Lista de obras -

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

artículo científico publicado en 2016

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

artículo científico publicado en 2014

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

artículo científico publicado en 2021

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado el 21 de julio de 2011

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

artículo científico publicado en 2014

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

artículo científico publicado en 2017

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.

artículo científico publicado en 2016

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

artículo científico publicado en 2020

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

artículo científico publicado en 2017

Transcriptome variation in human tissues revealed by long-read sequencing

artículo científico publicado en 2021

Lista de obras de

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