Yanhua Wu

ORCID

Publication Activity (10 Years)

Years Active: 2019-2022
Publications (10 Years): 6

Top Venues

Human genetics

Molecular genetics & genomic medicine

Journal of medical genetics

Human molecular genetics

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

Publications

Zixue Zhou, Xi Yang, Yuncheng Pan, Lingyue Shang, Siyuan Chen, Jialin Yang, Li Jin, Feng Zhang, Yanhua Wu
Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging. Human molecular genetics 30 (21) (2022)
Yingchen Wang, Qing Chen, Feng Zhang, Xi Yang, Lingyue Shang, Shuting Ren, Yuncheng Pan, Zixue Zhou, Guoqing Li, Yunzheng Fang, Li Jin, Yanhua Wu, Xiaojin Zhang
Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient. Molecular genetics & genomic medicine (2021)
Guoqing Li, Xi Yang, Lingbo Wang, Yuncheng Pan, Siyuan Chen, Lingyue Shang, Yicheng Zhang, Yucheng Wu, Zixue Zhou, Qing Chen, Xue Zhang, Ling Zhang, Yingchen Wang, Jinsong Li, Li Jin, Yanhua Wu, Xiaojin Zhang, Feng Zhang
Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice. Journal of medical genetics (2021)
Xi Yang, Feng Zhang, Qinghua Shi, Yanhua Wu
"Response to the letter to the editor "Concerns regarding the potentially causal role of FANCA heterozygous variants in human primary ovarian insufficiency"". Human genetics 140 (4) (2020)
Yuncheng Pan, Xi Yang, Feng Zhang, Siyuan Chen, Zixue Zhou, Hao Yin, Hui Ma, Lingyue Shang, Jialin Yang, Guoqing Li, Yingchen Wang, Li Jin, Qinghua Shi, Yanhua Wu
A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice. Molecular genetics and genomics : MGG 296 (1) (2020)
Xi Yang, Xiaojin Zhang, Jiao Jiao, Feng Zhang, Yuncheng Pan, Qiqi Wang, Qing Chen, Baozhu Cai, Shuyan Tang, Zixue Zhou, Siyuan Chen, Hao Yin, Wei Fu, Yang Luo, Da Li, Guoqing Li, Lingyue Shang, Jialing Yang, Li Jin, Qinghua Shi, Yanhua Wu
Rare variants in FANCA induce premature ovarian insufficiency. Human genetics 138 (11-12) (2019)

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Publication Activity (10 Years)

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Yanhua Wu