Zhao Chen

发表

Alterations of the Gut Microbiota in Multiple System Atrophy Patients

K. Xia, B. Tang, Hong Jiang, 2019, Front. Neurosci..

MR Imaging of SCA3/MJD

B. Tang, Hong Jiang, Linlin Wan, 2020, Frontiers in Neuroscience.

Spinocerebellar Ataxia Type 28 (SCA28) is an Uncommon Cause of Dominant Ataxia Among Chinese Kindreds

Li Zhang, K. Xia, B. Tang, 2012, The International journal of neuroscience.

Spinocerebellar ataxia type 27 (SCA27) is an uncommon cause of dominant ataxia among Chinese Han population

Li Zhang, K. Xia, Q. Pan, 2012, Neuroscience Letters.

Biallelic Intronic AAGGG Expansion of RFC1 is Related to Multiple System Atrophy

T. Ashizawa, K. Xia, B. Tang, 2020, Annals of neurology.

Lithium Chloride Alleviates Neurodegeneration Partly by Inhibiting Activity of GSK3β in a SCA3 Drosophila Model

Li Zhang, K. Xia, B. Tang, 2013, The Cerebellum.

Association of serum neurofilament light and disease severity in patients with spinocerebellar ataxia type 3

T. Klockgether, B. Tang, W. Liao, 2020, Neurology.

Central motor conduction time in spinocerebellar ataxia: a meta-analysis

B. Tang, Hong Jiang, Linlin Wan, 2020, Aging.

Genetic etiology of a Chinese ataxia cohort: Expanding the mutational spectrum of hereditary ataxias.

K. Xia, B. Tang, Hong Jiang, 2021, Parkinsonism & related disorders.

K. Xia, B. Tang, Hong Jiang, 2019, Front. Neurol..

Genetic and clinical analyses of spinocerebellar ataxia type 8 in mainland China

K. Xia, B. Tang, Hong Jiang, 2019, Journal of Neurology.

Spinocerebellar Ataxia Type 13 is an Uncommon SCA Subtype in the Chinese Han Population

B. Tang, Hong Jiang, Junling Wang, 2013, The International journal of neuroscience.

Increase of the plasma α‐synuclein levels in patients with multiple system atrophy

Li Zhang, K. Xia, B. Tang, 2014, Movement disorders : official journal of the Movement Disorder Society.

The progression rate of spinocerebellar ataxia type 3 varies with disease stage

K. Xia, B. Tang, Hong Jiang, 2022, Journal of translational medicine.

High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression

T. Klockgether, T. Ashizawa, B. Tang, 2015, The Cerebellum.

Sodium Valproate Alleviates Neurodegeneration in SCA3/MJD via Suppressing Apoptosis and Rescuing the Hypoacetylation Levels of Histone H3 and H4

Li Zhang, B. Tang, Hong Jiang, 2013, PloS one.

No genetic evidence for the involvement of GGC repeat expansions of the NOTCH2NLC gene in Chinese patients with multiple system atrophy

B. Tang, Hong Jiang, Linlin Wan, 2020, Neurobiology of Aging.

SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population

K. Xia, B. Tang, Hong Jiang, 2015, The International journal of neuroscience.

The Natural History of Spinocerebellar Ataxia Type 3 in Mainland China: A 2-Year Cohort Study

T. Klockgether, K. Xia, B. Tang, 2022, Frontiers in Aging Neuroscience.

Polymorphisms in DNA methylation–related genes are linked to the phenotype of Machado-Joseph disease

T. Ashizawa, K. Xia, B. Tang, 2019, Neurobiology of Aging.

New Model for Estimation of the Age at Onset in Spinocerebellar Ataxia Type 3

T. Klockgether, K. Xia, Jinchen Li, 2021, Neurology.

Association of TNF-α rs1799964 and IL-1β rs16944 polymorphisms with multiple system atrophy in Chinese Han population

K. Xia, B. Tang, Hong Jiang, 2018, The International journal of neuroscience.

A Variant in Genes of the NPY System as Modifier Factor of Machado-Joseph Disease in the Chinese Population

Hong Jiang, Xiang Tang, Lu-lu Zhang, 2022, Frontiers in Aging Neuroscience.

Is the High Frequency of Machado-Joseph Disease in China Due to New Mutational Origins?

K. Xia, Zhengmao Hu, B. Tang, 2019, Front. Genet..

Investigation on modulation of DNA repair pathways in Chinese MJD patients

K. Xia, B. Tang, J. Sequeiros, 2018, Neurobiology of Aging.

Two Novel SNPs in ATXN3 3’ UTR May Decrease Age at Onset of SCA3/MJD in Chinese Patients

T. Ashizawa, K. Xia, Q. Pan, 2015, PloS one.

Mental health of spinocerebellar ataxia patients during COVID-19 pandemic: a cross-sectional study

K. Xia, B. Tang, Hong Jiang, 2020 .

Characterization of the central motor conduction time in a large cohort of spinocerebellar ataxia type 3 patients.

