SNP information rs1746048

Research and publications:

  19198609   Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

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

  20440292   Early identification of cardiovascular risk using genomics and proteomics.

  20729558   Improved prediction of cardiovascular disease based on a panel of single nucleotide polymorphisms identified through genome-wide association studies.

  20835900   Genetics of diabetes complications.

  20971364   A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.

  21239051   Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.

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

  21369780   Genome-wide association studies in atherosclerosis.

  21378990   Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

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

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

  21875899   Thirty-five common variants for coronary artery disease: the fruits of much collaborative labour.

  22144573   Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction.

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

  22152955   Genetic susceptibility to coronary heart disease in type 2 diabetes: 3 independent studies.

  22216278   Large scale association analysis identifies three susceptibility loci for coronary artery disease.

  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

  22363065   Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?

  22429504   Genetic predisposition to coronary heart disease and stroke using an additive genetic risk score: a population-based study in Greece.

  22588700   Genetics of coronary artery disease in the 21st century.

  22807925   Touch of chemokines.

  22882272   Genetic variants associated with myocardial infarction in the PSMA6 gene and Chr9p21 are also associated with ischaemic stroke.

  23468967   Improvement in prediction of coronary heart disease risk over conventional risk factors using SNPs identified in genome-wide association studies.

  23531450   Relationship between chemokine (C-X-C motif) ligand 12 gene variant (rs1746048) and coronary heart disease: case-control study and meta-analysis.

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

  24475106   Genetic variants associated with myocardial infarction and the risk factors in Chinese population.

  24725463   Analysis of common and coding variants with cardiovascular disease in the Diabetes Heart Study.

  24932356   Genetics of coronary artery disease: an update.

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

  25804320   Association Between Coronary Artery Disease Genetic Variants and Subclinical Atherosclerosis: An Association Study and Meta-analysis.

  26324845   Association of chemokine CXC ligand 12 gene polymorphism (rs1746048) with cardiovascular mortality in patients with rheumatoid arthritis: results from the Norfolk Arthritis Register.

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

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

  26971241   Influence of Genetic Risk Factors on Coronary Heart Disease Occurrence in Afro-Caribbeans.

  27189168   The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

  27294088   Genetics of the acute coronary syndrome.

  27461004   Association of six CpG-SNPs in the inflammation-related genes with coronary heart disease.

  27716211   A 19-SNP coronary heart disease gene score profile in subjects with type 2 diabetes: the coronary heart disease risk in type 2 diabetes (CoRDia study) study baseline characteristics.

  27888760   Relationship between selected DNA polymorphisms and coronary artery disease complications.

  28138111   Association of CDKN2B-AS1 rs1333049 with Brain Diseases: A Case-control Study and a Meta-analysis.

  28167353   Genetic risk analysis of coronary artery disease in Pakistani subjects using a genetic risk score of 21 variants.

  28426714   A genetic risk score for CAD, psychological stress, and their interaction as predictors of CAD, fatal MI, non-fatal MI and cardiovascular death.

  28614256   Association between chemokine CXC ligand 12 gene polymorphism (rs1746048) and coronary heart disease: A MOOSE-compliant meta-analysis.

  28705542   Effect of Coronary Artery Disease risk SNPs on serum cytokine levels and cytokine imbalance in Premature Coronary Artery Disease.

  28856136   Impact of a Genetic Risk Score for Coronary Artery Disease on Reducing Cardiovascular Risk: A Pilot Randomized Controlled Study.

  29557746   Significant Association of CXCL12 rs1746048 with LDL-C Level in Intracranial Aneurysms.

  29673405   GWAS implicated risk variants in different genes contribute additively to increase the risk of coronary artery disease (CAD) in the Pakistani subjects.

  31294628   Identification of Novel CXCL12 Genetic Polymorphisms Associated with Type 2 Diabetes Mellitus: A Chinese Sib-Pair Study.

  31845553   Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

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

  31933744   Influence of rs1746048 SNPs on clinical manifestations and incidence of acute myocardial infarction in Guangxi Han population.

  33488114   Impact of PCSK9, WDR12, CDKN2A, and CXCL12 Polymorphisms in Jordanian Cardiovascular Patients on Warfarin Responsiveness and Sensitivity.