A SNPshot of PubMed to associate genetic variants with drugs, diseases, and adverse reactions-Reference-Cited by-同舟云学术

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A SNPshot of PubMed to associate genetic variants with drugs, diseases, and adverse reactions

Published:2012-10 Issue:5 Volume:45 Page:842-850
ISSN:1532-0464
Container-title:Journal of Biomedical Informatics
language:en
Short-container-title:Journal of Biomedical Informatics

Author:

Hakenberg Jörg,Voronov Dmitry,Nguyên Võ Hà,Liang Shanshan,Anwar Saadat,Lumpkin Barry,Leaman Robert,Tari Luis,Baral Chitta

Funder

National Science Foundation

Science Foundation Arizona

Fulbright International Student Program Russia

Arizona State University

Publisher

Elsevier BV

Subject

Health Informatics,Computer Science Applications

Reference27 articles.

1. Increased frequency of cytochrome P450 2D6 poor metabolizers among patients with metoprolol-associated adverse effects

2. Polymorphism of Human Cytochrome P450 2D6 and Its Clinical Significance

3. CYP2D6 and CYP2C19 genotype-based dose recommendations for antidepressants: a first step towards subpopulation-specific dosages

4. Incidence of Adverse Drug Reactions in Hospitalized Patients

5. Integrating genotype and phenotype information: an overview of the PharmGKB project

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