Silvia Vettore

1.0k total citations
39 papers, 719 citations indexed

About

Silvia Vettore is a scholar working on Hematology, Surgery and Genetics. According to data from OpenAlex, Silvia Vettore has authored 39 papers receiving a total of 719 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Hematology, 7 papers in Surgery and 7 papers in Genetics. Recurrent topics in Silvia Vettore's work include Platelet Disorders and Treatments (20 papers), Blood Coagulation and Thrombosis Mechanisms (20 papers) and Hemophilia Treatment and Research (15 papers). Silvia Vettore is often cited by papers focused on Platelet Disorders and Treatments (20 papers), Blood Coagulation and Thrombosis Mechanisms (20 papers) and Hemophilia Treatment and Research (15 papers). Silvia Vettore collaborates with scholars based in Italy, United States and Japan. Silvia Vettore's co-authors include Antonio Girolami, Raffaella Scandellari, Fabiana Tezza, Bruno Girolami, Margherita Scapin, Maria Teresa Sartori, Anna Maria Lombardi, Luisa Gorza, Elisabetta Ruzzon and Maurizio Vitadello and has published in prestigious journals such as Blood, Annals of the New York Academy of Sciences and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Silvia Vettore

39 papers receiving 703 citations

Peers

Countries citing papers authored by Silvia Vettore

Since Specialization

Citations

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

Fields of papers citing papers by Silvia Vettore

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Silvia Vettore

This figure shows the co-authorship network connecting the top 25 collaborators of Silvia Vettore. A scholar is included among the top collaborators of Silvia Vettore 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 Vettore. Silvia Vettore 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	Serum Thrombopoietin and cMpl Expression in Thrombocytopenia of Different Etiologies 2014 ·Hematology Reports ·Fabrizio Vianello, Silvia Vettore, Fabiana Tezza, Luca De Toni, Raffaella Scandellari, Luisa Sambado, (unknown), Fabrizio Fabris	7
2	Conformational Changes of Congenital FVII Variants with Defective Binding to Tissue Factor ARG304GLN (FVII Padua), ARG 304TRP (FVII Nagoya) and ARG79GLN (FVII Shinjo or Tondabayashi) 2013 ·International Journal of Biomedical Science ·Antonio Girolami, Silvia Vettore, Luisa Sambado, (unknown), Stefano Moro, Alessandro Bulfone, (unknown)	3
3	Occurrence of thrombosis in congenital thrombocytopenic disorders 2012 ·Blood Coagulation & Fibrinolysis ·Antonio Girolami, Luisa Sambado, (unknown), Silvia Vettore, Anna Maria Lombardi	13
4	Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard–Soulier syndrome 2012 ·Journal of Thrombosis and Thrombolysis ·Antonio Girolami, Silvia Vettore, Fabrizio Vianello, (unknown), Fabrizio Fabris	6
5	Heparin-induced thrombocytopenia: The role of platelets genetic polymorphisms 2012 ·Platelets ·Pamela Scarparo, (unknown), Elena Duner, (unknown), (unknown), Silvia Vettore, (unknown), (unknown), Fabrizio Fabris	19
6	Presence of anti‐ADAMTS13 antibodies in obesity 2012 ·European Journal of Clinical Investigation ·Anna Maria Lombardi, Roberto Fabris, A. Scarda, (unknown), Chiara Dal Prà, Pamela Scarparo, Silvia Vettore, Marnie Granzotto, (unknown), Mirto Foletto, Roberto Serra, (unknown), Mario Plebani, Fabrizio Fabris, Roberto Vettor	13
7	Platelets express and release osteocalcin and co‐localize in human calcified atherosclerotic plaques 2012 ·Journal of Thrombosis and Haemostasis ·Carlo Foresta, Giacomo Strapazzon, Luca De Toni, F. Fabris, Franco Grego, Gino Gerosa, Silvia Vettore, Andrea Garolla	27
8	Congenital FVII deficiency and thrombotic events after replacement therapy 2011 ·Journal of Thrombosis and Thrombolysis ·Antonio Girolami, Irene Bertozzi, (unknown), Rodolfo Muzzolon, Silvia Vettore	29
9	Similarities and Discrepancies in Homozygous Factor VII Defects due to Mutations in the Region of Residues Met298 to Cys310 (Exon 8) in the Catalytic Domain of Factor VII 2011 ·PubMed ·Antonio Girolami, (unknown), (unknown), Silvia Vettore	2
10	Ox Brain versus Rabbit Brain Thromboplastin Assays Are the Best Tool for a Preliminary Diagnosis of the Arg304Gln Factor VII Defect (FVII Padua) 2010 ·Acta Haematologica ·Antonio Girolami, (unknown), (unknown), Roberta Sartori, Silvia Vettore	10
11	Persistent validity of a classification of congenital factor X defects based on clotting, chromogenic and immunological assays even in the molecular biology era 2010 ·Haemophilia ·Antonio Girolami, Silvia Vettore, Pamela Scarparo, Anna Maria Lombardi	11
12	A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect 2010 ·European Journal of Medical Genetics ·Silvia Vettore, Daniela De Rocco, B. Gerber, Raffaella Scandellari, Anna Monica Bianco, Carlo L. Balduini, Alessandro Pecci, Fabrizio Fabris, Anna Savoia	8
13	The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency 2009 ·Journal of Thrombosis and Thrombolysis ·Antonio Girolami, (unknown), Silvia Vettore, Anna Maria Lombardi, Bruno Girolami	18
14	Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature 2009 ·Journal of Thrombosis and Thrombolysis ·Antonio Girolami, Fabiana Tezza, Raffaella Scandellari, Silvia Vettore, Bruno Girolami	38
15	Congenital Bleeding Disorders of the Vitamin K‐Dependent Clotting Factors 2008 ·Vitamins and hormones ·Antonio Girolami, Raffaella Scandellari, Margherita Scapin, Silvia Vettore	24
16	Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review 2006 ·Haemophilia ·Antonio Girolami, Elisabetta Ruzzon, Fabiana Tezza, Raffaella Scandellari, Silvia Vettore, Bruno Girolami	68
17	Congenital Combined Defects of Factor VII: A Critical Review 2006 ·Acta Haematologica ·Antonio Girolami, Elisabetta Ruzzon, Fabiana Tezza, (unknown), Silvia Vettore	12
18	Regional and Age-related Differences in mRNA Composition of Intracellular Ca2+-release Channels of Rat Cardiac Myocytes 1997 ·Journal of Molecular and Cellular Cardiology ·Luisa Gorza, Silvia Vettore, (unknown), Vincenzo Sorrentino, Maurizio Vitadello	28
19	Identification of an 18 basepair deletion in the PAI-1 gene promoter region in a family with thrombotic disease 1997 ·Fibrinolysis & proteolysis ·Gunnar Falk, Maria Sartori, G Patrassi, Silvia Vettore, A Girolami, B. Wiman	1
20	Molecular and cellular diversity of heart conduction system myocytes 1994 ·Trends in Cardiovascular Medicine ·Luisa Gorza, Silvia Vettore, Maurizio Vitadello	27

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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