(Q35080564)

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Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels

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scholarly article

1 reference

Europe PubMed Central

6 August 2017

Mayo Genome Consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels (English)

1 reference

Europe PubMed Central

6 August 2017

genome-wide association study

0 references

1 reference

based on heuristic

inferred from title

Jyotishman Pathak

3

object named as

Jyotishman Pathak

1 reference

Europe PubMed Central

6 August 2017

Christopher G. Chute

15

object named as

Christopher G Chute

1 reference

Europe PubMed Central

6 August 2017

Gloria M Petersen

13

object named as

Gloria M Petersen

1 reference

Europe PubMed Central

6 August 2017

Paul J. Limburg

5

object named as

Paul J Limburg

1 reference

Europe PubMed Central

6 August 2017

Mariza de Andrade

14

object named as

Mariza de Andrade

1 reference

Europe PubMed Central

6 August 2017

Iftikhar J Kullo

11

object named as

Iftikhar J Kullo

1 reference

Europe PubMed Central

6 August 2017

8

object named as

Eric W Klee

1 reference

Europe PubMed Central

6 August 2017

author name string

Suzette J Bielinski

1

1 reference

Europe PubMed Central

6 August 2017

High Seng Chai

2

1 reference

Europe PubMed Central

6 August 2017

Jayant A Talwalkar

4

1 reference

Europe PubMed Central

6 August 2017

Rachel E Gullerud

6

1 reference

Europe PubMed Central

6 August 2017

Hugues Sicotte

7

1 reference

Europe PubMed Central

6 August 2017

Jason L Ross

9

1 reference

Europe PubMed Central

6 August 2017

Jean-Pierre A Kocher

10

1 reference

Europe PubMed Central

6 August 2017

John A Heit

12

1 reference

Europe PubMed Central

6 August 2017

language of work or name

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publication date

6 June 2011

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

86

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Europe PubMed Central

6 August 2017

606-614

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Europe PubMed Central

6 August 2017

7

1 reference

Europe PubMed Central

6 August 2017

The eMERGE Network: a consortium of biorepositories linked to electronic medical records data for conducting genomic studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Genetic influences on serum bilirubin in American Indians: The Strong Heart Family Study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Leveraging informatics for genetic studies: use of the electronic medical record to enable a genome-wide association study of peripheral arterial disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Genome-wide association of serum bilirubin levels in Korean population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Genome-wide association meta-analysis for total serum bilirubin levels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

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=3127556

8 July 2018

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=3127556

8 July 2018

Role of cysteine residues in the function of human UDP glucuronosyltransferase isoform 1A1 (UGT1A1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Genetic factors related to unconjugated hyperbilirubinemia amongst adults

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Evidence for a substantial genetic influence on biochemical liver function tests: results from a population-based Danish twin study.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Human UDP-glucuronosyltransferases: metabolism, expression, and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

8 July 2018

Common variants of four bilirubin metabolism genes and their association with serum bilirubin and coronary artery disease in Chinese Han population.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

27 September 2018

OATP1B1 POLYMORPHISM IS A MAJOR DETERMINANT OF SERUM BILIRUBIN LEVEL BUT NOT ASSOCIATED WITH RIFAMPICIN-MEDIATED BILIRUBIN ELEVATION

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3127556

16 November 2018

Influence of common variants in the pharmacokinetic genes (OATP-C, UGT1A1, and MRP2) on serum bilirubin levels in healthy subjects

1 reference

https://pubmed.ncbi.nlm.nih.gov/21646302

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/21646302

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotypes in the UGT1A1 gene and their role as genetic determinants of bilirubin concentration in healthy German volunteers

1 reference

https://pubmed.ncbi.nlm.nih.gov/21646302

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.4065/MCP.2011.0178

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

1 reference

Europe PubMed Central

6 August 2017

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