Author

Shu Xie

Observed name: Xie, Shu

Institution: Chinese National Human Genome Center

Observed institution: Chinese National Human Genome Center

ORCID: 0009-0000-7648-7941

Observed ORCID: 0009-0000-7648-7941

OpenAlex ID: A5071552049

Association of Catechol-O-Methyltransferase and monoamine oxidase B gene polymorphisms with motor complications in parkinson's disease in a Chinese population

2014 · Hongying Hao, Ming Shao, et al. · Parkinsonism & Related Disorders · 33

Linkage analysis and whole-exome sequencing exclude extra mutations responsible for the parkinsonian phenotype of spinocerebellar ataxia-2

2014 · Chaodong Wang, Yanming Xu, et al. · Neurobiology of Aging · 21

Parkin dosage mutations in patients with early-onset sporadic and familial Parkinson's disease in Chinese: An independent pathogenic role

2010 · Chaodong Wang, Huili Ma, et al. · Brain Research · 16

High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease

2024 · Chaodong Wang, Hankui Liu, et al. · npj Parkinson s Disease · 12

Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease

2013 · Chaodong Wang, Xiuli Feng, et al. · Neurobiology of Aging · 4

[Polymorphisms of catechol-O-methyltransferase and monoamine oxidase B genes among Chinese patients with Parkinson's disease].

2015 · Hongying Hao, Ming Shao, et al. · PubMed · 2

Works count: 8

Citation count: 88

H-index: 4

I10-index: 4