Eva Trevisson

5.7k total citations
70 papers, 2.6k citations indexed

About

Eva Trevisson is a scholar working on Molecular Biology, Neurology and Biochemistry. According to data from OpenAlex, Eva Trevisson has authored 70 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 20 papers in Neurology and 16 papers in Biochemistry. Recurrent topics in Eva Trevisson's work include Coenzyme Q10 studies and effects (21 papers), Neurofibromatosis and Schwannoma Cases (19 papers) and Mitochondrial Function and Pathology (14 papers). Eva Trevisson is often cited by papers focused on Coenzyme Q10 studies and effects (21 papers), Neurofibromatosis and Schwannoma Cases (19 papers) and Mitochondrial Function and Pathology (14 papers). Eva Trevisson collaborates with scholars based in Italy, Spain and United States. Eva Trevisson's co-authors include Leonardo Salviati, Plácido Navas, María Andrea Desbats, Mara Doimo, Salvatore DiMauro, Michio Hirano, Cristina Cerqua, Catarina M. Quinzii, Alberto Casarin and Matteo Cassina and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Scientific Reports.

In The Last Decade

Eva Trevisson

69 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eva Trevisson Italy 29 2.0k 624 584 337 308 70 2.6k
Catarina M. Quinzii United States 41 3.9k 1.9× 1.1k 1.8× 1.1k 1.9× 259 0.8× 797 2.6× 75 4.6k
María Andrea Desbats Italy 21 1.8k 0.9× 292 0.5× 304 0.5× 65 0.2× 172 0.6× 28 2.2k
Saba Tadesse United States 20 1.3k 0.6× 139 0.2× 172 0.3× 125 0.4× 625 2.0× 28 1.5k
Costanza Lamperti Italy 27 2.3k 1.1× 85 0.1× 224 0.4× 127 0.4× 1.1k 3.5× 74 3.0k
Beatriz Dorado Spain 17 657 0.3× 65 0.1× 77 0.1× 241 0.7× 149 0.5× 34 1.3k
Andrea Lapucci Italy 24 1.1k 0.5× 78 0.1× 58 0.1× 75 0.2× 62 0.2× 54 1.7k
Cristina Cerqua Italy 12 863 0.4× 109 0.2× 108 0.2× 26 0.1× 94 0.3× 14 1.1k
Daniel Platt United States 10 948 0.5× 58 0.1× 122 0.2× 29 0.1× 137 0.4× 13 1.8k
Elena Rapizzi Italy 25 1.4k 0.7× 50 0.1× 30 0.1× 127 0.4× 95 0.3× 61 2.5k
Dieter A. Kubli United States 17 1.5k 0.8× 35 0.1× 53 0.1× 156 0.5× 140 0.5× 24 2.3k

Countries citing papers authored by Eva Trevisson

Since Specialization
Citations

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

Fields of papers citing papers by Eva Trevisson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Trevisson

