Associated Papers
PON1, APOE and SDF-1 Gene Polymorphisms and Risk of Retinal Vein Occlusion: A Case-Control Study.
Ragkousis A et al.
Genes, 2024
Impact of pharmacogenetics on aspirin resistance: a systematic review.
Silva GFD et al.
Arquivos De Neuro-psiquiatria, 2023
Association of BglII Polymorphism in ITGA2 and (894G/T and -786T/C) Polymorphisms in eNOS Gene With Stroke Susceptibility in Tunisian Patients α2 Gene Polymorphism in α2β1 Integrin and eNOS Gene Variants and Stroke.
Jalel A et al.
Biological Research for Nursing, 2021
CENTRAL RETINAL VEIN OCCLUSION IN OTHERWISE HEALTHY CHILDREN AND ADOLESCENTS: Association With Multigenetic Variants of Thrombophilia.
Bremond-Gignac D et al.
Retina (philadelphia, Pa.), 2020
Integrin ß1 polymorphisms and bleeding risk after coronary artery stenting.
Thienel M et al.
Molecular Biology Reports, 2019
Genetic polymorphisms associated with the prevalence of retinal vein occlusion in a Greek population.
Christodoulou A et al.
International Ophthalmology, 2019
Association of GPIa and COX-2 gene polymorphism with aspirin resistance.
Wang H et al.
Journal of Clinical Laboratory Analysis, 2018
Association between platelet glycoprotein Ia C807T gene polymorphism and ischemic stroke: a meta-analysis in a separate ethnic group.
Huang XY et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2017
Association between C807T(C/T) polymorphism of platelet glycoprotein gene and sensitivity to ischemic stroke: a meta-analysis.
Luo C et al.
Genetics and Molecular Research : Gmr, 2017
Platelet glycoprotein gene Ia C807T, HPA-3, and Ibα VNTR polymorphisms are associated with increased ischemic stroke risk: Evidence from a comprehensive meta-analysis.
Liu H et al.
International Journal of Stroke : Official Journal of the International Stroke Society, 2017
Platelet response to a small molecule inhibitor of α2β1 integrin is associated with ITGA2 C807T dimorphism.
Nissinen L et al.
Platelets, 2016
Association of CVD candidate gene polymorphisms with ischemic stroke and cerebral hemorrhage in Chinese individuals.
Ou W et al.
Plos One, 2014
Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: a case control study of genetic factors.
Gupta T et al.
American Journal of Medical Genetics. Part A, 2013
Gene polymorphisms contributing to hypertension in immunoglobulin A nephropathy.
Shinzawa M et al.
Clinical and Experimental Nephrology, 2012
Predictive role of multilocus genetic polymorphisms in cardiovascular disease and inflammation-related genes on chronic kidney disease in Type 2 diabetes--an 8-year prospective cohort analysis of 1163 patients.
Wang Y et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2012
Platelet receptor gain-of-function single nucleotide polymorphisms in carotid and vertebral stenosis patients.
Lugli AK et al.
Journal of Thrombosis and Thrombolysis, 2011
Predictive role of polymorphisms in interleukin-5 receptor alpha-subunit, lipoprotein lipase, integrin A2 and nitric oxide synthase genes on ischemic stroke in type 2 diabetes--an 8-year prospective cohort analysis of 1327 Chinese patients.
Luk AO et al.
Atherosclerosis, 2011
Platelet polymorphisms: frequency distribution and association with coronary artery disease in an Indian population.
Ashavaid TF et al.
Platelets, 2011
Functional effect of platelet membrane glycoprotein ia gene polymorphism in the pathogenesis of unstable angina pectoris.
Zhao YH et al.
The Journal of International Medical Research, 2011
Enzymes that hydrolyze adenine nucleotides in platelets and polymorphisms in the alpha2 gene of integrin alpha2beta1 in patients with von Willebrand disease.
Santos KF et al.
Molecular and Cellular Biochemistry, 2010
Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
Kuehl K et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2010
Adrenergic beta-1 receptor genetic variation predicts longitudinal rate of GFR decline in hypertensive nephrosclerosis.
