ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP

ASSOCIATION STUDY OF CORONARY ARTERY DISEASE (CAD) USING HUMANCVD 50K CHIP

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون:	Goel, A, Clarke, R, Hopewell, J, Kyriakou, T, Heath, S, Parish, S, Barlera, S, Franzosi, MG, Rust, S, Bennett, D, Silveira, A, Malarstig, A, Green, F, Lathrop, M, Gigante, B, Leander, K, Faire, U, Seedorf, U, Hamsten, A, Collins, R, Watkins, H, Farrall, M, Peden, J, Consortium, PROCARDIS
التنسيق:	Conference item
منشور في:	2009

مواد مشابهة

Genetic variants associated with Lp(a) lipoprotein level and coronary disease.
حسب: Clarke, R, وآخرون
منشور في: (2009)

COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE
حسب: Seedorf, U, وآخرون
منشور في: (2010)

Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease
حسب: Clarke, R, وآخرون
منشور في: (2009)

Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease
حسب: Hopewell, J, وآخرون
منشور في: (2014)

Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.
حسب: Hopewell, J, وآخرون
منشور في: (2014)

Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels
حسب: Hopewell, J, وآخرون
منشور في: (2010)

Independent relevance of renal function for coronary artery disease
حسب: Hopewell, J, وآخرون
منشور في: (2010)

Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.
حسب: Lasse Folkersen, وآخرون
منشور في: (2009-11-01)

A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk
حسب: Kyriakou, T, وآخرون
منشور في: (2014)

A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
حسب: Kyriakou, T, وآخرون
منشور في: (2014)

LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS
حسب: Kyriakou, T, وآخرون
منشور في: (2014)

Multiple QTL influence the serum Lp(a) concentration: A genome-wide linkage screen in the PROCARDIS study
حسب: Barlera, وآخرون
منشور في: (2007)

Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.
حسب: Folkersen, L, وآخرون
منشور في: (2009)

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
حسب: Broadbent, H, وآخرون
منشور في: (2008)

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
حسب: Broadbent, H, وآخرون
منشور في: (2008)

Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study.
حسب: Barlera, S, وآخرون
منشور في: (2007)

Identification of ZNF366 and PTPRD as novel determinants of plasma homocysteine in a family-based genome-wide association study.
حسب: Mälarstig, A, وآخرون
منشور في: (2009)

Evidence from a family based study of gene association of lymphotoxin alpha with coronary artery disease (CAD)
حسب: Green, F, وآخرون
منشور في: (2004)

Quantitative trait genetic linkage analysis of body mass index in familial coronary artery disease.
حسب: Specchia, C, وآخرون
منشور في: (2008)

Oxidized phospholipids, Lp(a) and coronary heart disease risk
حسب: Clarke, R, وآخرون
منشور في: (2012)

ANRIL, THE NON CODING RNA PRESENT IN THE CHROMOSOME 9 CAD ASSOCIATED LOCUS, HAS MULTIPLE SPLICE VARIANTS AND A POTENTIAL REGULATORY ROLE IN CDKN2B EXPRESSION
حسب: Kyriakou, T, وآخرون
منشور في: (2009)

Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.
حسب: Paré, G, وآخرون
منشور في: (2009)

USE OF ENCODE DATA TO IDENTIFY PUTATIVE FUNCTIONAL VARIANTS IN CORONARY ARTERY DISEASE GWAS
حسب: Goel, A, وآخرون
منشور في: (2014)

A Genome-Wide Association Study of Risk of Coronary Artery Disease in European and South Asian Populations
حسب: Hopewell, J, وآخرون
منشور في: (2010)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17
حسب: Farrall, M, وآخرون
منشور في: (2006)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
حسب: Farrall, M, وآخرون
منشور في: (2006)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on Chromosome 17
حسب: Farrall, M, وآخرون
منشور في: (2006)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
حسب: Farrall, M, وآخرون
منشور في: (2006)

Fast and general tests of genetic interaction for genome-wide association studies.
حسب: Mattias Frånberg, وآخرون
منشور في: (2017-06-01)

Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease
حسب: Grace, PC, وآخرون
منشور في: (2018)

Plasma cytokines and risk of coronary heart disease in the PROCARDIS study
حسب: Clarke, R, وآخرون
منشور في: (2018)

Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease
حسب: Magosi, LE, وآخرون
منشور في: (2019)

Identifying systematic heterogeneity patterns in genetic association meta-analysis studies
حسب: Magosi, L, وآخرون
منشور في: (2017)

Remnant lipoproteins are related to intima-media thickness of the carotid artery independently of LDL cholesterol and plasma triglycerides.
حسب: Karpe, F, وآخرون
منشور في: (2001)

Dyslipoproteinemic changes in borderline hypertension.
حسب: Lemne, C, وآخرون
منشور في: (1994)

Magnitude of alimentary lipemia is related to intima-media thickness of the common carotid artery in middle-aged men.
حسب: Karpe, F, وآخرون
منشور في: (1998)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
حسب: Martin Farrall, وآخرون
منشور في: (2006-05-01)

The interaction between coagulation factor 2 receptor and interleukin 6 haplotypes increases the risk of myocardial infarction in men.
حسب: Bruna Gigante, وآخرون
منشور في: (2010-01-01)

The risk of type 2 diabetes in men is synergistically affected by parental history of diabetes and overweight.
حسب: Cecilia Wikner, وآخرون
منشور في: (2013-01-01)

Differential gene expression in macrophages from human atherosclerotic plaques shows convergence on pathways implicated by genome-wide association study risk variants
حسب: Chai, J, وآخرون
منشور في: (2018)