human | Q5 |
P496 | ORCID iD | 0000-0002-8365-7731 |
P69 | educated at | Aix-Marseille University Faculty of Sciences | Q3064322 |
P108 | employer | Assistance Publique-Hôpitaux de Marseille | Q15974693 |
P106 | occupation | researcher | Q1650915 |
Q57611776 | A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1 |
Q33772964 | A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1. |
Q43719755 | A meta-analysis of genome-wide association studies identifies ORM1 as a novel gene controlling thrombin generation potential. |
Q34471057 | Association of soluble endothelial protein C receptor plasma levels and PROCR rs867186 with cardiovascular risk factors and cardiovascular events in coronary artery disease patients: the Athero Gene study |
Q33931897 | C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies |
Q28728919 | Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis |
Q51773327 | Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. |
Q28744518 | Genetics of venous thrombosis: insights from a new genome wide association study |
Q57611749 | Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project |
Q57611683 | Human thymopoiesis is influenced by a common genetic variant within the TCRA-TCRD locus |
Q57605719 | KNG1 Ile581Thr and susceptibility to venous thrombosis |
Q35266365 | Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism |