Quannan Zhuang
Shanghai Key Laboratory Of Birth Defects And Pediatric Heart Center
Shanghai, China
Shanghai, China
Last Updated: 09/26/2026
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Found 9 publications
A cardiac-related, promoter-proximal, regulatory element shapes chromatin and JAG1 transcription.
Journal: Life science alliance
Published: December 15, 2025
Defects in PDIA4 increase individuals' susceptibility to congenital heart disease.
Journal: Frontiers in genetics
Published: November 25, 2025
Essential role of NONO-HOXA1-Wnt axis in cardiomyocyte differentiation.
Journal: Nature communications
Published: May 28, 2025
Identification of candidate genes harboring pathogenic variants in congenital heart disease and laterality defects in Chinese population.
Journal: Frontiers in genetics
Published: February 24, 2025
MST1R Gene Variants Predispose Individuals to Tetralogy of Fallot.
Journal: Phenomics (Cham, Switzerland)
Published: February 28, 2024
Association of copy number variation in X chromosome-linked PNPLA4 with heterotaxy and congenital heart disease.
Journal: Chinese medical journal
Published: October 25, 2023
Analysis of the CHD7 gene mutations in patients of congenital heart disease with extracardiac malformations.
Journal: Translational pediatrics
Published: November 30, 2022
An X-linked PLXNB3 mutation identified in patients with congenital heart disease with neurodevelopmental disabilities.
Journal: Translational pediatrics
Published: October 09, 2022
Showing 1-9 of 9
Last Updated: 09/26/2026