Wenjing Sun

Publication Activity (10 Years)

Years Active: 2020-2022
Publications (10 Years): 4

Top Topics

Polycystic Kidney Disease

Autism Spectrum Disorder

Top Venues

Molecular genetics & genomic medicine

Disease markers

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

Publications

Yusi Wang, Xuguang Hao, Xueyuan Jia, Wei Ji, Shuai Yuan, Estelle Judith Abla Gnamey, Min Huang, Lidan Xu, Xuelong Zhang, Jing Bai, Wenjing Sun, Songbin Fu, Yong Liu, Jie Wu
A novel variant of GLI3, p.Asp1514Thrfs*5, is identified in a Chinese family affected by polydactyly. Molecular genetics & genomic medicine 10 (7) (2022)
Kexian Dong, Xiaogang Liu, Xueyuan Jia, Huanhuan Miao, Wei Ji, Jie Wu, Yun Huang, Lidan Xu, Xuelong Zhang, Hui Su, Guohua Ji, Peng Liu, Rongwei Guan, Jing Bai, Songbin Fu, Xianli Zhou, Wenjing Sun
Disease causing property analyzation of variants in 12 Chinese families with polycystic kidney disease. Molecular genetics & genomic medicine 8 (11) (2020)
Tahir Zaib, Chunhui Zhang, Komal Saleem, Lidan Xu, Qian Qin, Yusi Wang, Wei Ji, Hanif Khan, Hanfei Yu, Siqi Zhu, Wei Gao, Yun Huang, Xueyuan Jia, Jie Wu, Hongtao Song, Yan-Qiao Zhang, Wenjing Sun, Songbin Fu
Functional Characterization of a Missense Variant of MLH1 Identified in Lynch Syndrome Pedigree. Disease markers 2020 (2020)
Komal Saleem, Qingbo Cui, Tahir Zaib, Siqi Zhu, Qian Qin, Yusi Wang, Jinxi Dam, Wei Ji, Peng Liu, Xueyuan Jia, Jie Wu, Jing Bai, Songbin Fu, Wenjing Sun
Evaluation of a Novel Missense Mutation in ABCB4 Gene Causing Progressive Familial Intrahepatic Cholestasis Type 3. Disease markers 2020 (2020)