Published in Circulation on April 04, 2000
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Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels. BMC Med Genet (2011) 1.02
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Functional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levels. Haematologica (2009) 0.91
Sequence variation and genetic evolution at the human F12 locus: mapping quantitative trait nucleotides that influence FXII plasma levels. Hum Mol Genet (2009) 0.89
Genetic regulation of plasma von Willebrand factor levels: quantitative trait loci analysis in a mouse model. J Thromb Haemost (2006) 0.89
A genome-wide association study of the Protein C anticoagulant pathway. PLoS One (2011) 0.85
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A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration. Hum Mol Genet (2015) 0.82
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Human F7 sequence is split into three deep clades that are related to FVII plasma levels. Hum Genet (2005) 0.80
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Combined cis-regulator elements as important mechanism affecting FXII plasma levels. Thromb Res (2009) 0.79
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Genetic determinants of variation in the plasma levels of the C4b-binding protein (C4BP) in Spanish families. Immunogenetics (2003) 0.78
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Associations of D-dimer and von Willebrand factor with atherosclerosis in Japanese and white men. Acta Cardiol (2010) 0.78
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Genetic Determinants of Thrombin Generation and Their Relation to Venous Thrombosis: Results from the GAIT-2 Project. PLoS One (2016) 0.77
Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci. PLoS One (2012) 0.77
Genetic variants associated with protein C levels. J Thromb Haemost (2013) 0.77
A quantitative trait locus on chromosome 5p influences d-dimer levels in the san antonio family heart study. Int J Vasc Med (2010) 0.76
No evidence for genome-wide interactions on plasma fibrinogen by smoking, alcohol consumption and body mass index: results from meta-analyses of 80,607 subjects. PLoS One (2014) 0.76
Interactions of established risk factors and a GWAS-based genetic risk score on the risk of venous thromboembolism. Thromb Haemost (2016) 0.76
A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study. Hum Mol Genet (2014) 0.75
Heritability of thromboxane A2 and prostaglandin E2 biosynthetic machinery in a Spanish population. Arterioscler Thromb Vasc Biol (2009) 0.75
D-Dimer in African Americans: Whole Genome Sequence Analysis and Relationship to Cardiovascular Disease Risk in the Jackson Heart Study. Arterioscler Thromb Vasc Biol (2017) 0.75
Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. Proc Natl Acad Sci U S A (2017) 0.75
Coagulation factor VIII levels are associated with long-term survival - interactions with gender in a large hospital-based cohort. Wien Klin Wochenschr (2010) 0.75
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Statistical properties of a variance components method for quantitative trait linkage analysis in nuclear families and extended pedigrees. Genet Epidemiol (1997) 2.43
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Evidence for linkage of regions on chromosomes 6 and 11 to plasma glucose concentrations in Mexican Americans. Genome Res (1996) 2.24
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A major locus for fasting insulin concentrations and insulin resistance on chromosome 6q with strong pleiotropic effects on obesity-related phenotypes in nondiabetic Mexican Americans. Am J Hum Genet (2001) 1.91
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The genetic basis of plasma variation in adiponectin, a global endophenotype for obesity and the metabolic syndrome. J Clin Endocrinol Metab (2001) 1.82
Endophenotypes as quantitative risk factors for psychiatric disease: rationale and study design. Am J Med Genet (2001) 1.78
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Genetics of microstructure of cerebral white matter using diffusion tensor imaging. Neuroimage (2010) 1.70
New rapid antigen test for diagnosis of pneumococcal meningitis. Lancet (2001) 1.70
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Familial thrombophilia and lifetime risk of venous thrombosis. J Thromb Haemost (2004) 1.44
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