Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience

Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing

(2015) Adam A. Nishimura et al.   GENETICS IN MEDICINE

Rescue morphine in mechanically ventilated newborns associated with combined OPRM1 and COMT genotype

(2014) Maja Matic et al.   PHARMACOGENOMICS

A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress

(2014) Beverly H. Brummett et al.   PLoS One

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

(2013) Robert C. Green et al.   GENETICS IN MEDICINE

A Functional Polymorphism in the 5HTR2C Gene Associated with Stress Responses Also Predicts Incident Cardiovascular Events

(2013) Beverly H. Brummett et al.   PLoS One

Paediatric pharmacogenomics: an overview

(2012) D. B. Hawcutt et al.   ARCHIVES OF DISEASE IN CHILDHOOD

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

(2012) Susan M. Wolf et al.   GENETICS IN MEDICINE

Association between polymorphisms of eNOS and GPx-1 genes, activity of free-radical processes and in-stent restenosis

(2012) Yu. A. Shuvalova et al.   MOLECULAR AND CELLULAR BIOCHEMISTRY

CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network

(2011) M V Relling et al.   CLINICAL PHARMACOLOGY & THERAPEUTICS

The NIH Undiagnosed Diseases Program

(2011) William A. Gahl   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

AlleleSeq: analysis of allele-specific expression and binding in a network framework

(2011) J. Rozowsky et al.   Molecular Systems Biology

A framework for variation discovery and genotyping using next-generation DNA sequencing data

(2011) Mark A DePristo et al.   NATURE GENETICS

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

(2010) A. McKenna et al.   GENOME RESEARCH

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

A Unified Approach to Genotype Imputation and Haplotype-Phase Inference for Large Data Sets of Trios and Unrelated Individuals

(2009) Brian L. Browning et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic Variants in Microsomal Epoxide Hydrolase Influence Carbamazepine Dosing

(2009) Mohd Makmor-Bakry et al.   CLINICAL NEUROPHARMACOLOGY