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

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

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς:	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
Μορφή:	Conference item
Έκδοση:	2009

Παρόμοια τεκμήρια

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Έκδοση: (2009)

COMMON GENETIC VARIANTS ASSOCIATED WITH LOW Lp(a) KRINGLE-IV COPY NUMBER, HIGH Lp(a) CONCENTRATION, AND INCREASED RISK OF CORONARY HEART DISEASE
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Common Genetic Variants Associated With Higher Lp(a) Concentrations and Increased Risk of Coronary Heart Disease
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Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease
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Impact of lipoprotein(a) levels and apolipoprotein(a) isoform size on risk of coronary heart disease.
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Association of Apolipoprotein(a) Isoforms With Coronary Heart Disease is Mediated Through Plasma Lipoprotein(a) Levels
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Independent relevance of renal function for coronary artery disease
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Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk
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A common LPA null allele associates with lower lipoprotein(a) levels and coronary artery disease risk.
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Έκδοση: (2014)

LPA NULL MUTATION GENOTYPING AND QPCR ANALYSIS REFINE KRINGLE ISOFORM ANALYSIS OF LP(A) LEVELS
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Multiple QTL influence the serum Lp(a) concentration: A genome-wide linkage screen in the PROCARDIS study
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Relationship between CAD risk genotype in the chromosome 9p21 locus and gene expression. Identification of eight new ANRIL splice variants.
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Έκδοση: (2009)

Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p.
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Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p
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Multiple QTL influence the serum Lp(a) concentration: a genome-wide linkage screen in the PROCARDIS study.
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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
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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.
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A Genome-Wide Association Study of Risk of Coronary Artery Disease in European and South Asian Populations
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Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17
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Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
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Έκδοση: (2006)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on Chromosome 17
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Έκδοση: (2006)

Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
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Lack of genetic support for shared aetiology of Coronary Artery Disease and Late-onset Alzheimer’s disease
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Plasma cytokines and risk of coronary heart disease in the PROCARDIS study
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Identifying small-effect genetic associations overlooked by the conventional fixed-effect model in a large-scale meta-analysis of coronary artery disease
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Identifying systematic heterogeneity patterns in genetic association meta-analysis studies
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Genome-wide mapping of susceptibility to coronary artery disease identifies a novel replicated locus on chromosome 17.
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Differential gene expression in macrophages from human atherosclerotic plaques shows convergence on pathways implicated by genome-wide association study risk variants
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