Maroulio Pertesi
- Co-authors
- Irene KonstantopoulouDrakoulis YannoukakosFlorence Le Calvez‐KelmGeorge FountzilasFlorentia FostiraFrancesca DamiolaFabienne LesueurJames McKay
- Topics
- BRCA gene mutations in cancer (11 papers)CRISPR and Genetic Engineering (5 papers)Genomic variations and chromosomal abnormalities (4 papers)
- Cited by
- Cancer ResearchGeneticsOncology
- Partner nations
- United StatesSwedenGreece
In The Last Decade
Maroulio Pertesi
20 papers receiving 422 citations
Peers
Comparison fields: 5 of 47
- Molecular Biology 242
- Genetics 218
- Cancer Research 140
- Oncology 114
- Pathology and Forensic Medicine 51
Countries citing papers authored by Maroulio Pertesi
This map shows the geographic impact of Maroulio Pertesi'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 Maroulio Pertesi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maroulio Pertesi more than expected).
Fields of papers citing papers by Maroulio Pertesi
This network shows the impact of papers produced by Maroulio Pertesi. 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 Maroulio Pertesi. The network helps show where Maroulio Pertesi may publish in the future.
Co-authorship network of co-authors of Maroulio Pertesi
This figure shows the co-authorship network connecting the top 25 collaborators of Maroulio Pertesi. A scholar is included among the top collaborators of Maroulio Pertesi 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 Maroulio Pertesi. Maroulio Pertesi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 4 | |
| 4 | 1 | |
| 5 | 18 | |
| 6 | 21 | |
| 7 | 13 | |
| 8 | 17 | |
| 9 | 59 | |
| 10 | 5 | |
| 11 | 28 | |
| 12 | 73 | |
| 13 | 26 | |
| 14 | 27 | |
| 15 | 53 | |
| 16 | 10 | |
| 17 | 5 | |
| 18 | 25 | |
| 19 | Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now? | 8 |
| 20 | 29 |
About Maroulio Pertesi
Maroulio Pertesi is a scholar working on Genetics, Hematology and Immunology, having authored 21 papers that have together received 430 indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (11 papers), CRISPR and Genetic Engineering (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Cancer Research (140 citations), Genetics (218 citations) and Oncology (114 citations). Maroulio Pertesi has collaborated with scholars based in United States, Sweden and Greece. Frequent co-authors include Irene Konstantopoulou, Drakoulis Yannoukakos, Florence Le Calvez‐Kelm, George Fountzilas, Florentia Fostira, Francesca Damiola, Fabienne Lesueur, James McKay, Graham Byrnes and Björn Nilsson. Their work appears in journals such as Nature Communications, Journal of Clinical Oncology and PLoS ONE.
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.