Associated Papers
Impact of Apolipoprotein E Variants: A Review of Naturally Occurring Variants and Clinical Features.
Matsunaga A et al.
Journal of Atherosclerosis and Thrombosis, 2025
Inherited Thrombophilia Associated With Ischemic Pediatric Stroke in Parent-Child Pairs.
Krleza JL et al.
Pediatric Neurology, 2023
Genetics of Alzheimer's disease: an East Asian perspective.
Miyashita A et al.
Journal of Human Genetics, 2023
Impact of pharmacogenetics on aspirin resistance: a systematic review.
Silva GFD et al.
Arquivos De Neuro-psiquiatria, 2023
Lysine acetylation regulates the interaction between proteins and membranes.
Okada AK et al.
Nature Communications, 2021
Genetic polymorphisms in early-onset myocardial infarction in a sample of Iraqi patients: a pilot study.
Mohammad AM et al.
Bmc Research Notes, 2020
Global genetic diversity of human apolipoproteins and effects on cardiovascular disease risk.
Zhou Y et al.
Journal of Lipid Research, 2018
Association of Polymorphisms in Coagulation Factor Genes and Enzymes of Homocysteine Metabolism With Arterial Ischemic Stroke in Children.
Coen Herak D et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2017
Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.
Fawzy MS et al.
Bmc Cardiovascular Disorders, 2017
Genetic association between FXIII and β-fibrinogen genes and women with recurrent spontaneous abortion: a meta- analysis.
Li J et al.
Journal of Assisted Reproduction and Genetics, 2015
Clinical proteome informatics workbench detects pathogenic mutations in hereditary amyloidoses.
Dasari S et al.
Journal of Proteome Research, 2014
Apolipoprotein E (Apo E) gene polymorphisms and recurrent pregnancy loss: a meta-analysis.
Li J et al.
Journal of Assisted Reproduction and Genetics, 2014
Prevalence of myocardial infarction polymorphisms in Afyonkarahisar, Western Turkey.
Onrat ST et al.
Molecular Biology Reports, 2012
Screening and Evaluation of Deleterious SNPs in APOE Gene of Alzheimer's Disease.
Masoodi TA et al.
Neurology Research International, 2012
A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
Yenicesu GI et al.
American Journal of Reproductive Immunology (new York, N.y. : 1989), 2010
Frequency distribution of the G/A alleles of the beta-fibrinogen gene in the Lebanese population.
Shammaa DM et al.
Molecular Biology Reports, 2008
Combined effect of hemostatic gene polymorphisms and the risk of myocardial infarction in patients with advanced coronary atherosclerosis.
Martinelli N et al.
Plos One, 2008
Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis.
Banerjee I et al.
Journal of Human Genetics, 2007
Genetic factors contribute to bleeding after cardiac surgery.
Welsby IJ et al.
Journal of Thrombosis and Haemostasis : Jth, 2005
Fibrinogen gene promoter -455 A allele as a risk factor for lacunar stroke.
Martiskainen M et al.
Stroke, 2003
[APOC3, CETP, beta-fibrinogen and MTHFR are genetic determinants of carotid intim-media thickness (Stanislas cohort)].
Pallaud C et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux, 2001
APOC3, CETP, fibrinogen, and MTHFR are genetic determinants of carotid intima-media thickness in healthy men (the Stanislas cohort).
Pallaud C et al.
Clinical Genetics, 2001
Fibrinogen polymorphisms and atherothrombotic disease.
Green FR
Annals of the New York Academy of Sciences, 2001
Two common, functional polymorphisms in the promoter region of the beta-fibrinogen gene contribute to regulation of plasma fibrinogen concentration.
van 't Hooft FM et al.
Arteriosclerosis, Thrombosis, and Vascular Biology, 1999
Molecular assessment of some cardiovascular genetic risk factors among Iraqi patients with ischemic heart diseases.
Mohammed WJ et al.
International Journal of Health Sciences, 0