Silvia Spena

840 total citations
25 papers, 527 citations indexed

About

Silvia Spena is a scholar working on Pulmonary and Respiratory Medicine, Hematology and Physiology. According to data from OpenAlex, Silvia Spena has authored 25 papers receiving a total of 527 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Pulmonary and Respiratory Medicine, 9 papers in Hematology and 8 papers in Physiology. Recurrent topics in Silvia Spena's work include Blood properties and coagulation (11 papers), Erythrocyte Function and Pathophysiology (7 papers) and Platelet Disorders and Treatments (5 papers). Silvia Spena is often cited by papers focused on Blood properties and coagulation (11 papers), Erythrocyte Function and Pathophysiology (7 papers) and Platelet Disorders and Treatments (5 papers). Silvia Spena collaborates with scholars based in Italy, United Kingdom and Spain. Silvia Spena's co-authors include Maria Luisa Tenchini, Rosanna Asselta, Stefano Duga, Flora Peyvandi, Massimo Malcovati, Cristina Gervasini, Donatella Milani, Pier Mannuccio Mannucci, Lidia Larizza and Angelo Selicorni and has published in prestigious journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

In The Last Decade

Silvia Spena

24 papers receiving 509 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Silvia Spena Italy	13	185	178	117	112	104	25	527
Anita Wischmeijer Italy	16	260 1.4×	96 0.5×	333 2.8×	27 0.2×	19 0.2×	29	622
Odile Boute France	13	162 0.9×	36 0.2×	222 1.9×	35 0.3×	8 0.1×	31	471
B. G. A. ter Haar Netherlands	15	212 1.1×	28 0.2×	160 1.4×	16 0.1×	22 0.2×	20	423
R M Winter United Kingdom	14	276 1.5×	60 0.3×	402 3.4×	24 0.2×	13 0.1×	32	683
Angeline Lai Singapore	10	152 0.8×	21 0.1×	133 1.1×	10 0.1×	11 0.1×	31	349
Mariateresa Di Stazio Italy	9	164 0.9×	49 0.3×	84 0.7×	4 0.0×	12 0.1×	21	451
Kutay Taysi United States	17	277 1.5×	22 0.1×	440 3.8×	49 0.4×	27 0.3×	48	710
Giorgio Filippi Italy	14	304 1.6×	61 0.3×	281 2.4×	25 0.2×	98 0.9×	27	581
Karen J. Harrison Canada	10	248 1.3×	77 0.4×	252 2.2×	4 0.0×	12 0.1×	17	461
Marjan M. Nezarati Canada	10	232 1.3×	27 0.2×	198 1.7×	7 0.1×	58 0.6×	17	447

Countries citing papers authored by Silvia Spena

Since Specialization

Citations

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

Fields of papers citing papers by Silvia Spena

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Spena

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

All Works

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20 of 20 papers shown

Gualtierotti, Roberta, et al.. (2024). Gender equity in hemophilia: need for healthcare, familial, and societal advocacy. Frontiers in Medicine. 11. 1345496–1345496. 2 indexed citations

Spena, Silvia, Francesca Gianniello, Emanuela Pappalardo, et al.. (2023). Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor. International Journal of Molecular Sciences. 24(18). 14167–14167.

Gualtierotti, Roberta, Chiara Suffritti, Silvia Spena, et al.. (2023). The Histopathological Landscape of Synovitis in Hemophilic Arthropathy. Blood. 142(Supplement 1). 5481–5481. 1 indexed citations

Iorio, Marilena V., et al.. (2022). Worldwide SARS-CoV-2 haplotype distribution in early pandemic. PLoS ONE. 17(2). e0263705–e0263705. 2 indexed citations

Spena, Silvia, Chiara Cordiglieri, Isabella Garagiola, & Flora Peyvandi. (2021). Development of a Specific Monoclonal Antibody to Detect Male Cells Expressing the RPS4Y1 Protein. International Journal of Molecular Sciences. 22(4). 2001–2001. 3 indexed citations

Esposito, Susanna, Paola Marchisio, Annalisa Orenti, et al.. (2015). Genetic Polymorphisms of Functional Candidate Genes and Recurrent Acute Otitis Media With or Without Tympanic Membrane Perforation. Medicine. 94(42). e1860–e1860. 11 indexed citations

Esposito, Susanna, Samantha Bosis, Annalisa Orenti, et al.. (2015). Genetic polymorphisms and the development of invasive bacterial infections in children. International Journal of Immunopathology and Pharmacology. 29(1). 99–104. 2 indexed citations

Spena, Silvia, Donatella Milani, Gloria Negri, et al.. (2014). Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients. Clinical Genetics. 88(5). 431–440. 43 indexed citations

Negri, Gloria, Donatella Milani, Francesca Forzano, et al.. (2014). Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene. Clinical Genetics. 87(2). 148–154. 60 indexed citations

10.

Rimoldi, Valeria, Giulia Soldà, Rosanna Asselta, et al.. (2013). Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript. PLoS ONE. 8(3). e59333–e59333. 5 indexed citations

11.

López‐Atalaya, José P., Cristina Gervasini, Federica Mottadelli, et al.. (2011). Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome. Journal of Medical Genetics. 49(1). 66–74. 57 indexed citations

12.

Guella, Ilaria, Giulia Soldà, Silvia Spena, et al.. (2008). Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect. Thrombosis and Haemostasis. 99(3). 523–530. 17 indexed citations

13.

Platé, Manuela, Rosanna Asselta, Silvia Spena, et al.. (2008). Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion. Blood Cells Molecules and Diseases. 41(3). 292–297. 12 indexed citations

14.

Asselta, Rosanna, Silvia Spena, Stefano Duga, & Maria Luisa Tenchini. (2007). Molecular Genetics of Quantitative Fibrinogen Disorders. Cardiovascular & Hematological Agents in Medicinal Chemistry. 5(2). 163–173. 10 indexed citations

15.

Spena, Silvia, Rosanna Asselta, Manuela Platé, et al.. (2007). Pseudo‐exon activation caused by a deep‐intronic mutation in the fibrinogen γ‐chain gene as a novel mechanism for congenital afibrinogenaemia. British Journal of Haematology. 139(1). 128–132. 19 indexed citations

16.

Spena, Silvia, Maria Luisa Tenchini, & Emanuele Buratti. (2006). Cryptic splice site usage in exon 7 of the human fibrinogen Bβ-chain gene is regulated by a naturally silent SF2/ASF binding site within this exon. RNA. 12(6). 948–958. 17 indexed citations

17.

Spena, Silvia, Stefano Duga, Rosanna Asselta, et al.. (2004). Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aα-chain gene. European Journal of Human Genetics. 12(11). 891–898. 43 indexed citations

18.

Spena, Silvia, Rosanna Asselta, Stefano Duga, et al.. (2003). Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bβ-chain gene. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1639(2). 87–94. 26 indexed citations

19.

Asselta, Rosanna, Stefano Duga, Silvia Spena, et al.. (2003). Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia. Blood. 103(8). 3051–3054. 23 indexed citations

20.

Asselta, Rosanna, Stefano Duga, Silvia Spena, et al.. (2001). Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs. Blood. 98(13). 3685–3692. 63 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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