Eva Trevisson
Impact in
- Biochemistry top 0.5%
- Biochemical Acid Research Studies
- Neurology top 1%
- Neurofibromatosis and Schwannoma Cases
Papers in
- Biochemistry 20
- Biochemical Acid Research Studies 16
- Neurology 27
- Neurofibromatosis and Schwannoma Cases 24
- Vascular Malformations Diagnosis and Treatment 6
- Co-authors
- Leonardo Salviati (47 shared papers)Plácido Navas (15 shared papers)María Andrea Desbats (13 shared papers)Mara Doimo (17 shared papers)Salvatore DiMauro (6 shared papers)Michio Hirano (5 shared papers)Cristina Cerqua (12 shared papers)Catarina Maria Quinzii (4 shared papers)
- Journals
- European Journal of Human Genetics (10 papers)Cancers (5 papers)Genetics in Medicine (5 papers)The American Journal of Human Genetics (5 papers)Clinical Genetics (4 papers)
- Partner nations
- ItalyUnited StatesSpain
In The Last Decade
Eva Trevisson
94 papers receiving 4.4k citations
Eva Trevisson's Hit Papers
Peers
Comparison fields: 5 of 107
- Biochemistry 739
- Neurology 1.2k
- Clinical Biochemistry 368
- Molecular Biology 2.8k
- Nephrology 212
Countries citing papers authored by Eva Trevisson
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
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-authors
The 25 scholars most cited alongside Eva Trevisson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 97 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation Hit paper breakdown → | 2021 | 459 |
| 2 | 2011 | 338 | |
| 3 | 2006 | 302 | |
| 4 | 2016 | 199 | |
| 5 | 2014 | 189 | |
| 6 | 2017 | 163 | |
| 7 | 2007 | 162 | |
| 8 | Updated diagnostic criteria and nomenclature for neurofibromatosis type 2 and schwannomatosis: An international consensus recommendation Hit paper breakdown → | 2022 | 160 |
| 9 | 2007 | 126 | |
| 10 | 2014 | 115 | |
| 11 | 2014 | 104 | |
| 12 | 2019 | 100 | |
| 13 | 2012 | 98 | |
| 14 | 2008 | 94 | |
| 15 | 2018 | 86 | |
| 16 | 2009 | 79 | |
| 17 | 2011 | 74 | |
| 18 | 2013 | 73 | |
| 19 | 2014 | 65 | |
| 20 | 2008 | 64 |
About Eva Trevisson
Eva Trevisson is a scholar working on Biochemistry, Neurology, Molecular Biology, Clinical Biochemistry and Rheumatology, having authored 97 papers that have together received 4.6k indexed citations. Recurring topics across this work include Coenzyme Q10 studies and effects (27 papers), Neurofibromatosis and Schwannoma Cases (24 papers), Mitochondrial Function and Pathology (17 papers), Biochemical Acid Research Studies (16 papers), Advanced battery technologies research (14 papers), Metabolism and Genetic Disorders (7 papers), Vascular Malformations Diagnosis and Treatment (6 papers) and Meningioma and schwannoma management (6 papers). The work is most often cited by research in Biochemistry (739 citations), Neurology (1.2k citations), Clinical Biochemistry (368 citations), Molecular Biology (2.8k citations) and Nephrology (212 citations). Eva Trevisson has collaborated with scholars based in Italy, United States and Spain. Frequent co-authors include Leonardo Salviati, Plácido Navas, María Andrea Desbats, Mara Doimo, Salvatore DiMauro, Michio Hirano, Cristina Cerqua, Catarina Maria Quinzii, Matteo Cassina and Alberto Casarin. Their work appears in journals such as European Journal of Human Genetics, Cancers, Genetics in Medicine, The American Journal of Human Genetics and Clinical Genetics.
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.