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Author Details

Andrew M Glazer
Vanderbilt University
2010
41
20
PMIDPaper TitleJournal TitlePublished Year
36524479Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.Circulation2023
37164047Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant.Heart Rhythm2023
37426450Minimum information and guidelines for reporting a Multiplexed Assay of Variant Effect.ArXiv2023
37162834High-throughput functional mapping of variants in an arrhythmia gene, <i>KCNE1</i>, reveals novel biology.bioRxiv2023
36716194Proactive Variant Effect Mapping Aids Diagnosis in Pediatric Cardiac Arrest.Circ Genom Precis Med2023
34930020Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.Circulation2022
35544069Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes.JAMA Cardiol2022
36368182Genetics of congenital arrhythmia syndromes: the challenge of variant interpretation.Curr Opin Genet Dev2022
36197721Functional Assays Reclassify Suspected Splice-Altering Variants of Uncertain Significance in Mendelian Channelopathies.Circ Genom Precis Med2022
35216338Veratridine Can Bind to a Site at the Mouth of the Channel Pore at Human Cardiac Sodium Channel Na<sub>V</sub>1.5.Int J Mol Sci2022
35305865Dominant negative effects of SCN5A missense variants.Genet Med2022
34994586Common Ancestry-Specific Ion Channel Variants Predispose to Drug-Induced Arrhythmias.Circulation2022
32171470Androgenic effects on ventricular repolarization: A translational study from the international pharmacovigilance database to iPSC-cardiomyocytes.Ann Endocrinol (Paris)2021
34987964Incessant atrial and ventricular tachycardias associated with an <i>SCN5A</i> mutation.HeartRhythm Case Rep2021
34495297Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes.JAMA Cardiol2021
34309407Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> Variants.Circ Genom Precis Med2021
32533946High-Throughput Reclassification of SCN5A Variants.Am J Hum Genet2020
31928070Deep Mutational Scan of an <i>SCN5A</i> Voltage Sensor.Circ Genom Precis Med2020
33141630<i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision Medicine.Circ Genom Precis Med2020
32522694High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel K<sub>V</sub>11.1.Heart Rhythm2020
32569262A Bayesian method to estimate variant-induced disease penetrance.PLoS Genet2020
31004778Patient-independent human induced pluripotent stem cell model: A new tool for rapid determination of genetic variant pathogenicity in long QT syndrome.Heart Rhythm2019
31378084Androgenic Effects on Ventricular Repolarization: A Translational Study From the International Pharmacovigilance Database to iPSC-Cardiomyocytes.Circulation2019
29590070Phenotype risk scores identify patients with unrecognized Mendelian disease patterns.Science2018
29967236Hypogonadism as a Reversible Cause of Torsades de Pointes in Men.Circulation2018
29728395<i>SCN5A</i> (Na<sub>V</sub>1.5) Variant Functional Perturbation and Clinical Presentation: Variants of a Certain Significance.Circ Genom Precis Med2018
29720397Increased long QT and torsade de pointes reporting on tamoxifen compared with aromatase inhibitors.Heart2018
29606593A Mechanism of Calmodulin Modulation of the Human Cardiac Sodium Channel.Structure2018
29709575Arrhythmia genetics: Not dark and lite, but 50 shades of gray.Heart Rhythm2018
28542097Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.Pharmacogenet Genomics2017
28207879Comparison of HLA allelic imputation programs.PLoS One2017
28490672Phenome-wide scanning identifies multiple diseases and disease severity phenotypes associated with HLA variants.Sci Transl Med2017
26947264Partially repeatable genetic basis of benthic adaptation in threespine sticklebacks.Evolution2016
27931609Clinical and Biological Insights Into Combined Post- and Pre-Capillary Pulmonary Hypertension.J Am Coll Cardiol2016
26062935Distinct developmental genetic mechanisms underlie convergently evolved tooth gain in sticklebacks.Development2015
26044731Genome Assembly Improvement and Mapping Convergently Evolved Skeletal Traits in Sticklebacks with Genotyping-by-Sequencing.G3 (Bethesda)2015
24652999Modular skeletal evolution in sticklebacks is controlled by additive and clustered quantitative trait Loci.Genetics2014
24966315Two developmentally temporal quantitative trait loci underlie convergent evolution of increased branchial bone length in sticklebacks.Proc Biol Sci2014
24851181Parallel developmental genetic features underlie stickleback gill raker evolution.Evodevo2014
19852954The Zn finger protein Iguana impacts Hedgehog signaling by promoting ciliogenesis.Dev Biol2010
20686598Exploring the genetic basis of variation in gene predictions with a synthetic association study.PLoS One2010
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Collaborators

Dan M Roden
Vanderbilt University Medical Center
Co-authored papers 28
Christian M Shaffer
Vanderbilt University
Co-authored papers 8
Quinn S Wells
Vanderbilt University Medical Center
Co-authored papers 8
Jonathan D Mosley
Vanderbilt University Medical Center
Co-authored papers 7
Moore Benjamin Shoemaker
Vanderbilt University Medical Center
Co-authored papers 5
Joshua C Denny
Vanderbilt University
Co-authored papers 5
Douglas M Fowler
University of Washington, USA Brotman Baty Institute for Precision Medicine
Co-authored papers 3
Kenneth C Anderson
Dana Farber Cancer Institute
Co-authored papers 3
Eric Farber-Eger
Vanderbilt University Medical Center
Co-authored papers 3
Jason H Karnes
Vanderbilt University Medical Center
Co-authored papers 3
Sara L Van Driest
National Institutes of Health
Co-authored papers 3
Lisa Bastarache
Vanderbilt University Medical Center
Co-authored papers 3
Kevin Bersell
Vanderbilt University
Co-authored papers 2
Frederick P Roth
University of Toronto
Co-authored papers 2
Scott J Hebbring
Marshfield Clinic Research Institute
Co-authored papers 2
Wei-Qi Wei
Vanderbilt University Medical Center
Co-authored papers 2
Thomas Stricker
Co-authored papers 2
Patrick T Ellinor
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 2
Elizabeth J Phillips
Vanderbilt University Medical Center
Co-authored papers 2
Steven A Lubitz
Cardiovascular Research Center, Massachusetts General Hospital
Co-authored papers 2
John A Capra
Bakar Computational Health Sciences Institute, University of California san francisco
Co-authored papers 2
Victoria N Parikh
Stanford University
Co-authored papers 2
Murray H Brilliant
Marshfield Clinic Research Institute
Co-authored papers 2
Alfred L George
Northwestern University Feinberg School of Medicine
Co-authored papers 2
Peter Weeke
Rigshospitalet, University of Copenhagen
Co-authored papers 1
Sunghwan Sohn
Mayo Clinic
Co-authored papers 1
Qiong Yang
Co-authored papers 1
Braxton D Mitchell
Co-authored papers 1
Jennifer A Pacheco
University of Pennsylvania
Co-authored papers 1
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 1
Release 1.2