Ruyi Liu
Shanghai, China
Last Updated: 09/26/2026
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Found 18 publications
Novel mutations in NLRP2 and NLRP7 cause early embryonic arrest and female infertility.
Journal: Journal of assisted reproduction and genetics
Published: May 30, 2026
Pathogenic variants in ACTRT3 lead to male infertility characterized by fertilization defects.
Journal: Human reproduction (Oxford, England)
Published: December 25, 2024
Homozygous variants in CDC23 cause female infertility characterized by oocyte maturation defects.
Journal: Human genetics
Published: June 04, 2023
ARRDC5 deficiency impairs spermatogenesis by affecting SUN5 and NDC1.
Journal: Development (Cambridge, England)
Published: May 08, 2023
Bi-allelic variants in ASTL cause abnormal fertilization or oocyte maturation defects.
Journal: Human molecular genetics
Published: April 04, 2023
A novel homozygous variant in ZFP36L2 cause female infertility due to oocyte maturation defect.
Journal: Clinical genetics
Published: March 27, 2023
PATL2 regulates mRNA homeostasis in oocytes by interacting with EIF4E and CPEB1.
Journal: Development (Cambridge, England)
Published: January 03, 2023
YBX2-dependent stabilization of oocyte mRNA through a reversible sponge-like cortical partition.
Journal: Cell research
Published: November 30, 2022
ADGB variants cause asthenozoospermia and male infertility.
Journal: Human genetics
Published: November 09, 2022
Genetic screening in patients with ovarian dysfunction.
Journal: Clinical genetics
Published: September 19, 2022
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: April 01, 2022
Last Updated: 09/26/2026