Research/art/teacher profile of a person
Name and surname:
MUDr. Tomáš Šimurda, PhD., MPH
Document type:
Research/art/teacher profile of a person
The name of the university:
Comenius University Bratislava
The seat of the university:
Šafárikovo námestie 6, 818 06 Bratislava

I. - Basic information

I.1 - Surname
Simurda
I.2 - Name
Tomas
I.3 - Degrees
MD., PhD., MPH
I.4 - Year of birth
1989
I.5 - Name of the workplace
Department of Hematology and Transfusiology
I.6 - Address of the workplace
Kollarova 2, Martin, 03601
I.7 - Position
university teacher
I.8 - E-mail address
tomas.simurda@uniba.sk
I.9 - Hyperlink to the entry of a person in the Register of university staff
https://www.portalvs.sk/regzam/detail/24279
I.10 - Name of the study field in which a person works at the university
general medicine
I.11 - ORCID iD
0000-0002-7626-9650

II. - Higher education and further qualification growth

II.1 - First degree of higher education
II.2 - Second degree of higher education
II.a - Name of the university or institution
Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin
II.b - Year
2014
II.c - Study field and programme
general medicine
II.3 - Third degree of higher education
II.a - Name of the university or institution
Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin
II.b - Year
2018
II.c - Study field and programme
internal medicine
II.4 - Associate professor
II.5 - Professor
II.6 - Doctor of Science (DrSc.)

III. - Current and previous employment

III.a - Occupation-position III.b - Institution III.c - Duration
physician and PhD Student Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, University hospital Martin, 2014-2018
physician and university teacher Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin, University hospital Martin, 2018-2023

IV. - Development of pedagogical, professional, language, digital and other skills

V. - Overview of activities within the teaching career at the university

V.1 - Overview of the profile courses taught in the current academic year according to study programmes
V.1.a - Name of the profile course V.1.b - Study programme V.1.c - Degree V.1.d - Field of study
Hematology and Transfusiology General Medicine I.+II. General Medicine
Diploma thesis seminar 1 General Medicine I.+II. General Medicine
Diploma thesis seminar 2 General Medicine I.+II. General Medicine
Diploma thesis seminar 3 General Medicine I.+II. General Medicine
Propedeutics in internal medicine 2 General Medicine I.+II. General Medicine
Internal medicine 5 General Medicine I.+II. General Medicine
Propedeutics in internal medicine 2 Dentistry, Dental Medicine I.+II. Dentistry, Dental Medicine
Diploma thesis and defence of diploma thesis General Medicine I.+II. General Medicine
V.2 - Overview of the responsibility for the delivery, development and quality assurance of the study programme or its part at the university in the current academic year
V.3 - Overview of the responsibility for the development and quality of the field of habilitation procedure and inaugural procedure in the current academic year
V.4 - Overview of supervised final theses
V.4.1 - Number of currently supervised theses
V.4.b - Diploma (second degree)
3
V.4.c - Dissertation (third degree)
2
V.4.2 - Number of defended theses
V.4.b - Diploma (second degree)
5
V.5 - Overview of other courses taught in the current academic year according to study programmes

VI. - Overview of the research/artistic/other outputs

VI.1 - Overview of the research/artistic/other outputs and the corresponding citations
VI.1.1 - Number of the research/artistic/other outputs
VI.1.a - Overall
174
VI.1.b - Over the last six years
127
VI.1.2 - Number of the research/artistic/other outputs registered in the Web of Science or Scopus databases
VI.1.a - Overall
29
VI.1.b - Over the last six years
19
VI.1.3 - Number of citations corresponding to the research/artistic/other outputs
VI.1.a - Overall
403
VI.1.b - Over the last six years
390
VI.1.4 - Number of citations registered in the Web of Science or Scopus databases
VI.1.a - Overall
356
VI.1.b - Over the last six years
343
VI.1.5 - Number of invited lectures at the international, national level
VI.1.a - Overall
3
VI.1.b - Over the last six years
3
VI.2 - The most significant research/artistic/other outputs
1

