Valeria Bozzi

2.2k total citations
28 papers, 821 citations indexed

About

Valeria Bozzi is a scholar working on Hematology, Immunology and Allergy and Immunology. According to data from OpenAlex, Valeria Bozzi has authored 28 papers receiving a total of 821 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Hematology, 11 papers in Immunology and Allergy and 8 papers in Immunology. Recurrent topics in Valeria Bozzi's work include Platelet Disorders and Treatments (19 papers), Cell Adhesion Molecules Research (11 papers) and Blood groups and transfusion (9 papers). Valeria Bozzi is often cited by papers focused on Platelet Disorders and Treatments (19 papers), Cell Adhesion Molecules Research (11 papers) and Blood groups and transfusion (9 papers). Valeria Bozzi collaborates with scholars based in Italy, United Kingdom and Argentina. Valeria Bozzi's co-authors include Alessandro Pecci, Patrizia Noris, Anna Savoia, Federica Melazzini, Carlo L. Balduini, Alessandra Balduini, Daniela De Rocco, Catherine Klersy, Alessandro Malara and Mauro Torti and has published in prestigious journals such as Blood, PLoS ONE and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Valeria Bozzi

28 papers receiving 816 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valeria Bozzi Italy 16 585 173 168 139 118 28 821
Karen L. Imfeld United States 8 299 0.5× 68 0.4× 68 0.4× 121 0.9× 91 0.8× 14 566
Belinda Chan United States 9 119 0.2× 72 0.4× 84 0.5× 58 0.4× 181 1.5× 38 647
P. Kostakis Australia 9 212 0.4× 91 0.5× 53 0.3× 91 0.7× 33 0.3× 11 842
Olga Addimanda Italy 21 143 0.2× 36 0.2× 170 1.0× 261 1.9× 25 0.2× 49 1.0k
Davide Martorana Italy 16 62 0.1× 62 0.4× 358 2.1× 126 0.9× 57 0.5× 46 896
Benjamin Uzan France 14 102 0.2× 42 0.2× 108 0.6× 114 0.8× 87 0.7× 24 702
Carly Selan Australia 15 99 0.2× 23 0.1× 29 0.2× 86 0.6× 88 0.7× 21 674
Noriyuki Seta Japan 12 66 0.1× 60 0.3× 41 0.2× 181 1.3× 39 0.3× 22 473
Christine Pérot France 17 441 0.8× 175 1.0× 132 0.8× 105 0.8× 178 1.5× 31 934
Dimitrios Margaritis Greece 11 246 0.4× 138 0.8× 158 0.9× 151 1.1× 24 0.2× 36 598

Countries citing papers authored by Valeria Bozzi

Since Specialization
Citations

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

Fields of papers citing papers by Valeria Bozzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valeria Bozzi

This figure shows the co-authorship network connecting the top 25 collaborators of Valeria Bozzi. A scholar is included among the top collaborators of Valeria Bozzi 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 Valeria Bozzi. Valeria Bozzi 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.
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.
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
4.
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
5.
Faleschini, Michela, Marie‐Christine Morel‐Kopp, Caterina Marconi, et al.. (2021). Dysregulation of oncogenic factors by GFI1B p32: investigation of a novel <I>GFI1B</I> germline mutation. Haematologica. 107(1). 260–267. 1 indexed citations
6.
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
7.
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
8.
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
9.
Ciccocioppo, Rachele, Peter Kružliak, Carla Badulli, et al.. (2015). Ex vivo immunosuppressive effects of mesenchymal stem cells on Crohn’s disease mucosal T cells are largely dependent on indoleamine 2,3-dioxygenase activity and cell-cell contact. Stem Cell Research & Therapy. 6(1). 137–137. 43 indexed citations
10.
Pecci, Alessandro, Ginevra Biino, Tiziana Fierro, et al.. (2012). Alteration of Liver Enzymes Is a Feature of the Myh9-Related Disease Syndrome. PLoS ONE. 7(4). e35986–e35986. 46 indexed citations
11.
Pecci, Alessandro, Paolo Gresele, Catherine Klersy, et al.. (2010). Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. Blood. 116(26). 5832–5837. 100 indexed citations
12.
Rocco, Daniela De, Emanuele Panza, Valeria Bozzi, et al.. (2010). Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thrombosis and Haemostasis. 103(4). 826–832. 66 indexed citations
13.
Savoia, Anna, Alessandro Pastore, Daniela De Rocco, et al.. (2010). Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations. Haematologica. 96(3). 417–423. 70 indexed citations
14.
Noris, Patrizia, Catherine Klersy, Marco Zecca, et al.. (2009). Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia. Journal of Thrombosis and Haemostasis. 7(12). 2131–2136. 73 indexed citations
15.
Malara, Alessandro, et al.. (2009). Megakaryocytes of patients with MYH9-related thrombocytopenia present an altered proplatelet formation. Thrombosis and Haemostasis. 102(7). 90–96. 64 indexed citations
16.
Rocco, Daniela De, Núria Pujol‐Moix, Alessandro Pecci, et al.. (2009). Identification of the first duplication in MYH9-related disease: A hot spot for unequal crossing-over within exon 24 of the MYH9 gene. European Journal of Medical Genetics. 52(4). 191–194. 14 indexed citations
17.
Rocco, Daniela De, Paula G. Heller, Giorgia Girotto, et al.. (2009). MYH9related disease: A novel missense Ala95Asp mutation of theMYH9gene. Platelets. 20(8). 598–602. 7 indexed citations
18.
Panza, Emanuele, Monica Marini, Alessandro Pecci, et al.. (2008). Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines. PubMed. 1(1). 5–5. 5 indexed citations
19.
Balduini, Alessandra, Alessandro Malara, Alessandro Pecci, et al.. (2008). Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano. Journal of Thrombosis and Haemostasis. 7(3). 478–484. 52 indexed citations
20.
Campo, Ilaria, Patrizia Morbini, Michele Zorzetto, et al.. (2006). Expression of Receptor for Advanced Glycation End Products in Sarcoid Granulomas. American Journal of Respiratory and Critical Care Medicine. 175(5). 498–506. 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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