Maura Servida

677 total citations
11 papers, 288 citations indexed

About

Maura Servida is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Maura Servida has authored 11 papers receiving a total of 288 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Maura Servida's work include Glioma Diagnosis and Treatment (4 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Maura Servida is often cited by papers focused on Glioma Diagnosis and Treatment (4 papers), Mitochondrial Function and Pathology (3 papers) and ATP Synthase and ATPases Research (3 papers). Maura Servida collaborates with scholars based in Italy, Switzerland and Germany. Maura Servida's co-authors include Marica Eoli, Elena Anghileri, Paolo Ferroli, Francesco Acerbi, Bianca Pollo, Carlo Boffano, Marco Schiariti, Alexander Brawanski, Camilla de Laurentis and Cristina Montomoli and has published in prestigious journals such as Journal of Clinical Oncology, Clinical Cancer Research and Biochemical and Biophysical Research Communications.

In The Last Decade

Maura Servida

11 papers receiving 283 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maura Servida Italy 7 170 82 75 74 46 11 288
Justin A. Neira United States 8 197 1.2× 93 1.1× 40 0.5× 85 1.1× 73 1.6× 15 332
Andrea Bianconi Italy 12 178 1.0× 65 0.8× 31 0.4× 70 0.9× 26 0.6× 35 311
Fabio Cofano Italy 10 175 1.0× 70 0.9× 47 0.6× 60 0.8× 16 0.3× 29 309
Yoshiteru Miyajima Japan 11 238 1.4× 105 1.3× 70 0.9× 150 2.0× 14 0.3× 22 415
Ashley Ghiaseddin United States 9 199 1.2× 27 0.3× 101 1.3× 72 1.0× 29 0.6× 41 320
Matheus P. Pereira United States 11 100 0.6× 73 0.9× 121 1.6× 32 0.4× 72 1.6× 24 422
Shengyue Huang China 9 115 0.7× 52 0.6× 63 0.8× 19 0.3× 36 0.8× 18 271
Maria Donzelli United States 7 186 1.1× 31 0.4× 74 1.0× 47 0.6× 35 0.8× 19 349
Scott Turner United States 8 215 1.3× 31 0.4× 91 1.2× 45 0.6× 15 0.3× 13 311
Daisuke Kawauchi Japan 12 152 0.9× 55 0.7× 199 2.7× 23 0.3× 21 0.5× 29 375

Countries citing papers authored by Maura Servida

Since Specialization
Citations

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

Fields of papers citing papers by Maura Servida

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maura Servida

This figure shows the co-authorship network connecting the top 25 collaborators of Maura Servida. A scholar is included among the top collaborators of Maura Servida 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 Maura Servida. Maura Servida is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Rigamonti, Andrea, G. Simonetti, Antonio Silvani, et al.. (2020). Adult brainstem glioma: a multicentre retrospective analysis of 47 Italian patients. Neurological Sciences. 42(5). 1879–1886. 5 indexed citations
2.
Caputi, Luigi, Alessandra Erbetta, Gianluca Marucci, et al.. (2019). Biopsy-proven primary angiitis of the central nervous system mimicking leukodystrophy: A case report and review of the literature. Journal of Clinical Neuroscience. 64. 42–44. 7 indexed citations
3.
Acerbi, Francesco, Morgan Broggi, Karl-Michael Schebesch, et al.. (2017). Fluorescein-Guided Surgery for Resection of High-Grade Gliomas: A Multicentric Prospective Phase II Study (FLUOGLIO). Clinical Cancer Research. 24(1). 52–61. 168 indexed citations
4.
Eoli, Marica, Valeria Cuccarini, Domenico Aquino, et al.. (2017). Apparent diffusion coefficient (ADC) decrease to predict longer survival in glioblastoma patients treated by dendritic cell immunotherapy plus standard of care.. Journal of Clinical Oncology. 35(15_suppl). 2065–2065. 2 indexed citations
5.
Pellegatta, Serena, Marica Eoli, Valeria Cuccarini, et al.. (2017). Survival gain in glioblastoma patients treated with dendritic cell immunotherapy is associated with increased NK but not CD8 + T cell activation in the presence of adjuvant temozolomide. OncoImmunology. 7(4). e1412901–e1412901. 52 indexed citations
6.
Finocchiaro, Gaetano, Marica Eoli, Serena Pellegatta, et al.. (2015). IMCT-06SURVIVAL GAIN AND IMMUNE RESPONSE IN GLIOBLASTOMA PATIENTS TREATED WITH DENDRITIC CELL IMMUNOTHERAPY BEFORE AND DURING ADJUVANT TEMOZOLOMIDE. Neuro-Oncology. 17(suppl 5). v108.2–v108. 1 indexed citations
7.
Lucchiari, Sabrina, Francesca Magri, Maura Servida, et al.. (2013). Clinical evaluation and cellular electrophysiology of a recessive CLCN1 patient.. PubMed. 64(5). 669–78. 9 indexed citations
8.
Ronchi, Dario, Andreina Bordoni, Mafalda Rizzuti, et al.. (2011). Unusual adult-onset Leigh syndrome presentation due to the mitochondrial m.9176T>C mutation. Biochemical and Biophysical Research Communications. 412(2). 245–248. 12 indexed citations
9.
Ranieri, Michela, Roberto Del Bo, Andreina Bordoni, et al.. (2011). Optic atrophy plus phenotype due to mutations in the OPA1 gene: Two more Italian families. Journal of the Neurological Sciences. 315(1-2). 146–149. 20 indexed citations
10.
Ronchi, Dario, Monica Sciacco, Andreina Bordoni, et al.. (2011). The novel mitochondrial tRNAAsn gene mutation m.5709T>C produces ophthalmoparesis and respiratory impairment. European Journal of Human Genetics. 20(3). 357–360. 3 indexed citations
11.
Lucchiari, Sabrina, Serena Pagliarani, Stefania Corti, et al.. (2008). Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion. Journal of the Neurological Sciences. 275(1-2). 159–163. 9 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 Justin A. Neira Breakdown of academic impact, for papers by Andrea Bianconi Breakdown of academic impact, for papers by Fabio Cofano Breakdown of academic impact, for papers by Yoshiteru Miyajima Breakdown of academic impact, for papers by Ashley Ghiaseddin Breakdown of academic impact, for papers by Matheus P. Pereira Breakdown of academic impact, for papers by Shengyue Huang Breakdown of academic impact, for papers by Maria Donzelli Breakdown of academic impact, for papers by Scott Turner Breakdown of academic impact, for papers by Daisuke Kawauchi
Rankless by CCL
2026