Fung MM et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association, 2009
Pharmacogenetics in cardiovascular antithrombotic therapy.
Marín F et al.
Journal of the American College of Cardiology, 2009
Identification of a prostate cancer susceptibility gene on chromosome 5p13q12 associated with risk of both familial and sporadic disease.
FitzGerald LM et al.
European Journal of Human Genetics : Ejhg, 2009
A meta-analysis of candidate gene polymorphisms and ischemic stroke in 6 study populations: association of lymphotoxin-alpha in nonhypertensive patients.
Wang X et al.
Stroke, 2009
Genetic polymorphisms for the study of multifactorial stroke.
Bersano A et al.
Human Mutation, 2008
Effects of interacting networks of cardiovascular risk genes on the risk of type 2 diabetes mellitus (the CODAM study).
van Greevenbroek MM et al.
Bmc Medical Genetics, 2008
Review on genetic variants and maternal smoking in the etiology of oral clefts and other birth defects.
Shi M et al.
Birth Defects Research. Part C, Embryo Today : Reviews, 2008
Pharmacogenomics in acute coronary syndrome.
Remmler C et al.
Expert Opinion on Pharmacotherapy, 2008
Role of glycoprotein Ia gene polymorphisms in determining platelet function in myocardial infarction patients undergoing percutaneous coronary intervention on dual antiplatelet treatment.
Giusti B et al.
Atherosclerosis, 2008
Association of integrin alpha2 gene variants with ischemic stroke.
Matarin M et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism, 2008
807C/T polymorphism in platelet glycoprotein Ia gene is not associated with retinal vein occlusion.
Gadelha T et al.
Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, 2007
Association between 49 infant gene polymorphisms and preterm delivery.
Chen BH et al.
American Journal of Medical Genetics. Part A, 2007
The glu298asp polymorphism in the nitric oxide synthase 3 gene is associated with the risk of ischemic stroke in two large independent case-control studies.
Berger K et al.
Human Genetics, 2007
Platelet glycoprotein Ia 807C/T and 873G/A polymorphisms in patients with venous thromboembolism.
Okumus G et al.
Clinical and Applied Thrombosis/hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/hemostasis, 2007
Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory response, and blood pressure regulation.
Carmichael SL et al.
American Journal of Medical Genetics. Part A, 2006
Candidate gene polymorphisms do not differ between newborns with stroke and normal controls.
Miller SP et al.
Stroke, 2006
Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis.
Torfs CP et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2006
Differential expression of platelet glycoprotein Ia/IIa in Taiwan Chinese corresponds to glycoprotein ia gene polymorphisms.
Liu CZ et al.
Journal of Pharmacological Sciences, 2006
Multi-locus candidate gene polymorphisms and risk of myocardial infarction: a population-based, prospective genetic analysis.
Zee RY et al.
Journal of Thrombosis and Haemostasis : Jth, 2006
Assessment of the role of genetic polymorphism in venous thrombosis through artificial neural networks.
Penco S et al.
Annals of Human Genetics, 2005
Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
Shaw GM et al.
American Journal of Medical Genetics. Part A, 2005
Glycoprotein Ia 807TT/873AA genotype is not associated with myocardial infarction.
Kömürcü E et al.
Anadolu Kardiyoloji Dergisi : Akd = the Anatolian Journal of Cardiology, 2005
The prevalence of C807T mutation of glycoprotein Ia gene among young male survivors of myocardial infarction: a relation with coronary angiography results.
Lewandowski K et al.
Kardiologia Polska, 2005
Association of the gene polymorphisms of platelet glycoprotein Ia and IIb/IIIa with myocardial infarction and extent of coronary artery disease in the Korean population.
Park S et al.
Yonsei Medical Journal, 2004
Platelet GPIaC807T polymorphism is associated with negative outcome of sudden hearing loss.
Rudack C et al.
Hearing Research, 2004
Ethnic differences in the linkage disequilibrium and distribution of single-nucleotide polymorphisms in 35 candidate genes for cardiovascular diseases.
Ng MC et al.
Genomics, 2004
Gene interactions and stroke risk in children with sickle cell anemia.
Hoppe C et al.
Blood, 2004