Name and surname:
|
doc. MUDr. Juraj Sokol, PhD., MBA
|
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
|
III.a - Occupation-position | III.b - Institution | III.c - Duration |
---|---|---|
assistent | Comenius University in Bratislava, Jessenius Faculty of Medicine in Martin | 1.9.2014 - 31.1.2020 |
Associate Professor | omenius University in Bratislava, Jessenius Faculty of Medicine in Martin | 1.2.2020 - |
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 Transfusion Medicine | General Medicine | I.+II. | General Medicine |
Hematology and Transfusion Medicine | General Medicine | I.+II. | General Medicine |
Hemostasis - Vascular Medicine | General Medicine | I.+II. | General Medicine |
Hemostasis - Vascular Medicine | General Medicine | I.+II. | General Medicine |
Internal diseases 1 | Internal diseases | III. | General Medicine |
Internal diseases 1 | Internal diseases | III. | General Medicine |
V.5.a - Name of the course | V.5.b - Study programme | V.5.c - Degree | V.5.d - Field of study |
---|---|---|---|
Propaedeutics of internal diseases | General Medicine | I.+II. | General Medicine |
Propaedeutics of internal diseases | General Medicine | I.+II. | General Medicine |
Internal diseases 5 | General Medicine | I.+II. | General Medicine |
Internal diseases 5 | General Medicine | I.+II. | General Medicine |
Internal diseases - gerontology and nursing 2 | Nursing | I. | Nursing |
Sokol, Juraj (aut) [KAUT] [UKOLJ308] (20%) - Nehaj, František (aut) [UKOLJ] (20%) - Mokáň, Michal (aut) [UKOLJ220] (20%) - Lisá, Lenka (aut) [UKOLJ308] (20%) - Staško, Ján (aut) [UKOLJ308] (20%): COVID19 infection in a patient with paroxysmalnocturnal hemoglobinuria [elektronický dokument] : a case report
Lit.: 19 zázn.
In: Medicine [elektronický dokument]. - Roč.
100, č. 20 (2021), s. [1-4], art. no. 25456 [print]. - ISSN (print) 0025-7974
článok
180 Lekárske, farmaceutické a nelekárske
zdravotnícke vedy
URL:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8137037/
Registrované
v:
CCC Current Content Connect
MEDLINE
SCO SCOPUS
WOS CC Web of Science Core Collection
SCIE Science Citation Index Expanded
Indikátor
časopisu:
SJR (SCOPUS) 2021=0.470
SNIP (SCOPUS) 2021=1.009
CiteScore (SCOPUS) 2021=2.7
IF (JCR) 2021=1.817
AIS (JCR) 2021=0.482
Ohlasy: 5/4
Sokol, Juraj [KAUT] [UKOLJ308] (65%) - Škereňová, Mária [UKOLJ110] (20%) - Jedináková, Zuzana (5%) - Šimurda, Tomáš [UKOLJ308] (2%) - Škorňová, Ingrid [UKOLJ] (2%) - Staško, Ján [UKOLJ308] (2%) - Kubisz, Peter [UKOLJ] (4%): Progress in the Understanding of Sticky Platelet Syndrome
In: Seminars in Thrombosis and Hemostasis. - Volume. 43, No. 1 (2017), p. 8-13. - ISSN 0094-6176
scopus and wos
IF (JCR) 2017=3.345
Citations: 26/20
Sokol, Juraj [UKOLJ308] (80%) - Timp, J. F. (2%) - Le cessie, S. (1%) - Van Hylckama-Vlieg, A. (1%) - Rosendaal, F. R. (1%) - Kubisz, Peter [UKOLJ308] (3%) - Cannegieter, S. C. (2%) - Lijfering, W. M. [KAUT] (10%): Mild antithrombin deficiency and risk of recurrent venous thromboembolism: results from the MEGA follow-up study
Lit.: 25 zázn.
