B. Tang

发表

Common genetic variants on 1p13.2 associate with risk of autism

Z. Hu, D. St. Clair, Y. Hu, 2014, Molecular Psychiatry.

Identifying the presence of Parkinson’s disease using low-frequency fluctuations in BOLD signals

B. Tang, Ji-feng Guo, Yan Tang, 2017, Neuroscience Letters.

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Nan Li, Li Fang, Qian Liu, 2018, Journal of Medical Genetics.

Novel mutation of SCN1A in familial generalized epilepsy with febrile seizures plus

K. Xia, B. Tang, Ji-feng Guo, 2010, Neuroscience Letters.

Clinical standards and interpretation of gene sequence variants in human Mendelian disorders

B. Tang, S. Zeng, Kai Li, 2017 .

Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.

K. Xia, B. Tang, Ji-feng Guo, 2013, Biochemical and biophysical research communications.

Study on diagnosis and treatment of hereditary ataxia

B. Tang, Hong Jiang, 2012 .

SUMO-1 Modification on K166 of PolyQ-Expanded aTaxin-3 Strengthens Its Stability and Increases Its Cytotoxicity

K. Xia, B. Tang, Juan Du, 2013, PloS one.

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

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

SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China

B. Tang, Juan Du, Lu Shen, 2016, Journal of Neurology.

Mutation in PITX2 is associated with ring dermoid of the cornea

K. Xia, Q. Pan, L. Wu, 2004, Journal of Medical Genetics.

Examining the causal role of leptin in bone mineral density: A Mendelian randomization study.

L. Tan, H. Deng, B. Tang, 2019, Bone.

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

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

The contribution of GIGYF2 to Parkinson’s disease: a meta-analysis

B. Tang, Ji-feng Guo, Yuan Zhang, 2015, Neurological Sciences.

Impaired meningeal lymphatic drainage in patients with idiopathic Parkinson’s disease

B. Tang, E. Wu, Jia-Yi Li, 2021, Nature Medicine.

GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson’s disease: a two-cohort case-control study

B. Tang, Zhenghuan Fang, Ji-feng Guo, 2020, Translational Neurodegeneration.

Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients

B. Tang, Ji-feng Guo, W. Liao, 2017, Front. Neuroanat..

Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants

B. Tang, 2016, Chinese medical journal.

Can brain impermeable BACE1 inhibitors serve as anti-CAA medicine?

B. Tang, Li-Ling Huang, Xiao-Xin Yan, 2017, BMC Neurology.

Genetic Identification Is Critical for the Diagnosis of Parkinsonism: A Chinese Pedigree with Early Onset of Parkinsonism

K. Xia, B. Tang, Ji-feng Guo, 2015, PloS one.

Assessment of the association between NUS1 variants and essential tremor

B. Tang, Ji-feng Guo, Ke Xu, 2020, Neuroscience Letters.

Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor.

K. Xia, B. Tang, Fan Liang, 2019, Brain : a journal of neurology.

Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2011, Brain Research.

FBXO7 gene mutations may be rare in Chinese early-onset Parkinsonism patients

K. Xia, Q. Pan, B. Tang, 2010, Neuroscience Letters.

Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China

K. Xia, Q. Pan, X. Yan, 2016, Clinical genetics.

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.

Spinocerebellar ataxia type 23 is an uncommon SCA subtype in the Chinese Han population

K. Xia, B. Tang, Hong Jiang, 2012, Neuroscience Letters.

Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han

K. Xia, Q. Pan, B. Tang, 2008, Journal of Genetics.

Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study

B. Tang, Ji-feng Guo, Jin-chen Li, 2022, Frontiers in Genetics.

Association study between SNP rs150689919 in the DNA demethylation gene, TET1, and Parkinson’s disease in Chinese Han population

K. Xia, B. Tang, Ji-feng Guo, 2013, BMC Neurology.

[Mutation analysis of ATP13A2 gene in Chinese patients with familial autosomal recessive early-onset parkinsonism].

