P Mondini

771 total citations
28 papers, 568 citations indexed

About

P Mondini is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, P Mondini has authored 28 papers receiving a total of 568 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Pathology and Forensic Medicine and 6 papers in Genetics. Recurrent topics in P Mondini's work include Renal and related cancers (8 papers), Genetic factors in colorectal cancer (7 papers) and BRCA gene mutations in cancer (4 papers). P Mondini is often cited by papers focused on Renal and related cancers (8 papers), Genetic factors in colorectal cancer (7 papers) and BRCA gene mutations in cancer (4 papers). P Mondini collaborates with scholars based in Italy, United States and United Kingdom. P Mondini's co-authors include Paolo Radice, Marco A. Pierotti, Paola Sala, Lucio Bertario, Monica Giarola, Liliana Varesco, Pasquale Spinelli, Antonio Russo, S. Pilotti and Daniela Perotti and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Gastroenterology.

In The Last Decade

P Mondini

28 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P Mondini Italy 14 290 205 186 112 110 28 568
G Michils Belgium 9 211 0.7× 152 0.7× 129 0.7× 111 1.0× 136 1.2× 13 525
Brita Thode Germany 10 101 0.3× 102 0.5× 140 0.8× 95 0.8× 39 0.4× 18 381
W. Weybora Austria 6 72 0.2× 83 0.4× 149 0.8× 108 1.0× 113 1.0× 13 354
Marion Mandl Germany 8 502 1.7× 103 0.5× 299 1.6× 84 0.8× 112 1.0× 8 572
Mariola Iliszko Poland 12 74 0.3× 117 0.6× 121 0.7× 72 0.6× 189 1.7× 27 363
P Cavazzini Italy 11 146 0.5× 71 0.3× 98 0.5× 33 0.3× 44 0.4× 13 365
Ulf Kristoffersson Sweden 11 69 0.2× 163 0.8× 95 0.5× 185 1.7× 142 1.3× 18 599
Johnbosco Tayebwa Sweden 12 121 0.4× 114 0.6× 256 1.4× 21 0.2× 511 4.6× 12 764
Jean-Paul Després Canada 4 237 0.8× 72 0.4× 136 0.7× 33 0.3× 156 1.4× 5 435
Edmund Cheesman United Kingdom 11 59 0.2× 238 1.2× 50 0.3× 85 0.8× 67 0.6× 26 461

Countries citing papers authored by P Mondini

Since Specialization
Citations

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

Fields of papers citing papers by P Mondini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P Mondini

This figure shows the co-authorship network connecting the top 25 collaborators of P Mondini. A scholar is included among the top collaborators of P Mondini 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 P Mondini. P Mondini 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.
Colombo, Mara, P Mondini, Elisa Minenza, et al.. (2023). A novel BRCA1 splicing variant detected in an early onset triple-negative breast cancer patient additionally carrying a pathogenic variant in ATM: A case report. Frontiers in Oncology. 13. 1102184–1102184. 1 indexed citations
2.
Molinari, Francesca, Stefano Signoroni, Andrea Lampis, et al.. (2014). BRAF mutation analysis is a valid tool to implement in Lynch syndrome diagnosis in patients classified according to the Bethesda guidelines.. PubMed. 100(3). 315–20. 6 indexed citations
3.
Ripamonti, Carla B., Mara Colombo, P Mondini, et al.. (2013). First description of an acinic cell carcinoma of the breast in a BRCA1 mutation carrier: a case report. BMC Cancer. 13(1). 46–46. 32 indexed citations
4.
Perotti, Daniela, P Mondini, Monica Terenziani, et al.. (2005). WT1 Gene Analysis in Sporadic Early-Onset and Bilateral Wilms Tumor Patients Without Associated Abnormalities. Journal of Pediatric Hematology/Oncology. 27(4). 197–201. 9 indexed citations
5.
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
6.
Gismondi, Viviana, L Bonelli, Stefania Sciallero, et al.. (2002). Prevalence of the E1317Q Variant of the APC Gene in Italian Patients with Colorectal Adenomas. Genetic Testing. 6(4). 313–317. 14 indexed citations
7.
Perotti, Daniela, M. Testi, P Mondini, et al.. (2001). Refinement within single yeast artificial chromosome clones of a minimal region commonly deleted on the short arm of chromosome 7 in Wilms tumours. Genes Chromosomes and Cancer. 31(1). 42–47. 13 indexed citations
8.
Giarola, Monica, Silvano Presciuttini, P Mondini, et al.. (1999). Screening for mutations of theAPC gene in 66 Italian familial adenomatous polyposis patients: Evidence for phenotypic differences in cases with and without identified mutation. Human Mutation. 13(2). 116–123. 40 indexed citations
9.
Perotti, Daniela, P Mondini, Roberto Giardini, et al.. (1998). No evidence of WT1 involvement in a Burkitt’s lymphoma in a patient with Denys–Drash syndrome. Annals of Oncology. 9(6). 627–631. 5 indexed citations
10.
Giarola, Monica, Dan E. Wells, P Mondini, et al.. (1998). Mutations of adenomatous polyposis coli (APC) gene are uncommon in sporadic desmoid tumours. British Journal of Cancer. 78(5). 582–587. 67 indexed citations
11.
Mondini, P, Barbara Pasini, Valeria Pensotti, et al.. (1998). P7 BRCA1 and BRCA2 germline mutations in early-onset breast carcinoma patients. European Journal of Cancer. 34. S16–S16. 1 indexed citations
12.
Pensotti, Valeria, Paolo Radice, Silvano Presciuttini, et al.. (1997). Mean age of tumor onset in hereditary nonpolyposis colorectal cancer (HNPCC) families correlates with the presence of mutations in DNA mismatch repair genes. Genes Chromosomes and Cancer. 19(3). 135–142. 2 indexed citations
13.
Miozzo, Monica, Daniela Perotti, Fabiola Minoletti, et al.. (1996). Mapping of a Putative Tumor Suppressor Locus to Proximal 7p in Wilms Tumors. Genomics. 37(3). 310–315. 41 indexed citations
14.
Radice, Paolo, P Mondini, Gianbattista Spatti, et al.. (1996). Screening for mutations in exon 11 of the BRCA1 gene in 70 Italian breast and ovarian cancer patients by protein truncation test.. PubMed. 13(6). 1353–7. 24 indexed citations
15.
Radice, Paolo, Daniela Perotti, P Mondini, et al.. (1995). Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11. Genomics. 27(3). 497–501. 19 indexed citations
16.
Radice, Paolo, Marco A. Pierotti, P Mondini, et al.. (1989). Loss of heterozygosity in human germinal tumors. Cytogenetic and Genome Research. 52(1-2). 72–76. 29 indexed citations
17.
Pierotti, Marco A., Paolo Radice, P Mondini, et al.. (1989). Loss of heterozygous DNA markers in human germ cell neoplasms. Cancer Genetics and Cytogenetics. 38(2). 176–176. 1 indexed citations
18.
Biunno, Ida, Maria Rosa Pozzi, Paolo Radice, et al.. (1988). BgIII polymorphisn of the epidermal growth factor receptor (EGF-R) gene. Nucleic Acids Research. 16(15). 7753–7753. 1 indexed citations
19.
Mondini, P, et al.. (1983). [Jaundice as a symptom of traumatic diaphragmatic hernia].. PubMed. 74(43). 2621–3. 1 indexed citations
20.
Mondini, P, et al.. (1958). [Oozing hemorrhage after extracorporeal oxygenation and circulation].. PubMed. 13(3). 163–7. 1 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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