Wenjing Wang
Shanghai, 200438, China
Last Updated: 09/26/2026
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Found 27 publications
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertility.
Journal: Human genetics
Published: September 06, 2023
Homozygous variants in CDC23 cause female infertility characterized by oocyte maturation defects.
Journal: Human genetics
Published: June 04, 2023
Bi-allelic variants in ASTL cause abnormal fertilization or oocyte maturation defects.
Journal: Human molecular genetics
Published: April 04, 2023
Bi-allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility.
Journal: EMBO molecular medicine
Published: November 15, 2022
ADGB variants cause asthenozoospermia and male infertility.
Journal: Human genetics
Published: November 09, 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
Karyopherin α deficiency contributes to human preimplantation embryo arrest.
Journal: The Journal of clinical investigation
Published: March 16, 2022
Bi-allelic variants in KCNU1 cause impaired acrosome reactions and male infertility.
Journal: Human reproduction (Oxford, England)
Published: January 10, 2022
Changing Gly311 to an acidic amino acid in the MATE family protein DTX6 enhances Arabidopsis resistance to the dihydropyridine herbicides.
Journal: Molecular plant
Published: February 06, 2021
FBXO43 variants in patients with female infertility characterized by early embryonic arrest.
Journal: Human reproduction (Oxford, England)
Published: January 30, 2021
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.
Journal: Human reproduction (Oxford, England)
Published: December 29, 2020
Last Updated: 09/26/2026