Significant genetic association of a functional TFPI variant with circulating fibrinogen levels and coronary artery disease

Genomic Variant in IL-37 Confers A Significant Risk of Coronary Artery Disease

(2017) Dan Yin et al.   Scientific Reports

Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction

(2016) Shanshan Chen et al.   ATHEROSCLEROSIS

Coronary artery disease susceptibility gene ADTRP regulates cell cycle progression, proliferation, and apoptosis by global gene expression regulation

(2016) Chunyan Luo et al.   PHYSIOLOGICAL GENOMICS

Deletion of Hyaluronan Synthase 3 Inhibits Neointimal Hyperplasia in MiceSignificance

(2015) Lena S. Kiene et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration

(2015) Paul S. de Vries et al.   HUMAN MOLECULAR GENETICS

New insights into the biology of tissue factor pathway inhibitor

(2015) S. A. Maroney et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Genetic determinants of tissue factor pathway inhibitor plasma levels

(2015) Jessica Dennis et al.   THROMBOSIS AND HAEMOSTASIS

Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation

(2015) Yufeng Huang et al.   PLoS Genetics

Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population

(2015) S. Chen et al.   Journal of the American Heart Association

Common Variants in Promoter of ADTRP Associate with Early-Onset Coronary Artery Disease in a Southern Han Chinese Population

(2015) Er-Wen Huang et al.   PLoS One

A Novel Molecular Diagnostic Marker for Familial and Early-Onset Coronary Artery Disease and Myocardial Infarction in the LRP8 Gene

(2014) G.-Q. Shen et al.   Circulation-Cardiovascular Genetics

Candidate Pathway-Based Genome-Wide Association Studies Identify Novel Associations of Genomic Variants in the Complement System Associated With Coronary Artery Disease

(2014) C. Xu et al.   Circulation-Cardiovascular Genetics

The relevance of coagulation in cardiovascular disease: what do the biomarkers tell us?

(2014) Ann Rumley et al.   THROMBOSIS AND HAEMOSTASIS

The IL-33-ST2L Pathway Is Associated with Coronary Artery Disease in a Chinese Han Population

(2013) Xin Tu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease

(2013) Xiuchun Li et al.   ATHEROSCLEROSIS

Multiethnic Meta-Analysis of Genome-Wide Association Studies in >100 000 Subjects Identifies 23 Fibrinogen-Associated Loci but No Strong Evidence of a Causal Association Between Circulating Fibrinogen and Cardiovascular Disease

(2013) Maria Sabater-Lleal et al.   CIRCULATION

Association of single nucleotide polymorphism rs6903956 on chromosome 6p24.1 with coronary artery disease and lipid levels in different ethnic groups of the Singaporean population

(2013) Naeimeh Tayebi et al.   CLINICAL BIOCHEMISTRY

Multi-allelic haplotype association identifies novel information different from single-SNP analysis: A new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI

(2013) Gong-Qing Shen et al.   GENE

BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3

(2013) Xin Xiong et al.   HUMAN GENETICS

Comparison of the inhibitory activities of human tissue factor pathway inhibitor (TFPI)α and TFPIβ

(2013) S. A. Maroney et al.   JOURNAL OF THROMBOSIS AND HAEMOSTASIS

Tissue factor pathway inhibitor-alpha inhibits prothrombinase during the initiation of blood coagulation

(2013) J. P. Wood et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Genetic Variant R952Q in LRP8 is Associated with Increased Plasma Triglyceride Levels in Patients with Early-Onset CAD and MI

(2012) Gong-Qing Shen et al.   ANNALS OF HUMAN GENETICS

Association of SNP Rs6903956 on Chromosome 6p24.1 with Angiographical Characteristics of Coronary Atherosclerosis in a Chinese Population

(2012) Chang-Yan Guo et al.   PLoS One

Laboratory Investigations for Bleeding Disorders

(2012) Karen Moffat et al.   SEMINARS IN THROMBOSIS AND HEMOSTASIS

Novel protein ADTRP regulates TFPI expression and function in human endothelial cells in normal conditions and in response to androgen

(2011) C. Lupu et al.   BLOOD

Genome-wide association identifies a susceptibility locus for coronary artery disease in the Chinese Han population

(2011) Fan Wang et al.   NATURE GENETICS

Association of genomic loci from a cardiovascular gene SNP array with fibrinogen levels in European Americans and African-Americans from six cohort studies: the Candidate Gene Association Resource (CARe)

(2010) C. L. Wassel et al.   BLOOD

Association of Novel Genetic Loci With Circulating Fibrinogen Levels

(2009) Abbas Dehghan et al.   Circulation-Cardiovascular Genetics

Four SNPs on Chromosome 9p21 in a South Korean Population Implicate a Genetic Locus That Confers High Cross-Race Risk for Development of Coronary Artery Disease

(2007) Gong-Qing Shen et al.   ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY

Analysis of a T-287C polymorphism in the tissue factor pathway inhibitor gene and identification of a repressor element in the promoter

(2007) Ali Amini Nekoo et al.   THROMBOSIS RESEARCH