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Author Details
Full Name
Moore Benjamin Shoemaker
Affiliation
Vanderbilt University Medical Center
ORCID
Career Start Year
1997
Papers
127
H Index
39
Expertise
CM4AI Collaborator
Sarah J Ratcliffe (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36241009
Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General Population.
Am J Kidney Dis
2023
37662265
WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE.
medRxiv
2023
37834023
Disruption of Z-Disc Function Promotes Mechanical Dysfunction in Human Myocardium: Evidence for a Dual Myofilament Modulatory Role by Alpha-Actinin 2.
Int J Mol Sci
2023
37495323
Pulmonary Vein Myocardial Sleeve Length and its Association With Sex and 4q25/PITX2 Genotype.
JACC Clin Electrophysiol
2023
37348055
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
Genetics
2023
37046083
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis.
Nature
2023
37034657
The impact of damaging epilepsy and cardiac genetic variant burden in sudden death in the young.
medRxiv
2023
37431591
Adding open spectral data to MassBank and PubChem using open source tools to support non-targeted exposomics of mixtures.
Environ Sci Process Impacts
2023
37164047
Multicenter clinical and functional evidence reclassifies a recurrent noncanonical filamin C splice-altering variant.
Heart Rhythm
2023
37396334
Cardiac Sarcoidosis and a Likely Pathogenic <i>TTN</i> Variant in a Patient Presenting With Ventricular Tachycardia.
JACC Case Rep
2023
37126548
The genetic determinants of recurrent somatic mutations in 43,693 blood genomes.
Sci Adv
2023
36778406
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants.
bioRxiv
2023
36305812
PubChem 2023 update.
Nucleic Acids Res
2023
34930020
Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study.
Circulation
2022
35544069
Mortality Among Patients With Early-Onset Atrial Fibrillation and Rare Variants in Cardiomyopathy and Arrhythmia Genes.
JAMA Cardiol
2022
35592775
The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations.
Front Endocrinol (Lausanne)
2022
35385311
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential.
Sci Adv
2022
36074954
Catheter Ablation for Atrial Fibrillation in Adult Congenital Heart Disease: An International Multicenter Registry Study.
Circ Arrhythm Electrophysiol
2022
36166682
A Mechanistic Clinical Trial Using (<i>R</i>)- Versus <i>(S</i>)-Propafenone to Test RyR2 (Ryanodine Receptor) Inhibition for the Prevention of Atrial Fibrillation Induction.
Circ Arrhythm Electrophysiol
2022
36284750
The NORMAN Suspect List Exchange (NORMAN-SLE): facilitating European and worldwide collaboration on suspect screening in high resolution mass spectrometry.
Environ Sci Eur
2022
36050321
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways.
Nat Commun
2022
35245370
Genome-wide association study reveals novel genetic loci: a new polygenic risk score for mitral valve prolapse.
Eur Heart J
2022
33151290
PubChem in 2021: new data content and improved web interfaces.
Nucleic Acids Res
2021
33720349
Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries.
Genetics
2021
33825250
Prevalence and predictors of pacing-induced cardiomyopathy in young adult patients (<60 years) with pacemakers.
J Cardiovasc Electrophysiol
2021
33516708
Genetic Testing for Early Onset Atrial Arrhythmias Changes Clinical Management: 2 Cases of Cardiac Emerinopathy.
JACC Clin Electrophysiol
2021
33647223
Predictive Accuracy of a Polygenic Risk Score for Postoperative Atrial Fibrillation After Cardiac Surgery.
Circ Genom Precis Med
2021
33895829
Genetic Thyrotropin Regulation of Atrial Fibrillation Risk Is Mediated Through an Effect on Height.
J Clin Endocrinol Metab
2021
34495297
Early-Onset Atrial Fibrillation and the Prevalence of Rare Variants in Cardiomyopathy and Arrhythmia Genes.
JAMA Cardiol
2021
34454591
2-Hydroxybenzylamine (2-HOBA) to prevent early recurrence of atrial fibrillation after catheter ablation: protocol for a randomized controlled trial including detection of AF using a wearable device.
Trials
2021
34238011
Management of Congenital Long-QT Syndrome: Commentary From the Experts.
Circ Arrhythm Electrophysiol
2021
31599812
Clinical and Genetic Contributors to New-Onset Atrial Fibrillation in Critically Ill Adults.
Crit Care Med
2020
31881284
Higher risk at the lower end of the age spectrum in Brugada syndrome.
Heart Rhythm
2020
32091590
Atropine-induced sinus tachycardia protects against exercise-induced ventricular arrhythmias in patients with catecholaminergic polymorphic ventricular tachycardia.
Europace
2020
32716712
How Will Genetics Inform the Clinical Care of Atrial Fibrillation?
Circ Res
2020
32819535
Conduction Recovery After Cavotricuspid Isthmus Ablation When Performed With or Without Concomitant Atrial Fibrillation Ablation.
JACC Clin Electrophysiol
2020
32614720
Atrial Fibrillation Is a Complex Trait: Very Complex.
Circ Res
2020
32553227
Structural Abnormalities on Cardiac Magnetic Resonance Imaging in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia.
JACC Clin Electrophysiol
2020
32439900
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.
Nat Commun
2020
30371825
PubChem 2019 update: improved access to chemical data.
Nucleic Acids Res
2019
31515883
Clinical predictors of acute hyponatremia following LARIAT ligation of the left atrial appendage.
J Cardiovasc Electrophysiol
2019
31045260
Premature battery depletion due to compromised low-voltage capacitor in a family of defibrillators.
Pacing Clin Electrophysiol
2019
31004778
Patient-independent human induced pluripotent stem cell model: A new tool for rapid determination of genetic variant pathogenicity in long QT syndrome.
Heart Rhythm
2019
28917558
Cardiac sympathectomy for the management of ventricular arrhythmias refractory to catheter ablation.
Heart Rhythm
2018
29892015
Multi-ethnic genome-wide association study for atrial fibrillation.
Nat Genet
2018
30025701
Association of Body Mass Index With Intracardiac Left Atrial Voltage in Patients With Atrial Fibrillation.
JACC Clin Electrophysiol
2018
29914646
Relation of Body Mass Index to Symptom Burden in Patients withAtrial Fibrillation.
Am J Cardiol
2018
30089570
Pulmonary Vein Sleeve Length and Association With Body Mass Index and Sex in Atrial Fibrillation.
JACC Clin Electrophysiol
2018
29868113
Identification of Central Regulators of Calcium Signaling and ECM-Receptor Interaction Genetically Associated With the Progression and Recurrence of Atrial Fibrillation.
Front Genet
2018
30535219
Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.
JAMA
2018
1 - 50 of 127
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row(s) 1 - 29 of 29
Collaborators
Dan M Roden
Vanderbilt University Medical Center
Co-authored papers
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National Center for Biotechnology Information
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Alvaro Alonso
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Ramachandran S Vasan
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Joshua C Denny
Vanderbilt University
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Stephen S Rich
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Jennifer A Brody
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Christian M Shaffer
Vanderbilt University
Co-authored papers
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Harvard Medical School, Harvard University
Co-authored papers
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