(Q36174824)

12 August 2017

Current State and Future Prospects of Direct-to-Consumer Pharmacogenetics (English)

1 reference

12 August 2017

E W Chua

1

1 reference

PMC publication ID

3422723

12 August 2017

M A Kennedy

series ordinal

2

1 reference

12 August 2017

20 August 2012

1 reference

Frontiers in Pharmacology

12 August 2017

1 reference

12 August 2017

3

1 reference

12 August 2017

152

1 reference

Adoption of pharmacogenomic testing by US physicians: results of a nationwide survey

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Frequency of undetected CYP2D6 hybrid genes in clinical samples: impact on phenotype prediction

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

The future of direct-to-consumer clinical genetic tests

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

IL28B single nucleotide polymorphisms in the treatment of hepatitis C.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Pharmacogenetics: from bench to byte--an update of guidelines

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

The rs8099917 polymorphism, when determined by a suitable genotyping method, is a better predictor for response to pegylated alpha interferon/ribavirin therapy in Japanese patients than other single nucleotide polymorphisms associated with interleuk

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Accuracy of CNV Detection from GWAS Data

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

1 October 2017

Knowing me, knowing you.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Medicine. The future of personal genomics

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Medical genetics: a marker for Stevens-Johnson syndrome

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

An additional defective allele, CYP2C19*5, contributes to the S-mephenytoin poor metabolizer phenotype in Caucasians

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

A new genetic defect in human CYP2C19: mutation of the initiation codon is responsible for poor metabolism of S-mephenytoin

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Direct-to-consumer genetic testing: reliable or risky?

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Pharmacogenomics: "noninferiority" is sufficient for initial implementation

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

An agenda for personalized medicine

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Can extremely low or high morphine formation from codeine be predicted prior to therapy initiation?

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

CYP2D6 phenotype prediction from genotype: which system is the best?

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

The CYP2D6 activity score: translating genotype information into a qualitative measure of phenotype

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: characterization of gene duplication events.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3422723

Direct-to-consumer genetic tests: flawed and unethical

23 September 2018

1 reference

12 December 2020

Illusions of scientific legitimacy: misrepresented science in the direct-to-consumer genetic-testing marketplace

1 reference

12 December 2020

Direct to consumer genetic testing

1 reference

12 December 2020

When consumers get their genomes

1 reference

12 December 2020

Identifiers

DOI

10.3389/FPHAR.2012.00152

1 reference

12 August 2017

1 reference

PMC publication ID

3422723

12 August 2017

PubMed publication ID

22934000

1 reference

PMC publication ID

3422723