V3 QualyAfib Study Group - Casini, Alessandro (ctb) (1.51%) - von Mackensen, Sylvia (ctb) (1.47%) - Santoro, Cristina (ctb) (1.47%) - Djambas Khayat, Claudia (ctb) (1.47%) - Belhani, Meriem (ctb) (1.47%) - Ross, Cecil (ctb) (1.47%) - Dorgalaleh,Akbar (ctb) (1.47%) - Naz, Arshi (ctb) (1.47%) - Unal, Ekrem (ctb) (1.47%) - Abdelwahab, Magy (ctb) (1.47%) - Dupuis Lozeron, Elise (ctb) (1.47%) - Trillot, Nathalie (ctb) (1.47%) - Susen, Sophie (ctb) (1.47%) - Peyvandi, Flora (ctb) (1.47%) - DeMoerloose, Philippe (ctb) (1.47%) - Šimurda, Tomáš (ctb) [UKOLJ308] (1.47%): Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia. Blood [elektronický dokument]. - Roč. 137, č. 22 (2021), s. 3127-3136 [print]. - ISSN (print) 0006-4971

IF (JCR) 2021=25,669; Citations (10)

2

V3 Hugon-Rodin, Justine (aut) (3.456%) - Carriere, Camille (aut) (3.448%) - Claeyssens, Ségolene (aut) (3.448%) - Trillot, Nathalie (aut) (3.448%) - Drillaud, Nicolas (aut) (3.448%) - Šimurda, Tomáš (aut) [UKOLJ308] (3.448%) - Casini, Alessandro(aut) [KAUT] (3.448%): Obstetrical complications in hereditary fibrinogen disorders [elektronický dokument] : the Fibrinogest study. In: Journal of Thrombosis and Haemostasis [elektronický dokument]. - Roč. 21, č. 8 (2023), s. 2126-2136 [print]. - ISSN (print) 1538-7933. IF (JCR) 2022=10,4; Citations (4)

3

ADC Šimurda, Tomáš[KAUT] [UKOLJ308] (51%) - Brunclíková, Monika [UKOLJ308] (15%) - Asselta, Rosanna (3%) - Caccia, Sonia (2%) - Žolková, Jana [UKOLJ] (5%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Škorňová, Ingrid [UKOLJ](3%) - Hudeček, Ján (2%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (4%) - Kubisz, Peter [UKOLJ308] (3%): 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 in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype. In: International Journal of Molecular Sciences - Roč. 21, č. 13 (2020), s. [1-19] [online]. - ISSN (online) 1422-0067. IF (JCR) 2020=5,924; Citations (42)

4

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Vilar, Rui (2%) - Žolková, Jana [UKOLJ] (10%) - Ceznerová, Eliška (10%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Neerman-Arbez, Marguerite (2%) - Casini, Alessandro (2%) - Brunclíková, Monika [UKOLJ308] (2%) - Škorňová, Ingrid [UKOLJ] (2%) - Dobrotová, Miroslava (2%) - Grendár, Marián [UKOLJ110] (3%) - Staško, Ján [UKOLJ308] (2%) - Kubisz, Peter [UKOLJ308] (2%): A novel nonsense mutation in fgb (C.1421g>a; p.trp474ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype. In: Biomedicines - Roč. 8, č. 12 (2020), s. [1-10], art. no. 605 [online]. - ISSN (online) 2227-9059. IF (JCR) 2020=6,081; Citations (24)

5

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Žolková, Jana [UKOLJ] (10%) - Kolková, Zuzana [UKOLJ110] (8%) - Loderer, Dušan [UKOLJ110] (8%) - Dobrotová, Miroslava (2%) - Škorňová, Ingrid [UKOLJ] (5%) - Brunclíková, Monika [UKOLJ308] (3%) - Grendár,Marián [UKOLJ110] (3%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (5%) - Kubisz, Peter [UKOLJ308] (3%): Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. In: International Journal of Hematology - Roč. 111, č. 6 (2020), s. 795-802 [print]. - ISSN (print) 0925-5710. IF (JCR) 2020=2.490;Citations (23)