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

All Works

20 of 20 papers shown
1.
Frizziero, Luisa, et al.. (2022). Choroidal Abnormalities in Pediatric NF1: A Cohort Natural History Study. Cancers. 14(6). 1423–1423. 5 indexed citations
2.
Corallo, Diana, Carlo Zanon, Gian Paolo Tonini, et al.. (2021). Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study. Cells. 10(10). 2695–2695. 2 indexed citations
3.
Cerqua, Cristina, Alberto Casarin, Fabien Pierrel, et al.. (2019). Vitamin K2 cannot substitute Coenzyme Q10 as electron carrier in the mitochondrial respiratory chain of mammalian cells. Scientific Reports. 9(1). 6553–6553. 18 indexed citations
4.
Cassina, Matteo, Luisa Frizziero, Enrico Opocher, et al.. (2019). Optic Pathway Glioma in Type 1 Neurofibromatosis: Review of Its Pathogenesis, Diagnostic Assessment, and Treatment Recommendations. Cancers. 11(11). 1790–1790. 32 indexed citations
5.
Pinto, Anna Maria, Eva Trevisson, Valeria Morbidoni, et al.. (2018). Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma. European Journal of Human Genetics. 26(7). 1026–1037. 16 indexed citations
6.
Cerqua, Cristina, Valeria Morbidoni, María Andrea Desbats, et al.. (2018). COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1859(4). 244–252. 25 indexed citations
7.
Acosta, M.J., Luis Vázquez-Fonseca, María Andrea Desbats, et al.. (2016). Coenzyme Q biosynthesis in health and disease. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1857(8). 1079–1085. 175 indexed citations
8.
Lucchetta, Marta, Renzo Manara, Giorgio Perilongo, Maurizio Clementi, & Eva Trevisson. (2015). Regression of gadolinium-enhanced lesions in patients affected by neurofibromatosis type 1. La radiologia medica. 121(3). 214–217. 3 indexed citations
9.
Nguyen, Theresa, Alberto Casarin, María Andrea Desbats, et al.. (2014). Molecular characterization of the human COQ5 C-methyltransferase in coenzyme Q10 biosynthesis. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1841(11). 1628–1638. 47 indexed citations
10.
Bartolini, Luca, Stefano Sartori, Elisabetta Lenzini, et al.. (2013). De novo trisomy 20p characterized by array comparative genomic hybridization: Report of a novel case and review of the literature. Gene. 524(2). 368–372. 21 indexed citations
11.
Doimo, Mara, Eva Trevisson, Rannar Airik, et al.. (2013). Effect of vanillic acid on COQ6 mutants identified in patients with coenzyme Q10 deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1842(1). 1–6. 67 indexed citations
12.
Salviati, Leonardo, Eva Trevisson, María Hernández, et al.. (2012). Haploinsufficiency of COQ4 causes coenzyme Q10 deficiency. Journal of Medical Genetics. 49(3). 187–191. 85 indexed citations
13.
Trevisson, Eva, Salvatore DiMauro, Plácido Navas, & Leonardo Salviati. (2011). Coenzyme Q deficiency in muscle. Current Opinion in Neurology. 24(5). 449–456. 62 indexed citations
14.
Casarin, Alberto, Mara Doimo, Eva Trevisson, et al.. (2009). X‐linked brachytelephalangic chondrodysplasia punctata: A simple trait that is not so simple. American Journal of Medical Genetics Part A. 149A(11). 2464–2468. 9 indexed citations
15.
Casarin, Alberto, Eva Trevisson, Vanessa Pertegato, et al.. (2008). Functional characterization of human COQ4, a gene required for Coenzyme Q10 biosynthesis. Biochemical and Biophysical Research Communications. 372(1). 35–39. 43 indexed citations
16.
López‐Martín, José María, Leonardo Salviati, Eva Trevisson, et al.. (2007). Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis. Human Molecular Genetics. 16(9). 1091–1097. 109 indexed citations
17.
Trevisson, Eva, Leonardo Salviati, Irene Toldo, et al.. (2007). Argininosuccinate lyase deficiency: mutational spectrum in Italian patients and identification of a novelASLpseudogene. Human Mutation. 28(7). 694–702. 39 indexed citations
18.
Quinzii, Catarina M., Ali Naini, Leonardo Salviati, et al.. (2006). A Mutation in Para-Hydroxybenzoate-Polyprenyl Transferase (COQ2) Causes Primary Coenzyme Q10 Deficiency. The American Journal of Human Genetics. 78(2). 345–349. 263 indexed citations
19.
Salviati, Leonardo, Eva Trevisson, Irene Toldo, et al.. (2006). A novel deletion in the GJA12 gene causes Pelizaeus–Merzbacher-like disease. Neurogenetics. 8(1). 57–60. 37 indexed citations
20.
Sacconi, Sabrina, Eva Trevisson, Francesca Pistollato, et al.. (2005). hCOX18 and hCOX19: Two human genes involved in cytochrome c oxidase assembly. Biochemical and Biophysical Research Communications. 337(3). 832–839. 26 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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