Zhiqiang Wang

Molecular analysis of 51 unrelated pedigrees with late-onset multiple acyl-CoA dehydrogenation deficiency (MADD) in southern China confirmed the most common ETFDH mutation and high carrier frequency of c.250G>A

Zhiqiang Wang, Xuejiao Chen, Shen-Xing Murong et al. · Journal of Molecular Medicine · 2011 · 98 citations

Mendelian Disorder, Genetic Disorder, Common Etfdh Mutation +8

Single-molecule optical mapping enables quantitative measurement of D4Z4 repeats in facioscapulohumeral muscular dystrophy (FSHD)

Yi Dai, Pidong Li, Zhiqiang Wang et al. · Journal of Medical Genetics · 2019 · 74 citations · Full text

Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study

Zhiqiang Wang, Liangliang Qiu, Min-Ting Lin et al. · The Lancet Regional Health - Western Pacific · 2021 · 38 citations · Full text

1,2-Dichloroethane-induced toxic encephalopathy: A case series with morphological investigations

Shiyan Chen, Zhijian Zhang, Hong Lin et al. · Journal of the Neurological Sciences · 2015 · 37 citations

Poisoning, Case Series, Toxicology +8

Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients

Danyu Song, Yi Dai, Xiaoyu Chen et al. · Clinical Genetics · 2020 · 37 citations