Maria Stella Vari

3.5k total citations
31 papers, 453 citations indexed

About

Maria Stella Vari is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Maria Stella Vari has authored 31 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Psychiatry and Mental health, 11 papers in Genetics and 9 papers in Molecular Biology. Recurrent topics in Maria Stella Vari's work include Epilepsy research and treatment (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Metabolism and Genetic Disorders (6 papers). Maria Stella Vari is often cited by papers focused on Epilepsy research and treatment (12 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Metabolism and Genetic Disorders (6 papers). Maria Stella Vari collaborates with scholars based in Italy, Netherlands and United States. Maria Stella Vari's co-authors include Pasquale Striano, Federico Zara, Carlo Minetti, Alberto Verrotti, Elisabetta Amadori, Antonella Riva, Giovanni Morana, Valeria Capra, Marcello Scala and Michele Iacomino and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Pharmacological Research.

In The Last Decade

Maria Stella Vari

30 papers receiving 445 citations

Peers

Maria Stella Vari

GENET

PMH

PPCH

Dawn Cordeiro Canada

M. Pineda Spain

Reetta Hinttala Finland

Saad AlShahwan Saudi Arabia

Emma Reid United Kingdom

Johann Penzien Germany

J.F. de Rijk-van Andel Netherlands

Sabine Grønborg Denmark

Aziza Chedrawi Saudi Arabia

Shinjiro Akaboshi Japan

Dawn Cordeiro Canada

Maria Stella Vari

200 ×1.0

233 ×1.8

GENET

145 ×1.3

PMH

55 ×0.6

PPCH

173 ×1.9

Citations per year, relative to Maria Stella Vari Maria Stella Vari (= 1×) peers Dawn Cordeiro

Countries citing papers authored by Maria Stella Vari

Since Specialization

Citations

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

Fields of papers citing papers by Maria Stella Vari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Stella Vari. 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 Maria Stella Vari. The network helps show where Maria Stella Vari may publish in the future.

Co-authorship network of co-authors of Maria Stella Vari

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Stella Vari. A scholar is included among the top collaborators of Maria Stella Vari 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 Maria Stella Vari. Maria Stella Vari 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

Riva, Antonella, Sebastiano Barco, Valeria Manca, et al.. (2025). Long‐term plasma monitoring of THC and CBD in pediatric drug‐resistant epilepsy: Implications for cannabidiol therapy with Epidyolex®. Epilepsia Open. 10(5). 1699–1704.

Balagura, Ganna, Elisabetta Amadori, Maria Stella Vari, et al.. (2024). Early Developmental Intervention and Enriched Environment in CDKL5 Developmental and Epileptic Encephalopathy. Neurology Clinical Practice. 14(3). e200287–e200287. 2 indexed citations

Riva, Antonella, Roberta Roberti, Gianluca D’Onofrio, et al.. (2023). A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy. Epilepsia Open. 8(3). 1142–1150. 7 indexed citations

Scala, Marcello, Emanuela Abiusi, Ilaria Contaldo, et al.. (2022). Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series. Seizure. 100. 82–86. 12 indexed citations

Riva, Antonella, Gianluca Piccolo, Noemi Brolatti, et al.. (2022). Acute Neurological Presentation in Children With SARS-CoV-2 Infection. Frontiers in Pediatrics. 10. 909849–909849. 6 indexed citations

Mancardi, Maria Margherita, Alfonso Romano, Margherita Santucci, et al.. (2022). Electroencephalographic findings in ATRX syndrome: A new case series and review of literature. European Journal of Paediatric Neurology. 40. 69–72. 3 indexed citations

Marchese, Francesca, Maria Stella Vari, Ganna Balagura, et al.. (2020). An Open Retrospective Study of a Standardized Cannabidiol Based-Oil in Treatment-Resistant Epilepsy. Cannabis and Cannabinoid Research. 7(2). 199–206. 11 indexed citations

Amadori, Elisabetta, Marcello Scala, Maria Stella Vari, et al.. (2020). Targeted re-sequencing for early diagnosis of genetic causes of childhood epilepsy: the Italian experience from the ‘beyond epilepsy’ project. The Italian Journal of Pediatrics/Italian journal of pediatrics. 46(1). 92–92. 22 indexed citations

Terrone, Gaetano, Francesca Marchese, Maria Stella Vari, et al.. (2020). A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome. Seizure. 79. 53–55. 11 indexed citations

10.

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

11.

Micalizzi, Concetta, Thea Giacomini, Matteo Gastaldi, et al.. (2019). Bortezomib-Responsive Refractory Anti-N-Methyl-d-Aspartate Receptor Encephalitis. Pediatric Neurology. 103. 61–64. 24 indexed citations

12.

Scala, Marcello, Elisabetta Amadori, Lucia Fusco, et al.. (2019). Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy. European Journal of Paediatric Neurology. 23(4). 657–661. 4 indexed citations

13.

Scala, Marcello, Annalaura Torella, Mariasavina Severino, et al.. (2019). Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled females. European Journal of Human Genetics. 27(8). 1254–1259. 36 indexed citations

14.

Iapadre, Giulia, Giovanni Morana, Maria Stella Vari, et al.. (2018). A novel homozygous MFN2 mutation associated with severe and atypical CMT2 phenotype. European Journal of Paediatric Neurology. 22(3). 563–567. 17 indexed citations

15.

Cappuccio, Gerarda, Michele Pinelli, Taraka Donti, et al.. (2017). Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet. PLoS ONE. 12(9). e0184022–e0184022. 40 indexed citations

16.

Falsaperla, Raffaele, Maria Stella Vari, Irene Toldo, et al.. (2017). Pyridoxine-dependent epilepsies: an observational study on clinical, diagnostic, therapeutic and prognostic features in a pediatric cohort. Metabolic Brain Disease. 33(1). 261–269. 21 indexed citations

17.

Accogli, Andrea, Michele Iacomino, Alessandro Orsini, et al.. (2017). Novel AMPD2 mutation in pontocerebellar hypoplasia, dysmorphisms, and teeth abnormalities. Neurology Genetics. 3(5). e179–e179. 15 indexed citations

18.

Accogli, Andrea, Monica Traverso, Francesca Madia, et al.. (2017). A novel Xp22.13 microdeletion in Nance‐Horan syndrome. Birth Defects Research. 109(11). 866–868. 12 indexed citations

19.

Striano, Pasquale, et al.. (2016). Management of genetic epilepsies: From empirical treatment to precision medicine. Pharmacological Research. 107. 426–429. 45 indexed citations

20.

Vari, Maria Stella, Elisabetta Mencaroni, Carlo Minetti, et al.. (2015). Safety of Overnight Switch from Brand-Name to Generic Levetiracetam. Clinical Drug Investigation. 36(1). 87–91. 19 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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