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Thrombin generation, D-dimer and protein S in uncomplicated pregnancy

Clinical chemistry and laboratory medicine, 2015-11, Vol.53 (12), p.1975

2015

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Economic analysis of pharmacogenomic-guided clopidogrel treatment in Serbian patients with myocardial infarction undergoing primary percutaneous coronary intervention

Pharmacogenomics, 2016-11, Vol.17 (16), p.1775-1784

2016

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The c.-1639G>A polymorphism of the VKORC1 gene in Serbian population: retrospective study of the variability in response to oral anticoagulant therapy

Blood coagulation & fibrinolysis, 2010-09, Vol.21 (6), p.558-563

2010

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Extreme sensitivity to acenocoumarol therapy in patient with both VKORC.-1639 A/A and CYP2C91/3 genotypes

Journal of thrombosis and thrombolysis, 2011-10, Vol.32 (3), p.368-371

2011

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Are Prothrombotic Mutations a Time-to-Event Risk Factor?

Laboratory medicine, 2017-11, Vol.48 (4), p.326-331

2017

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Pharmacogenetic tests could be helpful in predicting of VKA maintenance dose in elderly patients at treatment initiation

Journal of thrombosis and thrombolysis, 2013, Vol.35 (1), p.90-94

2013

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Rationalized DNA sequencing-based protocol for genotyping patients receiving coumarin therapy

Scandinavian journal of clinical and laboratory investigation, 2013-09, Vol.73 (6), p.523-527

2013

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Risk factors for thrombosis in Serbian children

Blood coagulation & fibrinolysis, 2014-01, Vol.25 (1), p.25-32

2014

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Screening of mutations and polymorphism in CFRT gene in men infertile due to oligo- or azospermia

Srpski arhiv za celokupno lekarstvo, 2002, Vol.130 (1-2), p.1-6

2002

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European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

European journal of human genetics : EJHG, 2019-12, Vol.27 (12), p.1763-1773

2019

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One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

European journal of human genetics : EJHG, 2018-01, Vol.26 (1), p.1-11

2018

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The Silence Speaks, but We Do Not Listen: Synonymous c.1824C>T Gene Variant in the Last Exon of the Prothrombin Gene as a New Prothrombotic Risk Factor

Clinical chemistry (Baltimore, Md.), 2020-02, Vol.66 (2), p.379-389

2020

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A₁ATVar: a relational database of human SERPINA1 gene variants leading to α₁-antitrypsin deficiency and application of the VariVis software

Human mutation, 2009-03, Vol.30 (3), p.308-313

2009

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A 1 ATVar: a relational database of human SERPINA1 gene variants leading to α 1 -antitrypsin deficiency and application of the VariVis software

Human mutation, 2009-03, Vol.30 (3), p.308-313

2009

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A sub(1)ATVar: a relational database of human SERPINA1 gene variants leading to alpha sub(1)-antitrypsin deficiency and application of the VariVis software

Human mutation, 2009-03, Vol.30 (3), p.308-313

2009

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FV Leiden, FII G20210A and MTHFR C677T mutations in patients with lower or upper limb deep vein thrombosis

Genetika (Beograd), 2011, Vol.43 (2), p.371-380

2011

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A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

Human mutation, 2009-03, Vol.30 (3), p.308-313

2009

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Development of a universal, flexible and freely available database management system for gene-centered data collection, curation and display of DNA variation

2008 8th IEEE International Conference on BioInformatics and BioEngineering, 2008, Vol.8, p.1-6

2008

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Frequency of the ΔF508 deletion and G551D, R553X and G542X mutations in Yugoslav CF patients

Human genetics, 1992-03, Vol.88 (6), p.699-700

1992

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Thrombin generation, D-dimer and protein S in uncomplicated pregnancy

Economic analysis of pharmacogenomic-guided clopidogrel treatment in Serbian patients with myocardial infarction undergoing primary percutaneous coronary intervention

The c.-1639G>A polymorphism of the VKORC1 gene in Serbian population: retrospective study of the variability in response to oral anticoagulant therapy

Extreme sensitivity to acenocoumarol therapy in patient with both VKORC.-1639 A/A and CYP2C91/3 genotypes

Are Prothrombotic Mutations a Time-to-Event Risk Factor?

Pharmacogenetic tests could be helpful in predicting of VKA maintenance dose in elderly patients at treatment initiation

Rationalized DNA sequencing-based protocol for genotyping patients receiving coumarin therapy

Risk factors for thrombosis in Serbian children

Screening of mutations and polymorphism in CFRT gene in men infertile due to oligo- or azospermia

European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death

One small edit for humans, one giant edit for humankind? Points and questions to consider for a responsible way forward for gene editing in humans

The Silence Speaks, but We Do Not Listen: Synonymous c.1824C>T Gene Variant in the Last Exon of the Prothrombin Gene as a New Prothrombotic Risk Factor

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

A₁ATVar: a relational database of human SERPINA1 gene variants leading to α₁-antitrypsin deficiency and application of the VariVis software

A 1 ATVar: a relational database of human SERPINA1 gene variants leading to α 1 -antitrypsin deficiency and application of the VariVis software

A sub(1)ATVar: a relational database of human SERPINA1 gene variants leading to alpha sub(1)-antitrypsin deficiency and application of the VariVis software

FV Leiden, FII G20210A and MTHFR C677T mutations in patients with lower or upper limb deep vein thrombosis

A1ATVar: a relational database of human SERPINA1 gene variants leading to alpha1-antitrypsin deficiency and application of the VariVis software

Development of a universal, flexible and freely available database management system for gene-centered data collection, curation and display of DNA variation

Frequency of the ΔF508 deletion and G551D, R553X and G542X mutations in Yugoslav CF patients

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