In: Journal of Thrombosis and Haemostasis. - Volume. 16, No. 4 (2018), p. 680-688. - ISSN (print) 1538-7933
scopus and wos
SJR (SCOPUS) 2018=2.026
SNIP (SCOPUS) 2018=1.526
CiteScore (SCOPUS) 2018=8.3
IF (JCR) 2018=4.662
Kvartil Q:
wos-jcr -- Q1 [Peripheral vascular disease] -- 2018
wos-jcr -- Q2 [Hematology] -- 2018
scimago-sjr -- Q1 [Hematology] -- 2018
scimago-sjr -- Q1 [Medicine (miscellaneous)] -- 2018
Citations: 26/21
Sokol, Juraj [KAUT] [UKOLJ308] (65%) - Škereňová, Mária [UKOLJ110A] (20%) - Ivanková, Jela (10%) - Šimurda, Tomáš [UKOLJ308] (3%) - Staško, Ján [UKOLJ308] (2%): Association of Genetic Variability in Selected Genes in Patients With Deep VeinThrombosis and Platelet Hyperaggregability [elektronický dokument]
In: Clinical and Applied Thrombosis/Hemostasis [elektronický dokument]. - Volume 24, No. 7 (2018), p. 1027-1032 [print]. - ISSN (print) 1076-0296
scopus and wos
SJR (SCOPUS) 2018=0.452
SNIP (SCOPUS) 2018=0.728
CiteScore (SCOPUS) 2018=2.5
IF (JCR) 2018=1.846
Kvartil Q:
wos-jcr -- Q4 [Hematology] -- 2018
wos-jcr -- Q4 [Peripheral vascular disease] -- 2018
scimago-sjr -- Q2 [Medicine (miscellaneous)] -- 2018
scimago-sjr -- Q3 [Hematology] -- 2018
Citations: 19/16
Sokol, Juraj [KAUT] [UKOLJ308] (60%) - Škereňová, Mária [UKOLJ110A] (25%) - Biringer, Kamil [UKOLJ150] (5%) - Šimurda, Tomáš [UKOLJ308] (5%) - Kubisz, Peter [UKOLJ308] (3%) - Staško, Ján [UKOLJ308] (2%): Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability [elektronický dokument]
In: Clinical and Applied Thrombosis/Hemostasis [elektronický dokument]. - Volume 24, No. 9 (2018), p. 202S-208S [print]. - ISSN (print) 1076-0296
wos and scopus
SJR (SCOPUS) 2018=0.452
SNIP (SCOPUS) 2018=0.728
CiteScore (SCOPUS) 2018=2.5
IF (JCR) 2018=1.846
Kvartil Q:
wos-jcr -- Q4 [Hematology] -- 2018
wos-jcr -- Q4 [Peripheral vascular disease] -- 2018
scimago-sjr -- Q2 [Medicine (miscellaneous)] -- 2018
scimago-sjr -- Q3 [Hematology] -- 2018
Citations: 13/11
Sokol, Juraj [KAUT] [UKOLJ308] (65%) - Škereňová, Mária [UKOLJ110] (20%) - Jedináková, Zuzana (5%) - Šimurda, Tomáš [UKOLJ308] (2%) - Škorňová, Ingrid [UKOLJ] (2%) - Staško, Ján [UKOLJ308] (2%) - Kubisz, Peter [UKOLJ] (4%): Progress in the Understanding of Sticky Platelet Syndrome
In: Seminars in Thrombosis and Hemostasis. - Volume. 43, No. 1 (2017), p. 8-13. - ISSN 0094-6176
scopus and wos
IF (JCR) 2017=3.345
Citations: 26/20
Sokol, Juraj [UKOLJ308] (80%) - Timp, J. F. (2%) - Le cessie, S. (1%) - Van Hylckama-Vlieg, A. (1%) - Rosendaal, F. R. (1%) - Kubisz, Peter [UKOLJ308] (3%) - Cannegieter, S. C. (2%) - Lijfering, W. M. [KAUT] (10%): Mild antithrombin deficiency and risk of recurrent venous thromboembolism: results from the MEGA follow-up study
Lit.: 25 zázn.
