En‐Lin Dong

Biallelic Mutations in MYORG Cause Autosomal Recessive Primary Familial Brain Calcification

Xiang‐Ping Yao, Xuewen Cheng, Chong Wang et al. · Neuron · 2018 · 156 citations · Full text

Life Sciences, Genetics, Molecular Genetics +10

Clinical spectrum and genetic landscape for hereditary spastic paraplegias in China

En‐Lin Dong, Chong Wang, Shuang Wu et al. · Molecular Neurodegeneration · 2018 · 77 citations · Full text

Life Sciences, Genetics, Neurology +11

Stop-gain mutations in UBAP1 cause pure autosomal-dominant spastic paraplegia

Xiang Lin, Hui‐Zhen Su, En‐Lin Dong et al. · Brain · 2019 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Analysis of gene expression and functional characterization of XPR1: a pathogenic gene for primary familial brain calcification

Xiang‐Ping Yao, Miao Zhao, Chong Wang et al. · Cell and Tissue Research · 2017 · 31 citations

Life Sciences, Genetics, Molecular Genetics +9

Modeling the phenotype of spinal muscular atrophy by the direct conversion of human fibroblasts to motor neurons

Qi‐Jie Zhang, Jin-Jing Li, Xiang Lin et al. · Oncotarget · 2017 · 25 citations · Full text

Medicine, Neurobiology, Neuroscience +11