Romina Romaniello

1.9k total citations
59 papers, 789 citations indexed

About

Romina Romaniello is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Romina Romaniello has authored 59 papers receiving a total of 789 indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Pediatrics, Perinatology and Child Health, 23 papers in Genetics and 20 papers in Molecular Biology. Recurrent topics in Romina Romaniello's work include Fetal and Pediatric Neurological Disorders (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Microtubule and mitosis dynamics (7 papers). Romina Romaniello is often cited by papers focused on Fetal and Pediatric Neurological Disorders (24 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Microtubule and mitosis dynamics (7 papers). Romina Romaniello collaborates with scholars based in Italy, United Kingdom and United States. Romina Romaniello's co-authors include Renato Borgatti, Maria Teresa Bassi, Filippo Arrigoni, Fabio Triulzi, Cinzia Baschirotto, Nereo Bresolin, Elena Panzeri, Claudio Zucca, Cosimo Urgesi and Thomas D. Cushion and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Romina Romaniello

50 papers receiving 783 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Romina Romaniello Italy	16	359	242	206	161	139	59	789
Vanessa Douet United States	16	272 0.8×	205 0.8×	43 0.2×	168 1.0×	81 0.6×	25	748
Judy S. Liu United States	10	309 0.9×	118 0.5×	67 0.3×	173 1.1×	281 2.0×	16	746
Cecilia Schmidt United States	14	670 1.9×	885 3.7×	163 0.8×	124 0.8×	143 1.0×	18	1.9k
J.-M. Pinard France	10	254 0.7×	266 1.1×	470 2.3×	141 0.9×	322 2.3×	12	983
Candace Castagna United States	5	305 0.8×	289 1.2×	33 0.2×	107 0.7×	223 1.6×	5	933
Irina Bystron Russia	4	323 0.9×	100 0.4×	302 1.5×	56 0.3×	226 1.6×	7	878
Jin Nakatani Japan	12	521 1.5×	509 2.1×	82 0.4×	91 0.6×	186 1.3×	24	1.0k
Siddharth Srivastava United States	21	700 1.9×	1000 4.1×	100 0.5×	76 0.5×	143 1.0×	80	1.7k
Britt‐Marie Anderlid Sweden	22	607 1.7×	813 3.4×	209 1.0×	75 0.5×	51 0.4×	56	1.3k
Heinz Krestel Switzerland	16	353 1.0×	118 0.5×	43 0.2×	36 0.2×	299 2.2×	31	805

Countries citing papers authored by Romina Romaniello

Since Specialization

Citations

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

Fields of papers citing papers by Romina Romaniello

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Romina Romaniello

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

Pasca, Ludovica, Federica Morelli, G. Catalano, et al.. (2025). Sleep profile in patients with septo-optic-pituitary dysplasia: protocol for a prospective cohort study. BMJ Open. 15(1). e090675–e090675.

Pasca, Ludovica, et al.. (2025). New Perspectives on Non-Invasive Cerebellar Stimulation for Social and Affective Functions in Children and Adolescents. The Cerebellum. 24(4). 88–88. 1 indexed citations

Morelli, Federica, Sabrina Signorini, Simone Gana, et al.. (2025). A de novo ZMYM2 gene variant associated to a Rett-like phenotype: Case report of a new phenotype and review of the literature. Brain and Development. 47(3). 104351–104351.

Oldrati, Viola, Elisabetta Ferrari, Sandra Strazzer, et al.. (2024). Neurorestorative effects of cerebellar transcranial direct current stimulation on social prediction of adolescents and young adults with congenital cerebellar malformations. NeuroImage Clinical. 41. 103582–103582. 3 indexed citations

Pasca, Ludovica, Francesca Ferraro, Simone Gana, et al.. (2024). Cerebellar heterotopia in an 11‐year‐old child with KDM6B‐related neurodevelopmental disorder: A case report and review of the literature. American Journal of Medical Genetics Part A. 194(6). e63555–e63555.