In: Journal of Thrombosis and Haemostasis. - Volume. 16, No. 4 (2018), p. 680-688. - ISSN (print) 1538-7933
scopus and wos
SJR (SCOPUS) 2018=2.026
SNIP (SCOPUS) 2018=1.526
CiteScore (SCOPUS) 2018=8.3
IF (JCR) 2018=4.662
Kvartil Q:
wos-jcr -- Q1 [Peripheral vascular disease] -- 2018
wos-jcr -- Q2 [Hematology] -- 2018
scimago-sjr -- Q1 [Hematology] -- 2018
scimago-sjr -- Q1 [Medicine (miscellaneous)] -- 2018
Citations: 26/21
Sokol, Juraj [KAUT] [UKOLJ308] (65%) - Škereňová, Mária [UKOLJ110A] (20%) - Ivanková, Jela (10%) - Šimurda, Tomáš [UKOLJ308] (3%) - Staško, Ján [UKOLJ308] (2%): Association of Genetic Variability in Selected Genes in Patients With Deep VeinThrombosis and Platelet Hyperaggregability [elektronický dokument]
In: Clinical and Applied Thrombosis/Hemostasis [elektronický dokument]. - Volume 24, No. 7 (2018), p. 1027-1032 [print]. - ISSN (print) 1076-0296
scopus and wos
SJR (SCOPUS) 2018=0.452
SNIP (SCOPUS) 2018=0.728
CiteScore (SCOPUS) 2018=2.5
IF (JCR) 2018=1.846
Kvartil Q:
wos-jcr -- Q4 [Hematology] -- 2018
wos-jcr -- Q4 [Peripheral vascular disease] -- 2018
scimago-sjr -- Q2 [Medicine (miscellaneous)] -- 2018
scimago-sjr -- Q3 [Hematology] -- 2018
Citations: 19/16
Sokol, Juraj [KAUT] [UKOLJ308] (60%) - Škereňová, Mária [UKOLJ110A] (25%) - Biringer, Kamil [UKOLJ150] (5%) - Šimurda, Tomáš [UKOLJ308] (5%) - Kubisz, Peter [UKOLJ308] (3%) - Staško, Ján [UKOLJ308] (2%): Glycoprotein VI Gene Variants Affect Pregnancy Loss in Patients With Platelet Hyperaggregability [elektronický dokument]
In: Clinical and Applied Thrombosis/Hemostasis [elektronický dokument]. - Volume 24, No. 9 (2018), p. 202S-208S [print]. - ISSN (print) 1076-0296
wos and scopus
SJR (SCOPUS) 2018=0.452
SNIP (SCOPUS) 2018=0.728
CiteScore (SCOPUS) 2018=2.5
IF (JCR) 2018=1.846
Kvartil Q:
wos-jcr -- Q4 [Hematology] -- 2018
wos-jcr -- Q4 [Peripheral vascular disease] -- 2018
scimago-sjr -- Q2 [Medicine (miscellaneous)] -- 2018
scimago-sjr -- Q3 [Hematology] -- 2018
Citations: 13/11
Sokol, Juraj [UKOLJ308] (40%) - Nehaj, František [KAUT] [UKOLJ] (40%) - Ivanková, Jela (10%) - Mokáň, Michal [UKOLJ220] (8%) - Mokáň, Marián [UKOLJ220] (2%): First evidence: rivaroxaban and apixaban reduce thrombin-dependent platelet aggregation[elektronický dokument]
Lit.: 7 zázn.
