Hongmei Zhang

Two pedigrees with arrhythmogenic right ventricular cardiomyopathy linked with R49H and F531C mutation in DSG2

Xiaoping Li, Chenqing Zheng, Xuepin Chen, 2019, Human Genome Variation.

Targeted next-generation sequencing identified a known EMD mutation in a Chinese patient with Emery-Dreifuss muscular dystrophy

Xiaoping Li, Chenqing Zheng, Xuepin Chen, 2019, Human Genome Variation.

Two pedigrees with arrhythmogenic right ventricular cardiomyopathy linked with R49H and F531C mutation in DSG2

Chenqing Zheng, Xuepin Chen, Hui Peng, 2019, Human Genome Variation.

Genome-Wide Gene Expression Profiles Reveal Distinct Molecular Characteristics of the Goose Granulosa Cells

Guangliang Gao, Xianzhi Zhao, Youhui Xie, 2021, Frontiers in Genetics.

A Novel EMD Mutation Identified by Whole-Exome Sequencing in Twins with Emery–Dreifuss Muscular Dystrophy

Xiaoping Li, Rong Luo, Chenqing Zheng, 2020, Case reports in genetics.

ANovelEMDMutation Identified byWhole-ExomeSequencing in Twins with Emery–Dreifuss Muscular Dystrophy

Xiaoping Li, Rong Luo, Chenqing Zheng, 2020 .

Prognosis of patients with familial hypertrophic cardiomyopathy: A single-center cohort study with ten-year follow-up by propensity score matching analysis

W. Hua, Xiaoping Li, Hongmei Zhang, 2023, Heliyon.