Ettore Rizzo

1.8k total citations
20 papers, 357 citations indexed

About

Ettore Rizzo is a scholar working on Genetics, Genetics and Hematology. According to data from OpenAlex, Ettore Rizzo has authored 20 papers receiving a total of 357 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Genetics and 7 papers in Hematology. Recurrent topics in Ettore Rizzo's work include Genomics and Rare Diseases (7 papers), Acute Myeloid Leukemia Research (6 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Ettore Rizzo is often cited by papers focused on Genomics and Rare Diseases (7 papers), Acute Myeloid Leukemia Research (6 papers) and Chronic Lymphocytic Leukemia Research (5 papers). Ettore Rizzo collaborates with scholars based in Italy, United States and Japan. Ettore Rizzo's co-authors include Mariangela Bonizzoni, Ronald P. van Rij, Zhijian Tu, Rebeca Carballar‐Lejarazú, Lino Ometto, Pascal Miesen, Umberto Palatini, Virginia Valeria Ferretti, Anna Gallì and Luca Malcovati and has published in prestigious journals such as Blood, Bioinformatics and PLoS ONE.

In The Last Decade

Ettore Rizzo

19 papers receiving 350 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ettore Rizzo Italy 9 127 107 95 81 74 20 357
S Y Zhao China 8 44 0.3× 32 0.3× 196 2.1× 15 0.2× 22 0.3× 17 354
Mattias Mattsson Sweden 11 210 1.7× 46 0.4× 49 0.5× 160 2.0× 20 0.3× 24 377
Eleonora Ottina Austria 12 25 0.2× 33 0.3× 276 2.9× 19 0.2× 25 0.3× 18 590
Joy Nakitandwe United States 12 23 0.2× 73 0.7× 304 3.2× 47 0.6× 33 0.4× 30 521
Britta S. Möhl Germany 11 92 0.7× 16 0.1× 59 0.6× 121 1.5× 12 0.2× 15 466
Travis Drucker United States 8 41 0.3× 55 0.5× 194 2.0× 45 0.6× 29 0.4× 10 523
Philip E. Carter United Kingdom 6 167 1.3× 90 0.8× 106 1.1× 31 0.4× 37 0.5× 8 374
Bernd Unger Austria 9 56 0.4× 24 0.2× 131 1.4× 23 0.3× 97 1.3× 10 397
Dominic Rose Germany 14 64 0.5× 102 1.0× 577 6.1× 9 0.1× 15 0.2× 25 713
Bo Gustav Lindberg Sweden 7 16 0.1× 91 0.9× 232 2.4× 4 0.0× 97 1.3× 10 462

Countries citing papers authored by Ettore Rizzo

Since Specialization
Citations

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

Fields of papers citing papers by Ettore Rizzo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ettore Rizzo

