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Andrology|June 15, 2026
Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal ArchitectureJianteng Zhou, Ghulam Mustafa, Tingting Lin, et al.
Human Reproduction (Oxford, England)|May 8, 2022
Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degreesXuefeng Xie, Ghulam Murtaza, Yang Li, et al.
Cell Discovery|August 23, 2023
A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formationSuixing Fan, Yuewen Wang, Hanwei Jiang, et al.
Cells & Development|May 26, 2025
AKAP14 is dispensable for mouse fertilityZishuo Xu, Ansar Hussain, Hanwei Jiang, et al.
Scientific Reports|March 15, 2017
Ndrg3 gene regulates DSB repair during meiosis through modulation the ERK signal pathway in the male germ cellsHongjie Pan, Xuan Zhang, Hanwei Jiang, et al.
American Journal of Human Genetics|January 28, 2021
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humansSuixing Fan, Yuying Jiao, Ranjha Khan, et al.
Iscience|July 24, 2023
Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humansJunyan Liu, Fazal Rahim, Jianteng Zhou, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|January 29, 2015
Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC manLiu Wang, Zhipeng Xu, Furhan Iqbal, et al.
Reproductive Biomedicine Online|April 21, 2015
Abnormal meiotic recombination with complex chromosomal rearrangement in an azoospermic manLiu Wang, Furhan Iqbal, Guangyuan Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 31, 2018
Correction: A homozygous FANCM frameshift pathogenic variant causes male infertilityHao Yin, Hui Ma, Sajjad Hussain, et al.
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