Giulia Prato

590 total citations
27 papers, 241 citations indexed

About

Giulia Prato is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Giulia Prato has authored 27 papers receiving a total of 241 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 7 papers in Molecular Biology and 7 papers in Psychiatry and Mental health. Recurrent topics in Giulia Prato's work include Genetics and Neurodevelopmental Disorders (9 papers), Epilepsy research and treatment (6 papers) and Autism Spectrum Disorder Research (5 papers). Giulia Prato is often cited by papers focused on Genetics and Neurodevelopmental Disorders (9 papers), Epilepsy research and treatment (6 papers) and Autism Spectrum Disorder Research (5 papers). Giulia Prato collaborates with scholars based in Italy, United States and Australia. Giulia Prato's co-authors include Maria Margherita Mancardi, Isabel Hagel, Neil R. Lynch, Reina López, M. G. Baglietto, Livia Pisciotta, Patrizia Ronchetto, Cristina Cuoco, Elisa Tassano and Giorgio Gimelli and has published in prestigious journals such as International Journal of Molecular Sciences, Frontiers in Neuroscience and Clinical & Experimental Allergy.

In The Last Decade

Giulia Prato

24 papers receiving 226 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Giulia Prato Italy	8	65	57	54	27	26	27	241
Shang‐Hung Lin Taiwan	10	95 1.5×	20 0.4×	90 1.7×	9 0.3×	29 1.1×	26	479
Andrzej Jaworek Poland	12	26 0.4×	10 0.2×	95 1.8×	37 1.4×	11 0.4×	63	379
Kathrin Mahler Walther Germany	4	79 1.2×	28 0.5×	19 0.4×	5 0.2×	11 0.4×	5	321
Tal Eidlitz‐Markus Israel	12	49 0.8×	28 0.5×	79 1.5×	43 1.6×	192 7.4×	23	425
Tom Dyer United States	10	72 1.1×	92 1.6×	24 0.4×	2 0.1×	18 0.7×	15	288
Himadri Datta India	12	37 0.6×	37 0.6×	26 0.5×	11 0.4×	8 0.3×	36	326
Laure Wingertsmann France	7	168 2.6×	17 0.3×	50 0.9×	3 0.1×	10 0.4×	14	442
Kristin A. Koch United States	9	29 0.4×	25 0.4×	19 0.4×	6 0.2×	3 0.1×	10	350
Asiya Pasha United States	6	95 1.5×	16 0.3×	45 0.8×	13 0.5×	28 1.1×	7	451
Nicole Y. Lai United States	8	197 3.0×	19 0.3×	70 1.3×	8 0.3×	13 0.5×	10	437

Countries citing papers authored by Giulia Prato

Since Specialization

Citations

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

Fields of papers citing papers by Giulia Prato

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giulia Prato

This figure shows the co-authorship network connecting the top 25 collaborators of Giulia Prato. A scholar is included among the top collaborators of Giulia Prato 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 Giulia Prato. Giulia Prato 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

Pelizza, Maria Federica, et al.. (2026). Use of fenfluramine in MECP2-related Rett syndrome: Findings from a retrospective multicenter pediatric case series. Epilepsy & Behavior. 178. 110920–110920.

Prato, Giulia, et al.. (2025). Parkinsonism and Dystonia Are Prevalent and Concomitant Movement Disorders in a Cohort of Patients with Rett Syndrome. Movement Disorders Clinical Practice. 12(11). 1843–1848.

Leoncini, Silvia, Valeria Scandurra, Aglaia Vignoli, et al.. (2024). 24-h continuous non-invasive multiparameter home monitoring of vitals in patients with Rett syndrome by an innovative wearable technology: evidence of an overlooked chronic fatigue status. Frontiers in Neurology. 15. 1388506–1388506. 4 indexed citations

Rodrigues, Gabriel Dias, Giulia Prato, Raffaele Ferri, et al.. (2024). Predominant cardiac sympathetic modulation during wake and sleep in patients with Rett syndrome. Sleep Medicine. 119. 188–191. 2 indexed citations

Tobaldini, Eleonora, Gabriel Dias Rodrigues, Nicola Disma, et al.. (2023). Cardiac autonomic control in Rett syndrome: Insights from heart rate variability analysis. Frontiers in Neuroscience. 17. 1048278–1048278. 4 indexed citations

