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Polymorphisms in the Annexin A5 gene influence circulating Annexin A5 levels in healthy controls

Thrombosis research, 2012-06, Vol.129 (6), p.815-817

2012

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Annexin A5 haplotypes in familial hypercholesterolemia: Lack of association with carotid intima-media thickness and cardiovascular disease risk

Atherosclerosis, 2015-02, Vol.238 (2), p.195-200

2015

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A Reduced Sensitivity for Activated Protein C in the Absence of Factor V Leiden Increases the Risk of Venous Thrombosis

Blood, 1999-02, Vol.93 (4), p.1271-1276

1999

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Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarction

Atherosclerosis, 2009-03, Vol.203 (1), p.201-205

2009

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Factor IX-R338L (Factor IX Padua) screening in a Dutch population of sibpairs with early onset venous thromboembolism

Thrombosis research, 2011-12, Vol.128 (6), p.603-603

2011

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Haplotypes of IL1B, IL1RN, IL1R1, and IL1R2 and the risk of venous thrombosis

Arteriosclerosis, thrombosis, and vascular biology, 2007-06, Vol.27 (6), p.1486-1491

2007

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Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism

American journal of human genetics, 2015-04, Vol.96 (4), p.532-542

2015

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Discovery of common variants associated with low TSH levels and thyroid cancer risk

Nature genetics, 2012-03, Vol.44 (3), p.319-322

2012

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Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study

Blood, 2013-10, Vol.122 (18), p.3210-3219

2013

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Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen γ′ levels

Blood, 2005-12, Vol.106 (13), p.4176-4183

2005

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A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

PLoS genetics, 2013-02, Vol.9 (2), p.e1003266-e1003266

2013

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A Reduced Sensitivity for Activated Protein C in the Absence of Factor V Leiden Increases the Risk of Venous Thrombosis

Blood, 1999-02, Vol.93 (4), p.1271-1276

1999

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ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens

Thrombosis and haemostasis, 2007-04, Vol.97 (4), p.534-541

2007

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Estimation of genetic effects in multiple cases family studies using penalized maximum likelihood methodology

Biostatistics (Oxford, England), 2013-04, Vol.14 (2), p.220-231

2013

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Fibrinogen gamma gene 3'-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population

Thrombosis and haemostasis, 2009-06, Vol.101 (6), p.1078-1084

2009

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Haplotypes of VKORC1, NQO1 and GGCX, their effect on activity levels of vitamin K-dependent coagulation factors, and the risk of venous thrombosis

Thrombosis and haemostasis, 2011-09, Vol.106 (3), p.563-565

2011

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The Marburg I polymorphism of factor VII-activating protease is not associated with venous thrombosis

Blood, 2005-06, Vol.105 (12), p.4898-4898

2005

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Copy Number Variation of PROS1 and Protein S Deficiency Are Rare in a Population-Based Case-Control Study On Venous Thrombosis (MEGA study)

Blood, 2009-11, Vol.114 (22), p.3166-3166

2009

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High Levels of Protein C Are Determinated by PROCR H3 in a Dutch Family

Blood, 2009-11, Vol.114 (22), p.2139-2139

2009

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The HR2 haplotype of factor V: effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis

Thrombosis and haemostasis, 2000-04, Vol.83 (4), p.577-582

2000

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Frequency of the TAFI -438 G/A and factor XIIIA Val34Leu polymorphisms in patients with objectively proven pulmonary embolism

Thrombosis and haemostasis, 2003-09, Vol.90 (3), p.439-445

2003

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Polymorphism 10034C>T Is Located in a Functional Cleavage Stimulation Factor (CstF) Binding Site of the Fibrinogen Gamma Gene and Influences the γ′/γA mRNA Ratio

Blood, 2006-11, Vol.108 (11), p.543-543

2006

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The effect of plasma caeruloplasmin levels on the sensitivity for activated protein C

British journal of haematology, 2002-09, Vol.118 (3), p.843-846

2002

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Generalizing Terwilliger's likelihood approach: a new score statistic to test for genetic association

BMC genetics, 2007-09, Vol.8 (1), p.63, Article 63

2007

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Polymorphisms in the Annexin A5 gene influence circulating Annexin A5 levels in healthy controls

Annexin A5 haplotypes in familial hypercholesterolemia: Lack of association with carotid intima-media thickness and cardiovascular disease risk

A Reduced Sensitivity for Activated Protein C in the Absence of Factor V Leiden Increases the Risk of Venous Thrombosis

Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarction

Factor IX-R338L (Factor IX Padua) screening in a Dutch population of sibpairs with early onset venous thromboembolism

Haplotypes of IL1B, IL1RN, IL1R1, and IL1R2 and the risk of venous thrombosis

Meta-analysis of 65,734 Individuals Identifies TSPAN15 and SLC44A2 as Two Susceptibility Loci for Venous Thromboembolism

Discovery of common variants associated with low TSH levels and thyroid cancer risk

Protein S levels and the risk of venous thrombosis: results from the MEGA case-control study

Identification of low-frequency variants associated with gout and serum uric acid levels

Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen γ′ levels

A meta-analysis of thyroid-related traits reveals novel loci and gender-specific differences in the regulation of thyroid function

A Reduced Sensitivity for Activated Protein C in the Absence of Factor V Leiden Increases the Risk of Venous Thrombosis

ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens

Estimation of genetic effects in multiple cases family studies using penalized maximum likelihood methodology

Fibrinogen gamma gene 3'-end polymorphisms and risk of venous thromboembolism in the African-American and Caucasian population

Haplotypes of VKORC1, NQO1 and GGCX, their effect on activity levels of vitamin K-dependent coagulation factors, and the risk of venous thrombosis

The Marburg I polymorphism of factor VII-activating protease is not associated with venous thrombosis

Copy Number Variation of PROS1 and Protein S Deficiency Are Rare in a Population-Based Case-Control Study On Venous Thrombosis (MEGA study)

High Levels of Protein C Are Determinated by PROCR H3 in a Dutch Family

The HR2 haplotype of factor V: effects on factor V levels, normalized activated protein C sensitivity ratios and the risk of venous thrombosis

Frequency of the TAFI -438 G/A and factor XIIIA Val34Leu polymorphisms in patients with objectively proven pulmonary embolism

Polymorphism 10034C>T Is Located in a Functional Cleavage Stimulation Factor (CstF) Binding Site of the Fibrinogen Gamma Gene and Influences the γ′/γA mRNA Ratio

The effect of plasma caeruloplasmin levels on the sensitivity for activated protein C

Generalizing Terwilliger's likelihood approach: a new score statistic to test for genetic association

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