SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink (Q24598793)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

meta-analysis

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title

SLCO1B1 genetic variant associated with statin-induced myopathy: a proof-of-concept study using the clinical practice research datalink (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

1

1 reference

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7 March 2020

Tjeerd P van Staa

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

Munir Pirmohamed

8

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7 March 2020

author name string

H O'Meara

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

A L Jorgensen

3

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7 March 2020

J Campbell

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

M Hobbs

5

1 reference

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7 March 2020

G McCann

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

language of work or name

English

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publication date

13 August 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

Clinical Pharmacology & Therapeutics

7 March 2020

published in

1 reference

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7 March 2020

volume

94

1 reference

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7 March 2020

issue

6

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7 March 2020

page(s)

695-701

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Statin adverse effects : a review of the literature and evidence for a mitochondrial mechanism

7 March 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

SLCO1B1 variants and statin-induced myopathy--a genomewide study

24 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Recent advances in the utility and use of the General Practice Research Database as an example of a UK Primary Care Data resource

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

The clinical pharmacogenomics implementation consortium: CPIC guideline for SLCO1B1 and simvastatin-induced myopathy.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Mechanisms of statin-induced myalgia assessed by physiogenomic associations

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

The phenotype standardization project: improving pharmacogenetic studies of serious adverse drug reactions.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Cerivastatin, genetic variants, and the risk of rhabdomyolysis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Statin-induced myopathy: a review and update

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Common nonsynonymous substitutions in SLCO1B1 predispose to statin intolerance in routinely treated individuals with type 2 diabetes: a go-DARTS study

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Basic science review: Statin therapy--Part I: The pleiotropic effects of statins in cardiovascular disease

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Transporter pharmacogenetics and statin toxicity

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

The SLCO1B1*5 genetic variant is associated with statin-induced side effects

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

The role of coenzyme Q10 in statin-associated myopathy: a systematic review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Statin safety: a systematic review

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

CYP2D6 and CYP2C19 genotypes of patients with terodiline cardiotoxicity identified through the yellow card system

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Facilitating pharmacogenetic studies using electronic health records and natural-language processing: a case study of warfarin

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

The role of vitamin D and SLCO1B1*5 gene polymorphism in statin-associated myalgias

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3831180

Genetic involvement in statins induced myopathy. Preliminary data from an observational case-control study

30 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23942138

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic influence in statin intolerance

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23942138

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/CLPT.2013.161

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

release_yl7gfqg5ijgsnb3k7225bztdkm

7 March 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/yl7gfqg5ijgsnb3k7225bztdkm

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json

7 March 2020

PubMed publication ID

23942138

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23942138%20AND%20SRC:MED&resulttype=core&format=json