Jingwei Ye
443 Huangshan Road
Hefei, 230027, China
Hefei, 230027, China
Last Updated: 09/26/2026
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Found 12 publications
Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture.
Journal: Andrology
Published: February 10, 2026
S100PBP interacts with nucleoporin TPR and facilitates XY crossover formation in mice.
Journal: EMBO reports
Published: June 21, 2024
A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family.
Journal: Basic and clinical andrology
Published: October 07, 2023
A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation.
Journal: Cell discovery
Published: January 31, 2023
M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination.
Journal: EMBO reports
Published: July 12, 2022
Cornichon protein CNIH4 is not essential for mice gametogenesis and fertility.
Journal: Developmental biology
Published: June 13, 2022
RAD51AP2 is required for efficient meiotic recombination between X and Y chromosomes.
Journal: Science advances
Published: January 12, 2022
Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Journal: Human reproduction (Oxford, England)
Published: October 12, 2021
Evolutionarily conserved and testis-specific gene, 4930524B15Rik, is not essential for mouse spermatogenesis and fertility.
Journal: Molecular biology reports
Published: March 06, 2020
Showing 1-12 of 12
Last Updated: 09/26/2026