H. Peng

发表

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.

Identifying SYNE1 Ataxia With Novel Mutations in a Chinese Population

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

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

Low Temperature Thermodynamic Study of the Stable and Metastable Phases of Silver

Yaozhuang Nie, H. Peng, Xiao-bo Li, 2007 .

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

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

Updated frequency analysis of spinocerebellar ataxia in China.

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

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.

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.

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.

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

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

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

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

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

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.

A novel pathogenic deletion in ISPD causes Walker-Warburg syndrome in a Chinese family

Yanhua Zhao, Zhouteng Tao, Huirong Peng, 2022, Genes & Genomics.

miR‐25 alleviates polyQ‐mediated cytotoxicity by silencing ATXN3

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

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.

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.

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

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

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 progression rate of spinocerebellar ataxia type 3 varies with disease stage

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

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.

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

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

Holocene climate dynamics derived from pollen record of Jiulongchi wetland in Fanjing Mountain, southwest China

K. Xiong, B. Song, K. Bao, 2019, Quaternary International.

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.

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.

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

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

Alterations of the Gut Microbiota in Multiple System Atrophy Patients

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

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.

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.

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.

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.

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.

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.

Investigation on modulation of DNA repair pathways in Chinese MJD patients

K. Xia, B. Tang, J. Sequeiros, 2018, 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.

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.

Self-calibration of photometric redshift scatter from DECaLS DR8 power spectrum and validation with simulated catalogues

Le Zhang, Yu Yu, Haojie Xu, 2022, 2203.14609.

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

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

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.

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.