Hong-yu Shi

Zhongshan Hospital Wusong Branch
Zhongshan, 200940, China

Last Updated: 09/26/2026

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Found 18 publications

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease.

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease.

Journal: Diagnostics (Basel, Switzerland)

Published: June 03, 2022

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

Journal: American journal of translational research

Published: August 08, 2021

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.

VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy.

Journal: European journal of medical genetics

Published: July 30, 2021

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.

Journal: Genes

Published: January 09, 2021

SOX17 loss-of-function variation underlying familial congenital heart disease.

SOX17 loss-of-function variation underlying familial congenital heart disease.

Journal: European journal of medical genetics

Published: December 14, 2020

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

Journal: The American journal of cardiology

Published: September 08, 2017

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Journal: Heart and vessels

Published: July 11, 2017

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.

Journal: International heart journal

Published: July 11, 2017

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.

Journal: Clinical chemistry and laboratory medicine

Published: May 24, 2017

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.

Journal: International journal of medical sciences

Published: October 06, 2016

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.

Journal: International journal of molecular medicine

Published: October 03, 2016

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Journal: Clinical chemistry and laboratory medicine

Published: July 10, 2016

Showing 1-12 of 18

Last Updated: 09/26/2026