(Q24658145)

1

0 references

Manuela Uda

20

0 references

Antonella Mulas

8

0 references

Silvia Naitza

14

0 references

Laura Crisponi

13

0 references

Antonio Cao

19

0 references

Mara Marongiu

12

0 references

Gianluca Usala

5

0 references

Andrea Maschio

3

0 references

Maria Grazia Piras

9

0 references

Mariano Dei

6

0 references

Marco Masala

11

0 references

Sandra Lai

object named as

Sandra Lai

7

0 references

Alan R. Shuldiner

object named as

Alan R Shuldiner

17

0 references

author name string

Patrick F McArdle

4

0 references

Lucia Perseu

10

0 references

Renzo Galanello

15

0 references

Gonçalo R Abecasis

A second generation human haplotype map of over 3.1 million SNPs

16

0 references

language of work or name

English

0 references

publication date

15 July 2009

0 references

published in

Human Molecular Genetics

0 references

volume

18

0 references

issue

14

0 references

page(s)

2711-8

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Localization and genomic organization of a new hepatocellular organic anion transporting polypeptide

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Identification of a novel gene family encoding human liver-specific organic anion transporter LST-1

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Genetic polymorphisms of human organic anion transporters OATP-C (SLC21A6) and OATP-B (SLC21A9): allele frequencies in the Japanese population and functional analysis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Hepatic uptake of bilirubin and its conjugates by the human organic anion transporter SLC21A6

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

A novel human organic anion transporting polypeptide localized to the basolateral hepatocyte membrane

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Assignment of the human UDP glucuronosyltransferase gene (UGT1A1) to chromosome region 2q37

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Phosphodiesterase 8B gene variants are associated with serum TSH levels and thyroid function

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

The genetic response to short-term interventions affecting cardiovascular function: rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Common variants in the GDF5-UQCC region are associated with variation in human height

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Family-based association tests for genomewide association scans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Heritability of cardiovascular and personality traits in 6,148 Sardinians

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Construction of multilocus genetic linkage maps in humans

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

ATP-dependent transport of bilirubin glucuronides by the multidrug resistance protein MRP1 and its hepatocyte canalicular isoform MRP2.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2701337

Xenobiotic transporters of the human organic anion transporting polypeptides (OATP) family

30 May 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP203

The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP203

Cholelithiasis in thalassemia major

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP203

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDP203

The rat canalicular conjugate export pump (Mrp2) is down-regulated in intrahepatic and obstructive cholestasis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19419973

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19419973

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19419973