VI.3 - The most significant research/artistic/other outputs over the last six years
1

V3 QualyAfib Study Group - Casini, Alessandro (ctb) (1.51%) - von Mackensen, Sylvia (ctb) (1.47%) - Santoro, Cristina (ctb) (1.47%) - Djambas Khayat, Claudia (ctb) (1.47%) - Belhani, Meriem (ctb) (1.47%) - Ross, Cecil (ctb) (1.47%) - Dorgalaleh,Akbar (ctb) (1.47%) - Naz, Arshi (ctb) (1.47%) - Unal, Ekrem (ctb) (1.47%) - Abdelwahab, Magy (ctb) (1.47%) - Dupuis Lozeron, Elise (ctb) (1.47%) - Trillot, Nathalie (ctb) (1.47%) - Susen, Sophie (ctb) (1.47%) - Peyvandi, Flora (ctb) (1.47%) - DeMoerloose, Philippe (ctb) (1.47%) - Šimurda, Tomáš (ctb) [UKOLJ308] (1.47%): Clinical phenotype, fibrinogen supplementation, and health-related quality of life in patients with afibrinogenemia. Blood [elektronický dokument]. - Roč. 137, č. 22 (2021), s. 3127-3136 [print]. - ISSN (print) 0006-4971

IF (JCR) 2021=25,669; Citations (10)

2

V3 Hugon-Rodin, Justine (aut) (3.456%) - Carriere, Camille (aut) (3.448%) - Claeyssens, Ségolene (aut) (3.448%) - Trillot, Nathalie (aut) (3.448%) - Drillaud, Nicolas (aut) (3.448%) - Šimurda, Tomáš (aut) [UKOLJ308] (3.448%) - Casini, Alessandro(aut) [KAUT] (3.448%): Obstetrical complications in hereditary fibrinogen disorders [elektronický dokument] : the Fibrinogest study. In: Journal of Thrombosis and Haemostasis [elektronický dokument]. - Roč. 21, č. 8 (2023), s. 2126-2136 [print]. - ISSN (print) 1538-7933. IF (JCR) 2022=10,4; Citations (4)

3

ADC Šimurda, Tomáš[KAUT] [UKOLJ308] (51%) - Brunclíková, Monika [UKOLJ308] (15%) - Asselta, Rosanna (3%) - Caccia, Sonia (2%) - Žolková, Jana [UKOLJ] (5%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Škorňová, Ingrid [UKOLJ](3%) - Hudeček, Ján (2%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (4%) - Kubisz, Peter [UKOLJ308] (3%): 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 in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype. In: International Journal of Molecular Sciences - Roč. 21, č. 13 (2020), s. [1-19] [online]. - ISSN (online) 1422-0067. IF (JCR) 2020=5,924; Citations (42)

4

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Vilar, Rui (2%) - Žolková, Jana [UKOLJ] (10%) - Ceznerová, Eliška (10%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Neerman-Arbez, Marguerite (2%) - Casini, Alessandro (2%) - Brunclíková, Monika [UKOLJ308] (2%) - Škorňová, Ingrid [UKOLJ] (2%) - Dobrotová, Miroslava (2%) - Grendár, Marián [UKOLJ110] (3%) - Staško, Ján [UKOLJ308] (2%) - Kubisz, Peter [UKOLJ308] (2%): A novel nonsense mutation in fgb (C.1421g>a; p.trp474ter) in the beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype. In: Biomedicines - Roč. 8, č. 12 (2020), s. [1-10], art. no. 605 [online]. - ISSN (online) 2227-9059. IF (JCR) 2020=6,081; Citations (24)

