Kai Li

发表

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

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

Relationship between GWAS-linked three new loci in Essential tremor and risk of Parkinson's disease in Chinese population.

B. Tang, Ji-feng Guo, Xinxiang Yan, 2017, Parkinsonism & related disorders.

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.

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.

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

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

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.

Rare GCH1 heterozygous variants contributing to Parkinson's disease.

K. Xia, B. Tang, Ji-feng Guo, 2017, Brain : a journal of neurology.

Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population.

B. Tang, Ji-feng Guo, Xinxiang Yan, 2012, Parkinsonism & related disorders.

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

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

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

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

Coding mutations in NUS1 contribute to Parkinson’s disease

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

Novel mutations in ADSL for Adenylosuccinate Lyase Deficiency identified by the combination of Trio-WES and constantly updated guidelines

Yuan Zhang, K. Xia, B. Tang, 2017, Scientific Reports.

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

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

Dynamic expression patterns of ATF3 and p53 in the hippocampus of a pentylenetetrazole-induced kindling model

Kai Li, F. Tian, Jingya He, 2014, Molecular medicine reports.

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.

Analysis of EIF4G1 in ethnic Chinese

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

Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population

Yuan Zhang, B. Tang, Ji-feng Guo, 2017, Scientific Reports.

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.

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.

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.

Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease

Yuan Zhang, B. Tang, Ji-feng Guo, 2015, Neurobiology of Aging.

TMEM230 mutation analysis in Parkinson's disease in a Chinese population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2017, Neurobiology of Aging.

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.

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

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

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

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

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.

Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2017, Scientific Reports.

Lack of association between IL-10 and IL-18 gene promoter polymorphisms and Parkinson’s disease with cognitive impairment in a Chinese population

B. Tang, Ji-feng Guo, Xinxiang Yan, 2016, Scientific Reports.

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.

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.

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.

The rs3756063 polymorphism is associated with SNCA methylation in the Chinese Han population

Xiongwei Zhu, B. Tang, Ji-feng Guo, 2016, Journal of the Neurological Sciences.

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 .