B. Tang, Ji-feng Guo, Lei Wang, 2009, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Autophagy and Its Comprehensive Impact on ALS

B. Tang, Ji-feng Guo, Yuan Liu, 2012, 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.

Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy

B. Tang, Xuebing Ding, E. Wu, 2020, Nature Communications.

PSAP variants in Parkinson's disease: a large cohort study in Chinese mainland population.

B. Tang, Guihu Zhao, Zhenghuan Fang, 2020, Brain : a journal of neurology.

Spinocerebellar ataxia type 2 in China

S. Tsuji, B. Tang, N. Sambuughin, 1998, Neurology.

Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic

K. Xia, Q. Pan, B. Tang, 2009, Journal of the Neurological Sciences.

Analysis of PLA2G6 gene mutation in sporadic early-onset parkinsonism patients from Chinese population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2012, Neuroscience Letters.

PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort

K. Xia, Q. Pan, B. Tang, 2011, Neurology.

Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism

B. Tang, Ji-feng Guo, Xinxiang Yan, 2010, Journal of Neurology.

Association of the DRD2 and DRD3 polymorphisms with response to pramipexole in Parkinson’s disease patients

B. Tang, Xinxiang Yan, Honghao Zhou, 2009, European Journal of Clinical Pharmacology.

VPS35 gene variants are not associated with Parkinson's disease in the mainland Chinese population.

K. Xia, B. Tang, Ji-feng Guo, 2012, Parkinsonism & related disorders.

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.

Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population

K. Xia, B. Tang, Hong Jiang, 2017, The International journal of neuroscience.

PRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases

B. Tang, Junling Wang, Changhe Shi, 2013, Movement disorders : official journal of the Movement Disorder Society.

Association of rare PPARGC1A variants with Parkinson’s disease risk

B. Tang, Ji-feng Guo, Xinxiang Yan, 2022, Journal of Human Genetics.

Low-frequency and rare coding variants of NUS1 contribute to pathogenesis and phenotype of Parkinson’s disease: a case-control study

B. Tang, Ji-feng Guo, J. Mei, 2020 .

Two novel functional single nucleotide polymorphisms of ADRB3 are associated with type 2 diabetes in the Chinese population.

B. Tang, Yuan-Shan Zhu, Jiye Yin, 2013, The Journal of clinical endocrinology and metabolism.

Mutation Analysis of the TATA box-binding protein (TBP) gene in Chinese Han patients with spinocerebellar ataxia

K. Xia, Q. Pan, B. Tang, 2009, Journal of Clinical Neuroscience.

A novel hemizygous SACS mutation identified by whole exome sequencing and SNP array analysis in a Chinese ARSACS patient

H. Li, D. Yu, K. Xia, 2016, Journal of the Neurological Sciences.

Novel mutations of the SPG11 gene in hereditary spastic paraplegia with thin corpus callosum

K. Xia, B. Tang, N. Li, 2008, Journal of the Neurological Sciences.

Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth

K. Xia, B. Tang, Zhengmao Hu, 2018, Chinese medical journal.

Mutation analysis of small heat-shock protein 22 gene in Chinese patients with Charcot-Marie-Tooth disease.

C. Zhang, K. Xia, B. Tang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

[The characteristics of gene mutations in Chinese patients with Charcot-Marie-Tooth disease].

K. Xia, Q. Pan, B. Tang, 2005, Zhonghua yi xue za zhi.

Lack of bidirectional association between age‐related macular degeneration and Alzheimer's disease: A Mendelian randomization study

B. Tang, Ji-feng Guo, Jin-chen Li, 2022, Alzheimer's & dementia : the journal of the Alzheimer's Association.

C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China

B. Tang, Hong Jiang, Lu Shen, 2016, Journal of the Neurological Sciences.

BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage

B. Tang, Ji-feng Guo, Jiahong Lu, 2017, Oxidative medicine and cellular longevity.

The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review

P. Jin, B. Tang, Xiurong Huang, 2021, Molecular neurobiology.

Reply: Assessing the NOTCH2NLC GGC expansion in essential tremor patients from eastern China.

