List of works - Ewa Wypasek

12-month patterns of serum markers of collagen synthesis, transforming growth factor and connective tissue growth factor are similar in new-onset and chronic dilated cardiomyopathy in patients both with and without cardiac fibrosis.

scientific article published on 28 April 2017

A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction

scientific article published on 3 May 2013

A prothrombotic state and denser clot formation in patients following acute limb ischemia of unknown cause

scientific article published on 10 January 2020

Adiponectin, leptin, and resistin in patients with aortic stenosis without concomitant atherosclerotic vascular disease

scientific article published on 01 October 2011

Alpha-2-antiplasmin Arg407Lys polymorphism and cryptogenic ischemic cerebrovascular events: Association with neurological deficit

scientific article

Altered plasma fibrin clot properties in hypertensive patients with obstructive sleep apnoea are improved by continuous positive airway pressure treatment

scientific article

Association of Interleukin-10 promoter polymorphisms with neurosyphilis

scientific article published on 19 June 2015

Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis

scientific article

Biomechanical strain regulates TNFR2 but not TNFR1 in TMJ cells

scientific article published on 16 October 2006

Bleeding predictors in patients following venous thromboembolism treated with vitamin K antagonists: Association with increased number of single nucleotide polymorphisms

scientific article published on 9 February 2018

CYP2C9 Polymorphism and Unstable Anticoagulation with Warfarin in Patients Within the First 3 Months Following Heart Valve Replacement

scientific article published on July 2015

Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation

scientific article published on 7 December 2017

Determinants of elevated factor VIII in patients screened for thrombophilia

scientific article published on 29 January 2020

Does Diabetes Accelerate the Progression of Aortic Stenosis through Enhanced Inflammatory Response within Aortic valves? ⬇️

scientific article published on June 1, 2012

Dynamic biophysical strain modulates proinflammatory gene induction in meniscal fibrochondrocytes

scientific article published on February 2006

Effect of the E-selectin gene polymorphism (S149R) on platelet activation and adverse events after coronary artery surgery

scientific article

Effects of rivaroxaban and dabigatran on local expression of coagulation and inflammatory factors within human aortic stenotic valves

scientific article published on 06 May 2020

Exercise stress testing enhances blood coagulation and impairs fibrinolysis in asymptomatic aortic valve stenosis

scientific article published on 26 August 2014

Factor XIII Val34Leu polymorphism and ischaemic stroke in patients with patent foramen ovale

scientific article published in December 2009

Factor XIII Val34Leu polymorphism as a modulator of fibrin clot permeability and resistance to lysis in patients with severe coronary artery disease.

scientific article published in August 2009

Factor XIII expression within aortic valves and its plasma activity in patients with aortic stenosis: association with severity of disease

scientific article

False-positive lupus anticoagulant in patients receiving rivaroxaban: 24 h since the last dose are needed to exclude antiphospholipid syndrome

scientific article published in June 2015

Fibrinogen beta-chain -C148T polymorphism is associated with increased fibrinogen, C-reactive protein, and interleukin-6 in patients undergoing coronary artery bypass grafting

scientific article published in April 2012

Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism

scientific article published on 21 November 2021

Fibrosis of extracellular matrix is related to the duration of the disease but is unrelated to the dynamics of collagen metabolism in dilated cardiomyopathy.

scientific article published on 11 August 2016

First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis ⬇️

scientific article published on March 6, 2013

First report of the genetic background of Marfan syndrome in Polish patients.

scientific article

Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.

scientific article published on 13 June 2017

Genetic determinants of acenocoumarol and warfarin maintenance dose requirements in Slavic population: a potential role of CYP4F2 and GGCX polymorphisms

scientific article

High levels of latent antithrombin in plasma from patients with antithrombin deficiency

scientific article published on 23 February 2017

ID: 228

scholarly article by Agnieszka Irena Mazur-Bialy et al published November 2015 in Cytokine

Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6.

