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

KNG1 Ile581Thr and susceptibility to venous thrombosis

(2011) P.-E. Morange et al.   BLOOD

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease

(2011) John F Peden et al.   NATURE GENETICS

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

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1

(2010) Pierre-Emmanuel Morange et al.   AMERICAN JOURNAL OF HUMAN GENETICS

GCTA: A Tool for Genome-wide Complex Trait Analysis

(2010) Jian Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Venous Thromboembolism

(2010) Michele G. Beckman et al.   AMERICAN JOURNAL OF PREVENTIVE MEDICINE

Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis

(2010) N. L. Smith et al.   BLOOD

Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study

(2010) W. Tang et al.   BLOOD

C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies

(2010) A. Buil 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

Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23

(2010) J. Erdmann et al.   EUROPEAN HEART JOURNAL

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

(2010) G. ANTONI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

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

(2010) P.-E. MORANGE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Common SNPs explain a large proportion of the heritability for human height

(2010) Jian Yang et al.   NATURE GENETICS

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach

(2009) D.-A. Tregouet et al.   BLOOD

Genetic variants associated with deep vein thrombosis: theF11locus

(2009) Y. LI et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Genetics of venous thrombosis

(2009) F. R. ROSENDAAL et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

New susceptibility locus for coronary artery disease on chromosome 3q22.3

(2009) Jeanette Erdmann et al.   NATURE GENETICS

Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease

(2009) David-Alexandre Trégouët et al.   NATURE GENETICS

Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants

(2009) Sekar Kathiresan et al.   NATURE GENETICS

Genomewide Association Studies of Stroke

(2009) M. Arfan Ikram et al.   NEW ENGLAND JOURNAL OF MEDICINE

SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap

(2008) A. D. Johnson et al.   BIOINFORMATICS

Gene Variants Associated With Deep Vein Thrombosis

(2008) Irene D. Bezemer   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION