Author details

Full Name

Nathan R Tucker

Affiliation

ORCID

Career Start Year

2009

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37449401	Loss of the Atrial Fibrillation-Related Gene, <i>Zfhx3</i>, Results in Atrial Dilation and Arrhythmias.	Circ Res	2023
35114252	Increased atrial effectiveness of flecainide conferred by altered biophysical properties of sodium channels.	J Mol Cell Cardiol	2022
35732739	Single-nucleus profiling of human dilated and hypertrophic cardiomyopathy.	Nature	2022
35922509	Transcriptome variation in human tissues revealed by long-read sequencing.	Nature	2022
34663679	SnRNA sequencing defines signaling by RBC-derived extracellular vesicles in the murine heart.	Life Sci Alliance	2021
33654293	Single-cell meta-analysis of SARS-CoV-2 entry genes across tissues and demographics.	Nat Med	2021
34341789	Molecular Pathophysiology of Cardiac Injury and Cardiac Microthrombi in Fatal COVID-19: Insights from Clinico-histopathologic and Single Nuclei RNA Sequencing Analyses.		2021
32717170	Epigenetic and Transcriptional Networks Underlying Atrial Fibrillation.	Circ Res	2020
32248749	Identification of Functional Variant Enhancers Associated With Atrial Fibrillation.	Circ Res	2020
32403949	Transcriptional and Cellular Diversity of the Human Heart.	Circulation	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
33155827	Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation.	Circ Genom Precis Med	2020
32795091	Myocyte-Specific Upregulation of <i>ACE2</i> in Cardiovascular Disease: Implications for SARS-CoV-2-Mediated Myocarditis.	Circulation	2020
32511660	Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 mediated myocarditis.	medRxiv	2020
31112420	Genome-Wide Association Study-Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse.	Circ Genom Precis Med	2019
31636200	Long-range <i>Pitx2c</i> enhancer-promoter interactions prevent predisposition to atrial fibrillation.	Proc Natl Acad Sci U S A	2019
31070942	Cardioprotective Effects of MTSS1 Enhancer Variants.	Circulation	2019
29540468	Genetic Reduction in Left Ventricular Protein Kinase C-Î± and Adverse Ventricular Remodeling in Human Subjects.	Circ Genom Precis Med	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018
30535219	Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation.	JAMA	2018
29748316	Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval.	Circ Genom Precis Med	2018
29650770	Response by Ma et al to Letter Regarding Article, "Novel Mutation in <i>FLNC</i> (Filamin C) Causes Familial Restrictive Cardiomyopathy".	Circ Genom Precis Med	2018
27756709	Gain-of-function mutations in GATA6 lead to atrial fibrillation.	Heart Rhythm	2017
28416818	Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
28974514	Diminished <i>PRRX1</i> Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential.	Circ Cardiovasc Genet	2017
28747752	Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.	Nat Genet	2017
29212899	Novel Mutation in <i>FLNC</i> (Filamin C) Causes Familial Restrictive Cardiomyopathy.	Circ Cardiovasc Genet	2017
27866707	A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a.	Am J Hum Genet	2016
26733238	Common variation in atrial fibrillation: navigating the path from genetic association to mechanism.	Cardiovasc Res	2016
27162171	Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures.	Elife	2016
27855642	Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families.	BMC Med Genet	2016
27792790	PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance.	PLoS Genet	2016
26301497	Genetic association analyses highlight biological pathways underlying mitral valve prolapse.	Nat Genet	2015
24607718	A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation.	Heart Rhythm	2014
24296650	Overexpression of KCNN3 results in sudden cardiac death.	Cardiovasc Res	2014
24763465	Emerging directions in the genetics of atrial fibrillation.	Circ Res	2014
25124494	Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.	Circulation	2014
21814572	HSF1 is essential for the resistance of zebrafish eye and brain tissues to hypoxia/reperfusion injury.	PLoS ONE	2011
19238587	Hsp27 is persistently expressed in zebrafish skeletal and cardiac muscle tissues but dispensable for their morphogenesis.	Cell Stress and Chaperones	2009
19580808	Hsp27 associates with the titin filament system in heat-shocked zebrafish cardiomyocytes.	Experimental Cell Research	2009