Donata Belvini

460 total citations
17 papers, 264 citations indexed

About

Donata Belvini is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Donata Belvini has authored 17 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Hematology, 10 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Donata Belvini's work include Hemophilia Treatment and Research (16 papers), Platelet Disorders and Treatments (8 papers) and Cancer-related gene regulation (7 papers). Donata Belvini is often cited by papers focused on Hemophilia Treatment and Research (16 papers), Platelet Disorders and Treatments (8 papers) and Cancer-related gene regulation (7 papers). Donata Belvini collaborates with scholars based in Italy and Canada. Donata Belvini's co-authors include Giuseppe Tagariello, Paolo Radossi, Giuseppe Castaldo, Roberto Sartori, Ezio Zanon, Anne Goodeve, Sofia H. Giacomelli, Giancarlo Castaman, Maura Acquila and Antonio Girolami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Hematology & Oncology and Human Mutation.

In The Last Decade

Donata Belvini

16 papers receiving 255 citations

Peers

Donata Belvini

HEMAT

GENET

PPCH

Anne Rafowicz France

Kristen Meldi United States

Claudia Haferlach Germany

Marie Jarošová Czechia

Sonja Rauhut Germany

Elizabeth Chalmers United Kingdom

Alice S. van Velzen Netherlands

Genki Yamato Japan

Y. Lucy Liu United States

Glaivy Batsuli United States

Anne Rafowicz France

Donata Belvini

217 ×0.9

HEMAT

52 ×0.4

38 ×0.6

GENET

5 ×0.4

GENET

6 ×1.2

PPCH

Citations per year, relative to Donata Belvini Donata Belvini (= 1×) peers Anne Rafowicz

Countries citing papers authored by Donata Belvini

Since Specialization

Citations

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

Fields of papers citing papers by Donata Belvini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Donata Belvini

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

All Works

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17 of 17 papers shown

Morfini, Massimo, et al.. (2026). Pharmacokinetics of extended half-life albumin-fused factor IX and heterogeneous <i>F9</i> variants in hemophilia B: a retrospective cohort study. SHILAP Revista de lepidopterología. 5(1).

Testa, Maria Francesca, Francesco Bernardi, Donata Belvini, et al.. (2022). Translational readthrough at <i>F8</i> nonsense variants in the factor VIII B domain contributes to residual expression and lowers inhibitor association. Haematologica. 108(2). 472–482. 4 indexed citations

Belvini, Donata, et al.. (2019). High resolution melting for F9 gene mutation analysis in patients with haemophilia B.. PubMed. 17(1). 72–82. 2 indexed citations

Belvini, Donata, et al.. (2017). Multiplex ligation‐dependent probe amplification as first mutation screening for large deletions and duplications in haemophilia. Haemophilia. 23(2). e124–e132. 4 indexed citations

Belvini, Donata, Maura Acquila, Maria Patrizia Bicocchi, et al.. (2013). Prenatal diagnosis of haemophilia B: the Italian experience. Haemophilia. 19(6). 898–903. 4 indexed citations

Tagariello, Giuseppe, Alfonso Iorio, Davide Matino, et al.. (2013). High rate of spontaneous inhibitor clearance during the long term observation study of a single cohort of 524 haemophilia A patients not undergoing immunotolerance. Journal of Hematology & Oncology. 6(1). 63–63. 13 indexed citations

Pinotti, Mirko, Alessandro Canella, Giuseppe Tagariello, et al.. (2012). Ribosome readthrough accounts for secreted full-length factor IX in hemophilia B patients with nonsense mutations. Human Mutation. 33(9). 1373–1376. 16 indexed citations

Tagariello, Giuseppe, Roberto Sartori, Donata Belvini, et al.. (2009). The JAK2(V617F) tyrosine kinase mutation in blood donors with upper-limit haematocrit levels.. PubMed. 7(2). 111–6. 13 indexed citations

Santacroce, Rosa, Maura Acquila, Donata Belvini, et al.. (2008). Identification of 217 unreported mutations in the F8 gene in a group of 1,410 unselected Italian patients with hemophilia A. Journal of Human Genetics. 53(3). 275–284. 34 indexed citations

10.

Tagariello, Giuseppe, et al.. (2007). In vitro reactivity of factor VIII inhibitors with von Willebrand factor in different commercial factor VIII concentrates. American Journal of Hematology. 82(6). 460–462. 17 indexed citations

11.

Belvini, Donata, Paolo Radossi, Roberto Sartori, et al.. (2007). F8 gene mutation profile and ITT response in a cohort of Italian haemophilia A patients with inhibitors. Haemophilia. 13(4). 361–372. 17 indexed citations

12.

Tagariello, Giuseppe, et al.. (2007). The Italian haemophilia B mutation database: a tool for genetic counselling, carrier detection and prenatal diagnosis.. PubMed. 5(3). 158–63. 7 indexed citations

13.

Belvini, Donata, et al.. (2005). Molecular genotyping of the Italian cohort of patients with hemophilia B.. PubMed. 90(5). 635–42. 70 indexed citations

14.

Tagariello, Giuseppe, M. Gerotto, Patrizia Pontisso, et al.. (2004). Hepatitis C virus quasispecies in the natural course of HCV‐related disease in patients with haemophilia. Haemophilia. 10(1). 81–86. 5 indexed citations

15.

Belvini, Donata, et al.. (2002). Large FVIII gene deletion confers very high risk of inhibitor development in three related severe haemophiliacs. Haemophilia. 8(1). 17–21. 6 indexed citations

16.

Vianello, Fabrizio, Donata Belvini, Federico Dal Bello, et al.. (2001). Mild bleeding diathesis in a boy with combined severe haemophilia B (C¹⁰⁴⁰⁰→T) and heterozygous factor V Leiden. Haemophilia. 7(5). 511–514. 24 indexed citations

17.

Tagariello, Giuseppe, et al.. (2000). Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosis.. PubMed. 85(5). 525–9. 28 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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