Tomáš Šimurda

650 total citations
25 papers, 361 citations indexed

About

Tomáš Šimurda is a scholar working on Hematology, Pulmonary and Respiratory Medicine and Surgery. According to data from OpenAlex, Tomáš Šimurda has authored 25 papers receiving a total of 361 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Hematology, 14 papers in Pulmonary and Respiratory Medicine and 5 papers in Surgery. Recurrent topics in Tomáš Šimurda's work include Blood properties and coagulation (14 papers), Platelet Disorders and Treatments (14 papers) and Blood groups and transfusion (6 papers). Tomáš Šimurda is often cited by papers focused on Blood properties and coagulation (14 papers), Platelet Disorders and Treatments (14 papers) and Blood groups and transfusion (6 papers). Tomáš Šimurda collaborates with scholars based in Slovakia, Czechia and Switzerland. Tomáš Šimurda's co-authors include Ján Staško, Peter Kubisz, Ingrid Škorňová, Dušan Loderer, Jana Žolková, Miroslava Dobrotová, Juraj Sokol, Zora Lasabová, Zuzana Kolková and Jan Hudeček and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and Journal of Clinical Medicine.

In The Last Decade

Tomáš Šimurda

22 papers receiving 358 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomáš Šimurda Slovakia 13 172 155 56 55 53 25 361
Jana Žolková Slovakia 10 112 0.7× 123 0.8× 43 0.8× 51 0.9× 32 0.6× 26 268
Miroslava Dobrotová Slovakia 13 175 1.0× 126 0.8× 135 2.4× 37 0.7× 75 1.4× 25 420
Sonja Alesci Germany 12 279 1.6× 91 0.6× 45 0.8× 40 0.7× 48 0.9× 32 441
Jean‐Jacques Huart France 6 137 0.8× 80 0.5× 41 0.7× 78 1.4× 50 0.9× 7 389
Rehana Sultana Lovely United States 9 197 1.1× 346 2.2× 32 0.6× 31 0.6× 25 0.5× 17 463
Marcos Pino Spain 11 179 1.0× 49 0.3× 102 1.8× 51 0.9× 59 1.1× 21 388
Joke Konings Netherlands 11 117 0.7× 51 0.3× 54 1.0× 19 0.3× 26 0.5× 18 291
Asashi Tanaka Japan 10 91 0.5× 41 0.3× 24 0.4× 41 0.7× 32 0.6× 51 332
Anthony R. Hubbard United Kingdom 11 273 1.6× 39 0.3× 35 0.6× 33 0.6× 49 0.9× 27 412
Juergen Roemisch Germany 4 223 1.3× 51 0.3× 61 1.1× 64 1.2× 52 1.0× 5 410

Countries citing papers authored by Tomáš Šimurda

Since Specialization
Citations

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

Fields of papers citing papers by Tomáš Šimurda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomáš Šimurda

