SNP information rs501120

Research and publications:

  17634449   Genomewide association analysis of coronary artery disease.

  18780302   Association studies of 22 candidate SNPs with late-onset Alzheimer's disease.

  18979498   The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.

  19164808   Large scale association analysis of novel genetic loci for coronary artery disease.

  19207022   Genome-wide association studies of coronary artery disease and heart failure: where are we going?

  19501493   A composite scoring of genotypes discriminates coronary heart disease risk beyond conventional risk factors in the Boston Puerto Rican Health Study

  19750184   Genome-wide association studies for atherosclerotic vascular disease and its risk factors.

  19955471   Genetic variants identified in a European genome-wide association study that were found to predict incident coronary heart disease in the atherosclerosis risk in communities study.

  19956433   Genetics of coronary artery disease: focus on genome-wide association studies.

  20017983   Evaluation of population impact of candidate polymorphisms for coronary heart disease in the Framingham Heart Study Offspring Cohort.

  20098575   Genetics and cardiovascular disease: Design and development of a DNA biobank.

  20440292   Early identification of cardiovascular risk using genomics and proteomics.

  20694560   Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans.

  20847302   Coronary artery disease-related genetic variant on chromosome 10q11 is associated with carotid intima-media thickness and atherosclerosis.

  20981302   Genome-wide association study of coronary artery disease.

  21242481   Genetic risk score and risk of myocardial infarction in Hispanics.

  21369780   Genome-wide association studies in atherosclerosis.

  21415067   The novel atherosclerosis locus at 10q11 regulates plasma CXCL12 levels.

  21463265   Association of SNP rs17465637 on chromosome 1q41 and rs599839 on 1p13.3 with myocardial infarction in an American caucasian population.

  21698238   Replication of putative susceptibility loci from genome-wide association studies associated with coronary atherosclerosis in Chinese Han population.

  21804106   Comparative analysis of genome-wide association studies signals for lipids, diabetes, and coronary heart disease: Cardiovascular Biomarker Genetics Collaboration.

  21860704   Implications of discoveries from genome-wide association studies in current cardiovascular practice.

  22042884   Association of genetic variants and incident coronary heart disease in multiethnic cohorts: the PAGE study.

  22151179   Genotype-informed estimation of risk of coronary heart disease based on genome-wide association data linked to the electronic medical record.

  22295058   Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Surv

  22386691   Lack of association between the CXCL12 rs501120 polymorphism and cardiovascular disease in Spanish patients with rheumatoid arthritis.

  22807925   Touch of chemokines.

  22848412   Genetic markers enhance coronary risk prediction in men: the MORGAM prospective cohorts.

  22927710   Genetic markers of cardiovascular disease in rheumatoid arthritis.

  23666823   Genetic variants on chromosome 10q11.21 are associated with ischemic stroke in the northern Chinese Han population.

  25542012   Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

  26847647   Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

  26892960   From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

  26950853   Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

  26958643   Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.

  28686695   Coronary artery disease-associated genetic variants and biomarkers of inflammation.

  28777867   [Association of endotheline receptor gene rs1878406 polymorphism with severe multi-vessel coronary disease].

  29695241   Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

  30764545   Common Polymorphisms Linked to Obesity and Cardiovascular Disease in Europeans and Asians are Associated with Type 2 Diabetes in Mexican Mestizos.

  31804579   The Mediterranean diet reduces the genetic risk of chromosome 9p21 for myocardial infarction in an Asian population community cohort.

  31862910   The CXCL12 SNPs and their haplotypes are associated with serum lipid traits.

  32604426   The ABO Locus is Associated with Increased Fibrin Network Formation in Patients with Stable Coronary Artery Disease.

  32858814   Association of the PSRC1 rs599839 Variant with Coronary Artery Disease in a Mexican Population.