Chaodong Wang

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 11

Top Topics

Dna Methylation

Amyotrophic Lateral Sclerosis

Top Venues

NPJ Parkinson's disease

Nature communications

Molecular genetics & genomic medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Chaodong Wang, Han-Kui Liu, Xu-Ying Li, Jinghong Ma, Zhuqin Gu, Xiuli Feng, Shu Xie, Bei-Sha Tang, Sheng-Di Chen, Wei Wang, Jian Wang, Jian-Guo Zhang, Piu Chan
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Chaodong Wang, Han-Kui Liu, Xu-Ying Li, Jinghong Ma, Zhuqin Gu, Xiuli Feng, Shu Xie, Bei-Sha Tang, Sheng-Di Chen, Wei Wang, Jian Wang, Jian-Guo Zhang, Piu Chan
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Chaodong Wang, Han-Kui Liu, Xu-Ying Li, Jinghong Ma, Zhuqin Gu, Xiuli Feng, Shu Xie, Bei-Sha Tang, Sheng-Di Chen, Wei Wang, Jian Wang, Jian-Guo Zhang, Piu Chan
High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson's disease. NPJ Parkinson's disease 10 (1) (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Jie Zhong, Chaodong Wang, Dan Zhang, Xiaoli Yao, Quanzhen Zhao, Xusheng Huang, Feng Lin, Chun Xue, Yaqing Wang, Ruojie He, Xu-Ying Li, Qibin Li, Mingbang Wang, Shaoli Zhao, Shabbir Khan Afridi, Wen-Hao Zhou, Zhanjun Wang, Yan-Ming Xu, Zhiheng Xu
PCDHA9 as a candidate gene for amyotrophic lateral sclerosis. Nature communications 15 (1) (2024)
Liping Zhang, Xu-Ying Li, Fanxi Xu, Lehong Gao, Zhanjun Wang, Xianling Wang, Xian Li, Mengyu Liu, Junge Zhu, Tingyan Yao, Jing Ye, Xiao-Hong Qi, Yaqing Wang, Guoguang Zhao, Chaodong Wang, null null
Multidisciplinary molecular consultation increases the diagnosis of pediatric epileptic encephalopathy and neurodevelopmental disorders. Molecular genetics & genomic medicine (2023)
Junge Zhu, Fanxi Xu, Hong Lai, Huiyao Yuan, Xu-Ying Li, Junya Hu, Wei Li, Lei Liu, Chaodong Wang
ACO2 deficiency increases vulnerability to Parkinson's disease via dysregulating mitochondrial function and histone acetylation-mediated transcription of autophagy genes. Communications biology 6 (1) (2023)
Lianghao Si, Zhanjun Wang, Xu-Ying Li, Yang Song, Tingyan Yao, Erhe Xu, Xianling Wang, Chaodong Wang
Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders. Neurogenetics (2023)
Xianling Wang, Xu-Ying Li, Yueshan Piao, Guobin Yuan, Yicong Lin, Hai Chen, Zhanjun Wang, Cunjiang Li, Chaodong Wang
Hartnup disease presenting as hereditary spastic paraplegia and severe peripheral neuropathy. American journal of medical genetics. Part A (2021)
Xu-Ying Li, Weiwei Yang, Xin Li, Xu-Ran Li, Wei Li, Qihan Song, Linjuan Sun, Feng Lin, Zhigang Chen, Chaodong Wang, Shun Yu
Phosphorylated Alpha-Synuclein in Red Blood Cells as a Potential Diagnostic Biomarker for Multiple System Atrophy: A Pilot Study. Parkinson's disease 2020 (2020)