Qiao Wei

发表

New clinical characteristics and novel pathogenic variants of patients with hereditary leukodystrophies

Zhi-ying Wu, Juan-juan Xie, W. Ni, 2019, CNS neuroscience & therapeutics.

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Zhi-ying Wu, Qiao Wei, Hong-Fu Li, 2019, Translational Neurodegeneration.

Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients

A. Gitler, W. Ni, Qiao Wei, 2018, Journal of Molecular Medicine.

Identification and functional analysis of novel mutations in the SOD1 gene in Chinese patients with amyotrophic lateral sclerosis

A. Gitler, Qiao Wei, Hong-Fu Li, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis

Qiao Wei, Zhi-Jun Liu, Zhi-Ying Wu, 2019, Aging and disease.

Identified novel heterozygous HTRA1 pathogenic variants in Chinese patients with HTRA1-associated dominant cerebral small vessel disease

Juan Zhang, W. Ni, Qiao Wei, 2022, Frontiers in Genetics.

Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2019, Molecular genetics & genomic medicine.

Targeted next-generation sequencing improves diagnosis of hereditary spastic paraplegia in Chinese patients

A. Gitler, W. Ni, Qiao Wei, 2018, Journal of Molecular Medicine.

Motor neuron disease‐like phenotype associated with anti‐IgLON5 disease

Qiao Wei, Qing-Qing Tao, Xin-Zhen Yin, 2018, CNS neuroscience & therapeutics.

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

Qiao Wei, Huan Ma, Ge Bai, 2019, Clinical genetics.

Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot‐Marie‐Tooth disease

Qiao Wei, Huan Ma, Ge Bai, 2020, Journal of the peripheral nervous system : JPNS.

Sensory nerve disturbance in amyotrophic lateral sclerosis

Qiao Wei, Qing-Qing Tao, Zhi-Ying Wu, 2018, Life sciences.

Clinical feature difference between juvenile amyotrophic lateral sclerosis with SPTLC1 and FUS mutations

Qiao Wei, Hong-Fu Li, Zhi-Ying Wu, 2023, Chinese medical journal.

Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy.

Qiao Wei, Ge Bai, Hong-Fu Li, 2021, Brain : a journal of neurology.

Spastic paraplegia as the only symptom in two adult‐onset patients carrying a novel pathogenic variant in PYCR2

W. Ni, Qiao Wei, Juan-Juan Xie, 2020, European journal of neurology.

Novel stop‐gain RNF170 variation detected in a Chinese family with adolescent‐onset hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Yu-Lan Chen, 2022, Clinical genetics.

Clinical features and genetic spectrum in Chinese patients with recessive hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Zhi-Jun Liu, 2019, Translational Neurodegeneration.

Nuclear DJ-1 Regulates DNA Damage Repair via the Regulation of PARP1 Activity

J. Pu, Qiao Wei, Zhi-Hao Lin, 2023, International journal of molecular sciences.

A novel UBAP1 truncated variant in a Chinese family with hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2022, Molecular genetics & genomic medicine.

Clinical and genetic characterization of a cohort of Chinese patients with hereditary spastic paraplegia

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2019, Clinical genetics.

Biallelic variants in the COQ4 gene caused hereditary spastic paraplegia predominant phenotype.

Qiao Wei, Hong-Fu Li, Hai-Lin Dong, 2023, CNS neuroscience & therapeutics.