Ann-kristin Dicke
Muenster, NW, Germany
Last Updated: 09/26/2026
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Found 11 publications
Genotype-specific differences in infertile men due to loss-of-function variants in M1AP or ZZS genes.
Journal: EMBO molecular medicine
Published: July 11, 2024
How exome sequencing improves the diagnostics and management of men with non-syndromic infertility.
Journal: Andrology
Published: March 03, 2024
Inherited defects of piRNA biogenesis cause transposon de-repression, impaired spermatogenesis, and human male infertility.
Journal: Nature communications
Published: December 20, 2023
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermia.
Journal: Communications biology
Published: December 03, 2022
Bi-allelic variants in INSL3 and RXFP2 cause bilateral cryptorchidism and male infertility.
Journal: Human reproduction (Oxford, England)
Published: October 14, 2022
The piRNA-pathway factor FKBP6 is essential for spermatogenesis but dispensable for control of meiotic LINE-1 expression in humans.
Journal: American journal of human genetics
Published: May 15, 2022
Rap1 controls epiblast morphogenesis in sync with the pluripotency states transition.
Journal: Developmental cell
Published: January 06, 2022
Genetic Architecture of Azoospermia-Time to Advance the Standard of Care.
Journal: European urology
Published: December 22, 2021
Expression and Function of Organic Cation Transporter 2 in Pancreas.
Journal: Frontiers in cell and developmental biology
Published: March 31, 2021
Showing 1-11 of 11
Last Updated: 09/26/2026