Junjie He

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 · 39 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency

Hong‐Xia Fu, Xinyi Liu, Zhiqiang Wang et al. · Neurological Sciences · 2016 · 31 citations

Life Sciences, Genetics, Molecular Genetics +11

Clinical and genetic features of patients with facial‐sparing facioscapulohumeral muscular dystrophy

Junjie He, Xiaodan Lin, Fei Lin et al. · European Journal of Neurology · 2017 · 29 citations

Medicine, Genetics, Molecular Genetics +14

Association of 4qA-Specific Distal D4Z4 Hypomethylation With Disease Severity and Progression in Facioscapulohumeral Muscular Dystrophy

Fuze Zheng, Liangliang Qiu, Long Chen et al. · Neurology · 2023 · 21 citations · Full text

Medicine, Genetics, Molecular Genetics +16

Skeletal Muscle Magnetic Resonance Imaging of the Lower Limbs in Late-onset Lipid Storage Myopathy with Electron Transfer Flavoprotein Dehydrogenase Gene Mutations

Xin-Yi Liu, Ming Jin, Zhiqiang Wang et al. · Chinese Medical Journal · 2016 · 13 citations · Full text

Medicine, Genetics, Neurology +17