W. Cohen

发表

A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis

L. Letenneur, D. Trégouët, M. Lathrop, 2013, BMC Medical Genetics.

Genetics of Venous Thrombosis: Insights from a New Genome Wide Association Study

F. Cambien, L. Letenneur, D. Trégouët, 2011, PloS one.

Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels

D. Tregouet, M. Lathrop, M. Germain, 2011, BMC Medical Genetics.

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project

D. Trégouët, M. Lathrop, D. Zélénika, 2012, British journal of haematology.

Anticoagulation with a new oral anticoagulant in heart transplant recipients.

W. Cohen, P. Morange, G. Habib, 2013, International journal of cardiology.

Effect of CYP2C19*2 and *17 genetic variants on platelet response to clopidogrel and prasugrel maintenance dose and relation to bleeding complications.

W. Cohen, P. Morange, M. Alessi, 2013, The American journal of cardiology.

Usefulness of high clopidogrel maintenance dose according to CYP2C19 genotypes in clopidogrel low responders undergoing coronary stenting for non ST elevation acute coronary syndrome.

W. Cohen, P. Morange, M. Alessi, 2011, The American journal of cardiology.

Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles-NImes prediction model.

D. Trégouët, W. Cohen, P. Morange, 2014, Journal of thrombosis and haemostasis : JTH.

ABO Blood Group and von Willebrand Factor Levels Partially Explained the Incomplete Penetrance of Congenital Thrombophilia

D. Tregouet, W. Cohen, P. Morange, 2012, Arteriosclerosis, thrombosis, and vascular biology.

Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: The Athero Gene Study

R. Schnabel, D. Tregouet, S. Blankenberg, 2012, BMC Medical Genetics.

Brief report KNG1 Ile581Thr and susceptibility to venous thrombosis

L. Letenneur, D. Trégouët, M. Lathrop, 2011 .

Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles‐NImes prediction model

D. Trégouët, W. Cohen, P. Morange, 2014, Journal of thrombosis and haemostasis : JTH.

ANKRD26-related thrombocytopenia and myeloid malignancies.

Paola Giordano, Marco Seri, Anna Savoia, 2013, Blood.

A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential.

F. Cambien, L. Letenneur, D. Trégouët, 2014, Blood.

Non-adherence to aspirin in patients undergoing coronary stenting: negative impact of comorbid conditions and implications for clinical management.

W. Cohen, P. Carrieri, T. Cuisset, 2011, Archives of cardiovascular diseases.

Ile581Thr and susceptibility to venous thrombosis KNG1

Lorna M. Lopez, L. Letenneur, J. Lambert, 2013 .