Giovanna De Vecchi

514 total citations
11 papers, 140 citations indexed

About

Giovanna De Vecchi is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Giovanna De Vecchi has authored 11 papers receiving a total of 140 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 3 papers in Pathology and Forensic Medicine and 3 papers in Genetics. Recurrent topics in Giovanna De Vecchi's work include Renal and related cancers (5 papers), Genomics and Rare Diseases (2 papers) and Renal cell carcinoma treatment (2 papers). Giovanna De Vecchi is often cited by papers focused on Renal and related cancers (5 papers), Genomics and Rare Diseases (2 papers) and Renal cell carcinoma treatment (2 papers). Giovanna De Vecchi collaborates with scholars based in Italy, United Kingdom and Australia. Giovanna De Vecchi's co-authors include Paolo Radice, Siranoush Manoukian, Mara Colombo, Paola Collini, Carla B. Ripamonti, Bernard Peissel, Monica Barile, Liliana Varesco, Daniela Perotti and Fernando Ravagnani and has published in prestigious journals such as PLoS ONE, Human Mutation and Cancers.

In The Last Decade

Giovanna De Vecchi

11 papers receiving 138 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Giovanna De Vecchi Italy 6 99 51 28 27 25 11 140
Ana Blatnik Slovenia 7 142 1.4× 57 1.1× 22 0.8× 26 1.0× 29 1.2× 29 208
Wendy A. van Zelst-Stams Netherlands 5 87 0.9× 53 1.0× 45 1.6× 58 2.1× 72 2.9× 5 168
Sonia Margarit Chile 7 111 1.1× 135 2.6× 37 1.3× 61 2.3× 33 1.3× 14 201
Adrià López‐Fernández Spain 7 112 1.1× 116 2.3× 33 1.2× 47 1.7× 53 2.1× 18 199
Mónica Salinas Spain 8 85 0.9× 87 1.7× 37 1.3× 41 1.5× 51 2.0× 15 163
Hélene Schlecht United Kingdom 7 100 1.0× 69 1.4× 60 2.1× 28 1.0× 27 1.1× 27 199
Bartłomiej Gliniewicz Poland 4 69 0.7× 94 1.8× 37 1.3× 41 1.5× 49 2.0× 9 168
Jaydutt Bhalshankar Singapore 4 49 0.5× 25 0.5× 19 0.7× 21 0.8× 19 0.8× 5 117
Tom Hofste Netherlands 7 119 1.2× 24 0.5× 10 0.4× 26 1.0× 15 0.6× 10 172
Paula Rofes Spain 6 65 0.7× 52 1.0× 30 1.1× 35 1.3× 48 1.9× 11 118

Countries citing papers authored by Giovanna De Vecchi

Since Specialization
Citations

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

Fields of papers citing papers by Giovanna De Vecchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Giovanna De Vecchi. 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 Giovanna De Vecchi. The network helps show where Giovanna De Vecchi may publish in the future.

Co-authorship network of co-authors of Giovanna De Vecchi

This figure shows the co-authorship network connecting the top 25 collaborators of Giovanna De Vecchi. A scholar is included among the top collaborators of Giovanna De Vecchi 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 Giovanna De Vecchi. Giovanna De Vecchi 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.
Brignola, C., Sara Volorio, Giovanna De Vecchi, et al.. (2023). De novo germline pathogenic variant in Lynch Syndrome: A rare event or the tip of the iceberg?. Tumori Journal. 110(1). 69–73. 4 indexed citations
2.
Maragliano, Roberta, Ileana Carnevali, Valeria Pensotti, et al.. (2021). Mixed Neuroendocrine/Non-neuroendocrine Neoplasm (MiNEN) of the Ovary Arising from Endometriosis: Molecular Pathology Analysis in Support of a Pathogenetic Paradigm. Endocrine Pathology. 33(3). 400–410. 5 indexed citations
3.
Azzollini, Jacopo, Elisabetta Schiavello, Francesca Romana Buttarelli, et al.. (2020). Pre- and Post-Zygotic TP53 De Novo Mutations in SHH-Medulloblastoma. Cancers. 12(9). 2503–2503. 1 indexed citations
4.
5.
Colombo, Mara, Giovanna De Vecchi, Laura Caleca, et al.. (2013). Comparative In Vitro and In Silico Analyses of Variants in Splicing Regions of BRCA1 and BRCA2 Genes and Characterization of Novel Pathogenic Mutations. PLoS ONE. 8(2). e57173–e57173. 39 indexed citations
6.
Vecchi, Giovanna De, Paolo Verderio, Sara Pizzamiglio, et al.. (2008). The p53 Arg72Pro and Ins16bp polymorphisms and their haplotypes are not associated with breast cancer risk in BRCA-mutation negative familial cases. Cancer Detection and Prevention. 32(2). 140–143. 17 indexed citations
7.
Spreafico, Filippo, Monica Terenziani, Elena Lualdi, et al.. (2006). Non‐chromosome 11‐p syndromes in Wilms tumor patients: Clinical and cytogenetic report of two Down syndrome cases and one Turner syndrome case. American Journal of Medical Genetics Part A. 143A(1). 85–88. 5 indexed citations
8.
Renzo, Francesca Di, Luisa Doneda, Elena Menegola, et al.. (2006). The Murine Pou6f2 Gene is Temporally and Spatially Regulated During Kidney Embryogenesis and its Human Homolog is Overexpressed in a Subset of Wilms Tumors. Journal of Pediatric Hematology/Oncology. 28(12). 791–797. 8 indexed citations
9.
Manoukian, Siranoush, John A. Crolla, M. Testi, et al.. (2005). Bilateral preaxial polydactyly in a WAGR syndrome patient. American Journal of Medical Genetics Part A. 134A(4). 426–429. 4 indexed citations
10.
Perotti, Daniela, Giovanna De Vecchi, Elena Lualdi, et al.. (2005). Wilms Tumor in Monozygous Twins. Journal of Pediatric Hematology/Oncology. 27(10). 521–525. 3 indexed citations
11.
Perotti, Daniela, Giovanna De Vecchi, M. Testi, et al.. (2004). Germline mutations of thePOU6F2 gene in Wilms tumors with loss of heterozygosity on chromosome 7p14. Human Mutation. 24(5). 400–407. 30 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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