Gong‐Lu Liu

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis

Zhijun Liu, Hui-Xia Lin, Qiao Wei et al. · Aging and Disease · 2019 · 66 citations · Full text

Life Sciences, Genetics, Neurology +17

<i>PRRT2</i> mutation correlated with phenotype of paroxysmal kinesigenic dyskinesia and drug response

Hong‐Fu Li, Wan‐Jin Chen, Ni Wang et al. · Neurology · 2013 · 57 citations

Life Sciences, Genetics, Molecular Genetics +6

Involvement of IRE1α signaling in the hippocampus in patients with mesial temporal lobe epilepsy

Gong‐Lu Liu, Hui Guo, Chunni Guo et al. · Brain Research Bulletin · 2010 · 36 citations

Medicine, Neurobiology, Neuroscience +12

Bi-allelic loss of function variants in <i>COX20</i> gene cause autosomal recessive sensory neuronopathy

Hai‐Lin Dong, Yin Ma, Hao Yu et al. · Brain · 2021 · 35 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Genetic spectrum and clinical profiles in a southeast Chinese cohort of Charcot‐Marie‐Tooth disease

Cong‐Xin Chen, Hai‐Lin Dong, Qiao Wei et al. · Clinical Genetics · 2019 · 32 citations

Life Sciences, Genetics, Molecular Genetics +16