Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels--the Framingham Heart Study. (Q37364279)

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scientific article published on 19 March 2009

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English	Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels--the Framingham Heart Study.	scientific article published on 19 March 2009

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scholarly article

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26 January 2020

Conditional linkage and genome-wide association studies identify UGT1A1 as a major gene for anti-atherogenic serum bilirubin levels--the Framingham Heart Study (English)

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26 January 2020

genome-wide association study

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atherosclerosis

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based on heuristic

inferred from title

Johannes P Schwaiger

2

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26 January 2020

Florian Kronenberg

9

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26 January 2020

L. Adrienne Cupples

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26 January 2020

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Steven C Hunt

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26 January 2020

Christopher J O'Donnell

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Christopher J O'Donnell

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26 January 2020

author name string

Jing-Ping Lin

1

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26 January 2020

Gang Zheng

5

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26 January 2020

Veit Schoenborn

6

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26 January 2020

Jungnam Joo

8

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26 January 2020

publication date

19 March 2009

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26 January 2020

Atherosclerosis

1 reference

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26 January 2020

206

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26 January 2020

1

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26 January 2020

228-233

1 reference

Europe PubMed Central

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26 January 2020

Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Serum bilirubin levels, UGT1A1 polymorphisms and risk for coronary artery disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Robust ranks of true associations in genome-wide case-control association studies

1 reference

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6 September 2017

Gilbert syndrome, UGT1A1*28 allele, and cardiovascular disease risk: possible protective effects and therapeutic applications of bilirubin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Human cell growth requires a functional cytoplasmic exosome, which is involved in various mRNA decay pathways

1 reference

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6 September 2017

Association between the UGT1A1*28 allele, bilirubin levels, and coronary heart disease in the Framingham Heart Study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Evidence for a gene influencing serum bilirubin on chromosome 2q telomere: a genomewide scan in the Framingham study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

6 September 2017

Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

14 September 2017

Coexpression of gene polymorphisms involved in bilirubin production and metabolism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

A common genetic variant is associated with adult and childhood obesity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

Comparative genomics analysis of human sequence variation in the UGT1A gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

A pharmacogenetic effect of factor XIII valine 34 leucine polymorphism on fibrinolytic therapy for acute myocardial infarction.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

Trend tests for case-control studies of genetic markers: power, sample size and robustness

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

2 September 2018

Genome-wide association studies of quantitative traits with related individuals: little (power) lost but much to be gained

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2752659

3 December 2018

Evidence for a major gene elevating serum bilirubin concentration in Utah pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Relationship between bilirubin, apolipoprotein B, and coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum bilirubin and risk of ischemic heart disease in middle-aged British men

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

UGT1A1*28 allele and coronary heart disease: the Rotterdam Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of plasma bilirubin with coronary heart disease and segregation of bilirubin as a major gene trait: the NHLBI family heart study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Further evidence that the UGT1A1*28 allele is not associated with coronary heart disease: The ECTIM Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Are Linkage Analysis and the Collection of Family Data Dead? Prospects for Family Studies in the Age of Genome-Wide Association

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

UDP-Glucuronosyltransferase 1A1 gene polymorphisms and total bilirubin levels in an ethnically diverse cohort of women

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome scan for loci influencing anti-atherogenic serum bilirubin levels

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of low serum concentration of bilirubin with increased risk of coronary artery disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association between the UGT1A1 TA-repeat polymorphism and bilirubin concentration in patients with intermittent claudication: results from the CAVASIC study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19389676

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/J.ATHEROSCLEROSIS.2009.02.039

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26 January 2020

1 reference

Europe PubMed Central

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26 January 2020

1 reference

Europe PubMed Central

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26 January 2020

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