Silvia Spena

840 citations

25 papers · 527 indexed · h-index 13

Co-authors: Maria Luisa Tenchini Rosanna Asselta Stefano Duga Flora Peyvandi Massimo Malcovati Cristina Gervasini Donatella Milani Pier Mannuccio Mannucci
Topics: Blood properties and coagulation (11 papers)Erythrocyte Function and Pathophysiology (7 papers)Platelet Disorders and Treatments (5 papers)
Cited by: Developmental Biology Hematology Pulmonary and Respiratory Medicine
Journals: Blood PLoS ONE International Journal of Molecular Sciences
Partner nations: Italy United Kingdom Spain

In The Last Decade

Silvia Spena

24 papers receiving 509 citations

Peers

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

#	Work	Indexed citations
1	Gender equity in hemophilia: need for healthcare, familial, and societal advocacy 2024 ·Frontiers in Medicine ·Roberta Gualtierotti,Isabella Garagiola,(unknown),Silvia Spena,(unknown),Flora Peyvandi	2
2	Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor 2023 ·International Journal of Molecular Sciences ·Silvia Spena,(unknown),Francesca Gianniello,Emanuela Pappalardo,(unknown),Isabella Garagiola,Ida Martinelli,Flora Peyvandi	0
3	The Histopathological Landscape of Synovitis in Hemophilic Arthropathy 2023 ·Blood ·Roberta Gualtierotti,Chiara Suffritti,(unknown),(unknown),Silvia Spena,(unknown),(unknown),(unknown),(unknown),(unknown),Alessandro Ciavarella,Marco Maggioni,Umberto Gianelli,Simona Maria Siboni,(unknown),Luigi Piero Solimeno,Flora Peyvandi	1
4	Worldwide SARS-CoV-2 haplotype distribution in early pandemic 2022 ·PLoS ONE ·(unknown),Marilena V. Iorio,Silvia Spena,Elda Tagliabue,Flora Peyvandi	2
5	Development of a Specific Monoclonal Antibody to Detect Male Cells Expressing the RPS4Y1 Protein 2021 ·International Journal of Molecular Sciences ·Silvia Spena,Chiara Cordiglieri,Isabella Garagiola,Flora Peyvandi	3
6	Genetic Polymorphisms of Functional Candidate Genes and Recurrent Acute Otitis Media With or Without Tympanic Membrane Perforation 2015 ·Medicine ·Susanna Esposito,Paola Marchisio,Annalisa Orenti,Silvia Spena,Sonia Bianchini,Erica Nazzari,(unknown),Alberto Zampiero,Elia Biganzoli,Nicola Principi	11
7	Genetic polymorphisms and the development of invasive bacterial infections in children 2015 ·International Journal of Immunopathology and Pharmacology ·Susanna Esposito,Samantha Bosis,Annalisa Orenti,Silvia Spena,(unknown),Sonia Bianchini,Alberto Zampiero,Nicola Principi	2
8	Insights into genotype–phenotype correlations from CREBBP point mutation screening in a cohort of 46 Rubinstein–Taybi syndrome patients 2014 ·Clinical Genetics ·Silvia Spena,Donatella Milani,(unknown),Gloria Negri,(unknown),Nursel Elçioğlu,(unknown),Alba Pilotta,Luigina Spaccini,Anna Ficcadenti,Cinzia Magnani,Gioacchino Scarano,Angelo Selicorni,Lidia Larizza,Cristina Gervasini	43
9	Clinical and molecular characterization of Rubinstein‐Taybi syndrome patients carrying distinct novel mutations of the EP300 gene 2014 ·Clinical Genetics ·Gloria Negri,Donatella Milani,(unknown),Francesca Forzano,Matteo Della Monica,(unknown),(unknown),Lorella Caffi,Palma Finelli,Gioacchino Scarano,Cinzia Magnani,Angelo Selicorni,Silvia Spena,Lidia Larizza,Cristina Gervasini	60
10	Dual Role of G-runs and hnRNP F in the Regulation of a Mutation-Activated Pseudoexon in the Fibrinogen Gamma-Chain Transcript 2013 ·PLoS ONE ·Valeria Rimoldi,Giulia Soldà,Rosanna Asselta,Silvia Spena,Cristiana Stuani,Emanuele Buratti,Stefano Duga	5
