Zixue Zhou

A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice

F. Zhang, L. Jin, Qinghua Shi, 2020, Molecular Genetics and Genomics.

Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice

L. Jin, Ling Zhang, Feng Zhang, 2021, Journal of Medical Genetics.

A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice

L. Jin, Feng Zhang, Hao Yin, 2020, Molecular Genetics and Genomics.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

Rare variants in FANCA induce premature ovarian insufficiency

L. Jin, Qinghua Shi, Feng Zhang, 2019, Human Genetics.

Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging

L. Jin, Feng Zhang, Yanhua Wu, 2021, Human molecular genetics.

Whole exome sequencing identified a rare WT1 loss‐of‐function variant in a non‐syndromic POI patient

L. Jin, Feng Zhang, Yanhua Wu, 2021, Molecular genetics & genomic medicine.

Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.

Feng Zhang, Yuncheng Pan, Xi Yang, 2023, Journal of genetics and genomics = Yi chuan xue bao.