Multi-phenotype analyses of hemostatic traits with cardiovascular events reveal novel genetic associations.
第一作者:
Gerard,Temprano-Sagrera
第一单位:
Genomics of Complex Disease Unit, Sant Pau Biomedical Research Institute. IIB-Sant Pau, Barcelona, Spain.
作者:
医学主题词
心血管疾病(Cardiovascular Diseases);因子Ⅺ(Factor XI);疾病遗传易感性(Genetic Predisposition to Disease);全基因组关联研究(Genome-Wide Association Study);止血(Hemostasis);止血药(Hemostatics);人类(Humans);表型(Phenotype);多态性, 单核苷酸(Polymorphism, Single Nucleotide);组织型纤溶酶原激活物(Tissue Plasminogen Activator)
DOI
10.1111/jth.15698
PMID
35285134
发布时间
2025-05-30
基金项目
R01 HL139553/HL/NHLBI NIH HHS/United States
HL141291/HL/NHLBI NIH HHS/United States
HL139553/HL/NHLBI NIH HHS/United States
HL134894/HL/NHLBI NIH HHS/United States
MC_PC_17228/MRC_/Medical Research Council/United Kingdom
UM1 DK126194/DK/NIDDK NIH HHS/United States
R01 HL141291/HL/NHLBI NIH HHS/United States
IK2 CX001780/CX/CSRD VA/United States
R01 HL134894/HL/NHLBI NIH HHS/United States
MC_QA137853/MRC_/Medical Research Council/United Kingdom
- 浏览2
Journal of thrombosis and haemostasis
1331-1349页
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