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Whole-Genome Sequencing in Pharmacogenetics

Authors: Thomas J, Urban;

Whole-Genome Sequencing in Pharmacogenetics

Abstract

on clinical disease prediction, and remarking on the problem of ‘missing heritability’ of risk for common diseases unaccounted for by common variants [1], the arena of pharmacogenetics was often singled out as an exception [2]. GWAS of drug response traits are quite exceptional in having provided a number of clinically significant genetic predictors of drug outcomes, with estimated effect sizes sometimes orders of magnitude greater than those seen for any human disease [3,4]. Despite this, GWAS of drug response traits currently represent only a small fraction of the total number of GWAS performed to date [101].

Related Organizations
Keywords

Genetic Markers, Drug-Related Side Effects and Adverse Reactions, Genome, Human, Pharmacogenetics, High-Throughput Nucleotide Sequencing, Humans, Biomarkers, Pharmacological, Genome-Wide Association Study

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
13
Average
Average
Top 10%
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