Jacopo Azzollini

3.7k total citations
25 papers, 324 citations indexed

About

Jacopo Azzollini is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Jacopo Azzollini has authored 25 papers receiving a total of 324 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 6 papers in Cancer Research. Recurrent topics in Jacopo Azzollini's work include BRCA gene mutations in cancer (11 papers), Genomics and Chromatin Dynamics (9 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jacopo Azzollini is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Genomics and Chromatin Dynamics (9 papers) and Genomic variations and chromosomal abnormalities (5 papers). Jacopo Azzollini collaborates with scholars based in Italy, France and Switzerland. Jacopo Azzollini's co-authors include Siranoush Manoukian, Bernard Peissel, Cristina Gervasini, Lidia Larizza, Silvia Russo, Angelo Selicorni, Anna Cereda, Maura Masciadri, Ilaria Parenti and Paolo Radice and has published in prestigious journals such as PLoS ONE, Scientific Reports and Neuroscience Letters.

In The Last Decade

Jacopo Azzollini

25 papers receiving 321 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jacopo Azzollini Italy 13 208 196 50 47 31 25 324
Dominique Stoppa-Lyonnet France 6 185 0.9× 217 1.1× 65 1.3× 58 1.2× 40 1.3× 6 350
Katharina Eirich Germany 6 313 1.5× 145 0.7× 65 1.3× 83 1.8× 34 1.1× 8 389
Matthew Lubin United States 5 263 1.3× 265 1.4× 52 1.0× 97 2.1× 53 1.7× 8 413
Hannah F. Almubarak Saudi Arabia 5 252 1.2× 94 0.5× 60 1.2× 110 2.3× 31 1.0× 7 371
Mara Colombo Italy 10 156 0.8× 118 0.6× 36 0.7× 50 1.1× 47 1.5× 15 250
Mike Stratton United Kingdom 5 136 0.7× 88 0.4× 26 0.5× 67 1.4× 30 1.0× 9 235
Jennifer McDaid United Kingdom 8 271 1.3× 99 0.5× 21 0.4× 29 0.6× 22 0.7× 8 325
Rashesh Sanghvi United Kingdom 7 188 0.9× 104 0.5× 26 0.5× 113 2.4× 28 0.9× 10 328
Alison Trainer United Kingdom 6 234 1.1× 157 0.8× 61 1.2× 41 0.9× 28 0.9× 7 363
Pei Xin Lim United States 9 347 1.7× 80 0.4× 162 3.2× 60 1.3× 16 0.5× 11 397

