Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 17 publications
Novel variants in YTHDC2 cause non-obstructive azoospermia by disrupting the mitotic-to-meiotic transition in humans and mice.
Journal: Human reproduction (Oxford, England)
Published: January 13, 2026
A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.
Journal: Human molecular genetics
Published: January 30, 2025
Homozygous CCDC146 mutation causes oligoasthenoteratozoospermia in humans and mice.
Journal: Zoological research
Published: September 08, 2024
A homozygous nonsense variant in HENMT1 causes male infertility in humans and mice.
Journal: Andrology
Published: April 26, 2024
A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans.
Journal: Frontiers in genetics
Published: August 11, 2022
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Journal: American journal of human genetics
Published: July 08, 2022
Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome.
Journal: Genetic testing and molecular biomarkers
Published: October 21, 2021
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
Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Journal: Human reproduction (Oxford, England)
Published: April 13, 2021
Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Journal: American journal of human genetics
Published: October 23, 2020
Last Updated: 09/26/2026