Xiao-li Liu

发表

Novel Mutations in Endoplasmic Reticulum Lipid Raft-associated Protein 2 Gene Cause Pure Hereditary Spastic Paraplegia Type 18

S. Chen, Wotu Tian, Jun-Yi Shen, 2016, Chinese medical journal.

Clinicopathologic characterization and abnormal autophagy of CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Jianfang Ma, 2019, Translational Neurodegeneration.

Altered structural and functional connectivity in CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Jiong Hu, 2020, Brain Imaging and Behavior.

The study of exercise tests in paroxysmal kinesigenic dyskinesia

S. Chen, Wotu Tian, Xiao-li Liu, 2018, Clinical Neurophysiology.

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

Huidong Tang, S. Chen, Wotu Tian, 2020, Movement disorders : official journal of the Movement Disorder Society.

Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review

Huidong Tang, S. Chen, Wotu Tian, 2019, Neuromuscular Disorders.

A community-based study of risk factors for probable rapid eye movement sleep behavior disorder.

Huidong Tang, Jianfang Ma, Xiang Gao, 2017, Sleep medicine.

Mechanisms of Short-Chain Fatty Acids Derived from Gut Microbiota in Alzheimer's Disease

Huidong Tang, S. Chen, Xiao-li Liu, 2022, Aging and disease.

Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia

Wotu Tian, Xiao-li Liu, Xiao-jun Huang, 2022, Journal of Neurology.

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

B. Tang, Huidong Tang, S. Chen, 2018, Movement disorders : official journal of the Movement Disorder Society.

Clinical and genetic analyses of 150 patients with paroxysmal kinesigenic dyskinesia

Wotu Tian, Xiao-li Liu, Xiao-jun Huang, 2022, Journal of Neurology.

Clinical phenotype and genetic characteristics of ataxia - telangiectasia: four cases report

Xiao-li Liu, Li Cao, Lan Zheng, 2017 .

Novel mutations in the SPAST gene cause hereditary spastic paraplegia.

Ying Wang, Huidong Tang, Shengdi Chen, 2019, Parkinsonism & related disorders.

De novo mutations in GFAP cause Alexander disease : clinical features , fMRI and functional 3 analysis 4 Running head : De novo mutations in Alexander disease 5 6

Huidong Tang, Wotu Tian, Xiao-li Liu, 2020 .

Novel Mutations in SCN4A Gene Cause Myotonia Congenita with Scoliosis

Huidong Tang, Wotu Tian, Xiao-li Liu, 2018, Chinese medical journal.

Clinical phenotype and genetic mutation of fatty acid hydroxylase - associated neurodegeneration: analysis of four cases

S. Chen, Jun-Yi Shen, Xiao-li Liu, 2017 .

Integrating peripheral blood and brain transcriptomics to identify immunological features associated with Alzheimer’s disease in mild cognitive impairment patients

Huidong Tang, Xiao-li Liu, Xiao-hang Qian, 2022, Frontiers in Immunology.

A novel homozygous mutation in ERLIN1 gene causing spastic paraplegia 62 and literature review.

Wotu Tian, Xiao-li Liu, Li Cao, 2022, European journal of medical genetics.

Long-read sequencing identified intronic (GGCCTG)n expansion in NOP56 in one SCA36 family and literature review

Wotu Tian, Xiao-li Liu, Li Cao, 2022, Clinical Neurology and Neurosurgery.

Injection of amyloid-β to lateral ventricle induces gut microbiota dysbiosis in association with inhibition of cholinergic anti-inflammatory pathways in Alzheimer’s disease

Huidong Tang, Xiao-li Liu, Xiao-hang Qian, 2022, Journal of Neuroinflammation.

Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

Huidong Tang, S. Chen, Xiao-li Liu, 2015, Channels.

Novel IBA57 mutations in two chinese patients and literature review of multiple mitochondrial dysfunction syndrome

Wotu Tian, Xiao-li Liu, X. Luan, 2021, Metabolic Brain Disease.

Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature review

Ying Wang, Huidong Tang, S. Chen, 2018, Seizure.

Depression, Anxiety, and Quality of Life in Paroxysmal Kinesigenic Dyskinesia Patients

S. Chen, Wotu Tian, Jun-Yi Shen, 2017, Chinese medical journal.

Inflammatory pathways in Alzheimer’s disease mediated by gut microbiota

Huidong Tang, S. Chen, Xiao-li Liu, 2021, Ageing Research Reviews.

Identification of Immune Hub Genes Associated With Braak Stages in Alzheimer’s Disease and Their Correlation of Immune Infiltration

Huidong Tang, Xiao-li Liu, Xiao-hang Qian, 2022, Frontiers in Aging Neuroscience.

Methylation status of DJ-1 in leukocyte DNA of Parkinson’s disease patients

Shengdi Chen, Jianqing Ding, Xiao-li Liu, 2016, Translational Neurodegeneration.

The Whole Exome Sequencing Clarifies the Genotype- Phenotype Correlations in Patients with Early-Onset Dementia

Huidong Tang, Jianfang Ma, Shengdi Chen, 2018, Aging and disease.

PRRT2 truncated mutations lead to nonsense-mediated mRNA decay in Paroxysmal Kinesigenic Dyskinesia.

Huidong Tang, S. Chen, Xiao-li Liu, 2014, Parkinsonism & related disorders.

Altered structural and functional connectivity in CSF1R-related leukoencephalopathy

Ying Wang, Huidong Tang, Wotu Tian, 2020, Brain Imaging and Behavior.

Case report: A Chinese child with Andersen–Tawil syndrome due to a de novo KCNJ2 mutation

Huidong Tang, S. Chen, Jun-Yi Shen, 2015, Journal of the Neurological Sciences.

Novel ATM mutations with ataxia-telangiectasia

S. Chen, Jun-Yi Shen, Xiao-li Liu, 2016, Neuroscience Letters.

c.1263+1G>A Is a Latent Hotspot for CYP27A1 Mutations in Chinese Patients With Cerebrotendinous Xanthomatosis

Xiao-li Liu, X. Luan, Xiao-jun Huang, 2020, Frontiers in Genetics.

Investigating the causal association between branched-chain amino acids and Alzheimer's disease: A bidirectional Mendelian randomized study

Huidong Tang, Xiao-li Liu, Xiao-hang Qian, 2023, Frontiers in Nutrition.

Paroxysmal kinesigenic dyskinesia

B. Tang, S. Chen, Jun-Yi Shen, 2015, Neurology.

Myotonia congenita: novel mutations in CLCN1 gene

Ying Wang, Huidong Tang, S. Chen, 2015, Channels.

Two patients with congenital myasthenic syndrome caused by COLQ gene mutations and the consequent ColQ protein defect

Xiao-li Liu, Qiting Zhang, K. Qiao, 2023, Heliyon.

ABCA7-Associated Clinical Features and Molecular Mechanisms in Alzheimer’s Disease

Huidong Tang, Xiao-li Liu, Xiao-hang Qian, 2023, Molecular Neurobiology.