Chuan Zhang

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 15

Top Topics

Attention Deficit Hyperactivity Disorder

Transcription Factor

Intellectual Disability

High Fat Diet Induced

Top Venues

Molecular psychiatry

Molecular genetics & genomic medicine

Journal of clinical laboratory analysis

The Journal of international medical research

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

Publications

Panpan Ma, Bingbo Zhou, Qichao Kang, Xue Chen, Xinyuan Tian, Ling Hui, Shengju Hao, Huiyan Wu, Chuan Zhang
Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants. Molecular genetics & genomic medicine 12 (6) (2024)
Panpan Ma, Bingbo Zhou, Qichao Kang, Xue Chen, Xinyuan Tian, Ling Hui, Shengju Hao, Huiyan Wu, Chuan Zhang
Mutation spectrum of hearing loss patients in Northwest China: Identification of 20 novel variants. Molecular genetics & genomic medicine 12 (6) (2024)
Xinyuan Tian, Xiaoni Zhang, Qinghua Zhang, Xue Chen, Bingbo Zhou, Panpan Ma, Lei Zheng, Shengju Hao, Junhe Ling, Chuan Zhang, Ling Hui
Immune skeletal dysplasia with neurodevelopmental abnormalities caused by a novel variant of EXTL3 gene in a Chinese family. Molecular genetics & genomic medicine (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry 28 (3) (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry 28 (3) (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry (2023)
Danyang Li, Bingbo Zhou, Xinyuan Tian, Xue Chen, Yupei Wang, Shengju Hao, Chuan Zhang, Ling Hui
Genetic analysis and literature review of a Poirier-Bienvenu neurodevelopmental syndrome family line caused by a de novo frameshift variant in CSNK2B. Molecular genetics & genomic medicine (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry 28 (3) (2023)
Jiayi Li, Chuan Zhang, Xinyuan Tian, Bingbo Zhou, Xue Chen, Yupei Wang, Shengju Hao, Ling Hui, Zhaoyan Meng
Novel de novo mutation in ZBTB20 in a Chinese Primrose syndrome family and a review of the literature. Molecular genetics & genomic medicine (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry (2023)
Tian Meng, Xiaoting Chen, Zheng-Jie He, Haofeng Huang, Shiyin Lin, Kunru Liu, Guo Bai, Hao Liu, Min-Dong Xu, Haixia Zhuang, Yunlong Zhang, Ahmed Waqas, Qian Liu, Chuan Zhang, Xiang-Dong Sun, Huansen Huang, Muhammad Umair, Yousheng Yan, Du Feng
ATP9A deficiency causes ADHD and aberrant endosomal recycling via modulating RAB5 and RAB11 activity. Molecular psychiatry 28 (3) (2023)
Chuan Zhang, Shengju Hao, Qinghua Zhang, Furong Liu, Bingbo Zhou, Feng Xuan, Wang Xing, Xue Chen, Yan Wang, Panpan Ma, Zongfu Cao, Xu Ma
Maternal UPD of chromosome 7 in a patient with Silver-Russell syndrome and Pendred syndrome. Journal of clinical laboratory analysis 34 (9) (2020)
Chuan Zhang, Lisha An, Huiqin Xue, Shengju Hao, Yousheng Yan, Qinghua Zhang, Xiaohua Jin, Qian Li, Bingbo Zhou, Xuan Feng, Panpan Ma, Xing Wang, Xue Chen, Cuixia Chen, Zongfu Cao, Xu Ma
Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients. Journal of clinical laboratory analysis 35 (1) (2020)
Chuan Zhang, Shengju Hao, Yali Liu, Bingbo Zhou, Furong Liu, Lei Zheng, Panpan Ma, Qing Liu, Xiaojuan Lin, Yousheng Yan, Qinghua Zhang
A novel LOXHD1 variant in a Chinese couple with hearing loss. The Journal of international medical research 47 (12) (2019)