Physician

Cardiology

Dr. G M. Vincent, MD

Vincent is an expert in the field of Cardiology. He researched medicine at University of Utah School of Medicine. He has 1 awards "Fellow (FACC)". Vincent is a published doctor as well. He has 99 publications published. The latest was: The expression of normal ventricular repolarization in the body surface distribution of T potentials.

Publications

Mutation and Gender Specific Risk in Type-2 Long QT Syndrome: Implications for Risk Stratification for Life-Threatening Cardiac Events in Patients with Long QT Syndrome.
Nonsense-Mediated mRNA Decay Caused by a Frameshift Mutation in a Large Kindred of Type 2 Long QT Syndrome.
Genotype-Specific QT Correction for Heart Rate and the Risk of Life Threatening Cardiac Events in Adolescents with the Congenital Long-QT Syndrome.
Risk for life-threatening cardiac events in patients with genotype-confirmed long-QT syndrome and normal-range corrected QT intervals.
Genotype-phenotype aspects of type 2 long QT syndrome.
Clinical implications for patients with long QT syndrome who experience a cardiac event during infancy.
Sudden cardiac arrest in the young due to inherited arrhythmias: the importance of family care.
High efficacy of beta-blockers in long-QT syndrome type 1: contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "fail...
Genotyping has a minor role in selecting therapy for congenital long-QT syndromes at present.
Risk of death in the long QT syndrome when a sibling has died.
Long-QT syndrome after age 40.
Risk factors for aborted cardiac arrest and sudden cardiac death in children with the congenital long-QT syndrome.
Nonsense mutations in hERG cause a decrease in mutant mRNA transcripts by nonsense-mediated mRNA decay in human long-QT syndrome.
Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene.
Long QT syndrome and pregnancy.
Long QT syndrome in adults.
Risk of aborted cardiac arrest or sudden cardiac death during adolescence in the long-QT syndrome.
Corrected QT variability in serial electrocardiograms in long QT syndrome: the importance of the maximum corrected QT for risk stratification.
Improved long-term survival associated with stent deployment during percutaneous coronary interventions: results from a registry of 3399 patients.
Inaccurate electrocardiographic interpretation of long QT: the majority of physicians cannot recognize a long QT when they see one.
Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.
Risk assessment in long QT syndrome: the Achilles heel of appropriate treatment.
The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death in children and young adults.
The role of genotyping in diagnosing cardiac channelopathies : progress to date.
An intronic mutation causes long QT syndrome.
Atrial arrhythmias in the inherited long QT syndrome: laboratory quirk or clinical arrhythmia?
The long-QT syndrome--bedside to bench to bedside.
Increased risk of arrhythmic events in long-QT syndrome with mutations in the pore region of the human ether-a-go-go-related gene potassium channel.
Clinical implications for affected parents and siblings of probands with long-QT syndrome.
Prevention of drug-induced long QT syndrome: gender, chemistry, and education.
Genotype-phenotype correlation in the long-QT syndrome: gene-specific triggers for life-threatening arrhythmias.
Spectrum of ST-T-wave patterns and repolarization parameters in congenital long-QT syndrome: ECG findings identify genotypes.
Commotio cordis: a deadly consequence of chest trauma.
Spectrum of mutations in long-QT syndrome genes. KVLQT1, HERG, SCN5A, KCNE1, and KCNE2.
Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome.
Clinical and genetic variables associated with acute arousal and nonarousal-related cardiac events among subjects with long QT syndrome.
Comparison of clinical and genetic variables of cardiac events associated with loud noise versus swimming among subjects with the long QT syndrome.
The inherited long QT syndrome: from ion channel to bedside.
Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases:hypertrophic cardiomyopathy, long-QT s...
Influence of genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.
ECG Quiz Sudden Death in a Young Athlete.
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.
Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome.
The molecular genetics of the long QT syndrome: genes causing fainting and sudden death.
Lipoprotein(a) interactions with lipid and nonlipid risk factors in early familial coronary artery disease.
George M. Cober Lecturer: Mark T. Keating. Molecular basis of the long-QT syndrome associated with deafness.
Molecular basis of the long-QT syndrome associated with deafness.
Age-gender influence on the rate-corrected QT interval and the QT-heart rate relation in families with genotypically characterized long QT syndrome.
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
Higher serum bilirubin is associated with decreased risk for early familial coronary artery disease.
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias.
ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome.
Higher plasma homocyst(e)ine and increased susceptibility to adverse effects of low folate in early familial coronary artery disease.
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome.
Heterogeneity in the inherited long QT syndrome.
Diagnosis of old inferior myocardial infarction by body surface isopotential mapping.
[Multiple sclerosis].
Reversible segmental myocardial dysfunction in septic shock.
Q-T interval syndromes.
Optothermal mathematical model and experimental studies for laser irradiation of arteries in the presence of blood flow.
Clinically practical lead systems for improved electrocardiography: comparison with precordial grids and conventional lead systems.
QRS-wave detector evaluation.
The financial impact of Medicare diagnosis-related groups. Effect upon hospitals receiving cardiac patients referred for tertiary care.
Multifiber gradient-index lens laser angioplasty probe.
Protamine allergy reactions during cardiac catheterization and cardiac surgery: risk in patients taking protamine-insulin preparations.
Mechanisms of ischemic ST-segment displacement. Evaluation by direct current recordings.
Coronary spasm producing coronary thrombosis and myocardial infarction.
The expression of normal ventricular repolarization in the body surface distribution of T potentials.
Catheter-directed neodymium:YAG laser injury of the left ventricle for arrhythmia ablation: dosimetry and hemodynamic, hematologic, and electrophysiologic effects.
The heart rate of Romano-Ward syndrome patients.
An evaluation of potential prognostic indicators in cardiac patients.
Role of DNA testing for diagnosis, management, and genetic screening in long QT syndrome, hypertrophic cardiomyopathy, and Marfan syndrome.
Long QT syndrome in children: the value of rate corrected QT interval and DNA analysis as screening tests in the general population.
Presence of blood significantly decreases transmission of 630 nm laser light.
Laser catheter ablation of simulated ventricular tachycardia.
Risk of Syncope in Family Members Who Are Genotype Negative for a Family-Associated Long QT Syndrome Mutation.
Application of body surface mapping to exercise testing: S-T80 isoarea maps in patients with coronary artery disease.
In vivo canine coronary artery laser irradiation: photodynamic therapy using dihematoporphyrin ether and 632 nm laser. A safety and dose-response relationship study.
Hypothesis for the molecular physiology of the Romano-Ward long QT syndrome.
Modulating effects of age and gender on the clinical course of long QT syndrome by genotype.
Diagnostic criteria for the long QT syndrome. An update.
Long QT syndrome in children: the value of the rate corrected QT interval in children who present with fainting.
Genetics and molecular biology of the inherited long QT syndrome.
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
Thermal laser probe angioplasty: influence of constant tip temperature, plaque composition, and probe/vessel diameter ratio.
KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death.
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotype.
Location of mutation in the KCNQ1 and phenotypic presentation of long QT syndrome.
A splice site mutation in hERG leads to cryptic splicing in human long QT syndrome.
Plasma homocyst(e)ine as a risk factor for early familial coronary artery disease.
Locus heterogeneity of autosomal dominant long QT syndrome.
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11.
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene.
The long QT syndrome. Prospective longitudinal study of 328 families.
Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome.
The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome.

Schools

University of Utah
Johns Hopkins Hospital
University Utah Med Center

Doctors Specialties

Cardiology

Accepted Insurances

Awards

Fellow (FACC)

Education

University of Utah
Johns Hopkins University
University of Utah School of Medicine

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