Xun Wang

Publication Activity (10 Years)

Years Active: 2022-2023
Publications (10 Years): 7

Top Topics

Mitochondrial Dna

Intellectual Disability

Duchenne Muscular Dystrophy

Cardiovascular Risk Factors

Top Venues

Diagnostics (Basel, Switzerland)

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

Publications

Wai Cheng Iao, Weixing Zhang, Xun Wang, Yuxuan Wu, Duoru Lin, Haotian Lin
Deep Learning Algorithms for Screening and Diagnosis of Systemic Diseases Based on Ophthalmic Manifestations: A Systematic Review. Diagnostics (Basel, Switzerland) 13 (5) (2023)
Wai Cheng Iao, Weixing Zhang, Xun Wang, Yuxuan Wu, Duoru Lin, Haotian Lin
Deep Learning Algorithms for Screening and Diagnosis of Systemic Diseases Based on Ophthalmic Manifestations: A Systematic Review. Diagnostics (Basel, Switzerland) 13 (5) (2023)
Qiwei Wang, Tingfeng Qin, Xun Wang, Jing Li, Xiaoshan Lin, Dongni Wang, Zhuoling Lin, Xulin Zhang, Xiaoyan Li, Haotian Lin, Weirong Chen
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome. Genes 13 (12) (2022)
Qiwei Wang, Tingfeng Qin, Xun Wang, Jing Li, Xiaoshan Lin, Dongni Wang, Zhuoling Lin, Xulin Zhang, Xiaoyan Li, Haotian Lin, Weirong Chen
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome. Genes 13 (12) (2022)
Qiwei Wang, Tingfeng Qin, Xun Wang, Jing Li, Xiaoshan Lin, Dongni Wang, Zhuoling Lin, Xulin Zhang, Xiaoyan Li, Haotian Lin, Weirong Chen
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome. Genes 13 (12) (2022)
Qiwei Wang, Tingfeng Qin, Xun Wang, Jing Li, Xiaoshan Lin, Dongni Wang, Zhuoling Lin, Xulin Zhang, Xiaoyan Li, Haotian Lin, Weirong Chen
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome. Genes 13 (12) (2022)
Qiwei Wang, Tingfeng Qin, Xun Wang, Jing Li, Xiaoshan Lin, Dongni Wang, Zhuoling Lin, Xulin Zhang, Xiaoyan Li, Haotian Lin, Weirong Chen
Whole-Exome Sequencing and Copy Number Analysis in a Patient with Warburg Micro Syndrome. Genes 13 (12) (2022)