B. Tang, Ji-feng Guo, Qi-ying Sun, 2020, Brain : a journal of neurology.

Reply: Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.

B. Tang, Ji-feng Guo, Qi-ying Sun, 2020, Brain : a journal of neurology.

3.077 NOVEL PLA2G6 GENE MUTATION IS ASSOCIATED WITH AUTOSOMAL RECESSIVE EARLY-ONSET PARKINSONISM

B. Tang, Ji-feng Guo, Xinxiang Yan, 2012 .

Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia

B. Tang, Hong Jiang, Lu Shen, 2018, The International journal of neuroscience.

Impaired iPLA2β activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA2β activity as the cause of iron deposition in PLAN

B. Tang, Ji-feng Guo, Xinxiang Yan, 2019, Brain Research.

Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson's Disease: A Diagnostic Accuracy Study

Yang Zhang, B. Tang, Ji-feng Guo, 2022, Movement disorders : official journal of the Movement Disorder Society.

Study of the Relationship between Gene Polymorphisms of Paraoxonase 2 and Stroke in a Chinese Population

B. Tang, J. Xia, Le Zhang, 2007, Cerebrovascular Diseases.

Cx32 gene mutation associated with X-linked recessive Charcot-Marie-Tooth disease

K. Xia, B. Tang, Yanlin Ma, 2003 .

[Clinical and mutational analysis of KCNQ3 gene in a Chinese family with benign familial neonatal convulsions].

K. Xia, B. Tang, Ji-feng Guo, 2006, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

NRBF2 is a RAB7 effector required for autophagosome maturation and mediates the association of APP-CTFs with active form of RAB7 for degradation

Yitao Wang, B. Tang, Huanxing Su, 2020, Autophagy.

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

J. Li, B. Tang, Wanjun Zhou, 2019, Brain : a journal of neurology.

SPG35 contributes to the second common subtype of AR‐HSP in China: frequency analysis and functional characterization of FA2H gene mutations

K. Xia, Q. Pan, X. Yan, 2015, Clinical genetics.

[Gene screening in five Chinese families with hereditary spastic paraplegia with thin corpus callosum].

K. Xia, B. Tang, Lu Shen, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Clinical features of hereditary spastic paraplegia with thin corpus callosum: report of 5 Chinese cases.

B. Tang, W. Luo, Hong Jiang, 2004, Chinese medical journal.

PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

B. Tang, Ji-feng Guo, Yu-pei Guo, 2018, Front. Neurol..

Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene

Zhixian Yang, K. Xia, B. Tang, 2018, Human molecular genetics.

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

Xin Jin, K. Xia, Q. Pan, 2010, Brain : a journal of neurology.

Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population

K. Xia, Q. Pan, B. Tang, 2010, Movement disorders : official journal of the Movement Disorder Society.

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias

K. Xia, B. Tang, Zhengmao Hu, 2011, Brain : a journal of neurology.

Identification of a locus for disseminated superficial actinic porokeratosis at chromosome 12q23.2-24.1.

K. Xia, H. Dai, B. Tang, 2000, The Journal of investigative dermatology.

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.

Contribution of coding/non-coding variants in NUS1 to late-onset sporadic Parkinson's disease.

B. Tang, Ji-feng Guo, Xinxiang Yan, 2021, Parkinsonism & related disorders.

Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2012, Neuroscience Letters.

The Progress of Induced Pluripotent Stem Cells as Models of Parkinson's Disease

B. Tang, Ji-feng Guo, Ji-feng Kang, 2016, Stem cells international.

Microglial Activation in the Pathogenesis of Huntington’s Disease

B. Tang, Ji-feng Guo, Su Yang, 2017, Front. Aging Neurosci..

Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L

K. Xia, Q. Pan, H. Dai, 2005, Human Genetics.

PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population

K. Xia, Q. Pan, B. Tang, 2011, Brain Research.

LRRK2 A419V variant is a risk factor for Parkinson's disease in Asian population

Yuan Zhang, K. Xia, B. Tang, 2015, Neurobiology of Aging.

PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B

B. Tang, Mugen Liu, P. Yi, 2017, Scientific Reports.

Research advances on neurite outgrowth inhibitor B receptor

B. Tang, Ji-feng Guo, Rui Zhang, 2020, Journal of cellular and molecular medicine.

Coding mutations in NUS1 contribute to Parkinson’s disease

H. Shang, P. Chan, K. Xia, 2018, Proceedings of the National Academy of Sciences.

Parkinson's Disease and Cognitive Impairment

B. Tang, Ji-feng Guo, Yang Yang, 2016, Parkinson's disease.

Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia.

K. Xia, B. Tang, Xinxiang Yan, 2013, European journal of medical genetics.

RAB39B gene mutations are not linked to familial Parkinson’s disease in China

B. Tang, Ji-feng Guo, Chang-min Wan, 2016, Scientific Reports.

A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24

K. Xia, Q. Pan, H. Dai, 2004, Human Genetics.

Mutation analysis of Parkin, PINK1, DJ‐1 and ATP13A2 genes in Chinese patients with autosomal recessive early‐onset Parkinsonism

K. Xia, Q. Pan, B. Tang, 2008, Movement disorders : official journal of the Movement Disorder Society.

Frequency of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansion in patients with hereditary spinocerebellar ataxia from Chinese kindreds.

Q. Pan, H. Dai, B. Tang, 2000, Archives of neurology.

[Mutation analysis of LITAF, RAB7, LMNA and MTMR2 genes in Chinese Charcot-Marie-Tooth disease.].

K. Xia, B. Tang, Zhengmao Hu, 2010, Yi chuan = Hereditas.

Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease

B. Tang, Ji-feng Guo, Rui Zhang, 2021, Neurobiology of Aging.

Analysis of Salivary Microbiome in Patients with Alzheimer's Disease.

B. Tang, Lu Shen, Zhenhua Yuan, 2019, Journal of Alzheimer's disease : JAD.

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.

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

K. Xia, Q. Pan, H. Dai, 1998, Nature Genetics.

CCG polymorphisms in the huntingtin gene have no effect on the pathogenesis of patients with Huntington's disease in mainland Chinese families

K. Xia, B. Tang, Jun Tian, 2012, Journal of the Neurological Sciences.

Distribution of Transglutaminase 6 in the Central Nervous System of Adult Mice

Yu-Qiang Ding, K. Xia, B. Tang, 2013, Anatomical record.

The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review

B. Tang, Xiurong Huang, Ji-feng Guo, 2021, Molecular Neurobiology.

Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants.

C. Tanner, J. Langston, P. Chan, 2012, Parkinsonism & related disorders.

Hypomethylation of SNCA in blood of patients with sporadic Parkinson's disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2014, Journal of the Neurological Sciences.

Analysis of EIF4G1 in ethnic Chinese

K. Xia, B. Tang, Ji-feng Guo, 2013, BMC Neurology.

Screening for two SNPs of LINGO1 gene in patients with essential tremor or sporadic Parkinson's disease in Chinese population

K. Xia, Q. Pan, B. Tang, 2010, Neuroscience Letters.

Sortilin Fragments Deposit at Senile Plaques in Human Cerebrum

H. Cai, Y. Chu, B. Tang, 2017, Front. Neuroanat..

VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

L. Mei, B. Tang, W. Xiong, 2015, Molecular Brain.

TNFSF4 gene polymorphism rs3861950 but not rs3850641 is associated with the risk of cerebral infarction in a Chinese population

K. Xia, B. Tang, Qi-dong Yang, 2013, Journal of Thrombosis and Thrombolysis.

Association study between two novel single nucleotide polymorphisms and sporadic Parkinson's disease in Chinese Han population

K. Xia, B. Tang, Ji-feng Guo, 2012, Neuroscience Letters.

C9orf72 mutation is rare in Alzheimer's disease, Parkinson's disease, and essential tremor in China

K. Xia, B. Tang, Ji-feng Guo, 2013, Front. Cell. Neurosci..

[Mutation analysis of MFN2 gene in Chinese patients with Charcot-Marie-Tooth disease].

