Maura Acquila

602 total citations
30 papers, 371 citations indexed

About

Maura Acquila is a scholar working on Hematology, Molecular Biology and Genetics. According to data from OpenAlex, Maura Acquila has authored 30 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Hematology, 15 papers in Molecular Biology and 9 papers in Genetics. Recurrent topics in Maura Acquila's work include Hemophilia Treatment and Research (15 papers), Cancer-related gene regulation (11 papers) and Blood Coagulation and Thrombosis Mechanisms (8 papers). Maura Acquila is often cited by papers focused on Hemophilia Treatment and Research (15 papers), Cancer-related gene regulation (11 papers) and Blood Coagulation and Thrombosis Mechanisms (8 papers). Maura Acquila collaborates with scholars based in Italy, United States and Japan. Maura Acquila's co-authors include Cristina Morerio, Claudio Panarello, Maria Patrizia Bicocchi, Cristina Rosanda, Elisa Tassano, Angelo Claudio Molinari, Carlo Dufour, Mirella Pasino, PG Mori and Tiziana Lanza and has published in prestigious journals such as Nucleic Acids Research, Blood and Cancer Research.

In The Last Decade

Maura Acquila

30 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maura Acquila Italy 12 214 182 74 43 42 30 371
S. K. China 11 176 0.8× 85 0.5× 61 0.8× 28 0.7× 28 0.7× 23 337
S Furusawa Japan 11 226 1.1× 129 0.7× 90 1.2× 35 0.8× 69 1.6× 35 396
Árpád Bátai Hungary 13 253 1.2× 138 0.8× 152 2.1× 47 1.1× 16 0.4× 32 386
Santina Acuto Italy 12 115 0.5× 215 1.2× 194 2.6× 18 0.4× 103 2.5× 34 387
Daiki Karigane Japan 10 140 0.7× 128 0.7× 54 0.7× 26 0.6× 24 0.6× 31 337
S. Rifkin United States 4 377 1.8× 208 1.1× 112 1.5× 12 0.3× 51 1.2× 5 493
Aage Drivsholm Denmark 12 257 1.2× 111 0.6× 101 1.4× 14 0.3× 37 0.9× 23 357
T Nagasawa Japan 7 113 0.5× 77 0.4× 33 0.4× 11 0.3× 27 0.6× 11 231
D.C. Setubal Brazil 9 302 1.4× 100 0.5× 95 1.3× 14 0.3× 23 0.5× 21 390
Kateřina Mužíková Czechia 9 209 1.0× 105 0.6× 81 1.1× 11 0.3× 47 1.1× 16 380

Countries citing papers authored by Maura Acquila

Since Specialization
Citations

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

Fields of papers citing papers by Maura Acquila

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maura Acquila

This figure shows the co-authorship network connecting the top 25 collaborators of Maura Acquila. A scholar is included among the top collaborators of Maura Acquila 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 Maura Acquila. Maura Acquila 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.
Mariani, Marcello, et al.. (2021). Antibodies against Receptor Binding Domain of SARS-CoV-2 spike protein induced by BNT162b2 vaccine: results from a pragmatic, real-life study. Journal of Infection and Public Health. 14(10). 1560–1562. 10 indexed citations
2.
Luca, Maia De, Francesca Ippolita Calò Carducci, Valeria Pansini, et al.. (2013). Unusual presentation of haemophilia in two paediatric patients. Blood Coagulation & Fibrinolysis. 24(6). 645–648. 3 indexed citations
3.
Cangemi, Giuliana, Angela Pistorio, Maurizio Miano, et al.. (2013). Diagnostic potential of hepcidin testing in pediatrics. European Journal Of Haematology. 90(4). 323–330. 30 indexed citations
4.
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
5.
Tassano, Elisa, et al.. (2010). MicroRNA‐125b‐1 and BLID upregulation resulting from a novel IGH translocation in childhood B‐Cell precursor acute lymphoblastic leukemia. Genes Chromosomes and Cancer. 49(8). 682–687. 26 indexed citations
6.
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
7.
Bicocchi, Maria Patrizia, Mirella Pasino, Camillo Rosano, et al.. (2006). Insight into molecular changes of the FIX protein in a series of Italian patients with haemophilia B. Haemophilia. 12(3). 263–270. 11 indexed citations
8.
Bicocchi, Maria Patrizia, Mirella Pasino, Tiziana Lanza, et al.. (2005). Small FVIII gene rearrangements in 18 hemophilia A patients: Five novel mutations. American Journal of Hematology. 78(2). 117–122. 3 indexed citations
9.
Bicocchi, Maria Patrizia, Barbara R. Migeon, Mirella Pasino, et al.. (2005). Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A. European Journal of Human Genetics. 13(5). 635–640. 34 indexed citations
10.
Morerio, Cristina, Maura Acquila, Cristina Rosanda, et al.. (2004). t(9;11)(p22;p15) with NUP98-LEDGF fusion gene in pediatric acute myeloid leukemia. Leukemia Research. 29(4). 467–470. 23 indexed citations
11.
Bicocchi, Maria Patrizia, Mirella Pasino, Tiziana Lanza, et al.. (2003). Analysis of 18 novel mutations in the factor VIII gene. British Journal of Haematology. 122(5). 810–817. 13 indexed citations
12.
Bicocchi, Maria Patrizia, et al.. (2003). Mutation analysis impact on the genetic counseling of sporadic hemophilia B families. American Journal of Medical Genetics Part A. 118A(4). 328–331. 5 indexed citations
13.
Acquila, Maura, Mirella Pasino, Cristina Santoro, et al.. (2003). Germ‐line origin of intron 1 inversion in two haemophilia A families. Haemophilia. 9(6). 717–720. 1 indexed citations
14.
Acquila, Maura, et al.. (2001). A new strategy for prenatal diagnosis in a sporadic haemophilia B family. Haemophilia. 7(4). 416–418. 6 indexed citations
15.
Gattorno, Marco, Angelo Claudio Molinari, Antonella Buoncompagni, et al.. (2000). Recurrent antiphospholipid-related deep vein thrombosis as presenting manifestation of systemic lupus erythematosus. European Journal of Pediatrics. 159(3). 211–214. 5 indexed citations
16.
Acquila, Maura, et al.. (1993). Carrier detection and prenatal diagnosis of hemophilia B with more advanced techniques. Annals of Hematology. 67(6). 289–293. 2 indexed citations
17.
Rossi, Giovanni, Elena Battistini, S. Oddera, et al.. (1992). Long‐term prednisone and azathioprine treatment of a patient with idiopathic pulmonary hemosiderosis. Pediatric Pulmonology. 13(3). 176–180. 29 indexed citations
18.
Panarello, Claudio, et al.. (1992). Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52. Cytogenetic and Genome Research. 59(4). 241–242. 20 indexed citations
19.
20.
Acquila, Maura, et al.. (1990). DGGE detection of Hhal polymorphism in the F9 gene. Nucleic Acids Research. 18(16). 4960–4960. 2 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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