Xing-Yuan Liu
Biographic Data
| ID | 10482271 |
|---|---|
| NAME | Xing-Yuan Liu |
| GIVEN NAMES | Xing-Yuan |
| FAMILY NAME | Liu |
| SIGNATURE | LIU X |
| AFFILIATIONS | Department of Pediatrics, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China |
| VERIFIED | No |
| TOTAL WORKS | 1 |
| TOTAL CITATIONS | 0 |
| AUTHOR COUNT | 1 |
| EDITOR COUNT | 0 |
| FIRST PUBLICATION YEAR | 2025 |
| LATEST PUBLICATION YEAR | 2025 |
| H-INDEX | 0 |
Identification and Functional Characterization of a Novel SOX4 Mutation Predisposing to Coffin–Siris Syndromic Congenital Heart Disease
Background/Objectives: Congenital heart disease (CHD) occurs in ~1% of all live neonates globally, rendering it the most prevalent developmental anomaly affecting humans; this condition confers substantial infant morbidity and mortality worldwide. Although there is ample evidence to suggest a paramount genetic basis for CHD, the genetic etiologies underpinning the majority of CHD remain elusive. In the present study, SOX4 was selected as a signif…
No prominent works on this page.
Identification and Functional Characterization of a Novel SOX4 Mutation Predisposing to Coffin–Siris Syndromic Congenital Heart Disease
Background/Objectives: Congenital heart disease (CHD) occurs in ~1% of all live neonates globally, rendering it the most prevalent developmental anomaly affecting humans; this condition confers substantial infant morbidity and mortality worldwide. Although there is ample evidence to suggest a paramount genetic basis for CHD, the genetic etiologies underpinning the majority of CHD remain elusive. In the present study, SOX4 was selected as a signif…
Biology (1 work) · Chromatin Remodeling and Cancer (1 work) · Congenital heart defects research (1 work) · Gene (1 work) · Gene expression (1 work) · Genetics (1 work) · Genetics and Neurodevelopmental Disorders (1 work) · Mutation (1 work) · Phenotype (1 work) · Proband (1 work)