K. Xia, Q. Pan, B. Tang, 2009, Zhonghua yi xue za zhi.

Identifying mild-moderate Parkinson’s disease using whole-brain functional connectivity

Yan Tang, Ji-feng Guo, Yuan Yang, 2018, Clinical Neurophysiology.

ASSOCIATION ANALYSIS OF SEROTONIN TRANSPORTER PROMOTER GENE POLYMORPHISM WITH ADHD AND RELATED SYMPTOMATOLOGY

B. Tang, L. Su, Yu-hu Zhang, 2005, The International journal of neuroscience.

Mutation analysis of PRRT2 in two Chinese BFIS families and nomenclature of PRRT2 related paroxysmal diseases

K. Xia, B. Tang, Zhengmao Hu, 2013, Neuroscience Letters.

Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Chinese Han patients with hereditary spastic paraplegia.

K. Xia, B. Tang, Hong Jiang, 2009, Chinese medical journal.

Expansion of the phenotypic spectrum of SPG6 caused by mutation in NIPA1

K. Xia, B. Tang, Hong Jiang, 2011, Clinical Neurology and Neurosurgery.

Mutation analysis of CAPN1 in Chinese populations with spastic paraplegia and related neurodegenerative diseases

B. Tang, Zhengmao Hu, Hong Jiang, 2020, Journal of the Neurological Sciences.

Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's disease.

A. Xie, P. Chan, Baorong Zhang, 2018, Parkinsonism & related disorders.

Effect of GBA Mutations on Phenotype of Parkinson's Disease: A Study on Chinese Population and a Meta-Analysis

B. Tang, Ji-feng Guo, Xinxiang Yan, 2015, Parkinson's disease.

Genetic Diagnosis of Two Dopa-Responsive Dystonia Families by Exome Sequencing

K. Xia, B. Tang, Zhengmao Hu, 2014, PloS one.

[TH gene mutation in Chinese patients with autosomal recessive dopa-responsive dystonia].

B. Tang, Wei Liu, Tao Chen, 2004, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stress

B. Tang, Ji-feng Guo, Xinxiang Yan, 2010, Brain Research.

[Molecular mechanism of idiopathic basal ganglia calcification].

M. Zhang, B. Tang, Lu Shen, 2015, Yi chuan = Hereditas.

Non-motor symptoms in Chinese Parkinson’s disease patients with and without LRRK2 G2385R and R1628P variants

P. Chan, Z. Gu, B. Tang, 2015, Journal of Neural Transmission.

The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients

B. Tang, Ji-feng Guo, Xinxiang Yan, 2016, Neuroscience Letters.

Lower serum UA levels in Parkinson's disease patients in the Chinese population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2012, Neuroscience Letters.

Spinocerebellar ataxia type 1 in China: molecular analysis and genotype-phenotype correlation in 5 families.

S. Tsuji, B. Tang, Y. Takiyama, 2001, Archives of neurology.

Follow-up study of variants of the GIGYF2 gene in Chinese patients with Parkinson’s disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2011, Journal of Clinical Neuroscience.

[Clinical and pathologic analysis of an autosomal recessive kindred with nemaline myopathy].

B. Tang, Hong Jiang, Dan-dan Jia, 2009, Zhonghua yi xue za zhi.

Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy

B. Tang, Xuebing Ding, E. Wu, 2020, Nature Communications.

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.

A neurophysiological profile in Parkinson’s disease with mild cognitive impairment and dementia in China

B. Tang, Ji-feng Guo, Xinxiang Yan, 2015, Journal of Clinical Neuroscience.

Involvement of Bcl-2-associated athanogene (BAG)-family proteins in the neuroprotection by rasagiline.

