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Endothelial to Mesenchymal Transition in Cardiovascular Disease: JACC State-of-the-Art Review

Journal of the American College of Cardiology, 2019-01, Vol.73 (2), p.190-209

2019

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Long Noncoding RNAs in Cardiac Development and Pathophysiology

Circulation research, 2012-10, Vol.111 (10), p.1349-1362

2012

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Basic Biology of Extracellular Matrix in the Cardiovascular System, Part 1/4: JACC Focus Seminar

Journal of the American College of Cardiology, 2020-05, Vol.75 (17), p.2169-2188

2020

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Cardiogenic Genes Expressed in Cardiac Fibroblasts Contribute to Heart Development and Repair

Circulation research, 2014-04, Vol.114 (9), p.1422-1434

2014

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Cardiac fibroblast heterogeneity and dynamics through the lens of single-cell dual 'omics

Cardiovascular research, 2022-05, Vol.118 (6), p.1380-1382

2022

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Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide

Journal of the American College of Cardiology, 2017-02, Vol.69 (7), p.859-870

2017

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Exclusion of the left atrial appendage with a novel device: Early results of a multicenter trial

The Journal of thoracic and cardiovascular surgery, 2011-11, Vol.142 (5), p.1002-1009.e1

2011

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Novel Mouse Model for Selective Tagging, Purification, and Manipulation of Cardiac Myofibroblasts

Circulation (New York, N.Y.), 2024-06, Vol.149 (24), p.1931-1934

2024

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Targeted Next-Generation Sequencing Identifies Pathogenic Variants in Familial Congenital Heart Disease

Journal of the American College of Cardiology, 2014-12, Vol.64 (23), p.2498-2506

2014

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Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genes

The American heart journal, 2022-02, Vol.244, p.1-13

2022

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Molecular Pathway for the Localized Formation of the Sinoatrial Node

Circulation research, 2007-02, Vol.100 (3), p.354-362

2007

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Introducing the Western Australian Cardiovascular Research Alliance (WACRA) – Why?, Why Now? And How Can Government Help?

Heart, lung & circulation, 2021-10, Vol.30 (10), p.e117-e118

2021

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Insights into the genetic architecture underlying complex, critical congenital heart disease

The American heart journal, 2022-12, Vol.254, p.166-171

2022

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Pitx2c and Nkx2-5 Are Required for the Formation and Identity of the Pulmonary Myocardium

Circulation research, 2007-10, Vol.101 (9), p.902-909

2007

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Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease

The American heart journal, 2018-07, Vol.201, p.33-39

2018

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Neuregulin 1 Sustains the Gene Regulatory Network in Both Trabecular and Nontrabecular Myocardium

Circulation research, 2010-09, Vol.107 (6), p.715-727

2010

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Irreversible Triggers for Hypertrophic Cardiomyopathy Are Established in the Early Postnatal Period

Journal of the American College of Cardiology, 2015-02, Vol.65 (6), p.560-569

2015

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Inhibition of Notch2 by Numb/Numblike controls myocardial compaction in the heart

Cardiovascular research, 2012-11, Vol.96 (2), p.276-285

2012

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Biased DNA Segregation and Cardiac Stem Cell Therapies

Circulation research, 2012-09, Vol.111 (7), p.827-830

2012

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The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease

International journal of cardiology, 2017-03, Vol.230, p.155-163

2017

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Formation of the Venous Pole of the Heart From an Nkx2–5–Negative Precursor Population Requires Tbx18

Circulation research, 2006-06, Vol.98 (12), p.1555-1563

2006

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Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy

Circulation. Cardiovascular genetics, 2013-06, Vol.6 (3), p.238-247

2013

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PDGF-AB Reduces Myofibroblast Differentiation Without Increasing Proliferation After Myocardial Infarction

JACC. Basic to translational science, 2023-06, Vol.8 (6), p.658-674

2023

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Cardiac homeobox gene NKX2-5 Mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome

Journal of the American College of Cardiology, 2003-06, Vol.41 (11), p.2072-2076

2003

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Nkx2-5 represses Gata1 gene expression and modulates the cellular fate of cardiac progenitors during embryogenesis

Circulation (New York, N.Y.), 2011-04, Vol.123 (15), p.1633-1641

2011

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Endothelial to Mesenchymal Transition in Cardiovascular Disease: JACC State-of-the-Art Review

Long Noncoding RNAs in Cardiac Development and Pathophysiology

Basic Biology of Extracellular Matrix in the Cardiovascular System, Part 1/4: JACC Focus Seminar

Cardiogenic Genes Expressed in Cardiac Fibroblasts Contribute to Heart Development and Repair

Cardiac fibroblast heterogeneity and dynamics through the lens of single-cell dual 'omics

Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide

Exclusion of the left atrial appendage with a novel device: Early results of a multicenter trial

Novel Mouse Model for Selective Tagging, Purification, and Manipulation of Cardiac Myofibroblasts

Targeted Next-Generation Sequencing Identifies Pathogenic Variants in Familial Congenital Heart Disease

Whole genome sequencing in transposition of the great arteries and associations with clinically relevant heart, brain and laterality genes

Molecular Pathway for the Localized Formation of the Sinoatrial Node

Introducing the Western Australian Cardiovascular Research Alliance (WACRA) – Why?, Why Now? And How Can Government Help?

Insights into the genetic architecture underlying complex, critical congenital heart disease

Pitx2c and Nkx2-5 Are Required for the Formation and Identity of the Pulmonary Myocardium

Genetic burden and associations with adverse neurodevelopment in neonates with congenital heart disease

Neuregulin 1 Sustains the Gene Regulatory Network in Both Trabecular and Nontrabecular Myocardium

Irreversible Triggers for Hypertrophic Cardiomyopathy Are Established in the Early Postnatal Period

Inhibition of Notch2 by Numb/Numblike controls myocardial compaction in the heart

Biased DNA Segregation and Cardiac Stem Cell Therapies

The promises and challenges of exome sequencing in familial, non-syndromic congenital heart disease

Formation of the Venous Pole of the Heart From an Nkx2–5–Negative Precursor Population Requires Tbx18

Functional characterization of a novel mutation in NKX2-5 associated with congenital heart disease and adult-onset cardiomyopathy

PDGF-AB Reduces Myofibroblast Differentiation Without Increasing Proliferation After Myocardial Infarction

Cardiac homeobox gene NKX2-5 Mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome

Nkx2-5 represses Gata1 gene expression and modulates the cellular fate of cardiac progenitors during embryogenesis

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