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Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

Journal of molecular medicine (Berlin, Germany), 2008-10, Vol.86 (10), p.1153-1161

2008

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Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

Journal of medical genetics, 2004-11, Vol.41 (11), p.814-825

2004

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Impact on venous thrombosis risk of newly discovered gene variants associated with FVIII and VWF plasma levels

Journal of thrombosis and haemostasis, 2011-01, Vol.9 (1), p.229-231

2011

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A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

Journal of thrombosis and haemostasis, 2010-12, Vol.8 (12), p.2671-2679

2010

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Association of plasminogen activator inhibitor (PAI)-1 (SERPINE1) SNPs with myocardial infarction, plasma PAI-1, and metabolic parameters: the HIFMECH study

Arteriosclerosis, thrombosis, and vascular biology, 2007-10, Vol.27 (10), p.2250-2257

2007

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Economic Analysis of Thrombo inCode, a Clinical–Genetic Function for Assessing the Risk of Venous Thromboembolism

Applied health economics and health policy, 2015-04, Vol.13 (2), p.233-242

2015

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The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility

Molecular human reproduction, 2000-09, Vol.6 (9), p.789-793

2000

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Relation between the antithrombin Cambridge II mutation, the risk of venous thrombosis, and the endogenous thrombin generation

Journal of thrombosis and haemostasis, 2008-11, Vol.6 (11), p.1975-1977

2008

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Effect of Cytochrome P450 Polymorphisms on Platelet Reactivity After Treatment With Clopidogrel in Acute Coronary Syndrome

The American journal of cardiology, 2008-04, Vol.101 (8), p.1088-1093

2008

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Interaction between the C-260T polymorphism of the CD14 gene and the plasma IL-6 concentration on the risk of myocardial infarction: the HIFMECH study

Atherosclerosis, 2005-04, Vol.179 (2), p.317-323

2005

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RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene

Nature genetics, 1999-07, Vol.22 (3), p.224-226

1999

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The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences

Journal of medical genetics, 1999-09, Vol.36 (9), p.670-677

1999

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The Mouse Y Chromosome Interval Necessary for Spermatogonial Proliferation is Gene Dense with Syntenic Homology to the Human AZFa Region

Human molecular genetics, 1998-10, Vol.7 (11), p.1713-1724

1998

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Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes

Journal of thrombosis and haemostasis, 2018-12, Vol.16 (12), p.2432-2441

2018

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Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man

Human reproduction (Oxford), 2010-10, Vol.25 (10), p.2655-2663

2010

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Factor V Leiden G1691A and prothrombin G20210A mutations are common in Tunisia

Journal of thrombosis and haemostasis, 2003-11, Vol.1 (11), p.2451-2452

2003

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A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis

Nature genetics, 2001-09, Vol.29 (1), p.49-53

2001

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Adrenergic receptor polymorphisms and platelet reactivity after treatment with dual antiplatelet therapy with aspirin and clopidogrel in acute coronary syndrome

Thrombosis and haemostasis, 2010-04, Vol.103 (4), p.774-779

2010

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TAFI antigen level variability in young healthy Asian Indians; First report from Asia

Clinical biochemistry, 2008-06, Vol.41 (9), p.750-753

2008

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Common variants in the thrombomodulin gene as a risk for myocardial infarction in the north of Europe (HIFMECH Study)

Thrombosis and haemostasis, 2004-03, Vol.91 (3), p.628-630

2004

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Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

American journal of human genetics, 2018-04, Vol.102 (4), p.636-648

2018

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Evaluation of vertical forces in the pads of German Shepherd dogs

Veterinary and comparative orthopaedics and traumatology, 2013, Vol.26 (1), p.6-11

2013

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Healing and expression of growth factors (TGF-β and PDGF) in canine radial ostectomy gap containing platelet-rich plasma

Veterinary and comparative orthopaedics and traumatology, 2012-01, Vol.25 (6), p.445-452

2012

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Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility

Impact on venous thrombosis risk of newly discovered gene variants associated with FVIII and VWF plasma levels

A multi‐stage multi‐design strategy provides strong evidence that the BAI3 locus is associated with early‐onset venous thromboembolism

Association of plasminogen activator inhibitor (PAI)-1 (SERPINE1) SNPs with myocardial infarction, plasma PAI-1, and metabolic parameters: the HIFMECH study

Economic Analysis of Thrombo inCode, a Clinical–Genetic Function for Assessing the Risk of Venous Thromboembolism

The human Y chromosome genes BPY2, CDY1 and DAZ are not essential for sustained fertility

Relation between the antithrombin Cambridge II mutation, the risk of venous thrombosis, and the endogenous thrombin generation

Effect of Cytochrome P450 Polymorphisms on Platelet Reactivity After Treatment With Clopidogrel in Acute Coronary Syndrome

Interaction between the C-260T polymorphism of the CD14 gene and the plasma IL-6 concentration on the risk of myocardial infarction: the HIFMECH study

RBMY evolved on the Y chromosome from a ubiquitously transcribed X-Y identical gene

The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences

The Mouse Y Chromosome Interval Necessary for Spermatogonial Proliferation is Gene Dense with Syntenic Homology to the Human AZFa Region

Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes

Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man

Factor V Leiden G1691A and prothrombin G20210A mutations are common in Tunisia

A Y-encoded subunit of the translation initiation factor Eif2 is essential for mouse spermatogenesis

Adrenergic receptor polymorphisms and platelet reactivity after treatment with dual antiplatelet therapy with aspirin and clopidogrel in acute coronary syndrome

TAFI antigen level variability in young healthy Asian Indians; First report from Asia

Common variants in the thrombomodulin gene as a risk for myocardial infarction in the north of Europe (HIFMECH Study)

Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice

Absence of CFAP69 Causes Male Infertility due to Multiple Morphological Abnormalities of the Flagella in Human and Mouse

Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation

Evaluation of vertical forces in the pads of German Shepherd dogs

Healing and expression of growth factors (TGF-β and PDGF) in canine radial ostectomy gap containing platelet-rich plasma

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