scientific article published on 21 March 2018

IgA Antiphospholipid Antibodies and Anti-Domain 1 of Beta 2 Glycoprotein 1 Antibodies are Associated with Livedo Reticularis and Heart Valve Disease in Antiphospholipid Syndrome

scientific article

Impaired Fibrinolysis in Patients with Isolated Aortic Stenosis is Associated with Enhanced Oxidative Stress

scientific article published on 25 June 2020

Increased levels of bone remodeling biomarkers (osteoprotegerin and osteopontin) in hypertensive individuals

scientific article

Interaction between functional polymorphisms in FCER1A and TLR2 and the severity of atopic dermatitis

scientific article published on 31 August 2020

Interleukin-6 receptor Asp358Ala gene polymorphism is associated with plasma C-reactive protein levels and severity of aortic valve stenosis

scientific article published on 01 July 2014

Iron deficiency: a novel risk factor of recurrence in patients after unprovoked venous thromboembolism

scientific article published on 04 March 2016

Left ventricular reverse remodeling is not related to biopsy-detected extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy, regardless of the definition used for LVRR

scientific article published on 21 December 2016

Lymphocyte and monocyte subpopulations in severe aortic stenosis at the time of surgical intervention

scientific article published on 07 April 2018

MPI-CDG with transient hypoglycosylation and antithrombin deficiency

scholarly article by María Eugenia de la Morena-Barrio et al published February 2019 in Haematologica

Mast cells are responsible for the lack of anti-inflammatory effects of morphine in CBA mice

scientific article published on December 2004

Mechanical signals control SOX-9, VEGF, and c-Myc expression and cell proliferation during inflammation via integrin-linked kinase, B-Raf, and ERK1/2-dependent signaling in articular chondrocytes

scientific article

Morphine-modulated mast cell migration and proliferation during early stages of zymosan-induced peritonitis in CBA mice

scientific article published on 01 January 2011

Non-classical and intermediate monocytes in patients following venous thromboembolism: Links with inflammation

scientific article published on 01 January 2019

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

scientific article published on 05 February 2014

Protein C and protein S deficiency - practical diagnostic issues

scientific article published in July 2013

Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.

scientific article

Quantification of airborne birch (Betula sp.) pollen grains and allergens in Krakow.

scientific article published in March 2005

Reduced plasma fibrin clot permeability and susceptibility to fibrinolysis are associated with increased intima-media thickness in patients with primary antiphospholipid syndrome

scientific article

Regulation of RANKL by biomechanical loading in fibrochondrocytes of meniscus

scientific article published on 21 July 2005

Relations between circulating microRNAs (miR-21, miR-26, miR-29, miR-30 and miR-133a), extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy.

scientific article published on 18 November 2016

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC12A and the CYP2C93/*3 alleles: genetic testing to support switching to new oral anticoagulants

scientific article

Residual iliofemoral thrombosis in a 31-year-old woman on oral contraceptives possessing heterozygous factor V Leiden, factor XIII Val34Leu allele and alpha-fibrinogen Thr312Ala allele: case report

scientific article published on 01 December 2009

Right ventricular morphology and function is not related with microRNAs and fibrosis markers in dilated cardiomyopathy.

scientific article published on 25 August 2017

Shorter preoperative fibrin clot lysis time predisposes to higher chest tube drainage in patients undergoing elective coronary artery bypass grafting surgery

scientific article published on 01 June 2010

Similar prevalence of platelet factor 4/heparin immunoglobulin G antibodies in patients following cardiac surgery and other patients suspected of heparin-induced thrombocytopaenia

scientific article published on 01 January 2018

Stenotic Bicuspid and Tricuspid Aortic Valves　- Micro-Computed Tomography and Biological Indices of Calcification

scientific article published on 24 March 2017

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

scientific article published on 5 June 2018

Toll-like receptors expression and NF-κB activation in peritoneal leukocytes in morphine-mediated impairment of zymosan-induced peritonitis in swiss mice

