Serena Barozzi

1.1k total citations
19 papers, 325 citations indexed

About

Serena Barozzi is a scholar working on Hematology, Immunology and Allergy and Genetics. According to data from OpenAlex, Serena Barozzi has authored 19 papers receiving a total of 325 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Hematology, 7 papers in Immunology and Allergy and 4 papers in Genetics. Recurrent topics in Serena Barozzi's work include Platelet Disorders and Treatments (15 papers), Cell Adhesion Molecules Research (7 papers) and Blood groups and transfusion (5 papers). Serena Barozzi is often cited by papers focused on Platelet Disorders and Treatments (15 papers), Cell Adhesion Molecules Research (7 papers) and Blood groups and transfusion (5 papers). Serena Barozzi collaborates with scholars based in Italy, United States and Greece. Serena Barozzi's co-authors include Alessandro Pecci, Anna Savoia, Patrizia Noris, Valeria Bozzi, Carlo L. Balduini, Alessandra Balduini, Carlo Zaninetti, Christian A. Di Buduo, Daniela De Rocco and Carlo Balduini and has published in prestigious journals such as Blood, International Journal of Molecular Sciences and eLife.

In The Last Decade

Serena Barozzi

19 papers receiving 322 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Serena Barozzi Italy 11 245 79 63 61 58 19 325
Nathalie Balayn France 5 255 1.0× 122 1.5× 56 0.9× 75 1.2× 42 0.7× 8 311
Sonja van den Oudenrijn Netherlands 9 313 1.3× 83 1.1× 66 1.0× 110 1.8× 125 2.2× 10 459
Fabien Pertuy France 7 216 0.9× 69 0.9× 14 0.2× 60 1.0× 42 0.7× 9 311
Hiroshi Nagahisa Japan 10 229 0.9× 80 1.0× 36 0.6× 122 2.0× 45 0.8× 14 401
Lucie Boyer Canada 12 295 1.2× 103 1.3× 25 0.4× 86 1.4× 84 1.4× 19 372
Martine Morales France 7 280 1.1× 49 0.6× 48 0.8× 93 1.5× 69 1.2× 8 392
Michela Faleschini Italy 7 107 0.4× 33 0.4× 48 0.8× 149 2.4× 39 0.7× 20 293
Guojing Zhu United States 10 60 0.2× 42 0.5× 40 0.6× 132 2.2× 72 1.2× 25 348
Iléana Antony‐Debré France 8 209 0.9× 96 1.2× 49 0.8× 97 1.6× 70 1.2× 15 300
Lihua Sun China 13 111 0.5× 20 0.3× 51 0.8× 90 1.5× 166 2.9× 18 348

Countries citing papers authored by Serena Barozzi

Since Specialization
Citations

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

Fields of papers citing papers by Serena Barozzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Serena Barozzi

