Genome-wide association studies identify genetic loci for low von Willebrand factor levels

CLEC4MandSTXBP5gene variations contribute to von Willebrand factor level variation in von Willebrand disease

(2015) Y. V. Sanders et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

The Ufm1 Cascade

(2014) Jens Daniel et al.   Cells

Genetic determinants of von Willebrand factor plasma levels and the risk of stroke: the Rotterdam Study

(2012) M. C. VAN SCHIE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Effect of Genetic Variation in STXBP5 and STX2 on von Willebrand Factor and Bleeding Phenotype in Type 1 von Willebrand Disease Patients

(2012) Janine E. van Loon et al.   PLoS One

Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association

(2012) K. C. Desch et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic determinants of plasma von Willebrand factor antigen levels: a target gene SNP and haplotype analysis of ARIC cohort

(2011) M. Campos et al.   BLOOD

Replication of LDL GWAs hits in PROSPER/PHASE as validation for future (pharmaco)genetic analyses

(2011) Stella Trompet et al.   BMC Medical Genetics

Genetic determinants of von Willebrand factor levels and activity in relation to the risk of cardiovascular disease: a review

(2011) M. C. VAN SCHIE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Common Variants of Large Effect in F12, KNG1, and HRG Are Associated with Activated Partial Thromboplastin Time

(2010) Lorna M. Houlihan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Variation in the von Willebrand factor gene is associated with von Willebrand factor levels and with the risk for cardiovascular disease

(2010) M. C. van Schie et al.   BLOOD

Novel Associations of Multiple Genetic Loci With Plasma Levels of Factor VII, Factor VIII, and von Willebrand Factor

(2010) Nicholas L. Smith et al.   CIRCULATION

Effect of Genetic Variations in Syntaxin-Binding Protein-5 and Syntaxin-2 on von Willebrand Factor Concentration and Cardiovascular Risk

(2010) Janine E. van Loon et al.   Circulation-Cardiovascular Genetics

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

(2009) Bruce M. Psaty et al.   Circulation-Cardiovascular Genetics

Runs of Homozygosity in European Populations

(2008) Ruth McQuillan et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Testing for association on the X chromosome

(2008) David Clayton   BIOSTATISTICS

A shorter von Willebrand factor survival in O blood group subjects explains how ABO determinants influence plasma von Willebrand factor

(2008) L. Gallinaro et al.   BLOOD

Von Willebrand Factor in Cardiovascular Disease

(2008) Alexander O. Spiel et al.   CIRCULATION

The ligand-binding profile of HARE: hyaluronan and chondroitin sulfates A, C, and D bind to overlapping sites distinct from the sites for heparin, acetylated low-density lipoprotein, dermatan sulfate, and CS-E

(2008) E. N. Harris et al.   GLYCOBIOLOGY

von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA)

(2008) W. L. NICHOLS et al.   HAEMOPHILIA

Novel Association of ABO Histo-Blood Group Antigen with Soluble ICAM-1: Results of a Genome-Wide Association Study of 6,578 Women

(2008) Guillaume Paré et al.   PLoS Genetics