Sabrina Rossi

2.2k total citations
64 papers, 830 citations indexed

About

Sabrina Rossi is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Sabrina Rossi has authored 64 papers receiving a total of 830 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Genetics, 21 papers in Molecular Biology and 19 papers in Neurology. Recurrent topics in Sabrina Rossi's work include Glioma Diagnosis and Treatment (24 papers), Neuroblastoma Research and Treatments (9 papers) and Skin and Cellular Biology Research (8 papers). Sabrina Rossi is often cited by papers focused on Glioma Diagnosis and Treatment (24 papers), Neuroblastoma Research and Treatments (9 papers) and Skin and Cellular Biology Research (8 papers). Sabrina Rossi collaborates with scholars based in Italy, United States and France. Sabrina Rossi's co-authors include C Andreoli, Riccardo Crebelli, Alessio Pitidis, P. Leopardi, Rossella Galati, Alessandra Verdina, Francesca Marcon, Andrea Zijno, M. Stasi and L Buscarini and has published in prestigious journals such as Journal of Clinical Oncology, SHILAP Revista de lepidopterología and International Journal of Molecular Sciences.

In The Last Decade

Sabrina Rossi

60 papers receiving 810 citations

Peers

Sabrina Rossi

GENET

HTM

PRM

Ken Hess United States

Claire Briet France

Seon‐Jin Yoon South Korea

Guangfei Li China

Yoshifumi Oda Japan

Krystyna Teichert-Kuliszewska Canada

Takakazu Sasaguri Japan

Michael T. Smith United States

Yeon Hee Cho South Korea

Ken Hess United States

Sabrina Rossi

118 ×0.5

172 ×0.7

159 ×0.9

GENET

62 ×0.5

HTM

122 ×1.0

PRM

Citations per year, relative to Sabrina Rossi Sabrina Rossi (= 1×) peers Ken Hess

Countries citing papers authored by Sabrina Rossi

Since Specialization

Citations

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

Fields of papers citing papers by Sabrina Rossi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sabrina Rossi

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

Rossi, Sabrina, Laura Masuelli, Angela Mastronuzzi, et al.. (2025). Circulating microRNAs: A remarkable opportunity as non-invasive biomarkers from adult to pediatric brain tumor patients. Critical Reviews in Oncology/Hematology. 208. 104650–104650. 1 indexed citations

Barresi, Sabina, Silvia Genovese, Isabella Giovannoni, et al.. (2025). An 11‐year‐old boy with a posterior fossa tumor. Brain Pathology. 35(2). e13332–e13332. 1 indexed citations

Baldo, Giada Del, Andrea Carai, Antonella Cacchione, et al.. (2024). A second case report of medulloblastoma in a patient carrying biallelic pathogenic MUTYH germline variants. Neuropathology and Applied Neurobiology. 50(2). e12968–e12968.

Barresi, Valeria, Evelina Miele, Lucia Pedace, et al.. (2024). CNS tumor with CREBBP::BCORL1 Fusion and pathogenic mutations in BCOR and CREBBP: expanding the spectrum of BCOR-altered tumors. Acta Neuropathologica Communications. 12(1). 8–8. 5 indexed citations

Giovannoni, Isabella, et al.. (2024). Identification of a novel SH3PXD2B::FER fusion in a case of plexiform myofibroblastic tumor and review of the literature. Genes Chromosomes and Cancer. 63(2). e23224–e23224. 3 indexed citations

Rossi, Sabrina, Sabina Barresi, Giovanna Stefania Colafati, et al.. (2022). Paediatric astroblastoma‐like neuroepithelial tumour of the spinal cord with a MAMLD1‐BEND2 rearrangement. Neuropathology and Applied Neurobiology. 48(5). e12814–e12814. 12 indexed citations

Broggi, Giuseppe, Francesca Gianno, Maura Massimino, et al.. (2022). Atypical teratoid/rhabdoid tumor in adults: a systematic review of the literature with meta-analysis and additional reports of 4 cases. Journal of Neuro-Oncology. 157(1). 1–14. 11 indexed citations

Carai, Andrea, Giada Del Baldo, Maria Vinci, et al.. (2022). Molecular Landscape in Infant High-Grade Gliomas: A Single Center Experience. Diagnostics. 12(2). 372–372. 11 indexed citations

Zenzo, Giovanni Di, Sabrina Rossi, Feliciana Mariotti, et al.. (2022). Case report: bullous pemphigoid development underlies dystrophic epidermolysis bullosa disease worsening. Frontiers in Immunology. 13. 929286–929286. 2 indexed citations

10.

Agolini, Emanuele, Elena Botta, M. Cristina Digilio, et al.. (2021). Expansion of the clinical and molecular spectrum of an XPD ‐related disorder linked to biallelic mutations in ERCC2 gene. Clinical Genetics. 99(6). 842–848. 5 indexed citations

11.

Rossi, Sabrina, Marco Gessi, Sabina Barresi, et al.. (2021). ALK ‐rearranged histiocytosis: Report of two cases with involvement of the central nervous system. Neuropathology and Applied Neurobiology. 47(6). 878–881. 12 indexed citations

12.

Barresi, Sabina, Isabella Giovannoni, Sabrina Rossi, et al.. (2021). A novel BRD4‐LEUTX fusion in a pediatric sarcoma with epithelioid morphology and diffuse S100 expression. Genes Chromosomes and Cancer. 60(9). 647–652. 7 indexed citations

13.

Rossi, Sabrina, Sabina Barresi, Stefano Chiaravalli, et al.. (2021). DICER1-associated malignancies mimicking germ cell neoplasms: Report of two cases and review of the literature. Pathology - Research and Practice. 225. 153553–153553. 12 indexed citations

14.

Diociaiuti, Andrea, Diego Martinelli, Francesco Nicita, et al.. (2021). Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis: Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization. Genes. 12(3). 343–343. 9 indexed citations

15.

Castiglia, Daniele, Paola Fortugno, Angelo Giuseppe Condorelli, et al.. (2021). A Novel Phenotype of Junctional Epidermolysis Bullosa with Transient Skin Fragility and Predominant Ocular Involvement Responsive to Human Amniotic Membrane Eyedrops. Genes. 12(5). 716–716. 7 indexed citations

16.

Pfister, Stefan M., Miguel Reyes‐Múgica, John K. C. Chan, et al.. (2021). A Summary of the Inaugural WHO Classification of Pediatric Tumors: Transitioning from the Optical into the Molecular Era. Cancer Discovery. 12(2). 331–355. 97 indexed citations

17.

Palma, Luca De, Alessandro De Benedictis, Nicola Pietrafusa, et al.. (2020). Early Onset Epilepsy Caused by Low-Grade Epilepsy-Associated Tumors and Focal Meningeal Involvement. Brain Sciences. 10(10). 752–752. 2 indexed citations

18.

Silveri, Massimiliano, Giovanni Cobellis, Agnese Roberti, et al.. (2020). Individualized robotic organ‐sparing surgery in a paediatric case of renal perivascular epithelioid cell tumour. International Journal of Medical Robotics and Computer Assisted Surgery. 16(5). 1–4. 4 indexed citations

19.

Benedictis, Alessandro De, Maria Camilla Rossi‐Espagnet, Francesca Diomedi‐Camassei, et al.. (2020). Intraventricular Ectopic Cerebellum. World Neurosurgery. 137. 158–163. 1 indexed citations

20.

Marcon, Francesca, Daniela Carotti, C Andreoli, et al.. (2012). DNA damage response in monozygotic twins discordant for smoking habits. Mutagenesis. 28(2). 135–144. 7 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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