5

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Žolková, Jana [UKOLJ] (10%) - Kolková, Zuzana [UKOLJ110] (8%) - Loderer, Dušan [UKOLJ110] (8%) - Dobrotová, Miroslava (2%) - Škorňová, Ingrid [UKOLJ] (5%) - Brunclíková, Monika [UKOLJ308] (3%) - Grendár,Marián [UKOLJ110] (3%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (5%) - Kubisz, Peter [UKOLJ308] (3%): Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia. In: International Journal of Hematology - Roč. 111, č. 6 (2020), s. 795-802 [print]. - ISSN (print) 0925-5710. IF (JCR) 2020=2.490;Citations (23)

VI.4 - The most significant citations corresponding to the research/artistic/other outputs
1

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Vilar, Rui (2%) - Žolková, Jana [UKOLJ] (10%) - Ceznerová, Eliška (10%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Neerman-Arbez, Marguerite (2%) - Casini, Alessandro (2%) - Brunclíková, Monika [UKOLJ308] (2%) - Škorňová, Ingrid [UKOLJ] (2%) - Dobrotová, Miroslava (2%) - Grendár, Marián [UKOLJ110] (3%) - Staško, Ján [UKOLJ308] (2%) - Kubisz, Peter [UKOLJ308] (2%): A novel nonsense mutation in fgb (C.1421g>a; p.trp474ter) inthe beta chain of fibrinogen causing hypofibrinogenemia with bleeding phenotype

In: Biomedicines [elektronický dokument]. - Roč. 8, č. 12 (2020), s. [1-10], art. no. 605 [online]. - ISSN (online) 2227-9059; IF (JCR) 2020=6,081; Citations (24)

[o1] 2021 Jansen, E. E. - Hartmann, M.: Biomedicines, roč. 9, č. 8, 2021, čl. č. 1064 - SCI ; SCOPUS;  IF (JCR) 2020=6,081;

2

ADC Šimurda, Tomáš [UKOLJ308] (51%) - Stančiaková, Lucia [KAUT] [UKOLJ308] (35%) - Staško, Ján [UKOLJ308] (5%) - Dobrotová, Miroslava (4%) - Kubisz, Peter [UKOLJ] (5%): Yes or no for secondary prophylaxis in afibrinogenemia?

In: Blood Coagulation and Fibrinolysis. - Roč. 26, č. 8 (2015), s. 978-980. - ISSN 0957-5235. IF (JCR) 2015=1,242; Ohlasy (16)

[n1] Juang, L. J. - Hur, W. S. - Silva, L. M. - Strilchuk, A. W. - Francisco, B. - Leung, J. - Robertson, M. K. - Groeneveld, D. J. - La Prairie, B. - Chun, E. M. - Cap, A. P. - Luyendyk, J. P. - Palumbo, J. S. - Cullis, P. R. -Bugge, T. H. - Flick, M. J. - Kastrup, C. J.: Blood, roč. 139, č. 9, 2022, s. 1302-1311 -- SCI ; SCOPUS; IF (JCR) 2020-2021=22,113

3

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (71%) - Kubisz, Peter [UKOLJ] (10%) - Dobrotová, Miroslava (7%) - Nečas, Libor [UKOLJ] (5%) - Staško, Ján [UKOLJ308] (7%): Perioperative Coagulation Management in a Patient with Congenital Afibrinogenemia during Revision Total Hip Arthroplasty.

In: Seminars in Thrombosis and Hemostasis. - Roč. 42, č. 6 (2016), s. 689-691. - ISSN 0094-6176. IF (JCR) 2016=3,629; Citations (17)

[o1] 2021 Casini, A. - Neerman-Arbez, M. - de Moerloose, P.: Blood Reviews, roč. 48, 2021, čl. č. 100793 - SCI ; SCOPUS; IF (JCR) 2021-2022=8,250.

