Associated Papers
Beyond CYP2C19: inflammation and angiogenesis gene variants drive clopidogrel resistance in CAD patients.
Hajer F et al.
Inflammation Research : Official Journal of the European Histamine Research Society ... [et Al.], 2025
Genetics of ischemic stroke functional outcome.
Carnwath TP et al.
Journal of Neurology, 2024
Association of KDR (rs2071559, rs1870377), CFH (rs1061170, rs1410996) genes variants and serum levels with pituitary adenoma.
Bruzaite A et al.
Molecular Genetics & Genomic Medicine, 2024
Association of single nucleotide variants in VEGFA and KDR with the risk and angiogenic features of diffuse large B-cell lymphoma.
Assis-Mendonça GR et al.
Leukemia & Lymphoma, 2023
Genetic polymorphisms in VEGFA and VEGFR2 genes associated with coronary heart disease susceptibility and severity.
Hajer F et al.
Molecular Biology Reports, 2023
Analysis of endothelial gene polymorphisms in Spanish patients with vascular dementia and Alzheimer´s disease.
Manso-Calderón R et al.
Scientific Reports, 2023
Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.
Shi M et al.
Journal of the American Heart Association, 2022
KDR polymorphism (1192G/A, 1719A/T) and modulation of ARV drug-induced hepatotoxicity.
Singh H et al.
Microbial Pathogenesis, 2021
Missense Variants in Hypoxia-Induced VEGFA/VEGFR2 Signaling Predict the Outcome of Large Artery Atherosclerotic Stroke.
Li Z et al.
Cellular and Molecular Neurobiology, 2021
Angiogenesis' related genetic variants alter clinical features and prognosis of diffuse large B-cell lymphoma patients.
Brito ABC et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2021
Germline Genetic Variants of the Renin-Angiotensin System, Hypoxia and Angiogenesis in Non-Small Cell Lung Cancer Progression: Discovery and Validation Studies.
Catarata MJ et al.
Cancers, 2020
A meta-analysis of the relationship between VEGFR2 polymorphisms and atherosclerotic cardiovascular diseases.
Wang L et al.
Clinical Cardiology, 2019
Associations of VEGFA and KDR single-nucleotide polymorphisms and increased risk and aggressiveness of high-grade gliomas.
Vasconcelos VCA et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine, 2019
Effect of gene-gene and gene-environment interaction on the risk of first-ever stroke and poststroke death.
Feng C et al.
Molecular Genetics & Genomic Medicine, 2019
The association of Q472H variant in the KDR gene with recurrent pregnancy loss in Southern Iran: A case-control study.
Keshavarz L et al.
International Journal of Reproductive Biomedicine, 2019
Investigation of angiogenesis genes with anterior cruciate ligament rupture risk in a South African population.
Rahim M et al.
Journal of Sports Sciences, 2018
Genetic and epigenetic variations associated with idiopathic recurrent pregnancy loss.
Arias-Sosa LA et al.
Journal of Assisted Reproduction and Genetics, 2018
KDR gene polymorphisms and idiopathic recurrent spontaneous abortion.
Honarvar N et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2016
VEGFR2 Gene Polymorphism Correlates with Deep Venous Thrombosis Risk in Chinese Han Population.
Wang X et al.
Genetic Testing and Molecular Biomarkers, 2015
Association of kinase insert domain-containing receptor (KDR) gene polymorphism/ haplotypes with recurrent spontaneous abortion and genetic structure.
Shahsavari S et al.
International Journal of Reproductive Biomedicine, 2015
Discovery and validation of vascular endothelial growth factor (VEGF) pathway polymorphisms in esophageal adenocarcinoma outcome.
Eng L et al.
Carcinogenesis, 2015
Clinical relevance of vascular endothelial growth factor type A (VEGFA) and VEGF receptor type 2 (VEGFR2) gene polymorphism in chronic lymphocytic leukemia.
Góra-Tybor J et al.
Blood Cells, Molecules & Diseases, 2015
Association of kinase insert domain-containing receptor (KDR) gene polymorphisms with idiopathic recurrent spontaneous abortion in Korean women.
Rah H et al.
Fertility and Sterility, 2013
Increased risk of ovarian hyperstimulation syndrome following controlled ovarian hyperstimulation in patients with vascular endothelial growth factor +405 cc genotype.
Hanevik HI et al.
Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2012
Vascular endothelial growth factor pathway polymorphisms as prognostic and pharmacogenetic factors in cancer: a systematic review and meta-analysis.
Eng L et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research, 2012
Association between kinase insert domain-containing receptor polymorphisms (-604T>C, 1192G>A, 1719A>T) and premature ovarian failure in Korean women.
Rah H et al.
Menopause (new York, N.y.), 2012
Association between kinase insert domain-containing receptor gene polymorphisms and silent brain infarction: a Korean study.
Han IB et al.
Journal of the Neurological Sciences, 2012
Potentially functional genetic variants in KDR gene as prognostic markers in patients with resected colorectal cancer.
Dong G et al.
Cancer Science, 2012
Influence of pharmacogenetic variability on the pharmacokinetics and toxicity of the aurora kinase inhibitor danusertib.
Steeghs N et al.
Investigational New Drugs, 2011
Association between kinase insert domain-containing receptor gene polymorphism and haplotypes and ischemic stroke.
Oh SH et al.
Journal of the Neurological Sciences, 2011
Pharmacogenetic interaction analysis for the efficacy of systemic treatment in metastatic colorectal cancer.
Pander J et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology, 2011
Pharmacogenetics of telatinib, a VEGFR-2 and VEGFR-3 tyrosine kinase inhibitor, used in patients with solid tumors.
Steeghs N et al.
Investigational New Drugs, 2011
Genes of Inflammation and Placental Function GWAS Associated with Idiopathic Recurrent Miscarriage in the Kazakh Population.
Murtazaliyeva A et al.
Journal of Human Reproductive Sciences, 0