Ke Li

Clinico-pathological features and mutational spectrum of 16 nemaline myopathy patients from a Chinese neuromuscular center

C. Pu, Zhenfu Wang, Hui-fang Wang, 2021, Acta Neurologica Belgica.

Proteomic study of sporadic inclusion body myositis

Xusheng Huang, C. Pu, Jie-xiao Liu, 2014, Proteome Science.

Two de novo variations identified by massively parallel sequencing in 13 Chinese families with children diagnosed with autism spectrum disorder.

Zhiye Chen, Shengyuan Yu, Jun Wang, 2018, Clinica chimica acta; international journal of clinical chemistry.

Case Report: Diagnosis of Human Alveolar Echinococcosis via Next-Generation Sequencing Analysis

Q. Shi, R. Ban, Ke Li, 2021, Frontiers in Genetics.

A Case of Myotonic Dystrophy Type I With Rimmed Vacuoles in Skeletal Muscle Pathology.

Q. Shi, R. Ban, Ke Li, 2020, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

A novel application of tau PET in the diagnosis of sporadic inclusion body myositis

Q. Shi, C. Pu, Jiajin Liu, 2020, Medicine.

11C-PIB PET of inclusion body myositis: Molecular imaging of amyloid beta expression improving imaging-pathology correlations.

Q. Shi, Haodan Dang, Ke Li, 2020, Clinical Neuropathology.

Clinicopathologic features of sporadic inclusion body myositis in China.

Xusheng Huang, C. Pu, Jie-xiao Liu, 2015, Neurologia i neurochirurgia polska.

High‐throughput transcriptomic profiling of mRNAs and lncRNAs in the dermatomyositis muscle by RNA sequencing

Q. Shi, Shanchun Zhang, R. Ban, 2023, Rheumatology & Autoimmunity.