List of works - Nathan R Tucker

A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a

scientific article published on 16 November 2016

A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation

scientific article

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Deep learning enables genetic analysis of the human thoracic aorta

scientific article published on 26 November 2021

Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential

scientific article

Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

scientific article (publication date: 10 May 2016)

Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

scientific article published on 06 November 2020

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

scientific article published in July 2017

Gain-of-function mutations in GATA6 lead to atrial fibrillation

scientific journal article

Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

scientific article published on 24 August 2015

HSF1 Is Essential for the Resistance of Zebrafish Eye and Brain Tissues to Hypoxia/Reperfusion Injury ⬇️

scientific article published on July 21, 2011

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

scientific article published on 14 August 2014

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

scientific article

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

scientific article published on 21 May 2020

Multi-ethnic genome-wide association study for atrial fibrillation

article

Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families.

scientific article

Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 Mediated Myocarditis

scientific article published on 22 June 2020

Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 mediated myocarditis

scientific article published on 14 April 2020

Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy

scientific article published in December 2017

Transcriptome variation in human tissues revealed by long-read sequencing

scientific article

List of works by Nathan R Tucker

A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a

A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation

Association Between Titin Loss-of-Function Variants and Early-Onset Atrial Fibrillation

Common and Rare Coding Genetic Variation Underlying the Electrocardiographic PR Interval

Deep learning enables genetic analysis of the human thoracic aorta

Diminished PRRX1 Expression Is Associated With Increased Risk of Atrial Fibrillation and Shortening of the Cardiac Action Potential

Discovery and validation of sub-threshold genome-wide association study loci using epigenomic signatures

Epigenetic Analyses of Human Left Atrial Tissue Identifies Gene Networks Underlying Atrial Fibrillation

Erratum: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation

Gain-of-function mutations in GATA6 lead to atrial fibrillation

Genetic Reduction in Left Ventricular Protein Kinase C-α and Adverse Ventricular Remodeling in Human Subjects

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

HSF1 Is Essential for the Resistance of Zebrafish Eye and Brain Tissues to Hypoxia/Reperfusion Injury ⬇️

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation.

Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

Multi-ethnic genome-wide association study for atrial fibrillation

Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families.

Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 Mediated Myocarditis

Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 mediated myocarditis

Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy

Transcriptome variation in human tissues revealed by long-read sequencing