B. Tang, Ji-feng Guo, Xinxiang Yan, 2015, International journal of clinical and experimental medicine.

Paroxysmal kinesigenic dyskinesia

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

The BAG2 and BAG5 proteins inhibit the ubiquitination of pathogenic ataxin3-80Q

B. Tang, Ji-feng Guo, Hong Jiang, 2015, The International journal of neuroscience.

[Detection of the CAG trinucleotide repeats of MJD1 gene by recombinant DNA technology].

K. Xia, Q. Pan, B. Tang, 2009, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Evaluating the role of ARSA in Chinese patients with Parkinson's disease

B. Tang, Yi Zhang, Zhenghuan Fang, 2021, Neurobiology of Aging.

Constructing Prediction Models for Freezing of Gait by Nomogram and Machine Learning: A Longitudinal Study

B. Tang, Ji-feng Guo, Xin Wu, 2021, Frontiers in Neurology.

Kleine–Levin syndrome with brain atrophy

B. Tang, Hong Jiang, Yu-ting Shi, 2013, Journal of clinical neuroscience.

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

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

Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China

K. Xia, Q. Pan, B. Tang, 2013, Journal of Clinical Neuroscience.

LRRK2 Pro755Leu variant in ethnic Chinese population with Parkinson's disease

K. Xia, Q. Pan, B. Tang, 2011, Neuroscience Letters.

Identification of Ser465 as a novel PINK1 autophosphorylation site

B. Tang, Ji-feng Guo, Xinxiang Yan, 2017, Translational Neurodegeneration.

Association analysis of STK39, MCCC1/LAMP3 and sporadic PD in the Chinese Han population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2014, Neuroscience Letters.

Exon dosage analysis of parkin gene in Chinese sporadic Parkinson’s disease

K. Xia, B. Tang, Ji-feng Guo, 2015, Neuroscience Letters.

The single nucleotide polymorphism Rs12817488 is associated with Parkinson’s disease in the Chinese population

Yuan Zhang, B. Tang, Ji-feng Guo, 2015, Journal of Clinical Neuroscience.

Relationship between Alzheimer's disease GWAS-linked top hits and risk of Parkinson's disease with or without cognitive decline: a Chinese population-based study

Qian Xu, Ji-feng Guo, Yang Yang, 2016, Neurobiology of Aging.

The relationship between the phenotype of Parkinson's disease and levodopa-induced dyskinesia

B. Tang, Ji-feng Guo, Xinxiang Yan, 2013, Neuroscience Letters.

Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's Disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2019, Front. Neurol..

Alzheimer’s disease susceptibility genes modify the risk of Parkinson disease and Parkinson’s disease-associated cognitive impairment

B. Tang, Ji-feng Guo, Chang-min Wan, 2018, Neuroscience Letters.

A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease

B. Tang, Ji-feng Guo, Xinxiang Yan, 2010, Neuroscience Letters.

[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population].

K. Xia, Q. Pan, B. Tang, 2010, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Transglutaminase 6 interacts with polyQ proteins and promotes the formation of polyQ aggregates.

K. Xia, B. Tang, Hong Jiang, 2013, Biochemical and biophysical research communications.

Clinical features and [11C]-CFT PET analysis of PARK2, PARK6, PARK7-linked autosomal recessive early onset Parkinsonism

B. Tang, Ji-feng Guo, Xinxiang Yan, 2011, Neurological Sciences.

A rare Von Hippel–Lindau disease that mimics acute myelitis: case report and review of the literature

B. Tang, Hong Jiang, D. Xiao, 2010, Neurological Sciences.

Case-control study of the UCH-L1 S18Y variant in sporadic Parkinson’s disease in the Chinese population

K. Xia, Q. Pan, B. Tang, 2011, Journal of Clinical Neuroscience.

Phenotypes and cellular effects of GJB1 mutations causing CMT1X in a cohort of 226 Chinese CMT families

K. Xia, B. Tang, B. Tang, 2017, Clinical genetics.

Identification of clinically actionable secondary genetic variants from whole‐genome sequencing in a large‐scale Chinese population

B. Tang, S. Khederzadeh, Jin-chen Li, 2022, Clinical and translational medicine.

Association study between SMPD1 p.L302P and sporadic Parkinson's disease in ethnic Chinese population.