In: Journal of Thrombosis and Thrombolysis [elektronický dokument]. - Volume 46, No. 3 (2018), p. 393-398 [print]. - ISSN (print) 0929-5305
scopus and wos
SJR (SCOPUS) 2018=0.995
SNIP (SCOPUS) 2018=1.115
CiteScore (SCOPUS) 2018=4.8
IF (JCR) 2018=2.941
Kvartil Q:
wos-jcr -- Q3 [Peripheral vascular disease] -- 2018
wos-jcr -- Q3 [Cardiac & cardiovascular systems] -- 2018
wos-jcr -- Q3 [Hematology] -- 2018
scimago-sjr -- Q1 [Cardiology and cardiovascular medicine] -- 2018
scimago-sjr -- Q2 [Hematology] -- 2018
Citations: 9/8
Croles FN, Mulder R, Mulder AB, Lukens MV, Meijer K. β-Antithrombin, subtype of antithrombin deficiency and the risk of venous thromboembolism in hereditary antithrombin deficiency: A family cohort study. Thromb Res. 2018 Aug;168:47-52. doi: 10.1016/j.thromres.2018.06.004. IF(2018)=3.266
de la Morena-Barrio ME, Wypasek E, Owczarek D, Miñano A, Vicente V, Corral J, Undas A. MPI-CDG with transient hypoglycosylation and antithrombin deficiency. Haematologica. 2019 Feb;104(2):e79-e82. doi: 10.3324/haematol.2018.211326. IF(2019)=7.116
Croles FN, Lukens MV, Mulder R, de Maat MPM, Mulder AB, Meijer K. Monitoring of heparins in antithrombin-deficient patients. Thromb Res. 2019 Mar;175:8-12. doi: 10.1016/j.thromres.2019.01.007. IF(2019)=2.869
Li-Gao R, Mook-Kanamori DO, Cannegieter SC, Willems van Dijk K, Rosendaal FR, van Hylckama Vlieg A. The association of genetic variants in the cholesteryl ester transfer protein gene with hemostatic factors and a first venous thrombosis. J Thromb Haemost. 2019 Sep;17(9):1535-1543. doi: 10.1111/jth.14528. IF(2019)=4.365
Van Cott EM, Orlando C, Moore GW, Cooper PC, Meijer P, Marlar R; Subcommittee on Plasma Coagulation Inhibitors. Recommendations for clinical laboratory testing for antithrombin deficiency; Communication from the SSC of the ISTH. J Thromb Haemost. 2020 Jan;18(1):17-22. doi: 10.1111/jth.14648. IF (2020)=5.824
Grant VEGA 1/0187/17 - "Genetic Background and Hemostatic Changes in the Patients with von Willebrand Disease", principal investigator
Characteristic: Von Willebrand disease (vWD) is the most common inherited bleeding disorder. It was proved that conventional diagnostic methods are not sensitive sufficiently for the assessment of the diagnosis. Therefore, vWF multimer analysis and genetic testing can classify the patients with vWD more properly. These all are the reasons for the centralization of the individuals with vWD in one reference dagnostic centre with the availability to classify the subject with vWD rapidly in the acute clinical situations, for the pharmacovigilance, national planning of the care for such patients and budget allocation. Currently, such comprehensive centre with universal diagnostic algorithm is missing in Slovak Republic. The prominent aim of the proposed project was therefore the correlation of the laboratory results and genetic analysis with clinical course of the disease, their use for the indication, monitoring and subsequent individual management of the substitution treatment of the individuals with vWD.
Grant APVV-17-0054 - "New Oral Anticoagulants in the Prevention of Major Cardiovascular Diseases, their Effect on Thrombocytes, Drug Interactions, Safety and Possibilities of the Therapy in Oncology Patients", co-investigator
Characteristic: Atrial fibrillation (AF) is the most common cardiac arrhythmia. Currently, four oral anticoagulants (NOAC), known as dabigatran, rivaroxaban, apixaban and edoxaban are currently used for anticoagulation therapy. The treatment with NOAC has been approved as alternatives to warfarin in patients with AF. The data of evidence-based and post-marketing literature on the benefit/risk ratio of NOACs are limited, conflicting, potentially biased and finally inconclusive in population of patients with AF. The aim of the study is to assess and compare the real benefits and harms of all three NOACs in routine practice. The main objective is to estimate and compare a composite event including major bleeding, thromboembolism (TE) and death from any cause.The secondary objectives are: to identify factors associated with the occurrence of major bleeding events and TE events in patients exposed to oral anticoagulant, to describe others adverse drug reactions, to compare the reliability of the monitoring of the NOACs by thrombelastometry, to assess the effect of NOACs on platelet aggregation and function, to assess the selected polymorphisms of drug-metabolising enzyme and to evaluate the drug interaction. The main outcome of the project is to improve the quality of health care and perioperative outcomes. The study could lead to a better understanding of the metabolic processes, platelet aggregation and genetic background of NOACs. The development of new monitoring methods will allow rapid assessment of coagulation activity in an emergency situation. This study has a major premise of interdisciplinary character, while the prevalence of patients taking NOAC refers to the high numbers in all fields of medicine.
