(Q37339440)

English

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

scientific article published on February 2009

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scholarly article

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

Genome-wide association studies for atherosclerotic vascular disease and its risk factors (English)

1 reference

Europe PubMed Central

19 August 2017

genome-wide association study

0 references

atherosclerosis

1 reference

based on heuristic

inferred from title

Iftikhar J Kullo

2

object named as

Iftikhar J Kullo

1 reference

Europe PubMed Central

19 August 2017

author name string

Keyue Ding

1

1 reference

Europe PubMed Central

19 August 2017

publication date

1 February 2009

1 reference

Europe PubMed Central

19 August 2017

Circulation: Cardiovascular Genetics

1 reference

Europe PubMed Central

19 August 2017

2

1 reference

Europe PubMed Central

19 August 2017

1

1 reference

Europe PubMed Central

19 August 2017

63-72

1 reference

Europe PubMed Central

19 August 2017

Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women

1 reference

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Revealing the architecture of gene regulation: the promise of eQTL studies

1 reference

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1 reference

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Common and rare variants in multifactorial susceptibility to common diseases

1 reference

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Common variants near MC4R are associated with fat mass, weight and risk of obesity

1 reference

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Common genetic variation near MC4R is associated with waist circumference and insulin resistance

1 reference

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A HapMap harvest of insights into the genetics of common disease

1 reference

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Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein

1 reference

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Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study

1 reference

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Genome-wide association studies for complex traits: consensus, uncertainty and challenges

1 reference

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Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes

1 reference

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How to interpret a genome-wide association study

1 reference

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LDL-cholesterol concentrations: a genome-wide association study

1 reference

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WGAViewer: software for genomic annotation of whole genome association studies

1 reference

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6 September 2017

Overview of DNA sequencing strategies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

1 reference

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Newly identified loci that influence lipid concentrations and risk of coronary artery disease

1 reference

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6 September 2017

Letting the genome out of the bottle--will we get our wish?

1 reference

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6 September 2017

Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

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Heart Disease and Stroke Statistics--2008 Update: A Report From the American Heart Association Statistics Committee and Stroke Statistics Subcommittee

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

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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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts

1 reference

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6 September 2017

Pathway-based approaches for analysis of genomewide association studies

1 reference

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6 September 2017

Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

The NCBI dbGaP database of genotypes and phenotypes

1 reference

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6 September 2017

Genome-wide association studies provide new insights into type 2 diabetes aetiology

1 reference

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6 September 2017

Genomewide association analysis of coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

Copy number variation in the human genome and its implications for cardiovascular disease

1 reference

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6 September 2017

A new multipoint method for genome-wide association studies by imputation of genotypes

1 reference

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6 September 2017

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

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6 September 2017

Replicating genotype-phenotype associations

1 reference

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6 September 2017

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

1 reference

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6 September 2017

Variation in FTO contributes to childhood obesity and severe adult obesity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

A common allele on chromosome 9 associated with coronary heart disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

A common variant on chromosome 9p21 affects the risk of myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

1 reference

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A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

1 reference

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6 September 2017

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

1 reference

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6 September 2017

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

1 reference

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6 September 2017

A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity

1 reference

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Population-based resequencing of ANGPTL4 uncovers variations that reduce triglycerides and increase HDL.

1 reference

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6 September 2017

No gene is an island: the flip-flop phenomenon

1 reference

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6 September 2017

Principal components analysis corrects for stratification in genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

6 September 2017

Structural variation of the human genome

1 reference

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6 September 2017

Effects of differential genotyping error rate on the type I error probability of case-control studies

1 reference

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6 September 2017

Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels

1 reference

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6 September 2017

Using linkage genome scans to improve power of association in genome scans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2740629

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A haplotype map of the human genome

1 reference

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Inflammation, atherosclerosis, and coronary artery disease

1 reference

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Low LDL cholesterol in individuals of African descent resulting from frequent nonsense mutations in PCSK9.

1 reference

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Population stratification and spurious allelic association

1 reference

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Genomic control for association studies

1 reference

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6 September 2017

Initial sequencing and analysis of the human genome

1 reference

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Use of unlinked genetic markers to detect population stratification in association studies.

1 reference

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The future of genetic studies of complex human diseases

1 reference

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1 reference

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6 September 2017

Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.

1 reference

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A treasure trove for lipoprotein biology

1 reference

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Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides

1 reference

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Evaluating and improving power in whole-genome association studies using fixed marker sets.

1 reference

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Mouse glucose transporter 9 splice variants are expressed in adult liver and kidney and are up-regulated in diabetes

1 reference

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2 September 2018

Comparison of C-reactive protein and low-density lipoprotein cholesterol levels in the prediction of first cardiovascular events

1 reference

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2 September 2018

Statistical false positive or true disease pathway?

1 reference

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20 October 2018

SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations

1 reference

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3 December 2018

Genetic Association Studies

1 reference

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3 December 2018

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

1 reference

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3 December 2018

Uric acid and cardiovascular risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/19750184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Casting a wider net for diabetes susceptibility genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19750184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Guilt beyond a reasonable doubt

1 reference

https://pubmed.ncbi.nlm.nih.gov/19750184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation is the spice of life

1 reference

https://pubmed.ncbi.nlm.nih.gov/19750184

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1161/CIRCGENETICS.108.816751

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

1 reference

Europe PubMed Central

19 August 2017

ResearchGate publication ID

0 references

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