Associated Papers
Impact of nonsynonymous single nucleotide polymorphisms in PROCR gene on protein stability and thrombotic risk: a molecular dynamic approach.
Abuagla HA et al.
Frontiers in Genetics, 2025
40370698 (PubMed )
Supplement: DataSheet1.pdf
EPCR Gene Ser219Gly Polymorphism and Venous Thromboembolism: A Meta-Analysis of 9,494 Subjects.
Li YY et al.
Frontiers in Physiology, 2017
Common genetic risk factors of venous thromboembolism in Western and Asian populations.
Huang SS et al.
Genetics and Molecular Research : Gmr, 2016
Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
Patil A et al.
Annals of Hematology, 2013
Endothelial cell protein C receptor gene 6936A/G polymorphism is associated with venous thromboembolism.
Yin G et al.
Experimental and Therapeutic Medicine, 2012
Genetic cardiovascular risk factors and age-related macular degeneration.
Haas P et al.
Acta Ophthalmologica, 2011
Congenital thrombotic risk factors in beta-thalassemia.
Sipahi T et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2009
Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
Shetty S et al.
European Journal of Haematology, 2008
Clinical applications of bioinformatics, genomics, and pharmacogenomics.
Iqbal O et al.
Methods in Molecular Biology (clifton, N.j.), 2006
Genetic susceptibility to venous thrombosis.
Seligsohn U et al.
The New England Journal of Medicine, 2001
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