B. Tang, Ji-feng Guo, Xinxiang Yan, 2015, International journal of clinical and experimental medicine.

Analysis of several loci from genome-wide association studies in Parkinson’s disease in mainland China

K. Xia, B. Tang, Ji-feng Guo, 2015, Neuroscience Letters.

Simvastatin Induces Neuroprotection in 6‐OHDA‐Lesioned PC12 via the PI3K/AKT/Caspase 3 Pathway and Anti‐Inflammatory Responses

B. Tang, Yunqi Xu, L. Long, 2013, CNS neuroscience & therapeutics.

A novel candidate locus on chromosome 11p14.1-p11.2 for autosomal dominant hereditary spastic paraplegia.

K. Xia, Q. Pan, B. Tang, 2008, Chinese medical journal.

Novel GIGYF2 gene variants in patients with Parkinson's disease in Chinese population

K. Xia, Q. Pan, B. Tang, 2010, Neuroscience Letters.

HCFC1 variants in the proteolysis domain are associated with X‐linked idiopathic partial epilepsy: Exploring the underlying mechanism

B. Tang, D. Zhou, Yi-wu Shi, 2023, Clinical and translational medicine.

Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase‐associated neurodegeneration

Ji-feng Guo, Kun Xia, K. Xia, 2005, Movement disorders : official journal of the Movement Disorder Society.

Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China

B. Tang, Ji-feng Guo, Xinxiang Yan, 2015, Neurobiology of Aging.

Polygenic determinants of Parkinson's disease in a Chinese population

Kai Li, Lu Shen, Hong Jiang, 2015, Neurobiology of Aging.

UQCRC1 variants in Parkinson's disease: A large cohort study in Chinese mainland population.

B. Tang, Zhenghuan Fang, Ji-feng Guo, 2021, Brain : a journal of neurology.

Marginal association between SNP rs2046571 of the HAS2 gene and Parkinson's disease in the Chinese female population

Kai Li, Ji-feng Guo, B. Tang, 2013, Neuroscience Letters.

Research on screening and identification of proteins interacting with ataxin-3.

K. Xia, Q. Pan, B. Tang, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

Xin Jin, K. Xia, Q. Pan, 2010, Brain : a journal of neurology.

EIF 4 G 1 gene variants are not associated with Parkinson ' s disease in the ethnic Chinese population

S. Lesage, B. Tang, Ji-feng Guo, 2012 .

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.

Associations between gut microbiota and Parkinson disease: A bidirectional Mendelian randomization analysis

B. Tang, Ji-feng Guo, Jin-chen Li, 2023, European journal of neurology.

Distribution of Transglutaminase 6 in the Central Nervous System of Adult Mice

Yu-Qiang Ding, K. Xia, B. Tang, 2013, Anatomical record.

A novel genetic locus for benign familial infantile seizures maps to chromosome 1p36.12‐p35.1

K. Xia, Q. Pan, B. Tang, 2008, Clinical genetics.

Influence of simvastatin on dopaminergic neurons of lipopolysaccharide-induced rat model of Parkinson's disease.

B. Tang, Xiao-wu Chen, Zhi-bin Chen, 2015, Asian Pacific journal of tropical medicine.

R492X mutation in PTEN-induced putative kinase 1 induced cellular mitochondrial dysfunction and oxidative stress

B. Tang, Ji-feng Guo, Xinxiang Yan, 2010, Brain Research.

C9ORF72 repeat expansion is not detected in sporadic ataxia patients in mainland China

B. Tang, Hong Jiang, Lu Shen, 2016, Journal of the Neurological Sciences.

Spinocerebellar ataxia type 35 (SCA35)-associated transglutaminase 6 mutants sensitize cells to apoptosis.

K. Xia, B. Tang, Ji-feng Guo, 2013, Biochemical and biophysical research communications.