This figure shows the co-authorship network connecting the top 25 collaborators of Ettore Rizzo. A scholar is included among the top collaborators of Ettore Rizzo 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 Ettore Rizzo. Ettore Rizzo 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.
Nicora, Giovanna, Andrea Gazzo, Riccardo Bellazzi, et al.. (2025). Digenic variant interpretation with hypothesis-driven explainable AI. NAR Genomics and Bioinformatics. 7(2). lqaf029–lqaf029.
2.
Limongelli, Ivan, et al.. (2024). VarChat: the generative AI assistant for the interpretation of human genomic variations. Bioinformatics. 40(4). 12 indexed citations
3.
Zucca, Susanna, Giovanna Nicora, Riccardo Bellazzi, et al.. (2024). An AI-based approach driven by genotypes and phenotypes to uplift the diagnostic yield of genetic diseases. Human Genetics. 144(2-3). 159–171. 8 indexed citations
4.
Molteni, Elisabetta, Elisa Bono, Anna Gallì, et al.. (2023). Prevalence and clinical expression of germ line predisposition to myeloid neoplasms in adults with marrow hypocellularity. Blood. 142(7). 643–657. 9 indexed citations
5.
Rossi, Marianna, Anna Gallì, Elisa Roncoroni, et al.. (2021). Enrichment of Double RUNX1 Mutations in Acute Leukemias of Ambiguous Lineage. Frontiers in Oncology. 11. 726637–726637. 4 indexed citations
6.
Gallì, Anna, Gabriele Todisco, Eulalia Catamo, et al.. (2021). Relationship between clone metrics and clinical outcome in clonal cytopenia. Blood. 138(11). 965–976. 61 indexed citations
7.
Tsaknakis, Grigorios, Anna Gallì, Peggy Kanellou, et al.. (2021). Incidence and prognosis of clonal hematopoiesis in patients with chronic idiopathic neutropenia. Blood. 138(14). 1249–1257. 13 indexed citations
8.
Defrancesco, Irene, Silvia Zibellini, Emanuela Boveri, et al.. (2020). Targeted next‐generation sequencing reveals molecular heterogeneity in non‐chronic lymphocytic leukemia clonal B‐cell lymphocytosis. Hematological Oncology. 38(5). 689–697. 4 indexed citations
9.
Rizzo, Ettore, Laura Raddrizzani, Sebastiano Di Bella, et al.. (2019). Comprehensive kinome NGS targeted expression profiling by KING-REX. BMC Genomics. 20(1). 307–307. 1 indexed citations
10.
Defrancesco, Irene, Silvia Zibellini, Emanuela Boveri, et al.. (2019). Targeted Next Generation Sequencing Reveals Molecular Heterogeneity in Non-CLL Clonal B-Cell Lymphocytosis. Blood. 134(Supplement_1). 1502–1502. 1 indexed citations
11.
12.
Palatini, Umberto, Pascal Miesen, Rebeca Carballar‐Lejarazú, et al.. (2017). Comparative genomics shows that viral integrations are abundant and express piRNAs in the arboviral vectors Aedes aegypti and Aedes albopictus. BMC Genomics. 18(1). 512–512. 116 indexed citations
13.
Varettoni, Marzia, Silvia Zibellini, Irene Defrancesco, et al.. (2017). Pattern of somatic mutations in patients with Waldenström macroglobulinemia or IgM monoclonal gammopathy of undetermined significance. Haematologica. 102(12). 2077–2085. 79 indexed citations
14.
Marini, Simone, Ivan Limongelli, Ettore Rizzo, et al.. (2016). A Data Fusion Approach to Enhance Association Study in Epilepsy. PLoS ONE. 11(12). e0164940–e0164940. 3 indexed citations
15.
Malcovati, Luca, Anna Gallì, Erica Travaglino, et al.. (2016). Predictive Value of Mutation Analysis in the Diagnostic Approach to Patients with Unexplained Cytopenia. Blood. 128(22). 298–298. 1 indexed citations
16.
17.
Elena, Chiara, Anna Gallì, Antonio Bianchessi, et al.. (2016). Somatic Mutations Are Frequently Detected in Chronic Myeloid Leukemia in Chronic Phase and Do Not Affect Response to Tyrosine-Kinase Inhibitors. Blood. 128(22). 1117–1117. 1 indexed citations
18.
Todisco, Gabriele, Anna Gallì, Erica Travaglino, et al.. (2016). SRSF2 Mutations Identify a Distinct Subtype of Myeloid Neoplasm Across Myelodysplastic Syndromes and Acute Myeloid Leukemia. Blood. 128(22). 4337–4337. 4 indexed citations
19.
Limongelli, Ivan, et al.. (2015). BigQ: a NoSQL based framework to handle genomic variants in i2b2. BMC Bioinformatics. 16(1). 415–415. 16 indexed citations
20.
Souilmi, Yassine, Alex K. Lancaster, Ettore Rizzo, et al.. (2015). Scalable and cost-effective NGS genotyping in the cloud. BMC Medical Genomics. 8(1). 64–64. 17 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

Breakdown of academic impact, for papers by S Y Zhao Breakdown of academic impact, for papers by Mattias Mattsson Breakdown of academic impact, for papers by Eleonora Ottina Breakdown of academic impact, for papers by Joy Nakitandwe Breakdown of academic impact, for papers by Britta S. Möhl Breakdown of academic impact, for papers by Travis Drucker Breakdown of academic impact, for papers by Philip E. Carter Breakdown of academic impact, for papers by Bernd Unger Breakdown of academic impact, for papers by Dominic Rose Breakdown of academic impact, for papers by Bo Gustav Lindberg
Rankless by CCL
2026