Daniela Zaffaroni

3.0k total citations
12 papers, 165 citations indexed

About

Daniela Zaffaroni is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Daniela Zaffaroni has authored 12 papers receiving a total of 165 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 3 papers in Pathology and Forensic Medicine. Recurrent topics in Daniela Zaffaroni's work include BRCA gene mutations in cancer (4 papers), DNA Repair Mechanisms (4 papers) and Genomics and Chromatin Dynamics (3 papers). Daniela Zaffaroni is often cited by papers focused on BRCA gene mutations in cancer (4 papers), DNA Repair Mechanisms (4 papers) and Genomics and Chromatin Dynamics (3 papers). Daniela Zaffaroni collaborates with scholars based in Italy, United States and Netherlands. Daniela Zaffaroni's co-authors include Bernard Peissel, Anna Saran, Tommaso A. Dragani, Giacomo Manenti, Vincenzo Covelli, Simonetta Rebessi, Valeria Pensotti, Paolo Radice, Simonetta Pazzaglia and Siranoush Manoukian and has published in prestigious journals such as PLoS ONE, Oncogene and International Journal of Cancer.

In The Last Decade

Daniela Zaffaroni

12 papers receiving 164 citations

Peers

Daniela Zaffaroni
S.J. Xu China
Olivier Ingster France
Yves Jean Bignon France
Helena Rudnicka Poland
Elodie Girard France
Rebecca Mathew Qatar
Hannah Carlson-Donohoe United States
Kelly McGoldrick United States
Hanan Khoury-Haddad Israel
Yael Laitman Israel
S.J. Xu China
Daniela Zaffaroni
Citations per year, relative to Daniela Zaffaroni Daniela Zaffaroni (= 1×) peers S.J. Xu

Countries citing papers authored by Daniela Zaffaroni

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Zaffaroni

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Zaffaroni

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

All Works

12 of 12 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.
Azzollini, Jacopo, Giulietta Scuvera, Eleonora Bruno, et al.. (2016). Mutation detection rates associated with specific selection criteria for BRCA1/2 testing in 1854 high-risk families: A monocentric Italian study. European Journal of Internal Medicine. 32. 65–71. 18 indexed citations
3.
Caleca, Laura, Anna Laura Putignano, Mara Colombo, et al.. (2014). Characterization of an Italian Founder Mutation in the RING-Finger Domain of BRCA1. PLoS ONE. 9(2). e86924–e86924. 20 indexed citations
4.
Bossi, Paola, Carla B. Ripamonti, Siranoush Manoukian, et al.. (2013). MC13-0082 Salivary gland cancer in two male BRCA gene mutation carriers. European Journal of Cancer. 49. S34–S35. 1 indexed citations
5.
Zuradelli, Monica, Bernard Peissel, Siranoush Manoukian, et al.. (2010). Four new cases of double heterozygosity for BRCA1 and BRCA2 gene mutations: clinical, pathological, and family characteristics. Breast Cancer Research and Treatment. 124(1). 251–258. 27 indexed citations
6.
Catucci, Irene, Paolo Verderio, Sara Pizzamiglio, et al.. (2010). The CASP8 rs3834129 polymorphism and breast cancer risk in BRCA1 mutation carriers. Breast Cancer Research and Treatment. 125(3). 855–860. 10 indexed citations
7.
Zaffaroni, Daniela, Monica Spinola, Antonella Galvan, et al.. (2004). Met proto-oncogene juxtamembrane rare variations in mouse and humans: differential effects of Arg and Cys alleles on mouse lung tumorigenesis. Oncogene. 24(6). 1084–1090. 19 indexed citations
8.
Gariboldi, Manuela, Bernard Peissel, Alessandra Fabbri, et al.. (2003). SCCA2-like serpins mediate genetic predisposition to skin tumors.. PubMed. 63(8). 1871–5. 13 indexed citations
9.
Saran, Anna, Daniela Zaffaroni, Simonetta Pazzaglia, et al.. (2001). Inhibition of both skin and lung tumorigenesis by Car‐R mouse‐derived cancer modifier loci. International Journal of Cancer. 97(5). 580–583. 5 indexed citations
10.
Peissel, Bernard, Daniela Zaffaroni, Simonetta Pazzaglia, et al.. (2001). Use of intercross outbred mice and single nucleotide polymorphisms to map skin cancer modifier loci. Mammalian Genome. 12(4). 291–294. 9 indexed citations
11.
Manenti, Giacomo, Bernard Peissel, Manuela Gariboldi, et al.. (2000). A cancer modifier role for parathyroid hormone-related protein. Oncogene. 19(47). 5324–5328. 26 indexed citations
12.
Peissel, Bernard, Daniela Zaffaroni, Nicola Zanesi, et al.. (2000). Linkage disequilibrium and haplotype mapping of a skin cancer susceptibility locus in outbred mice. Mammalian Genome. 11(11). 979–981. 13 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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2026