Veronica Medici

573 total citations
10 papers, 182 citations indexed

About

Veronica Medici is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Veronica Medici has authored 10 papers receiving a total of 182 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 3 papers in Cancer Research. Recurrent topics in Veronica Medici's work include BRCA gene mutations in cancer (8 papers), CRISPR and Genetic Engineering (4 papers) and Cancer Genomics and Diagnostics (3 papers). Veronica Medici is often cited by papers focused on BRCA gene mutations in cancer (8 papers), CRISPR and Genetic Engineering (4 papers) and Cancer Genomics and Diagnostics (3 papers). Veronica Medici collaborates with scholars based in Italy and United States. Veronica Medici's co-authors include Laura Cortesi, Isabella Marchi, Massimo Federico, Giacomo Carlo Sturniolo, Maria Grazia Vettorato, Fabio Pomerri, E. Dal Pont, R. D’Incà, Vincenza Di Leo and Antonio Ferronato and has published in prestigious journals such as International Journal of Molecular Sciences, Annals of Oncology and Clinica Chimica Acta.

In The Last Decade

Veronica Medici

10 papers receiving 178 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Veronica Medici Italy	8	102	46	46	45	32	10	182
Jolanta Szymańska-Pasternak Poland	9	74 0.7×	33 0.7×	93 2.0×	45 1.0×	37 1.2×	15	220
Marita Skarstedt Sweden	11	14 0.1×	25 0.5×	93 2.0×	40 0.9×	17 0.5×	15	210
Michael Fatouros Greece	9	77 0.8×	88 1.9×	50 1.1×	33 0.7×	21 0.7×	16	236
Ruth Gershoni Baruch Israel	6	89 0.9×	11 0.2×	121 2.6×	21 0.5×	17 0.5×	8	199
Sheila Goff United Kingdom	5	73 0.7×	24 0.5×	38 0.8×	44 1.0×	149 4.7×	5	219
Jakkapan Khunnarong Thailand	11	31 0.3×	36 0.8×	45 1.0×	26 0.6×	15 0.5×	26	234
Eligia Juárez-Torres Mexico	7	34 0.3×	31 0.7×	101 2.2×	60 1.3×	7 0.2×	7	209
Achilleas Achilleos Cyprus	10	56 0.5×	37 0.8×	62 1.3×	40 0.9×	15 0.5×	16	197
Marion Piedmonte United States	4	56 0.5×	61 1.3×	9 0.2×	14 0.3×	20 0.6×	4	155
Jeremy L. Pautu India	9	22 0.2×	51 1.1×	86 1.9×	26 0.6×	18 0.6×	23	183

Countries citing papers authored by Veronica Medici

Since Specialization

Citations

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

Fields of papers citing papers by Veronica Medici

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Veronica Medici

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

Zuntini, Roberta, Elena Bonora, Laura Benedetta Amato, et al.. (2021). Detecting Variants in the NBN Gene While Testing for Hereditary Breast Cancer: What to Do Next?. International Journal of Molecular Sciences. 22(11). 5832–5832. 10 indexed citations

Cortesi, Laura, Elisabetta De Matteis, Angela Toss, et al.. (2017). Evaluation of Transvaginal Ultrasound plus CA-125 Measurement and Prophylactic Salpingo-Oophorectomy in Women at Different Risk Levels of Ovarian Cancer: The Modena Study Group Cohort Study. Oncology. 93(6). 377–386. 21 indexed citations

Zuntini, Roberta, Laura Cortesi, Daniele Calistri, et al.. (2017). BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotype. Oncotarget. 8(14). 22640–22648. 12 indexed citations

Cortesi, Laura, Elisabetta Razzaboni, Angela Toss, et al.. (2013). A rapid genetic counselling and testing in newly diagnosed breast cancer is associated with high rate of risk-reducing mastectomy in BRCA1/2-positive Italian women. Annals of Oncology. 25(1). 57–63. 29 indexed citations

Pedroni, Monica, Carmela Di Gregorio, Laura Cortesi, et al.. (2013). Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors. Techniques in Coloproctology. 18(3). 285–289. 12 indexed citations

Cortesi, Laura, Arcangela De Nicolo, Veronica Medici, et al.. (2012). Collective evidence supports neutrality of BRCA1 V1687I, a novel sequence variant in the conserved THV motif of the first BRCT repeat. Breast Cancer Research and Treatment. 134(1). 435–441. 1 indexed citations

Cortesi, Laura, Cristina Masini, Claudia Cirilli, et al.. (2010). Favourable ten-year overall survival in a Caucasian population with high probability of hereditary breast cancer. BMC Cancer. 10(1). 90–90. 32 indexed citations

Marino, Marco, Claudio Rabacchi, Maria Luisa Simone, et al.. (2009). A novel deletion of BRCA1 gene that eliminates the ATG initiation codon without affecting the promoter region. Clinica Chimica Acta. 403(1-2). 249–253. 9 indexed citations

D’Incà, R., Fabio Pomerri, Maria Grazia Vettorato, et al.. (2007). Interaction between rifaximin and dietary fibre in patients with diverticular disease. Alimentary Pharmacology & Therapeutics. 25(7). 771–779. 51 indexed citations

10.

Temperani, Paola, Mario Luppi, Francesca Giacobbi, et al.. (2000). Late-Appearing PML/RARα Fusion Transcript with Coincidental t(12;13)(p13.2;q14) in Acute Promyelocytic Leukemia Lacking the t(15;17) Cytogenetic Anomaly. Cancer Genetics and Cytogenetics. 119(2). 121–126. 5 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