Xiaoming Wei (Wei Li)

ORCID

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 9

Top Venues

Clinical genetics

Molecular genetics & genomic medicine

eLife

Human genome variation

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

Publications

Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Xiaoming Wei, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. Clinical genetics 103 (4) (2023)
Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Xiaoming Wei, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. Clinical genetics 103 (4) (2023)
Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Xiaoming Wei, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. Clinical genetics 103 (4) (2023)
Yanqiu Liu, Liangwei Mao, Hui Huang, Wei Li, Jianfen Man, Wenqian Zhang, Lina Wang, Long Li, Yan Sun, Teng Zhai, Xueqin Guo, Lique Du, Jin Huang, Hao Li, Yang Wan, Xiaoming Wei
Clinical diagnosis of genetic disorders at both single-nucleotide and chromosomal levels based on BGISEQ-500 platform. Human genome variation 10 (1) (2023)
Juan Wu, Dongna Chen, Hui Huang, Ning Luo, Huishuang Chen, Junjie Zhao, Yanyan Wang, Tian Zhao, Siyuan Huang, Yang Ren, Teng Zhai, Weibin Sun, Houxuan Li, Xiaoming Wei
A novel gene ZNF862 causes hereditary gingival fibromatosis. eLife 11 (2022)
Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Xiaoming Wei, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. Clinical genetics (2022)
Liangpu Xu, Xinrui Wang, Jia Li, Lingji Chen, Haiwei Wang, Shiyi Xu, Yanhong Zhang, Xiaoming Wei, Pengcheng Yao, Meihua Tan, Si Zhou, Meihuan Chen, Yali Pan, Xuemei Chen, Xiaolan Chen, Yunliang Liu, Na Lin, Hailong Huang, Hua Cao
A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family. Clinical genetics (2022)
Xiaoming Wei, Fanwei Zeng, Baitong Fan, Nan Yu, Jing Wu, Yun Yang, Hui Huang, Sheng-Li Li, Zhiyu Peng
Impact of ultrasonography on identifying noninvasive prenatal screening false-negative aneuploidy. Molecular genetics & genomic medicine 8 (6) (2020)
Lianshu Han, Chao Chen, Fengyu Guo, Jun Ye, Zhiyu Peng, Wenjuan Qiu, Yaoshen Wang, Xiaoming Wei, Huiwen Zhang, Lili Liang, Yu Wang, Huanhuan Wang, Xing Ji, Jun Sun, Xuefan Gu
Noninvasive prenatal diagnosis of cobalamin C (cblC) deficiency through target region sequencing of cell-free DNA in maternal plasma. Prenatal diagnosis 40 (3) (2019)

Xiaoming Wei.css-eqlu8i{font-size:small;padding-left:4px;} (Wei Li)

Publication Activity (10 Years)

Top Topics

Top Venues

Xiaoming Wei (Wei Li)