| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Karl C Desch | |
| P2860 | cites work | Identifying novel genetic determinants of hemostatic balance | Q36230809 |
| The C-type lectin receptor CLEC4M binds, internalizes, and clears von Willebrand factor and contributes to the variation in plasma von Willebrand factor levels | Q37043558 | ||
| A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium | Q37708719 | ||
| Influence of hereditary or acquired thrombophilias on the treatment of venous thromboembolism | Q38023637 | ||
| Dysfunction of protein C anticoagulant system, main genetic risk factor for venous thromboembolism in northeast Asians | Q38162754 | ||
| The role of regulatory variation in complex traits and disease | Q38364456 | ||
| Extremely low-coverage sequencing and imputation increases power for genome-wide association studies | Q41882858 | ||
| A multi-stage multi-design strategy provides strong evidence that the BAI3 locus is associated with early-onset venous thromboembolism | Q43894795 | ||
| Influence of thrombophilia on risk of recurrent venous thromboembolism while on warfarin: results from a randomized trial | Q46368145 | ||
| The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls | Q50324464 | ||
| Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. | Q51773327 | ||
| Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project | Q57611749 | ||
| Genome-wide linkage analysis of von Willebrand factor plasma levels: results from the GAIT project | Q59590827 | ||
| CLEC4MandSTXBP5gene variations contribute to von Willebrand factor level variation in von Willebrand disease | Q62107228 | ||
| High levels of factor VIII and venous thrombosis | Q73434262 | ||
| High plasma concentration of factor VIIIc is a major risk factor for venous thromboembolism | Q73434266 | ||
| Gene variants associated with deep vein thrombosis | Q80893876 | ||
| Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels | Q24318690 | ||
| Complement factor H polymorphism in age-related macular degeneration | Q24553334 | ||
| Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C | Q24563608 | ||
| The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | Q24568334 | ||
| Genome-wide association study for circulating tissue plasminogen activator levels and functional follow-up implicates endothelial STXBP5 and STX2. | Q28658007 | ||
| 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 | Q28661433 | ||
| Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol | Q30411390 | ||
| Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation | Q30415902 | ||
| Syntaxin-binding protein STXBP5 inhibits endothelial exocytosis and promotes platelet secretion. | Q30590837 | ||
| A genome-wide search for common SNP x SNP interactions on the risk of venous thrombosis | Q31113588 | ||
| von Willebrand factor: two sides of a coin | Q33367858 | ||
| Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time | Q33772986 | ||
| Synthetic associations created by rare variants do not explain most GWAS results | Q33803707 | ||
| Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium | Q33817075 | ||
| Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia | Q34144305 | ||
| Congenital thrombophilic states associated with venous thrombosis: a qualitative overview and proposed classification system | Q34170635 | ||
| Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association | Q34319603 | ||
| Mutation in blood coagulation factor V associated with resistance to activated protein C. | Q34340007 | ||
| A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. | Q34407258 | ||
| Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study | Q34450740 | ||
| Genetic variants in PLG, LPA, and SIGLEC 14 as well as smoking contribute to plasma plasminogen levels | Q34508365 | ||
| Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis | Q35037432 | ||
| Genetic markers associated with plasma protein C level in African Americans: the atherosclerosis risk in communities (ARIC) study | Q35162846 | ||
| Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level | Q35200124 | ||
| Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism | Q35266365 | ||
| Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways | Q35624305 | ||
| Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease | Q36096131 | ||
| A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q. | Q36166323 | ||
| P433 | issue | 5 | |
| P921 | main subject | thrombosis | Q261327 |
| P304 | page(s) | 428-436 | |
| P577 | publication date | 2015-09-01 | |
| P1433 | published in | Current Opinion in Hematology | Q15757961 |
| P1476 | title | Dissecting the genetic determinants of hemostasis and thrombosis | |
| P478 | volume | 22 |
Search more.