Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience
出版年份 2016 全文链接
标题
Pharmacogenomic incidental findings in 308 families: The NIH Undiagnosed Diseases Program experience
作者
关键词
-
出版物
GENETICS IN MEDICINE
Volume 18, Issue 12, Pages 1303-1307
出版商
Springer Nature
发表日期
2016-06-03
DOI
10.1038/gim.2016.47
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- 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
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