scientific article published on 23 August 2012

Vascular Ehlers-Danlos syndrome in 2 Polish patients: identification of 2 novel COL3A1 gene mutations

scientific article published on 01 October 2019

Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review

scientific article published in December 2017

Warfarin Metabolites in Patients Following Cardiac Valve Implantation: A Contribution of Clinical and Genetic Factors

scientific article published on June 2015

List of works by Ewa Wypasek

12-month patterns of serum markers of collagen synthesis, transforming growth factor and connective tissue growth factor are similar in new-onset and chronic dilated cardiomyopathy in patients both with and without cardiac fibrosis.

A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction

A prothrombotic state and denser clot formation in patients following acute limb ischemia of unknown cause

Adiponectin, leptin, and resistin in patients with aortic stenosis without concomitant atherosclerotic vascular disease

Alpha-2-antiplasmin Arg407Lys polymorphism and cryptogenic ischemic cerebrovascular events: Association with neurological deficit

Altered plasma fibrin clot properties in hypertensive patients with obstructive sleep apnoea are improved by continuous positive airway pressure treatment

Association of Interleukin-10 promoter polymorphisms with neurosyphilis

Association of the C-Reactive Protein Gene (CRP) rs1205 C>T Polymorphism with Aortic Valve Calcification in Patients with Aortic Stenosis

Biomechanical strain regulates TNFR2 but not TNFR1 in TMJ cells

Bleeding predictors in patients following venous thromboembolism treated with vitamin K antagonists: Association with increased number of single nucleotide polymorphisms

CYP2C9 Polymorphism and Unstable Anticoagulation with Warfarin in Patients Within the First 3 Months Following Heart Valve Replacement

Detection and a functional characterization of the novel FBN1 intronic mutation underlying Marfan syndrome: case presentation

Determinants of elevated factor VIII in patients screened for thrombophilia

Does Diabetes Accelerate the Progression of Aortic Stenosis through Enhanced Inflammatory Response within Aortic valves? ⬇️

Dynamic biophysical strain modulates proinflammatory gene induction in meniscal fibrochondrocytes

Effect of the E-selectin gene polymorphism (S149R) on platelet activation and adverse events after coronary artery surgery

Effects of rivaroxaban and dabigatran on local expression of coagulation and inflammatory factors within human aortic stenotic valves

Exercise stress testing enhances blood coagulation and impairs fibrinolysis in asymptomatic aortic valve stenosis

Factor XIII Val34Leu polymorphism and ischaemic stroke in patients with patent foramen ovale

Factor XIII Val34Leu polymorphism as a modulator of fibrin clot permeability and resistance to lysis in patients with severe coronary artery disease.

Factor XIII expression within aortic valves and its plasma activity in patients with aortic stenosis: association with severity of disease

False-positive lupus anticoagulant in patients receiving rivaroxaban: 24 h since the last dose are needed to exclude antiphospholipid syndrome

Fibrinogen beta-chain -C148T polymorphism is associated with increased fibrinogen, C-reactive protein, and interleukin-6 in patients undergoing coronary artery bypass grafting

Fibrinogen β chain and FXIII polymorphisms affect fibrin clot properties in acute pulmonary embolism

Fibrosis of extracellular matrix is related to the duration of the disease but is unrelated to the dynamics of collagen metabolism in dilated cardiomyopathy.

First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis ⬇️

First report of the genetic background of Marfan syndrome in Polish patients.

Genetic characterization of antithrombin, protein C, and protein S deficiencies in Polish patients.

Genetic determinants of acenocoumarol and warfarin maintenance dose requirements in Slavic population: a potential role of CYP4F2 and GGCX polymorphisms

High levels of latent antithrombin in plasma from patients with antithrombin deficiency

ID: 228

Identification of a New Mechanism of Antithrombin Deficiency Hardly Detected by Current Methods: Duplication of SERPINC1 Exon 6.

