Francesca Fava

3.2k total citations
13 papers, 128 citations indexed

About

Francesca Fava is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Francesca Fava has authored 13 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Oncology. Recurrent topics in Francesca Fava's work include BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Francesca Fava is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Cancer Genomics and Diagnostics (3 papers) and Acute Myeloid Leukemia Research (2 papers). Francesca Fava collaborates with scholars based in Italy, France and Switzerland. Francesca Fava's co-authors include Christophe Marzac, Ollivier Legrand, Pierre Hirsch, Jean‐Yves Lallemand, Efraí­n Garrido, J. P. Marie, R. Tang, Eric Jacquet, Simona Lapusan and Alessandra Renieri and has published in prestigious journals such as International Journal of Molecular Sciences, Cells and Cancers.

In The Last Decade

Francesca Fava

12 papers receiving 126 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Francesca Fava Italy 5 62 51 35 32 16 13 128
Katarzyna Pawińska-Wąsikowska Poland 7 35 0.6× 20 0.4× 11 0.3× 9 0.3× 24 1.5× 15 93
Guillaume Hypolite France 8 21 0.3× 77 1.5× 59 1.7× 14 0.4× 8 0.5× 10 151
Federico Monaco Italy 7 45 0.7× 37 0.7× 45 1.3× 11 0.3× 10 0.6× 21 130
Valeria Cancelli Italy 9 62 1.0× 82 1.6× 138 3.9× 24 0.8× 4 0.3× 24 200
Péter Reményi Hungary 9 44 0.7× 34 0.7× 144 4.1× 31 1.0× 22 1.4× 36 217
Halldora K. Thorarinsdottir United States 7 37 0.6× 67 1.3× 10 0.3× 8 0.3× 54 3.4× 7 192
Mahsa Talbott United States 5 40 0.6× 22 0.4× 32 0.9× 13 0.4× 13 0.8× 10 141
Sara Gazaneo Italy 6 99 1.6× 78 1.5× 7 0.2× 20 0.6× 9 0.6× 6 173
Ferran Vall‐Llovera Spain 6 47 0.8× 42 0.8× 64 1.8× 6 0.2× 21 1.3× 12 132
Haifaa Abdulhaq United States 7 39 0.6× 79 1.5× 152 4.3× 10 0.3× 6 0.4× 29 225

Countries citing papers authored by Francesca Fava

Since Specialization
Citations

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

Fields of papers citing papers by Francesca Fava

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Francesca Fava

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

All Works

13 of 13 papers shown
1.
Serrano, Davide, Cristina Zanzottera, Francesca Fava, et al.. (2025). Hereditary Breast Cancer: Comprehensive Risk Assessment and Prevention Strategies. Genes. 16(1). 82–82. 1 indexed citations
2.
Fava, Francesca, Monica Marabelli, Mariarosaria Calvello, et al.. (2025). MLH1 promoter hypermethylation and Lynch Syndrome: When to test for constitutional epimutations of MLH1 gene?. Tumori Journal. 3887655698–3887655698. 1 indexed citations
3.
Polidoro, Silvia, Harriet Johansson, Giovanni Cugliari, et al.. (2025). Impact of Epigenome-Wide Methylation and Breast Cancer Recurrence in Women Tested Negative for BRCA Genes: The Breast Methylation Risk (BREMERI) Study. Cancers. 17(19). 3132–3132.
4.
Marabelli, Monica, Mariarosaria Calvello, Sara Gandini, et al.. (2025). Germline Testing in Breast Cancer: A Single-Center Analysis Comparing Strengths and Challenges of Different Approaches. Cancers. 17(9). 1419–1419. 1 indexed citations
5.
Zhang, Sai, Johnathan Cooper‐Knock, Annika K. Weimer, et al.. (2022). Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity. Cell Systems. 13(8). 598–614.e6. 14 indexed citations
6.
Zguro, Kristina, Chiara Fallerini, Francesca Fava, Simone Furini, & Alessandra Renieri. (2022). Host genetic basis of COVID-19: from methodologies to genes. European Journal of Human Genetics. 30(8). 899–907. 12 indexed citations
7.
Baldassarri, Margherita, Kristina Zguro, Valeria Tomati, et al.. (2022). Gain- and Loss-of-Function CFTR Alleles Are Associated with COVID-19 Clinical Outcomes. Cells. 11(24). 4096–4096. 4 indexed citations
8.
Zanella, Isabella, Simone Piva, Massimiliano Filosto, et al.. (2021). C9orf72 Intermediate Repeats Confer Genetic Risk for Severe COVID-19 Pneumonia Independently of Age. International Journal of Molecular Sciences. 22(13). 6991–6991. 10 indexed citations
9.
Tognetti, Linda, Margherita Baldassarri, Francesca Fava, et al.. (2020). A novel mutation in LMX1B gene in a newborn with nail‐patella syndrome: Clinical and dermoscopic findings. Pediatric Dermatology. 37(6). 1205–1206. 2 indexed citations
10.
Palmieri, Maria, Margherita Baldassarri, Francesca Fava, et al.. (2019). PIK3CA-CDKN2A clonal evolution in metastatic breast cancer and multiple points cell-free DNA analysis. Cancer Cell International. 19(1). 274–274. 1 indexed citations
11.
Hirsch, Pierre, Christophe Marzac, Jean‐Yves Perrot, et al.. (2011). Prognostic impact of high ABC transporter activity in 111 adult acute myeloid leukemia patients with normal cytogenetics when compared to FLT3, NPM1, CEBPA and BAALC. Haematologica. 97(2). 241–245. 20 indexed citations
12.
13.
Neri, Giovanni, et al.. (1975). Viral expression, oncogenicity, and antigenicity of a mouse salivary gland tumor and two cell lines derived from it.. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 35(9). 2394–402. 3 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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