11	Histone acetylation deficits in lymphoblastoid cell lines from patients with Rubinstein–Taybi syndrome 2011 ·Journal of Medical Genetics ·José P. López‐Atalaya,Cristina Gervasini,Federica Mottadelli,Silvia Spena,Maria Piccione,Gioacchino Scarano,Angelo Selicorni,Ángel Barco,Lidia Larizza	57
12	Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect 2008 ·Thrombosis and Haemostasis ·Ilaria Guella,Giulia Soldà,Silvia Spena,Rosanna Asselta,(unknown),Maria Luisa Tenchini,Giancarlo Castaman,Stefano Duga	17
13	Congenital hypofibrinogenemia: Characterization of two missense mutations affecting fibrinogen assembly and secretion 2008 ·Blood Cells Molecules and Diseases ·Manuela Platé,Rosanna Asselta,Silvia Spena,Marta Spreafico,Sharmila Fagoonee,Flora Peyvandi,Maria Luisa Tenchini,Stefano Duga	12
14	Molecular Genetics of Quantitative Fibrinogen Disorders 2007 ·Cardiovascular & Hematological Agents in Medicinal Chemistry ·Rosanna Asselta,Silvia Spena,Stefano Duga,Maria Luisa Tenchini	10
15	Pseudo‐exon activation caused by a deep‐intronic mutation in the fibrinogen γ‐chain gene as a novel mechanism for congenital afibrinogenaemia 2007 ·British Journal of Haematology ·Silvia Spena,Rosanna Asselta,Manuela Platé,Giancarlo Castaman,Stefano Duga,Maria Luisa Tenchini	19
16	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 2006 ·RNA ·Silvia Spena,Maria Luisa Tenchini,Emanuele Buratti	17
17	Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aα-chain gene 2004 ·European Journal of Human Genetics ·Silvia Spena,Stefano Duga,Rosanna Asselta,Flora Peyvandi,C Mahasandana,Massimo Malcovati,Maria Luisa Tenchini	43
18	Congenital afibrinogenemia: intracellular retention of fibrinogen due to a novel W437G mutation in the fibrinogen Bβ-chain gene 2003 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Silvia Spena,Rosanna Asselta,Stefano Duga,Massimo Malcovati,Flora Peyvandi,Pier Mannuccio Mannucci,Maria Luisa Tenchini	26
19	Missense or splicing mutation? The case of a fibrinogen Bβ-chain mutation causing severe hypofibrinogenemia 2003 ·Blood ·Rosanna Asselta,Stefano Duga,Silvia Spena,Flora Peyvandi,Giancarlo Castaman,Massimo Malcovati,Pier Mannuccio Mannucci,Maria Luisa Tenchini	23
20	Congenital afibrinogenemia: mutations leading to premature termination codons in fibrinogen Aα-chain gene are not associated with the decay of the mutant mRNAs 2001 ·Blood ·Rosanna Asselta,Stefano Duga,Silvia Spena,Elena Santagostino,Flora Peyvandi,(unknown),(unknown),Massimo Malcovati,Pier Mannuccio Mannucci,Maria Luisa Tenchini	63

About Silvia Spena

Silvia Spena is a scholar working on Developmental Biology, Hematology and Pulmonary and Respiratory Medicine, having authored 25 papers that have together received 527 indexed citations. Recurring topics across this work include Blood properties and coagulation (11 papers), Erythrocyte Function and Pathophysiology (7 papers) and Platelet Disorders and Treatments (5 papers). The work is most often cited by research in Developmental Biology (112 citations), Hematology (89 citations) and Pulmonary and Respiratory Medicine (178 citations). Silvia Spena has collaborated with scholars based in Italy, United Kingdom and Spain. Frequent 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. Their work appears in journals such as Blood, PLoS ONE and International Journal of Molecular Sciences.

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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