Grant APVV-16-0020 - "Specific laboratory monitoring of platelet reactivity in patients with acute myocardial infarction treated with new P2Y12 receptor antagonists", co-investigator
Characteristic: P2Y12 ADP receptor blocker (ADPRB) treatment forms currently the basis of pharmacotherapy in acute coronary syndrome (ACS) patients, and in patients after percutaneous coronary interventions (PCI). However, nowadays, there are lots of data demonstrating an association between insufficient ADPRB on-treatment response and the risk of ischemic events, including stent trombosis, which is an uncommon but life-threatening complication in patients after PCI. High on-treatment platelet reactivity may be detected with several laboratory tests. Light transsmition aggregometry with ADP induction is so far con- sidered to be a „golden standard“, and VASP (vasodilator stimulated phosphoprotein) phosphorylation assessement using flow cytometry is probably the most specific test for the assessment of insuficient platelet response. If high on-treatment platelet reactivity is detected, this phenomenon migh be overcome with increased ADPRB dosing, ADPRB switch (e. g. switch of clopidogrel to prasugrel), or with the addition of other antiplatelet agent. The administration of cangrelor – a new par- enteral ADPRB – might be another perspective way how to overcome the phenomenon of insuficient ADPRB on-treatment response.
Grant VEGA 1/0479/21 - "Molecular-genetic aspects of platelet hyperagregability in patients with venous thromboembolism", Deputy Principal Investigator
Characteristic: Platelet hyperaggregability after low concentrations of platelet agonists adenosine diphoshate (ADP) and/or epinephrine (EPI), referred to as sticky platelet syndrome (SPS), was first described by Holiday at the Ninth Conference on Stroke and Cerebral Circulation in Arizona in 1983. Clinical symptoms of SPS include unexplained arterial and venous thrombotic events, commonly occurring in stressful situations, and frequently recurrent under oral anticoagulant therapy. Furthermore, there is evidence for a causal relation between SPS and abortion. SPS is classified as type I (hyperaggregation after both ADP and EPI), type II (hyperaggregation after EPI alone) and type III (hyperaggregation after ADP alone). SPS type II seems to be the most common form. SPS is probably a hereditary, autosomal dominant thrombophilia, although the exact genetic cause has not as yet been identified. It has been suggested that defects of the platelet membrane glycoproteins or intracellular signal pathways involved in platelet activation and aggregation are responsible for the disorder.
VII.a - Activity, position | VII.b - Name of the institution, board | VII.c - Duration |
---|---|---|
member | Slovak Society on Haemostasis and Thrombosis | from 2010 |
member | Slovak Society of Hematology and Transfusion Medicine | from 2010 |
the president | HematologySK, civic association | from 2015 |
VIII.a - Name of the institution | VIII.b - Address of the institution | VIII.c - Duration (indicate the duration of stay) | VIII.d - Mobility scheme, employment contract, other (describe) |
---|---|---|---|
Leiden University Medical Center, Leiden, The Nederlands | Albinusdreef 2, 2333 ZA Leiden, The Nederlands | May 1 to July 31, 2015 | European Social Fund |
University of North Carolina, Chapel Hill, North Carolina, USA | 101 Manning Dr, Chapel Hill, NC 27514, USA | August 27, 2017 - February 28, 2018 | Fulbright Program |