This figure shows the co-authorship network connecting the top 25 collaborators of Tomáš Šimurda. A scholar is included among the top collaborators of Tomáš Šimurda 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 Tomáš Šimurda. Tomáš Šimurda 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.
Šimurda, Tomáš, Rita Marchi, Alessandro Casini, et al.. (2024). Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia. Blood Coagulation & Fibrinolysis. 35(2). 56–61. 1 indexed citations
2.
3.
Šimurda, Tomáš, et al.. (2023). Perioperative Monitoring with Rotational Thromboelastometry in a Severe Hemophilia A Patient Undergoing Elective Ankle Surgery. Seminars in Thrombosis and Hemostasis. 50(2). 310–313. 2 indexed citations
4.
Škorňová, Ingrid, Tomáš Šimurda, Lucia Stančiaková, et al.. (2023). A Functional Assay for the Determination of Heparin-Induced Thrombocytopenia via Flow Cytometry. Diagnostics. 13(18). 3019–3019. 1 indexed citations
5.
Šimurda, Tomáš, Jana Žolková, Ingrid Škorňová, et al.. (2022). Heterogeneity of Genotype–Phenotype in Congenital Hypofibrinogenemia—A Review of Case Reports Associated with Bleeding and Thrombosis. Journal of Clinical Medicine. 11(4). 1083–1083. 25 indexed citations
6.
Slavík, Luděk, Radek Vodička, Martin Procházka, et al.. (2022). Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing. Diagnostics. 12(5). 1060–1060. 3 indexed citations
7.
Šimurda, Tomáš, Rosanna Asselta, Jana Žolková, et al.. (2021). Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management. Diagnostics. 11(11). 2140–2140. 39 indexed citations
8.
Škorňová, Ingrid, Tomáš Šimurda, Ján Staško, et al.. (2021). Multimer Analysis of Von Willebrand Factor in Von Willebrand Disease with a Hydrasys Semi-Automatic Analyzer—Single-Center Experience. Diagnostics. 11(11). 2153–2153. 8 indexed citations
9.
Šimurda, Tomáš, R. Vilar, Jana Žolková, et al.. (2020). A Novel Nonsense Mutation in FGB (c.1421G>A; p.Trp474Ter) in the Beta Chain of Fibrinogen Causing Hypofibrinogenemia with Bleeding Phenotype. Biomedicines. 8(12). 605–605. 28 indexed citations
10.
Šimurda, Tomáš, Jana Žolková, Zuzana Kolková, et al.. (2020). Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. International Journal of Hematology. 111(6). 795–802. 23 indexed citations
11.
Šimurda, Tomáš, Rosanna Asselta, Sonia Caccia, et al.. (2020). Genetic Variants in the FGB and FGG Genes Mapping in the Beta and Gamma Nodules of the Fibrinogen Molecule in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype. International Journal of Molecular Sciences. 21(13). 4616–4616. 46 indexed citations
12.
Žolková, Jana, Juraj Sokol, Tomáš Šimurda, et al.. (2019). The Importance and Complications of Sequencing of Von Willebrand Gene in Von Willebrand Disease. SHILAP Revista de lepidopterología. 19(1). 5–11.
13.
Sokol, Juraj, Mária Škereňová, Kamil Biringer, et al.. (2018). Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability. Clinical and Applied Thrombosis/Hemostasis. 24(9_suppl). 202S–208S. 10 indexed citations
14.
Sokol, Juraj, Mária Škereňová, Jela Ivanková, Tomáš Šimurda, & Ján Staško. (2018). Association of Genetic Variability in Selected Genes in Patients With Deep Vein Thrombosis and Platelet Hyperaggregability. Clinical and Applied Thrombosis/Hemostasis. 24(7). 1027–1032. 18 indexed citations
15.
Šimurda, Tomáš, Jana Žolková, Dušan Loderer, et al.. (2017). Identification of Two Novel Fibrinogen Bβ Chain Mutations in Two Slovak Families with Quantitative Fibrinogen Disorders. International Journal of Molecular Sciences. 19(1). 100–100. 22 indexed citations
16.
Dobrotová, Miroslava, Ingrid Škorňová, Juraj Sokol, et al.. (2017). Successful Use of a Highly Purified Plasma von Willebrand Factor Concentrate Containing Little FVIII for the Long-Term Prophylaxis of Severe (Type 3) von Willebrand's Disease. Seminars in Thrombosis and Hemostasis. 43(6). 639–641. 17 indexed citations
17.
Kubisz, Peter, et al.. (2016). Perioperative Coagulation Management in a Patient with Congenital Afibrinogenemia during Revision Total Hip Arthroplasty. Seminars in Thrombosis and Hemostasis. 42(6). 689–692. 19 indexed citations
18.
Škereňová, Mária, Tomáš Šimurda, Ingrid Škorňová, et al.. (2016). Progress in the Understanding of Sticky Platelet Syndrome. Seminars in Thrombosis and Hemostasis. 43(1). 8–13. 22 indexed citations
19.
Loderer, Dušan, Juraj Sokol, Ján Staško, et al.. (2016). Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia. Seminars in Thrombosis and Hemostasis. 42(4). 455–458. 23 indexed citations
20.
Šimurda, Tomáš, Ján Staško, Dušan Loderer, et al.. (2015). Novel Fibrinogen Bbeta Chain Mutation as an Underlying Mechanism of Afibrinogenemia?. Seminars in Thrombosis and Hemostasis. 41(8). 901–902. 3 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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