4

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Žolková, Jana [UKOLJ] (10%) - Kolková, Zuzana [UKOLJ110] (8%) - Loderer, Dušan [UKOLJ110] (8%) - Dobrotová, Miroslava (2%) - Škorňová, Ingrid [UKOLJ] (5%) - Brunclíková, Monika [UKOLJ308] (3%) - Grendár,Marián [UKOLJ110] (3%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (5%) - Kubisz, Peter [UKOLJ308] (3%): Comparison of clinical phenotype with genetic and laboratory results in 31 patients with congenital dysfibrinogenemia in northern Slovakia.

In: International Journal of Hematology - Roč. 111, č. 6 (2020), s. 795-802 [print]. - ISSN (print) 0925-5710. IF (JCR) 2020=2.490; Citations (23)

[o1] 2021 Casini, A. - de Moerloose, P.: Blood, roč. 138, č. 21, 2021, s. 2021-2030 – SCI; IF (JCR) 2020-2021=22,113

5

ADC Šimurda, Tomáš [KAUT] [UKOLJ308] (51%) - Brunclíková, Monika [UKOLJ308] (15%) - Asselta, Rosanna (3%) - Caccia, Sonia (2%) - Žolková, Jana [UKOLJ] (5%) - Kolková, Zuzana [UKOLJ110] (5%) - Loderer, Dušan [UKOLJ110] (5%) - Škorňová, Ingrid [UKOLJ](3%) - Hudeček, Ján (2%) - Lasabová, Zora [UKOLJ121] (2%) - Staško, Ján [UKOLJ308] (4%) - Kubisz, Peter [UKOLJ308] (3%): 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 in Congenital Quantitative Fibrinogen Disorders Associated with a Thrombotic Phenotype.

In: International Journal of Molecular Sciences - Roč. 21, č. 13 (2020), s. [1-19] [online]. - ISSN (online) 1422-0067. IF (JCR) 2020=5,924; Citations (42)

[o1] 2021 Shen, Y. - Chen, L. - Guan, X. - Han, X. - Bo, X. - Li, S. - Sun, L. - Chen, Y. - Yue, W. - Xu, H.: ACS Nano, roč. 15, č. 12, 2021, s. 20414-20429 - SCI ; SCOPUS;       IF (JCR) 2020-2021=15,882

VI.5 - Participation in conducting (leading) the most important research projects or art projects over the last six years
1

VEGA 1/0436/21 (01.01.2021-31.12.2024):

„Genetic background of migraine conditions in patients with sticky platelet syndrome.“

principal investigator Tomas Simurda, MD, PhD.

link: e-VEGA (minedu.sk)

2

VEGA 1/0168/16 (01.01.2016-31.12.2019): 

“The use of monitoring of changes in haemostasis and detection of microRNA in the prediction of pregnancy complications in women with high-risk pregnancies“

principal investigator prof. Jan Stasko, MD, PhD.

link: e-VEGA (minedu.sk) (password is necessary)

3

VEGA 1/0187/17 (01.01.2017-31.12.2020):

“Genetic background and monitoring of changes in hemostasis in the management of von Willebrand disease“

principal investigator assoc. prof. Juraj Sokol, MD, PhD.

link: e-VEGA (minedu.sk) (password is necessary)




4

APVV-16-0020 (01.07.2017-30.09.2021):

“ Specific laboratory monitoring of platelet reactivity in the patients with acute myocardial infarction treated with new P2Y12-receptor antagonists“;

principal investigator prof. Jan Stasko, MD, PhD.

link: https://portal.apvv.sk/index.aspx?Module=Application&Page=Project&MenuID=287&ProjectID=21211&Area=preview

VII. - Overview of organizational experience related to higher education and research/artistic/other activities

VII.a - Activity, position VII.b - Name of the institution, board VII.c - Duration
Member of the Academic Senate JFM CU in Martin Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin 2016-2018; 2019-2023
Member of the Academic Senate CU in Bratislava Comenius University in Bratislava 2015-2018
Member of the Student Council for Higher Education Student Council for Higher Education 2017-2018

VIII. - Overview of international mobilities and visits oriented on education and research/artistic/other activities in the given field of study

IX. - Other relevant facts

Date of last update
2025-02-11