Nanchao Hong

Sun Yat-sen University — China

Biochemistry, Genetics and Molecular Biology · Life Sciences

8h-index208citations23works0.32yr avg
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Research Topics

Congenital heart defects research(11), Congenital Heart Disease Studies(9), Cardiac Valve Diseases and Treatments(6), Aortic Disease and Treatment Approaches(5), Infective Endocarditis Diagnosis and Management(4)

Publications23 total

TCT-628 Ascending Aorta is the Key Predictor for Pure Native Aortic Regurgitation Patients Underwent Self-expandable Transfemoral Transcatheter Aortic Valve Replacement: From the Multicenter National NTCVR Database in China
Journal of the American College of Cardiology·2025
Age-related outcomes of transcatheter aortic valve replacement in patients with pure severe aortic regurgitation
Cardiology·2025
Deficiency of Sox7 leads to congenital aortic stenosis via abnormal valve remodeling
Journal of Molecular and Cellular Cardiology·2025· 1 cited
Transcatheter Aortic Valve Replacement for Bicuspid vs. Tricuspid Aortic Stenosis among Patients at Low Surgical Risk in China: From the Multicenter National NTCVR Database
Journal of Clinical Medicine·2023· 6 citedOpen Access
Deficiency of Sox7 Leads to Congenital Aortic Stenosis via Abnormal Valve Remodeling
SSRN Electronic Journal·2023Open Access
The China Heart Valve Center and National Transcatheter Valve Therapeutics Registry database
Cardiology Plus·2022· 8 citedOpen Access
Transcatheter Aortic Valve Replacement in Low-Risk Patients With Severe Aortic Valve Stenosis in Chinese Patients
JACC Asia·2022· 5 citedOpen Access
Predisposition to atrioventricular septal defects may be caused by SOX7 variants that impair interaction with GATA4
Molecular Genetics and Genomics·2022· 2 cited
Coronary Artery Fistula: To Close or Not Close, That Is the Question
Cardiology Plus·2021Open Access
The transcription factor Sox7 modulates endocardiac cushion formation contributed to atrioventricular septal defect through Wnt4/Bmp2 signaling
Cell Death and Disease·2021· 17 citedOpen Access
MESP2 variants contribute to conotruncal heart defects by inhibiting cardiac neural crest cell proliferation
Journal of Molecular Medicine·2020· 6 cited
Three rare variants of SOX7 impairing its interaction with GATA4 may be a predisposing factor to complete AVSD
2020Open Access
LncRNAs as Therapeutic Targets for Autophagy-involved Cardiovascular Diseases: A Review of Molecular Mechanism and T herapy Strategy
Current Medicinal Chemistry·2020· 10 cited
[In-utero interventional treatment of two cases with critical aortic stenosis].
PubMed·2020· 1 cited
Oversized composite braided biodegradable stents with post-dilatation for pediatric applications: mid-term results of a porcine study
Biomaterials Science·2020· 11 cited
Self-expanding apical closure device for full-percutaneous closed-chest transapical valve procedures with large-sized introducer sheaths: first study in an animal model
Interactive Cardiovascular and Thoracic Surgery·2019· 3 citedOpen Access
A novel braided biodegradable stent for use in congenital heart disease: Short‐term results in porcine iliac artery
Journal of Biomedical Materials Research Part A·2019· 18 cited
Identification of Rare Copy Number Variants Associated With Pulmonary Atresia With Ventricular Septal Defect
Frontiers in Genetics·2019· 28 citedOpen Access
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
Journal of Translational Medicine·2018· 5 citedOpen Access
Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing
Human Genomics·2018· 25 citedOpen Access
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Frequent Co-authors

Kun Sun(13), Yu Yu(11), Erge Zhang(6), Chen Sun(6), Lihui Jin(6), Wenzhi Pan(6), Qihua Fu(5), Fen Li(5), Junbo Ge(5), Huilin Xie(4), Qi Zhang(4), Yanan Lu(4), Daxin Zhou(4), Hanbo Hu(3), Alex F. Chen(3), Sun Chen(3), Zhuoyan Li(3), Jianping Yang(3), Yuejuan Xu(3), Chen Sun(2)