Hong-yan Wang
State Key Laboratory Of Genetic
Shanghai, 200011, China
Shanghai, 200011, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 16 publications
Identification and Functional Analysis of Rare HECTD1 Missense Variants in Human Neural Tube Defects.
Journal: Research square
Published: January 23, 2024
Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects.
Journal: Human genetics
Published: December 23, 2023
Novel mutations of AXIN2 identified in a Chinese Congenital Heart Disease Cohort.
Journal: Journal of human genetics
Published: November 01, 2018
Variants identified in PTK7 associated with neural tube defects.
Journal: Molecular genetics & genomic medicine
Published: September 13, 2018
A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population.
Journal: Cell discovery
Published: May 02, 2017
A missense mutation in TCN2 is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin.
Journal: Oncotarget
Published: November 15, 2016
Mild decrease in TBX20 promoter activity is a potentially protective factor against congenital heart defects in the Han Chinese population.
Journal: Scientific reports
Published: September 06, 2015
Quantitative assessment of maternal biomarkers related to one-carbon metabolism and neural tube defects.
Journal: Scientific reports
Published: September 29, 2014
A functional variant in the cystathionine β-synthase gene promoter significantly reduces congenital heart disease susceptibility in a Han Chinese population.
Journal: Cell research
Published: September 19, 2012
Last Updated: 09/26/2026