Genetic variation of the blood coagulation regulator tissue factor pathway inhibitor and venous thromboembolism among middle‐aged and older adults: A population‐based cohort study - Manderstedt, Eric; Lind‐Halldén, Christina; Halldén, Christer; Elf, Johan; Svensson, Peter J.; Engström, Gunnar; Melander, Olle; Baras, Aris; Lotta, Luca A.; Zöller, Bengt; Abecasis, Goncalo; Baras, Aris; et al. (Research and practice in thrombosis and haemostasis, 2022)
Keywords: adult; Anticoagulants; Basic Medicine; blood clotting; blood coagulation; Brief Report; Brief Reports; Cardiac and Cardiovascular Systems; Cardiology and Cardiovascular Disease; Clinical Medicine; Cohort analysis; deep vein thrombosis; exosome; female; Gene expression; gene frequency; gene mutation; genetic analysis; genetic screening; genetic variation; Genomes; haplotype; Hematologi; Hematology; human; ICD-10; ICD-9; Kardiologi; Kardiologi och kardiovaskulära sjukdomar; Klinisk medicin; loss of function mutation; major clinical study; male; Medical and Health Sciences; Medical Genetics; Medical Genetics and Genomics (including Gene Therapy); Medicin och hälsovetenskap; Medicinsk genetik; Medicinsk genetik och genomik (Här ingår: Genterapi); Medicinska och farmaceutiska grundvetenskaper; missense mutation; molecular epidemiology; Older people; Population; Population-based studies; principal component analysis; single nucleotide polymorphism; Thromboembolism; thrombophilia; thrombophlebitis; Thrombosis; tissue factor pathway inhibitor; vein thrombosis; Veins & arteries; venous thromboembolism; whole exome sequencing; Sweden; molecular epidemiology; thrombophilia; genetic variation; blood coagulation; venous thromboembolism