Yu Wang

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 11

Top Topics

Left Ventricular

Endoplasmic Reticulum

Photodynamic Therapy

Top Venues

Prenatal diagnosis

Cardiology research and practice

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaohui Dai, Yu Wang, Hanmin Liu, Jiao Chen
Novel compound heterozygous variants in EMC1: Overlapping phenotypes of left ventricular noncompaction and long QT syndrome warranting in-depth exploration. Prenatal diagnosis 44 (6-7) (2023)
Lihong Pu, Xiaohui Dai, Dan Liu, Yu Wang, Hanmin Liu, Xiaolan He, Jiao Chen
A novel PIEZO2 mutation in a fetus from a Chinese family with Gordon syndrome. Prenatal diagnosis (2023)
Xiaohui Dai, Yu Wang, Hanmin Liu, Jiao Chen
Novel compound heterozygous variants in EMC1: Overlapping phenotypes of left ventricular noncompaction and long QT syndrome warranting in-depth exploration. Prenatal diagnosis 44 (6-7) (2023)
Xiaohui Dai, Yu Wang, Hanmin Liu, Jiao Chen
Novel compound heterozygous variants in EMC1: Overlapping phenotypes of left ventricular noncompaction and long QT syndrome warranting in-depth exploration. Prenatal diagnosis (2023)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis 43 (3) (2022)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis 43 (3) (2022)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis 43 (3) (2022)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis (2022)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis 43 (3) (2022)
Yu Wang, Xiaohui Dai, Hanmin Liu, Jin Peng, Jiao Chen
A novel ZIC3 mutation in a Chinese family with heterotaxy and multiple types of congenital heart defect. Prenatal diagnosis (2022)
Yu Wang, Mingqi Li, Lishan Zhong, Siqi Ren, Hezhi Li, Yongwen Tang, Zhilian Li, Hongwen Fei
Left Atrial Strain as Evaluated by Two-Dimensional Speckle Tracking Predicts Left Atrial Appendage Dysfunction in Chinese Patients with Atrial Fibrillation. Cardiology research and practice 2020 (2020)