Tortora, Domenico, Mariasavina Severino, Alessandro Consales, et al.. (2022). Comparison of Qualitative and Quantitative Analyses of MR-Arterial Spin Labeling Perfusion Data for the Assessment of Pediatric Patients with Focal Epilepsies. Diagnostics. 12(4). 811–811. 8 indexed citations

Pisciotta, Livia, Maria Margherita Mancardi, Michela Stagnaro, et al.. (2021). Alternating Hemiplegia of Childhood in a Child Harboring a Novel TBC1D24 Mutation: Case Report and Literature Review. Neuropediatrics. 53(1). 69–74. 1 indexed citations

Uccella, Sarà, Livia Pisciotta, Mariasavina Severino, et al.. (2021). Photoparoxysmal response in ADCK3 autosomal recessive ataxia: a case report and literature review. Epileptic Disorders. 23(1). 153–160. 8 indexed citations

Pacetti, Mattia, Thea Giacomini, Massimo Cossu, et al.. (2021). Hemispheric surgery for severe epilepsy in early childhood: a case series. Epileptic Disorders. 23(4). 611–622. 2 indexed citations

10.

Prato, Giulia, Elisa De Grandis, Maria Margherita Mancardi, et al.. (2020). Schimke immuno-osseous dysplasia, two new cases with peculiar EEG pattern. Brain and Development. 42(5). 408–413. 1 indexed citations

11.

Bertamino, Marta, Sara Signa, Roberta Caorsi, et al.. (2020). An atypical case of post-varicella stroke in a child presenting with hemichorea followed by late-onset inflammatory focal cerebral arteriopathy. Quantitative Imaging in Medicine and Surgery. 11(1). 463–471. 4 indexed citations

12.

Giacomini, Thea, Maria Stella Vari, Giulia Prato, et al.. (2019). Epileptic Encephalopathy, Myoclonus–Dystonia, and Premature Pubarche in Siblings with a Novel C-Terminal Truncating Mutation in ATRX Gene. Neuropediatrics. 50(5). 327–331. 6 indexed citations

13.

Giacomini, Thea, Livia Pisciotta, Giulia Prato, et al.. (2019). Severe early-onset developmental and epileptic encephalopathy (DEE) associated with novel compound heterozygous pathogenic variants in SLC25A22: Case report and literature review. Seizure. 70. 56–58. 5 indexed citations

14.

Calevo, Maria Grazia, R. Gaggero, Giulia Prato, et al.. (2019). Personality profile and health-related quality of life in adults with previous continuous spike-waves during slow sleep syndrome. Brain and Development. 41(6). 522–530. 2 indexed citations

15.

Accogli, Andrea, Marcello Scala, Annalisa Calcagno, et al.. (2018). CNNM2 homozygous mutations cause severe refractory hypomagnesemia, epileptic encephalopathy and brain malformations. European Journal of Medical Genetics. 62(3). 198–203. 22 indexed citations

16.

Stagnaro, Michela, Livia Pisciotta, Maja Di Rocco, et al.. (2018). ATP1A3 spectrum disorders: A video-documented history of 7 genetically confirmed early onset cases. European Journal of Paediatric Neurology. 22(2). 264–271. 10 indexed citations

17.

Tambasco, Nicola, Federico Paolini Paoletti, Giulia Prato, et al.. (2018). Long-term follow-up in pediatric patients with paroxysmal hypothermia (Shapiro's syndrome). European Journal of Paediatric Neurology. 22(6). 1081–1086. 6 indexed citations

18.

Baglietto, M. G., Gianluca Caridi, Giorgio Gimelli, et al.. (2013). RORB gene and 9q21.13 microdeletion: Report on a patient with epilepsy and mild intellectual disability. European Journal of Medical Genetics. 57(1). 44–46. 31 indexed citations

19.

Prato, Giulia, Maria Margherita Mancardi, M. G. Baglietto, et al.. (2013). Congenital Segmental Lymphedema in Tuberous Sclerosis Complex With Associated Subependymal Giant Cell Astrocytomas Treated with Mammalian Target of Rapamycin Inhibitors. Journal of Child Neurology. 29(9). NP54–NP57. 11 indexed citations

20.

Rossi, Andrea, Isabella Ceccherini, Marianna Pezzella, et al.. (2012). Magnetic Resonance Imaging “Tigroid Pattern” in Alexander Disease. Neuropediatrics. 44(3). 174–176. 4 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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