相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A. DePristo et al.
NATURE GENETICS (2011)
Defining a New Paradigm for Human Arrhythmia Syndromes Phenotypic Manifestations of Gene Mutations in Ion Channel- and Transporter-Associated Proteins
Michael J. Ackerman et al.
CIRCULATION RESEARCH (2010)
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron McKenna et al.
GENOME RESEARCH (2010)
A map of human genome variation from population-scale sequencing
David Altshuler et al.
NATURE (2010)
A method and server for predicting damaging missense mutations
Ivan A. Adzhubei et al.
NATURE METHODS (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Latent Genetic Backgrounds and Molecular Pathogenesis in Drug-Induced Long-QT Syndrome
Hideki Itoh et al.
CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY (2009)
Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia
S. Volpi et al.
MOLECULAR PSYCHIATRY (2009)
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
Arne Pfeufer et al.
NATURE GENETICS (2009)
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
Christopher Newton-Cheh et al.
NATURE GENETICS (2009)
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry
Emelia J. Benjamin et al.
NATURE GENETICS (2009)
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
Prateek Kumar et al.
NATURE PROTOCOLS (2009)
Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias
William S. Bush et al.
PHARMACOGENOMICS (2009)
Cellular basis of drug-induced torsades de pointes
D. M. Roden
BRITISH JOURNAL OF PHARMACOLOGY (2008)
SLCO1B1Variants and Statin-Induced Myopathy — A Genomewide Study
NEW ENGLAND JOURNAL OF MEDICINE (2008)
HLA-B*5701 screening for hypersensitivity to abacavir
Simon Mallal et al.
NEW ENGLAND JOURNAL OF MEDICINE (2008)
Mutation in glycerol-3-phosphate dehydrogenase 1-like gene (GPD1-L) decreases cardiac Na+ current and causes inherited Arrhythmias
Barry London et al.
CIRCULATION (2007)
Identifying genetic risk factors for serious adverse drug reactions: current progress and challenges
Russell A. Wilke et al.
NATURE REVIEWS DRUG DISCOVERY (2007)
The Pharmacogenetics Research Network: From SNP discovery to clinical drug response
K. M. Giacomini et al.
CLINICAL PHARMACOLOGY & THERAPEUTICS (2007)
Pharmacogenomics: Challenges and opportunities
Dan M. Roden et al.
ANNALS OF INTERNAL MEDICINE (2006)
Long QT syndrome: reduced repolarization reserve and the genetic link
DM Roden
JOURNAL OF INTERNAL MEDICINE (2006)
Genetics of acquired long QT syndrome
DM Roden et al.
JOURNAL OF CLINICAL INVESTIGATION (2005)
Distribution and intensity of constraint in mammalian genomic sequence
GM Cooper et al.
GENOME RESEARCH (2005)
Drug-induced Torsades de Pointes and implications for drug development
RR Fenichel et al.
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY (2004)
Genetic variations of KCNQ1, KCNH2, SCN5A, KCNE1, and KCNE2 in drug-induced long QT syndrome patients
ADC Paulussen et al.
JOURNAL OF MOLECULAR MEDICINE-JMM (2004)
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
P Yang et al.
CIRCULATION (2002)