,
, Tr egou? et
, Torrance
Mechanistic view of risk factors for venous thromboembolism, Arterioscler Thromb Vasc Biol, vol.32, pp.563-571, 2012. ,
Longitudinal analysis of hemostasis biomarkers in cancer patients during antitumor treatment, J Thromb Haemost, vol.14, pp.294-305, 2016. ,
Thrombin activatable fibrinolysis inhibitor and the risk for deep vein thrombosis, Blood, vol.95, pp.2855-2864, 2000. ,
Venous thrombosis risk associated with plasma hypofibrinolysis is explained by elevated plasma levels of TAFI and PAI-1, Blood, vol.116, pp.113-134, 2010. ,
Coagulation factors, inflammation markers, and venous thromboembolism: the longitudinal investigation of thromboembolism etiology (LITE), Am J Med, vol.113, pp.636-678, 2002. ,
Coagulation factors IX through XIII and the risk of future venous thrombosis: the Longitudinal Investigation of Thromboembolism Etiology, Blood, vol.114, pp.2878-83, 2009. ,
Mean platelet volume is a risk factor for venous thromboembolism: the Tromsø Study, J Thromb Haemost, vol.8, pp.157-62, 2010. ,
Platelet function as a risk factor for venous thromboembolism in the Framingham Heart Study, Thromb Res, vol.151, pp.57-62, 2017. ,
Genetics of venous thrombosis, J Thromb Haemost, vol.7, pp.301-305, 2009. ,
The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies, Hum Genet, vol.136, pp.665-77, 2017. ,
Meta-analysis of 65 734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism, Am J Hum Genet, vol.96, pp.532-574, 2015. ,
URL : https://hal.archives-ouvertes.fr/hal-01259946
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis, METASTROKE Consortium, INVENT Consortium, Sabater-Lleal M, vol.25, pp.1867-74, 2016. ,
A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1, Am J Hum Genet, vol.86, pp.592-597, 2010. ,
URL : https://hal.archives-ouvertes.fr/hal-00930143
Genetic susceptibility to thrombosis and its relationship to physiological risk factors: the GAIT study. Genetic Analysis of Idiopathic Thrombophilia, Am J Hum Genet, vol.67, pp.1452-1461, 2000. ,
Christensen K. Major genetic susceptibility for venous thromboembolism in men: a study of Danish twins, Epidemiology, vol.14, issue.3, pp.328-360, 2003. ,
Familial segregation of venous thromboembolism, J Thromb Haemost, vol.2, pp.731-737, 2004. ,
Genetics of venous thrombosis: insights from a new genome wide association study, PLoS ONE, vol.6, p.25581, 2011. ,
The value of family history as a risk indicator for venous thrombosis, Arch Intern Med, vol.169, issue.6, pp.610-625, 2009. ,
Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis, J Thromb Haemost, vol.11, pp.1228-1267, 2013. ,
Malignancies, prothrombotic mutations, and the risk of venous thrombosis, JAMA, vol.293, pp.715-737, 2005. ,
The risk of a first and a recurrent venous thrombosis associated with an elevated D-dimer level and an elevated thrombin potential: results of the THE-VTE study, J Thromb Haemost, vol.13, pp.1642-52, 2015. ,
A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders, Blood, vol.127, pp.2791-803, 2016. ,
URL : https://hal.archives-ouvertes.fr/hal-01478129
Predictive value of factor VIII levels for recurrent venous thrombosis: results from the MEGA follow-up study, J Thromb Haemost, vol.13, pp.1823-1855, 2015. ,
The human genome browser at UCSC ,
, Genome Res, vol.12, pp.996-1006, 2002.
Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline, BMC Bioinformatics, vol.15, p.30, 2014. ,
Fast and accurate short read alignment with Burrows-Wheeler transform, Bioinformatics, vol.25, pp.1754-60, 2009. ,
Durbin R; 1000 Genome Project Data Processing Subgroup. The Sequence Alignment/Map format and SAMtools, Bioinformatics, vol.25, pp.2078-2087, 2009. ,
A framework for variation discovery and genotyping using next-generation DNA sequencing data, Nat Genet, vol.43, pp.491-499, 2011. ,
An integrative variant analysis suite for whole exome next-generation sequencing data, BMC Bioinformatics, vol.13, p.8, 2012. ,
Durbin R; 1000 Genomes Project Analysis Group. The variant call format and VCFtools, Bioinformatics, vol.27, pp.2156-2164, 2011. ,
PLINK: a tool set for whole-genome association and population-based linkage analyses, Am J Hum Genet, vol.81, pp.559-75, 2007. ,
A global reference for human genetic variation, Nature, vol.526, pp.68-74, 2015. ,
Rare-variant association testing for sequencing data with the sequence kernel association test, Am J Hum Genet, vol.89, pp.82-93, 2011. ,
Genetic variants associated with deep vein thrombosis: the F11 locus, J Thromb Haemost, vol.7, pp.1802-1810, 2009. ,
Gene variants associated with deep vein thrombosis, JAMA, vol.299, pp.1306-1320, 2008. ,
A new type of plasma prekallikrein deficiency associated with homozygosity for Gly104Arg and Asn124Ser in apple domain 2 of the heavy-chain region, Eur J Haematol, vol.79, pp.59-68, 2007. ,
Genetic variation in the fibrinogen gamma gene increases the risk for deep venous thrombosis by reducing plasma fibrinogen gamma' levels, Blood, vol.106, pp.4176-83, 2005. ,
Assessment of genetic determinants of the association of c' fibrinogen in relation to cardiovascular disease, Arterioscler Thromb Vasc Biol, vol.31, pp.2345-52, 2011. ,
Association of genetic variations with nonfatal venous thrombosis in postmenopausal women, JAMA, vol.297, pp.489-98, 2007. ,
Multiple roles of complement MASP-1 at the interface of innate immune response and coagulation, Mol Immunol, vol.61, pp.69-78, 2014. ,
Effects of MASP-1 of the complement system on activation of coagulation factors and plasma clot formation, PLoS ONE, vol.7, p.35690, 2012. ,
The lectin complement pathway serine proteases (MASPs) represent a possible crossroad between the coagulation and complement systems in thromboinflammation, J Thromb Haemost, vol.14, pp.531-576, 2016. ,
The natural history of homocystinuria due to cystathionine b-synthase deficiency, Am J Hum Genet, vol.37, pp.1-31, 1997. ,
Hollenberg MD. Kallikrein-mediated cell signalling: targeting proteinase-activated receptors (PARs), Biol Chem, vol.387, pp.817-841, 2006. ,
Resistance to activated protein C in an unselected population of patients with pulmonary embolism, Lancet, vol.347, pp.1374-1379, 1996. ,
The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease, PLoS Genet, vol.11, p.1005165, 2015. ,
Incorporating non-coding annotations into rare variant analysis, PLoS ONE, vol.11, p.154181, 2016. ,