Countries citing papers authored by Jacopo Azzollini

Since Specialization
Citations

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

Fields of papers citing papers by Jacopo Azzollini

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacopo Azzollini

This figure shows the co-authorship network connecting the top 25 collaborators of Jacopo Azzollini. A scholar is included among the top collaborators of Jacopo Azzollini 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 Jacopo Azzollini. Jacopo Azzollini 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.
Azzollini, Jacopo, Luca Agnelli, Elena Conca, et al.. (2023). Prevalence of BRCA homopolymeric indels in an ION Torrent-based tumour-to-germline testing workflow in high-grade ovarian carcinoma. Scientific Reports. 13(1). 7781–7781. 2 indexed citations
2.
Zattarin, Emma, Riccardo Lobefaro, Rita Leporati, et al.. (2023). Breast cancers arising in subjects with germline BRCA1 or BRCA2 mutations: Different biological and clinical entities with potentially diverse therapeutic opportunities. Critical Reviews in Oncology/Hematology. 190. 104109–104109. 2 indexed citations
3.
Tomasello, Giovanni, Donatella Gambini, Fausto Petrelli, et al.. (2022). Characterization of the HER2 status in BRCA-mutated breast cancer: a single institutional series and systematic review with pooled analysis. ESMO Open. 7(4). 100531–100531. 12 indexed citations
4.
Azzollini, Jacopo, Andrea Ferrari, Stefano Chiaravalli, et al.. (2021). Clinical heterogeneity and reduced penetrance in DICER1 syndrome: a report of three families. Tumori Journal. 107(6). NP144–NP148. 2 indexed citations
5.
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
6.
Manoukian, Siranoush, Sara Alfieri, Elisabetta Bianchi, et al.. (2019). Risk‐reducing surgery in BRCA1/BRCA2 mutation carriers: Are there factors associated with the choice?. Psycho-Oncology. 28(9). 1871–1878. 12 indexed citations
7.
Villa, Roberta, Jacopo Azzollini, Bernard Peissel, & Siranoush Manoukian. (2019). Co-occurrence of Mayer-Rokitansky-Küster-Hauser syndrome and ovarian cancer: A case report and review of the literature. Gynecologic Oncology Reports. 28. 68–70. 4 indexed citations
8.
Azzollini, Jacopo, Chiara Pesenti, Sara Pizzamiglio, et al.. (2019). Constitutive BRCA1 Promoter Hypermethylation Can Be a Predisposing Event in Isolated Early-Onset Breast Cancer. Cancers. 11(1). 58–58. 22 indexed citations
9.
Pasanisi, Patrizia, Eleonora Bruno, Elisabetta Venturelli, et al.. (2018). A Dietary Intervention to Lower Serum Levels of IGF-I in BRCA Mutation Carriers. Cancers. 10(9). 309–309. 16 indexed citations
10.
Caleca, Laura, Irene Catucci, Gisella Figlioli, et al.. (2018). Two Missense Variants Detected in Breast Cancer Probands Preventing BRCA2-PALB2 Protein Interaction. Frontiers in Oncology. 8. 11 indexed citations
11.
Azzollini, Jacopo, Chiara Pesenti, Luca Ferrari, et al.. (2017). Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies. PLoS ONE. 12(2). e0171663–e0171663. 14 indexed citations
12.
Verde, Nicla La, Fabio Corsi, Anna Moretti, et al.. (2015). A Targeted Approach to Genetic Counseling in Breast Cancer Patients: The Experience of an Italian Local Project. Tumori Journal. 102(1). 45–50. 6 indexed citations
13.
Berrino, Franco, Silvia Francisci, Bernard Peissel, et al.. (2014). Estimate of the penetrance of BRCA mutation and the COS software for the assessment of BRCA mutation probability. Familial Cancer. 14(1). 117–128. 11 indexed citations
14.
Parenti, Ilaria, Maura Masciadri, Anna Cereda, et al.. (2014). Overall and allele-specific expression of theSMC1Agene in female Cornelia de Lange syndrome patients and healthy controls. Epigenetics. 9(7). 973–979. 8 indexed citations
15.
Gervasini, Cristina, Silvia Russo, Anna Cereda, et al.. (2013). Cornelia de Lange individuals with new and recurrent SMC1A mutations enhance delineation of mutation repertoire and phenotypic spectrum. American Journal of Medical Genetics Part A. 161(11). 2909–2919. 24 indexed citations
16.
Gervasini, Cristina, Ilaria Parenti, Jacopo Azzollini, et al.. (2013). Molecular characterization of a mosaic NIPBL deletion in a Cornelia de Lange patient with severe phenotype. European Journal of Medical Genetics. 56(3). 138–143. 17 indexed citations
17.
Gervasini, Cristina, Jacopo Azzollini, Maura Masciadri, et al.. (2013). Genomic imbalances in patients with a clinical presentation in the spectrum of Cornelia de Lange syndrome. BMC Medical Genetics. 14(1). 41–41. 16 indexed citations
18.
Nanetti, Lorenzo, Silvia Baratta, Marta Panzeri, et al.. (2012). Novel and recurrent spastin mutations in a large series of SPG4 Italian families. Neuroscience Letters. 528(1). 42–45. 5 indexed citations
19.
Russo, Silvia, Maura Masciadri, Cristina Gervasini, et al.. (2012). Intragenic and large NIPBL rearrangements revealed by MLPA in Cornelia de Lange patients. European Journal of Human Genetics. 20(7). 734–741. 16 indexed citations
20.
Castronovo, Paola, Andrée Delahaye‐Duriez, Cristina Gervasini, et al.. (2010). Somatic mosaicism in Cornelia de Lange syndrome: a further contributor to the wide clinical expressivity?. Clinical Genetics. 78(6). 560–564. 24 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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