Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. - Wikidata - awgldk - TriplyDB

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

http://www.wikidata.org/entity/Q35828701

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Mitochondrial Regulation of the Muscle Microenvironment in Critical Limb Ischemia The association of 9p21-3 locus with coronary atherosclerosis: a systematic review and meta-analysis Genetics of coronary artery disease Genome-wide association studies of late-onset cardiovascular disease Genetic variants underlying risk of endometriosis: insights from meta-analysis of eight genome-wide association and replication datasets The ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study.Peripheral artery disease: epidemiology and global perspectives.Deficient CDKN2B Expression: A Double Hit for PAD.Therapeutic angiogenesis for critical limb ischaemia.Common genetic variants do not associate with CAD in familial hypercholesterolemia.Meta-analysis of low density lipoprotein receptor (LDLR) rs2228671 polymorphism and coronary heart disease.Common variants in and near IRS1 and subclinical cardiovascular disease in the Framingham Heart Study.The combination of 9p21.3 genotype and biomarker profile improves a peripheral artery disease risk prediction model.The relationship between diastolic blood pressure and coronary artery calcification is dependent on single nucleotide polymorphisms on chromosome 9p21.3.SNPflow: a lightweight application for the processing, storing and automatic quality checking of genotyping assays.Association between 9p21 genomic markers and ischemic stroke risk: evidence based on 21 studies The genetic basis of peripheral arterial disease: current knowledge, challenges, and future directions.Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?The Rotterdam Study: 2016 objectives and design update.Gene-arsenic interaction in longitudinal changes of blood pressure: Findings from the Health Effects of Arsenic Longitudinal Study (HEALS) in Bangladesh Cryptic relatedness in epidemiologic collections accessed for genetic association studies: experiences from the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) study and the National Health and Nutrition Examination Surveys (NHANE Effect of 9p21 genetic variation on coronary heart disease is not modified by other risk markers. The Atherosclerosis Risk in Communities (ARIC) Study Sex Differences in Correlates of Intermediate Phenotypes and Prevalent Cardiovascular Disease in the General Population.CDKN2B Regulates TGFβ Signaling and Smooth Muscle Cell Investment of Hypoxic Neovessels Genetic determinants of the ankle-brachial index: a meta-analysis of a cardiovascular candidate gene 50K SNP panel in the candidate gene association resource (CARe) consortium.Association between the chromosome 9p21 locus and angiographic coronary artery disease burden: a collaborative meta-analysis.Resequencing and clinical associations of the 9p21.3 region: a comprehensive investigation in the Framingham heart study.Lack of associations of ten candidate coronary heart disease risk genetic variants and subclinical atherosclerosis in four US populations: the Population Architecture using Genomics and Epidemiology (PAGE) study.9p21 locus rs10757278 is associated with advanced carotid atherosclerosis in a gender-specific manner.Heterozygote Advantage of the rs3794624 Polymorphism in CYBA for Resistance to Tuberculosis in Two Chinese Populations.From genotype to phenotype in human atherosclerosis--recent findings Current Insights into the Joint Genetic Basis of Type 2 Diabetes and Coronary Heart Disease.Functional genomics of the 9p21.3 locus for atherosclerosis: clarity or confusion?The genetics of diabetic complications.Molecular genetics of coronary artery disease.A GDF15 3' UTR variant, rs1054564, results in allele-specific translational repression of GDF15 by hsa-miR-1233-3p Gene-based therapies in patients with critical limb ischemia.Peripheral Artery Disease and Aortic Disease.The Rotterdam Study: 2014 objectives and design update.Association between the rs1333040 polymorphism on the chromosomal 9p21 locus and sporadic brain arteriovenous malformations.

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Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies.

http://www.wikidata.org/entity/Q35828701

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CIRCGENETICS.111.961292

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Circulation: Cardiovascular Genetics

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Aaron R Folsom

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Andrea Senft

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Astrid Petersmann

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Barbara Kollerits

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P2860

Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study

Genome-wide and candidate gene association study of cigarette smoking behaviors

Potential etiologic and functional implications of genome-wide association loci for human diseases and traits

A common allele on chromosome 9 associated with coronary heart disease

A second generation human haplotype map of over 3.1 million SNPs

Genomewide association analysis of coronary artery disease

Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium: Design of prospective meta-analyses of genome-wide association studies from 5 cohorts

Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm

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

A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.

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100-112

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10.1161/CIRCGENETICS.111.961292

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Florian Kronenberg

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2011-12-23T00:00:00Z

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22199011

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genome-wide association study

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3303225

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