IgA Antiphospholipid Antibodies and Anti-Domain 1 of Beta 2 Glycoprotein 1 Antibodies are Associated with Livedo Reticularis and Heart Valve Disease in Antiphospholipid Syndrome

Impaired Fibrinolysis in Patients with Isolated Aortic Stenosis is Associated with Enhanced Oxidative Stress

Increased levels of bone remodeling biomarkers (osteoprotegerin and osteopontin) in hypertensive individuals

Interaction between functional polymorphisms in FCER1A and TLR2 and the severity of atopic dermatitis

Interleukin-6 receptor Asp358Ala gene polymorphism is associated with plasma C-reactive protein levels and severity of aortic valve stenosis

Iron deficiency: a novel risk factor of recurrence in patients after unprovoked venous thromboembolism

Left ventricular reverse remodeling is not related to biopsy-detected extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy, regardless of the definition used for LVRR

Lymphocyte and monocyte subpopulations in severe aortic stenosis at the time of surgical intervention

MPI-CDG with transient hypoglycosylation and antithrombin deficiency

Mast cells are responsible for the lack of anti-inflammatory effects of morphine in CBA mice

Mechanical signals control SOX-9, VEGF, and c-Myc expression and cell proliferation during inflammation via integrin-linked kinase, B-Raf, and ERK1/2-dependent signaling in articular chondrocytes

Morphine-modulated mast cell migration and proliferation during early stages of zymosan-induced peritonitis in CBA mice

Non-classical and intermediate monocytes in patients following venous thromboembolism: Links with inflammation

Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism

Protein C and protein S deficiency - practical diagnostic issues

Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.

Quantification of airborne birch (Betula sp.) pollen grains and allergens in Krakow.

Reduced plasma fibrin clot permeability and susceptibility to fibrinolysis are associated with increased intima-media thickness in patients with primary antiphospholipid syndrome

Regulation of RANKL by biomechanical loading in fibrochondrocytes of meniscus

Relations between circulating microRNAs (miR-21, miR-26, miR-29, miR-30 and miR-133a), extracellular matrix fibrosis and serum markers of fibrosis in dilated cardiomyopathy.

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC1*2A and the CYP2C9*3/*3 alleles: genetic testing to support switching to new oral anticoagulants

Residual iliofemoral thrombosis in a 31-year-old woman on oral contraceptives possessing heterozygous factor V Leiden, factor XIII Val34Leu allele and alpha-fibrinogen Thr312Ala allele: case report

Right ventricular morphology and function is not related with microRNAs and fibrosis markers in dilated cardiomyopathy.

Shorter preoperative fibrin clot lysis time predisposes to higher chest tube drainage in patients undergoing elective coronary artery bypass grafting surgery

Similar prevalence of platelet factor 4/heparin immunoglobulin G antibodies in patients following cardiac surgery and other patients suspected of heparin-induced thrombocytopaenia

Stenotic Bicuspid and Tricuspid Aortic Valves - Micro-Computed Tomography and Biological Indices of Calcification

The New *G29A and G1222A of HCRTR1, 5-HTTLPR of SLC6A4 Polymorphisms and Hypocretin-1, Serotonin Concentrations in Migraine Patients.

Toll-like receptors expression and NF-κB activation in peritoneal leukocytes in morphine-mediated impairment of zymosan-induced peritonitis in swiss mice

Vascular Ehlers-Danlos syndrome in 2 Polish patients: identification of 2 novel COL3A1 gene mutations

Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review

Warfarin Metabolites in Patients Following Cardiac Valve Implantation: A Contribution of Clinical and Genetic Factors

Repeated bleeding complications during therapy with vitamin K antagonists in a patient with the VKORC12A and the CYP2C93/*3 alleles: genetic testing to support switching to new oral anticoagulants

Stenotic Bicuspid and Tricuspid Aortic Valves　- Micro-Computed Tomography and Biological Indices of Calcification