Ferrari, Elisabetta, Viola Oldrati, Emilia Biffi, et al.. (2024). News insights into social cognition in Williams syndrome from a comprehensive assessment and a virtual reality task. Scientific Reports. 14(1). 28020–28020. 1 indexed citations

Strazzer, Sandra, Renato Borgatti, Romina Romaniello, et al.. (2024). Examining the Implementation of the Italian Version of the Teen Online Problem-Solving Program Coupled With Remote Psychological Support: Protocol for a Randomized Controlled Trial. JMIR Research Protocols. 14. e64178–e64178.

Oldrati, Viola, Sandra Strazzer, Geraldina Poggi, et al.. (2023). Randomized clinical trial on the effects of a computerized cognitive training for pediatric patients with acquired brain injury or congenital malformation. Scientific Reports. 13(1). 14559–14559. 3 indexed citations

Romaniello, Romina, Ludovica Pasca, Elena Panzeri, et al.. (2022). Superior Cerebellar Atrophy: An Imaging Clue to Diagnose ITPR1-Related Disorders. International Journal of Molecular Sciences. 23(12). 6723–6723. 5 indexed citations

10.

Goergen, Stacy, Michael Fahey, Kieran Frawley, et al.. (2021). The Fetus with Ganglionic Eminence Abnormality: Head Size and Extracranial Sonographic Findings Predict Genetic Diagnoses and Postnatal Outcomes. American Journal of Neuroradiology. 42(8). 1528–1534. 8 indexed citations

11.

Epifanio, Roberta, Roberto Giorda, Nicoletta Zanotta, et al.. (2021). SCN2A Pathogenic Variants and Epilepsy: Heterogeneous Clinical, Genetic and Diagnostic Features. Brain Sciences. 12(1). 18–18. 3 indexed citations

12.

Arrigoni, Filippo, Romina Romaniello, Filippo Manti, et al.. (2021). Get Your Molar Tooth Right: Joubert Syndrome Misdiagnosis Unmasked by Whole-Exome Sequencing. The Cerebellum. 21(6). 1144–1150. 9 indexed citations

13.

Arrigoni, Filippo, Denis Peruzzo, Simone Mandelstam, et al.. (2020). Characterizing White Matter Tract Organization in Polymicrogyria and Lissencephaly: A Multifiber Diffusion MRI Modeling and Tractography Study. American Journal of Neuroradiology. 41(8). 1495–1502. 10 indexed citations

14.

Arrigoni, Filippo, Romina Romaniello, Denis Peruzzo, et al.. (2017). Anterior Mesencephalic Cap Dysplasia: Novel Brain Stem Malformative Features Associated with Joubert Syndrome. American Journal of Neuroradiology. 38(12). 2385–2390. 11 indexed citations

15.

Romaniello, Romina, Francesco Saettini, Elena Panzeri, et al.. (2015). A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype. Neuroreport. 26(5). 254–257. 36 indexed citations

16.

Romaniello, Romina, Filippo Arrigoni, Maria Teresa Bassi, & Renato Borgatti. (2014). Mutations in α- and β-tubulin encoding genes: Implications in brain malformations. Brain and Development. 37(3). 273–280. 55 indexed citations

17.

Vantaggiato, Chiara, Orazio Cantoni, Andrea Guidarelli, et al.. (2013). Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents. Brain and Development. 36(8). 682–689. 6 indexed citations

18.

Romaniello, Romina, Claudio Zucca, Erika Tenderini, et al.. (2013). A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern. Journal of Child Neurology. 29(2). 249–253. 14 indexed citations

19.

Romaniello, Romina, Alessandra Tonelli, Filippo Arrigoni, et al.. (2012). A novel mutation in the β‐tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance. Developmental Medicine & Child Neurology. 54(8). 765–769. 45 indexed citations

20.

Romaniello, Romina, Claudio Zucca, A. Tonelli, et al.. (2010). A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation. Journal of Neurology Neurosurgery & Psychiatry. 81(8). 840–843. 45 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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