shows the co-authorship network connecting the top 25 collaborators of Roberta Solazzi. A scholar is included among the top collaborators of Roberta Solazzi 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 Roberta Solazzi. Roberta Solazzi 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.
Castellotti, Barbara, Francesca Ragona, Elena Freri, et al.. (2024). Next‐generation sequencing in pediatric‐onset epilepsies: Analysis with target panels and personalized therapeutic approach. Epilepsia Open. 9(5). 1922–1930. 2 indexed citations
2.
Mosca, Ilaria, Elena Freri, Paolo Ambrosino, et al.. (2024). Case report: Marked electroclinical improvement by fluoxetine treatment in a patient with KCNT1-related drug-resistant focal epilepsy. Frontiers in Cellular Neuroscience. 18. 1367838–1367838. 4 indexed citations
3.
Invernizzi, Federica, Barbara Castellotti, Chiara Reale, et al.. (2024). CLN6‐related continuum phenotype caused by aberrant splicing. Epilepsia Open. 10(1). 348–354. 1 indexed citations
4.
Ambrosino, Paolo, Francesca Ragona, Ilaria Mosca, et al.. (2023). A novel KCNC1 gain‐of‐function variant causing developmental and epileptic encephalopathy: “Precision medicine” approach with fluoxetine. Epilepsia. 64(7). e148–e155. 10 indexed citations
5.
Solazzi, Roberta, Elena Fiorini, Giulia Galati, et al.. (2023). Gelastic seizures and “smiling spasms”: A peculiar ictal pattern. Epileptic Disorders. 25(2). 269–273. 1 indexed citations
6.
Specchio, Nicola, Marina Trivisano, Matteo Lenge, et al.. (2023). CDKL5 deficiency disorder: progressive brain atrophy may be part of the syndrome. Cerebral Cortex. 33(17). 9709–9717. 7 indexed citations
7.
Solazzi, Roberta, Silvia Esposito, Margherita Estienne, et al.. (2023). Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome. Pediatric Neurology. 147. 24–27. 1 indexed citations
8.
Solazzi, Roberta, Marco Moscatelli, Davide Rossi Sebastiano, et al.. (2022). Severe Epilepsy and Movement Disorder May Be Early Symptoms of TMEM106B -Related Hypomyelinating Leukodystrophy. Neurology Genetics. 8(5). e200022–e200022. 2 indexed citations
9.
Varesio, Costanza, Elena Freri, Francesca Darra, et al.. (2021). CDKL5 deficiency disorder in males: Five new variants and review of the literature. European Journal of Paediatric Neurology. 33. 9–20. 19 indexed citations
10.
Franceschetti, Silvana, Elisa Visani, Davide Rossi Sebastiano, et al.. (2021). Cortico-muscular and cortico-cortical coherence changes resulting from Perampanel treatment in patients with cortical myoclonus. Clinical Neurophysiology. 132(5). 1057–1063. 6 indexed citations
11.
Freri, Elena, Barbara Castellotti, Laura Canafoglia, et al.. (2021). Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol. Seizure. 88. 143–145. 7 indexed citations
12.
Kamińska, Anna, Roberta Solazzi, Claude Cancés, et al.. (2021). SYNGAP1-DEE: A visual sensitive epilepsy. Clinical Neurophysiology. 132(4). 841–850. 17 indexed citations
13.
Solazzi, Roberta, Elena Fiorini, Elena Parrini, et al.. (2021). Early‐onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome. Epileptic Disorders. 23(5). 745–748. 4 indexed citations
14.
Solazzi, Roberta, Barbara Castellotti, Laura Canafoglia, et al.. (2021). Paroxysmal tonic upgaze in a child with SCN8A‐related encephalopathy∗. Epileptic Disorders. 23(4). 643–647. 3 indexed citations
15.
Soldovieri, Maria Virginia, Elena Freri, Paolo Ambrosino, et al.. (2020). Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy. Pharmacological Research. 160. 105200–105200. 13 indexed citations
16.
Vetri, Luigi, Francesco Calı̀, Mirella Vinci, et al.. (2020). A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy. European Journal of Medical Genetics. 63(4). 103848–103848. 18 indexed citations
17.
Ragona, Francesca, Laura Canafoglia, Barbara Castellotti, et al.. (2020). Early Parkinsonism in a Senegalese girl with Lafora disease. Epileptic Disorders. 22(2). 233–236. 2 indexed citations
18.
Castellotti, Barbara, Francesca Ragona, Elena Freri, et al.. (2019). Screening of SLC2A1 in a large cohort of patients suspected for Glut1 deficiency syndrome: identification of novel variants and associated phenotypes. Journal of Neurology. 266(6). 1439–1448. 26 indexed citations
19.
Solazzi, Roberta, Elena Fiorini, Elena Parrini, et al.. (2018). Diaper changing‐induced reflex seizures in CDKL5‐related epilepsy. Epileptic Disorders. 20(5). 428–433. 5 indexed citations
20.
Lamperti, Costanza, Federica Invernizzi, Roberta Solazzi, et al.. (2015). Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients. European Journal of Paediatric Neurology. 20(1). 152–157. 14 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

Breakdown of academic impact, for papers by Maura Ruzhnikov Breakdown of academic impact, for papers by Raffaella Minardi Breakdown of academic impact, for papers by Cheuk Wing Fung Breakdown of academic impact, for papers by Ahmed Abdelmoity Breakdown of academic impact, for papers by Giacomo Garone Breakdown of academic impact, for papers by Emmanuelle Lagrue Breakdown of academic impact, for papers by Yasuhiro Suzuki Breakdown of academic impact, for papers by Livia Pisciotta Breakdown of academic impact, for papers by Vandana Shashi
Rankless by CCL
2026