SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group (Q34047278)

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English	SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group	scientific article

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

SLCO1B1 rs4149056 polymorphism associated with statin-induced myopathy is differently distributed according to ethnicity in the Brazilian general population: Amerindians as a high risk ethnic group (English)

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

José Eduardo Krieger

object named as

José E Krieger

6

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author name string

Paulo C J L Santos

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Renata A G Soares

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Raimundo M Nascimento

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

George L L Machado-Coelho

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

José G Mill

5

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Europe PubMed Central

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30 July 2017

Alexandre C Pereira

7

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Europe PubMed Central

PubMed publication ID

30 July 2017

publication date

12 October 2011

1 reference

Europe PubMed Central

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30 July 2017

BMC Medical Genetics

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Europe PubMed Central

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30 July 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

136

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

CYP2C19 and ABCB1 gene polymorphisms are differently distributed according to ethnicity in the Brazilian general population

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

Organic anion transporting polypeptide 1B1: a genetically polymorphic transporter of major importance for hepatic drug uptake

1 reference

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5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

APOE polymorphism is associated with lipid profile, but not with arterial stiffness in the general population

1 reference

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5 July 2018

HFE gene mutations in patients with primary iron overload: is there a significant improvement in molecular diagnosis yield with HFE sequencing?

1 reference

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5 July 2018

Exploring genetic susceptibility to cancer in diverse populations

1 reference

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5 July 2018

The genetics of statin-induced myopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

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

1 reference

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5 July 2018

Prevalence and risk factors associated with peripheral arterial disease in the Hearts of Brazil Project

1 reference

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5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

Comparison of SLCO1B1 sequence variability among German, Turkish, and African populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

Does statin therapy initiation increase the risk for myopathy? An observational study of 32,225 diabetic and nondiabetic patients

1 reference

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5 July 2018

Effect of drug transporter genotypes on pravastatin disposition in European- and African-American participants

1 reference

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5 July 2018

The safety of statins in clinical practice

1 reference

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5 July 2018

Statin safety: a systematic review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

Statins, cardiovascular disease, and drug safety

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

5 July 2018

Efficacy and safety of cholesterol-lowering treatment: prospective meta-analysis of data from 90,056 participants in 14 randomised trials of statins

1 reference

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5 July 2018

Polymorphisms in OATP-C: identification of multiple allelic variants associated with altered transport activity among European- and African-Americans

1 reference

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5 July 2018

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

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5 July 2018

Ethnicity and arterial stiffness in Brazil

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-136

21 January 2018

Frequency of the SLCO1B1 388A>G and the 521T>C polymorphism in Tanzania genotyped by a new LightCycler®-based method

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3204270

28 October 2018

Different Effects of SLCO1B1 Polymorphism on the Pharmacokinetics of Atorvastatin and Rosuvastatin

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-136

21 January 2018

SLCO1B1 polymorphism markedly affects the pharmacokinetics of simvastatin acid

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-12-136

21 January 2018

An assessment of statin safety by muscle experts

1 reference

https://pubmed.ncbi.nlm.nih.gov/21992719

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21992719

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000® instrument.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21992719

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-12-136

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

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