K. Xia, B. Tang, Hong Jiang, 2022, Parkinsonism & related disorders.

Human stem cell models of polyglutamine diseases: Sources for disease models and cell therapy

B. Tang, Hong Jiang, Zhao Chen, 2020, Experimental Neurology.

Primary erythromelalgia: a review

B. Tang, Hong Jiang, Zhao Chen, 2015, Orphanet Journal of Rare Diseases.

Identification of a de novo DYNC1H1 mutation via WES according to published guidelines

K. Xia, B. Tang, Hong Jiang, 2016, Scientific Reports.

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

P. Jin, K. Xia, B. Tang, 2019, American journal of human genetics.

Polyglutamine-expanded ataxin3 alter specific gene expressions through changing DNA methylation status in SCA3/MJD

K. Xia, B. Tang, Hong Jiang, 2020, Aging.

Investigation of Gene Regulatory Networks Associated with Autism Spectrum Disorder Based on MiRNA Expression in China

K. Xia, Zhengmao Hu, B. Tang, 2015, PloS one.

Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population

B. Tang, Hong Jiang, Xin Zhou, 2018, Front. Neurol..

Generation of an induced pluripotent stem cell line (XHCSUi001-A) from urine cells of a patient with spinocerebellar ataxia type 3.

B. Tang, Xiaobo B Han, Hong Jiang, 2019, Stem cell research.

Coffin-Siris syndrome in two chinese patients with novel pathogenic variants of ARID1A and SMARCA4

B. Tang, Hong Jiang, Yun Peng, 2022, Genes & Genomics.

H. Shang, T. Ashizawa, Baorong Zhang, 2017, Brain : a journal of neurology.

Updated frequency analysis of spinocerebellar ataxia in China.

K. Xia, B. Tang, J. Sequeiros, 2018, Brain : a journal of neurology.

CRISPR/Cas9 mediated gene correction ameliorates abnormal phenotypes in spinocerebellar ataxia type 3 patient-derived induced pluripotent stem cells

B. Tang, Xiaobo B Han, Hong Jiang, 2021, Translational Psychiatry.

Anxiety and depression in spinocerebellar ataxia patients during the COVID-19 pandemic in China: A cross-sectional study

K. Xia, B. Tang, Hong Jiang, 2021, Journal of Clinical Neuroscience.

Age is an important independent modifier of SCA3 phenotype severity

B. Tang, Hong Jiang, Chun-rong Wang, 2020, Neuroscience Letters.

Profiling of mitochondrial genomes in SCA3/MJD patients from mainland China.

B. Tang, Hong Jiang, V. Zhang, 2020, Gene.

RNA Expression Profile and Potential Biomarkers in Patients With Spinocerebellar Ataxia Type 3 From Mainland China

K. Xia, B. Tang, Hong Jiang, 2019, Front. Genet..

Cerebellar lncRNA Expression Profile Analysis of SCA3/MJD Mice

K. Xia, B. Tang, Hong Jiang, 2018, International journal of genomics.

Using next-generation sequencing as a genetic diagnostic tool in rare autosomal recessive neurologic Mendelian disorders

T. Ashizawa, K. Xia, Q. Pan, 2013, Neurobiology of Aging.

miRNA profiling in autism spectrum disorder in China

Hong Jiang, Z. Long, Chun-rong Wang, 2015, Genomics data.

miR‐25 alleviates polyQ‐mediated cytotoxicity by silencing ATXN3

Li Zhang, D. Chuang, K. Xia, 2014, FEBS letters.

Genetic modifiers of age-at-onset in polyglutamine diseases

B. Tang, J. Sequeiros, Hong Jiang, 2018, Ageing Research Reviews.

Alteration of methylation status in the ATXN3 gene promoter region is linked to the SCA3/MJD

K. Xia, B. Tang, Hong Jiang, 2017, Neurobiology of Aging.

Prediction of the Age at Onset of Spinocerebellar Ataxia Type 3 with Machine Learning

Zuping Zhang, K. Xia, Jinchen Li, 2020, Movement disorders : official journal of the Movement Disorder Society.

The APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population

K. Xia, B. Tang, Hong Jiang, 2014, Neurobiology of Aging.

Targeted Next-Generation Sequencing Revealed Novel Mutations in Chinese Ataxia Telangiectasia Patients: A Precision Medicine Perspective

K. Xia, B. Tang, Hong Jiang, 2015, PloS one.

A deletion mutation of the VHL gene associated with a patient with sporadic von Hippel-Lindau disease

Li Zhang, K. Xia, B. Tang, 2013, Journal of Clinical Neuroscience.

Analysis of the GGGGCC Repeat Expansions of the C9orf72 Gene in SCA3/MJD Patients from China

T. Ashizawa, K. Xia, B. Tang, 2015, PloS one.

Roles of Post-translational Modifications in Spinocerebellar Ataxias

B. Tang, Hong Jiang, Linlin Wan, 2018, Front. Cell. Neurosci..

Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography

Yiyun Huang, M. Zhou, T. Ashizawa, 2023, Movement disorders : official journal of the Movement Disorder Society.

CAG Repeat Expansion in THAP11 Is Associated with a Novel Spinocerebellar Ataxia

X. Bao, Hong Jiang, Yuwu Jiang, 2023, Movement disorders : official journal of the Movement Disorder Society.

Diagnostic and prognostic performance of plasma neurofilament light chain in multiple system atrophy: a cross-sectional and longitudinal study

Jinchen Li, B. Tang, Hong Jiang, 2023, Journal of Neurology.

Identification of the Largest SCA36 Pedigree in Asia: with Multimodel Neuroimaging Evaluation for the First Time

K. Xia, B. Tang, Zhengmao Hu, 2021, The Cerebellum.

High Serum GFAP Levels in SCA3/MJD May Not Correlate with Disease Progression

T. Klockgether, T. Ashizawa, B. Tang, 2015, The Cerebellum.

ATXN2 polymorphism modulates age at onset in Machado-Joseph disease.

K. Xia, B. Tang, Hong Jiang, 2016, Brain : a journal of neurology.

(CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China.

H. Shang, T. Klockgether, T. Ashizawa, 2016, Brain : a journal of neurology.

Lithium Chloride Alleviates Neurodegeneration Partly by Inhibiting Activity of GSK3β in a SCA3 Drosophila Model

Li Zhang, K. Xia, B. Tang, 2013, The Cerebellum.

Blood Neurofilament Light Chain in Genetic Ataxia: A Meta‐Analysis

T. Klockgether, T. Ashizawa, K. Xia, 2021, Movement disorders : official journal of the Movement Disorder Society.

Serum vitamin levels in multiple system atrophy: A case-control study

B. Tang, Hong Jiang, Linlin Wan, 2023, Frontiers in Aging Neuroscience.

Identification of novel mutations in TSC1 and TSC2 for tuberous sclerosis complex by targeted next-generation sequencing and ACMG guidelines

Hong Jiang, Zhao Chen, Lang He, 2020, Child's Nervous System.

No Correlation between Plasma GPNMB Levels and Multiple System Atrophy in Chinese Cohorts

B. Tang, Hong Jiang, Z. Long, 2023, Movement disorders : official journal of the Movement Disorder Society.

Multidimensional biomarkers for multiple system atrophy: an update and future directions

B. Tang, Hong Jiang, Linlin Wan, 2023, Translational Neurodegeneration.

Corrigendum: Gene-Related Cerebellar Neurodegeneration in SCA3/MJD: A Case-Controlled Imaging-Genetic Study

K. Xia, B. Tang, Hong Jiang, 2020, Frontiers in Neurology.

Myeleterosis in an ALPS5 patient with primary immune dysregulation syndrome

B. Tang, B. Xiao, Hong Jiang, 2020, CNS neuroscience & therapeutics.

Efficacy of cerebellar transcranial magnetic stimulation in spinocerebellar ataxia type 3: a randomized, single-blinded, controlled trial

B. Tang, Hong Jiang, Lu Shen, 2023, Journal of Neurology.

Reply to: “THAP11 CAG Expansion Beyond Chinese‐Ancestry Cohorts: An Examination of 1000 Genomes and UK Biobank”

Zhao Chen, Cui-jie Wei, Dandan Tan, 2023, Movement disorders : official journal of the Movement Disorder Society.

SNP rs11931074 of the SNCA gene may not be associated with multiple system atrophy in Chinese population

K. Xia, B. Tang, Hong Jiang, 2015, International Journal of Neuroscience.

Increase of the plasma α‐synuclein levels in patients with multiple system atrophy

Li Zhang, K. Xia, B. Tang, 2014, Movement disorders : official journal of the Movement Disorder Society.

Analysis of (CAG)n expansion in ATXN1, ATXN2 and ATXN3 in Chinese patients with multiple system atrophy

K. Xia, H. Peng, B. Tang, 2018, Scientific Reports.