Opportunities and challenges for the integration of massively parallel genomic sequencing into clinical practice: lessons from the ClinSeq project
|
journal
|
February 2012 |
Modulation of Cardiac Performance by Motor Protein Gene Transfer
|
journal
|
March 2008 |
Hearing silence: non-neutral evolution at synonymous sites in mammals
|
journal
|
February 2006 |
Vascular System: Role of Nitric Oxide in Cardiovascular Diseases
|
journal
|
April 2008 |
GPS-SNO: Computational Prediction of Protein S-Nitrosylation Sites with a Modified GPS Algorithm
|
journal
|
June 2010 |
CAPON modulates cardiac repolarization via neuronal nitric oxide synthase signaling in the heart
|
journal
|
March 2008 |
Identification of S-nitrosylation motifs by site-specific mapping of the S-nitrosocysteine proteome in human vascular smooth muscle cells
|
journal
|
April 2006 |
Increased Plasma S-Nitrosothiol Concentrations Predict Cardiovascular Outcomes among Patients with End-Stage Renal Disease: A Prospective Study
|
journal
|
February 2004 |
Characteristics and Prognostic Implications of Myosin Missense Mutations in Familial Hypertrophic Cardiomyopathy
|
journal
|
April 1992 |
The efficiency of folding of some proteins is increased by controlled rates of translation in vivo
|
journal
|
January 1987 |
Taxol, a microtubule stabilizer, prevents ischemic ventricular arrhythmias in rats
|
journal
|
June 2010 |
Congenital and acquired long QT syndrome
|
journal
|
August 2000 |
Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome
|
journal
|
January 2014 |
Identifying potential functional impact of mutations and polymorphisms: linking heart failure, increased risk of arrhythmias and sudden cardiac death
|
journal
|
January 2013 |
Antithrombotic Therapy for Atrial Fibrillation
|
journal
|
February 2012 |
Modeling the Heart--from Genes to Cells to the Whole Organ
|
journal
|
March 2002 |
Common variants in KCNN3 are associated with lone atrial fibrillation
|
journal
|
February 2010 |
Fine Tuning of Proteomic Technologies to Improve Biological Findings: Advancements in 2011–2013
|
journal
|
November 2013 |
Identification of RNA editing sites in the SNP database
|
journal
|
August 2005 |
The sounds of silence: synonymous mutations affect function
|
journal
|
June 2007 |
Associations between Genetic Variants in the NOS1AP (CAPON) Gene and Cardiac Repolarization in the Old Order Amish
|
journal
|
January 2007 |
Myocardial Diseases
|
journal
|
November 2000 |
A framework for organizing cancer-related variations from existing databases, publications and NGS data using a High-performance Integrated Virtual Environment (HIVE)
|
journal
|
January 2014 |
A Bioinformatics Workflow for Variant Peptide Detection in Shotgun Proteomics
|
journal
|
March 2011 |
Human Catechol-O-Methyltransferase Haplotypes Modulate Protein Expression by Altering mRNA Secondary Structure
|
journal
|
December 2006 |
Monogenic atrial fibrillation as pathophysiological paradigms
|
journal
|
November 2010 |
A method and server for predicting damaging missense mutations
|
journal
|
April 2010 |
SNVDis: A Proteome-wide Analysis Service for Evaluating nsSNVs in Protein Functional Sites and Pathways
|
journal
|
April 2013 |
Secondary Variants in Individuals Undergoing Exome Sequencing: Screening of 572 Individuals Identifies High-Penetrance Mutations in Cancer-Susceptibility Genes
|
journal
|
July 2012 |
Silent (Synonymous) SNPs: Should We Care About Them?
|
book
|
January 2009 |
S -Nitrosylation in Cardiovascular Signaling
|
journal
|
March 2010 |
Common variants at ten loci modulate the QT interval duration in the QTSCD Study
|
journal
|
March 2009 |
The “missing” link in atrial fibrillation heritability
|
journal
|
November 2011 |
Protein S-nitrosylation: purview and parameters
|
journal
|
February 2005 |
Cardiac electrophysiological effects of nitric oxide
|
journal
|
June 2010 |
FFAS03: a server for profile-profile sequence alignments
|
journal
|
July 2005 |
Proteome-Wide Analysis of Disease-Associated SNPs That Show Allele-Specific Transcription Factor Binding
|
journal
|
September 2012 |
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization
|
journal
|
April 2006 |
Proteome-Wide Analysis of Single-Nucleotide Variations in the N-Glycosylation Sequon of Human Genes
|
journal
|
May 2012 |
Screening of KCNN3 in patients with early-onset lone atrial fibrillation
|
journal
|
March 2011 |
Database resources of the National Center for Biotechnology Information
|
journal
|
December 2011 |
Aberrant S-nitrosylation mediates calcium-triggered ventricular arrhythmia in the intact heart
|
journal
|
October 2012 |
Human Genome Sequencing in Health and Disease
|
journal
|
February 2012 |
Cardiac channelopathies
|
journal
|
January 2002 |
Identification of a Schizophrenia-Associated Functional Noncoding Variant in NOS1AP
|
journal
|
April 2009 |
Genetic variation in SCN10A influences cardiac conduction
|
journal
|
January 2010 |
Post-translational modifications of the cardiac Na channel: contribution of CaMKII-dependent phosphorylation to acquired arrhythmias
|
journal
|
August 2013 |
Detection and Validation of Non-synonymous Coding SNPs from Orthogonal Analysis of Shotgun Proteomics Data
|
journal
|
June 2007 |
Genomics, heart failure and sudden cardiac death
|
journal
|
April 2008 |
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|
journal
|
October 2013 |
Congenital long QT syndrome: The race to refine risk
|
journal
|
January 2014 |
The role of the cytoskeleton in heart failure
|
journal
|
January 2000 |
Regulation of Protein Function and Signaling by Reversible Cysteine S-Nitrosylation
|
journal
|
September 2013 |
Global analysis of disease-related DNA sequence variation in 10 healthy individuals: Implications for whole genome-based clinical diagnostics
|
journal
|
February 2011 |
Red Blood Cell Nitric Oxide as an Endocrine Vasoregulator: A Potential Role in Congestive Heart Failure
|
journal
|
March 2004 |
Hypertrophic cardiomyopathy mutation is expressed in messenger RNA of skeletal as well as cardiac muscle.
|
journal
|
February 1993 |
Genetic and Molecular Basis of Cardiac Arrhythmias: Impact on Clinical Management Parts I and II
|
journal
|
February 1999 |
Common Variants in Myocardial Ion Channel Genes Modify the QT Interval in the General Population: Results From the KORA Study
|
journal
|
April 2005 |
Increased Expression of Cytoskeletal, Linkage, and Extracellular Proteins in Failing Human Myocardium
|
journal
|
April 2000 |
Myocardial Diseases
|
journal
|
November 2000 |
Interpreting Secondary Cardiac Disease Variants in an Exome Cohort
|
journal
|
August 2013 |