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

All Works

19 of 19 papers shown
1.
Barozzi, Serena, Valeria Bozzi, Rosana F. Marta, et al.. (2024). Two novel families with RUNX1 variants indicate glycine 168 as a new mutational hotspot: Implications for FPD/AML diagnosis. British Journal of Haematology. 205(6). 2315–2320. 1 indexed citations
2.
Marzollo, Antonio, Stefania Zampieri, Serena Barozzi, et al.. (2024). Thrombocytopenia 4 (THC4): Six novel families with mutations of the cytochrome c gene. British Journal of Haematology. 205(1). 306–315. 6 indexed citations
3.
Barozzi, Serena, Caterina Marconi, Roberta Bottega, et al.. (2024). ACTN1‐related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype. British Journal of Haematology. 204(6). 2453–2457. 2 indexed citations
4.
Marconi, Caterina, Alessandro Pecci, Flavia Palombo, et al.. (2022). Exome sequencing in 116 patients with inherited thrombocytopenia that remained of unknown origin after systematic phenotype-driven diagnostic workup. Haematologica. 108(7). 1909–1919. 1 indexed citations
5.
Barozzi, Serena, Valeria Bozzi, Daniela De Rocco, et al.. (2021). A Novel Mutation in GP1BB Reveals the Role of the Cytoplasmic Domain of GPIbβ in the Pathophysiology of Bernard-Soulier Syndrome and GPIb-IX Complex Assembly. International Journal of Molecular Sciences. 22(19). 10190–10190. 6 indexed citations
6.
Buduo, Christian A. Di, Pierre Laurent, Carlo Zaninetti, et al.. (2021). Miniaturized 3D bone marrow tissue model to assess response to Thrombopoietin-receptor agonists in patients. eLife. 10. 12 indexed citations
7.
Barozzi, Serena, Christian A. Di Buduo, Caterina Marconi, et al.. (2020). Pathogenetic and clinical study of a patient with thrombocytopenia due to the p.E527K gain-of-function variant of SRC. Haematologica. 106(3). 918–922. 11 indexed citations
8.
Zaninetti, Carlo, Paolo Gresele, Antonella Bertomoro, et al.. (2019). Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial. Haematologica. 105(3). 820–828. 47 indexed citations
9.
Marconi, Caterina, Christian A. Di Buduo, Serena Barozzi, et al.. (2018). Loss-of-function mutations in PTPRJ cause a new form of inherited thrombocytopenia. Blood. 133(12). 1346–1357. 37 indexed citations
10.
Zaninetti, Carlo, Daniela De Rocco, Tania Giangregorio, et al.. (2018). MYH9-Related Thrombocytopenia: Four Novel Variants Affecting the Tail Domain of the Non-Muscle Myosin Heavy Chain IIA Associated with a Mild Clinical Evolution of the Disorder. Hämostaseologie. 39(1). 87–94. 1 indexed citations
11.
Zaninetti, Carlo, et al.. (2017). Inherited thrombocytopenia caused by ANKRD26 mutations misdiagnosed and treated as myelodysplastic syndrome: report on two cases. Journal of Thrombosis and Haemostasis. 15(12). 2388–2392. 26 indexed citations
12.
Pecci, Alessandro, Iman Ragab, Valeria Bozzi, et al.. (2017). Thrombopoietin mutation in congenital amegakaryocytic thrombocytopenia treatable with romiplostim. EMBO Molecular Medicine. 10(1). 63–75. 41 indexed citations
13.
Vanoli, Alessandro, Vittorio Necchi, Serena Barozzi, et al.. (2015). Chaperone molecules concentrate together with the ubiquitin–proteasome system inside particulate cytoplasmic structures: possible role in metabolism of misfolded proteins. Histochemistry and Cell Biology. 144(2). 179–184. 7 indexed citations
14.
Pecci, Alessandro, Vittorio Necchi, Serena Barozzi, et al.. (2015). Particulate cytoplasmic structures with high concentration of ubiquitin-proteasome accumulate in myeloid neoplasms. Journal of Hematology & Oncology. 8(1). 71–71. 8 indexed citations
15.
Pecci, Alessandro, Daniela De Rocco, Samppa Ryhänen, et al.. (2014). R705H mutation of MYH9 is associated with MYH9‐related disease and not only with non‐syndromic deafness DFNA17. Clinical Genetics. 88(1). 85–89. 14 indexed citations
16.
Economou, Marina, Spyros Batzios, Alessandro Pecci, et al.. (2012). MYH9-related Disorders. Journal of Pediatric Hematology/Oncology. 34(6). 412–415. 14 indexed citations
17.
Necchi, Vittorio, Alessandra Balduini, Patrizia Noris, et al.. (2012). Ubiquitin/proteasome-rich particulate cytoplasmic structures (PaCSs) in the platelets and megakaryocytes of ANKRD26-related thrombocytopenia. Thrombosis and Haemostasis. 109(2). 263–271. 46 indexed citations
18.
Rocco, Daniela De, Barbara Zieger, Helen Platokouki, et al.. (2012). MYH9-related disease: Five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations. European Journal of Medical Genetics. 56(1). 7–12. 22 indexed citations
19.
Bozzi, Valeria, Emanuele Panza, Serena Barozzi, et al.. (2011). Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells. Thrombosis and Haemostasis. 106(10). 693–704. 23 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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