Liangliang Qiu

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

Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese families

Haizhu Chen, Guorong Xu, Lin Feng et al. · Neuromuscular Disorders · 2019 · 29 citations

Medicine, Genetics, Molecular Genetics +10

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

<i>ATP1A1</i>mutations cause intermediate Charcot‐Marie‐Tooth disease

J. He, Lingling Guo, Shan Lin et al. · Human Mutation · 2019 · 16 citations

Life Sciences, Genetics, Molecular Genetics +17

Dysferlinopathy in a cohort of Chinese patients: clinical features, mutation spectrum, and imaging findings

Qi‐Fu Guo, Zhixian Ye, Liangliang Qiu et al. · Chinese Medical Journal · 2021 · 16 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17