List of works - Kun Sun

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

scientific article published on 08 March 2017

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

article

A nonsense variation p.Arg325X in thevascular endothelial growth factor-Agene may be associated with congenital tricuspid aortic valve stenosis ⬇️

scientific article published on 09 November 2011

Cheatham-Platinum stent implantation for pulmonary artery stenosis in children and adolescents: immediate and mid-term outcome ⬇️

scientific article published on November 16, 2010

Chinese fetal biometry: reference equations and comparison with charts from other populations

scientific article published on 7 December 2017

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

scientific article

Doppler myocardial performance index in assessment of ventricular function in children with single ventricles

scientific article published on 01 May 2008

Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection

scientific article

Duplication and deletion of CFC1 associated with heterotaxy syndrome

scientific article

Effects of chronic hypoxia on the expression of calmodulin and calcicum/calmodulin-dependent protein kinase II and the calcium activity in myocardial cells in young rats

scientific article published in June 2008

Evaluation of the development of pulmonary vessels with pulmonary venous index in congenital heart disease with decreased pulmonary blood flow

scientific article published in December 2007

Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect

scientific article published on 12 February 2020

Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect

scholarly article by Huilin Xie et al published 2019 in Frontiers in Genetics

Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

scientific article published on 17 September 2018

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients

scientific article

Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing

scientific article published on 12 February 2020

Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease

scientific article published on 12 June 2015

MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation

scientific article published on 22 June 2020

Novel CRELD1 gene mutations in patients with atrioventricular septal defect

scientific article

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion

scientific article

Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect

scientific article published in June 2014

Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects.

scientific article

Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects

scientific article published on 31 October 2017

[Clinical diagnosis of anomalous origin of the left coronary artery from the pulmonary artery in 22 cases]

scientific article published on 01 December 2008

[Exercise capacity evaluation after percutaneous balloon pulmonary valvuloplasty in children with pulmonary valve stenosis]

scientific article published on 01 January 2007

[Risk factors for arrhythmia early after transcatheter closure of perimembranous ventricular septal defects]

scientific article published on 01 October 2005

[Therapeutic effect of Cheatham-Platinum stent implantation for vessel stenosis associated with congenital heart disease in children and adolescents]

scientific article published on 01 April 2009

[Transcatheter closure of secundum atrial septal defect in children]

scientific article published on 01 April 2004

List of works by Kun Sun

A 3 base pair deletion in TBX1 leads to reduced protein expression and transcriptional activity

A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication

A nonsense variation p.Arg325X in thevascular endothelial growth factor-Agene may be associated with congenital tricuspid aortic valve stenosis ⬇️

Cheatham-Platinum stent implantation for pulmonary artery stenosis in children and adolescents: immediate and mid-term outcome ⬇️

Chinese fetal biometry: reference equations and comparison with charts from other populations

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus

Doppler myocardial performance index in assessment of ventricular function in children with single ventricles

Duplication and Deletion of 22q11 Associated with Anomalous Pulmonary Venous Connection

Duplication and deletion of CFC1 associated with heterotaxy syndrome

Effects of chronic hypoxia on the expression of calmodulin and calcicum/calmodulin-dependent protein kinase II and the calcium activity in myocardial cells in young rats

Evaluation of the development of pulmonary vessels with pulmonary venous index in congenital heart disease with decreased pulmonary blood flow

Identification of FOXH1 mutations in patients with sporadic conotruncal heart defect

Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect

Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing

Identification of ZFPM2 mutations in sporadic conotruncal heart defect patients

Identification of rare variants in novel candidate genes in pulmonary atresia patients by next generation sequencing

Investigation of Somatic NKX2-5 Mutations in Chinese Children with Congenital Heart Disease

MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation

Novel CRELD1 gene mutations in patients with atrioventricular septal defect

Novel TBX1 loss-of-function mutation causes isolated conotruncal heart defects in Chinese patients without 22q11.2 deletion

Potential role of CRELD1 gene in the pathogenesis of atrioventricular septal defect

Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects.

Targeted sequencing identifies novel GATA6 variants in a large cohort of patients with conotruncal heart defects

[Clinical diagnosis of anomalous origin of the left coronary artery from the pulmonary artery in 22 cases]

[Exercise capacity evaluation after percutaneous balloon pulmonary valvuloplasty in children with pulmonary valve stenosis]

[Risk factors for arrhythmia early after transcatheter closure of perimembranous ventricular septal defects]

[Therapeutic effect of Cheatham-Platinum stent implantation for vessel stenosis associated with congenital heart disease in children and adolescents]

[Transcatheter closure of secundum atrial septal defect in children]