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

Genetic Associations for Activated Partial Thromboplastin Time and Prothrombin Time, their Gene Expression Profiles, and Risk of Coronary Artery Disease

(2012) Weihong Tang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

High-throughput analysis of epistasis in genome-wide association studies with BiForce

(2012) Attila Gyenesei et al.   BIOINFORMATICS

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

(2012) Tiphaine Oudot-Mellakh et al.   BRITISH JOURNAL OF HAEMATOLOGY

Powerful Cocktail Methods for Detecting Genome-Wide Gene-Environment Interaction

(2012) Li Hsu et al.   GENETIC EPIDEMIOLOGY

Genetic variation in F3 (tissue factor) and the risk of incident venous thrombosis: meta-analysis of eight studies

(2012) N. L. SMITH et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Improved Statistics for Genome-Wide Interaction Analysis

(2012) Masao Ueki et al.   PLoS Genetics

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

(2011) Guillemette Antoni et al.   BMC Medical Genetics

Travelling the world of gene-gene interactions

(2011) K. Van Steen   BRIEFINGS IN BIOINFORMATICS

Lessons from genome-wide association studies in venous thrombosis

(2011) P. E. MORANGE et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

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

(2011) Marine Germain et al.   PLoS One

Missing heritability and strategies for finding the underlying causes of complex disease

(2010) Evan E. Eichler et al.   NATURE REVIEWS 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

Deciphering the molecular basis of venous thromboembolism: where are we and where should we go?

(2009) Pierre-Emmanuel Morange et al.   BRITISH JOURNAL OF HAEMATOLOGY

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

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

Detecting gene–gene interactions that underlie human diseases

(2009) Heather J Cordell   NATURE REVIEWS GENETICS

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

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