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American Journal of Human Genetics|August 4, 2018
Bi-allelic Recessive Loss-of-Function Variants in FANCM Cause Non-obstructive AzoospermiaLaura Kasak, Margus Punab, Liina Nagirnaja, et al.
Journal of the Endocrine Society|March 6, 2025
Azoospermia/Oligozoospermia and Prostate Cancer Are Increased in Families of Women With Primary Ovarian InsufficiencyKristina Allen-Brady, Samantha Kodama, Lauren E Verrilli, et al.
Communications Biology|March 30, 2023
DDX3Y is likely the key spermatogenic factor in the AZFa region that contributes to human non-obstructive azoospermiaAnn-Kristin Dicke, Adrian Pilatz, Margot J Wyrwoll, et al.
Developmental Cell|May 3, 2022
Single-cell analysis of human testis aging and correlation with elevated body mass indexXichen Nie, Sarah K Munyoki, Meena Sukhwani, et al.
Human Genetics|November 19, 2020
Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermiaAlbert Salas-Huetos, Frank Tüttelmann, Margot J Wyrwoll, et al.
Plos Genetics|June 11, 2020
NRF2 loss recapitulates heritable impacts of paternal cigarette smoke exposurePatrick J Murphy, Jingtao Guo, Timothy G Jenkins, et al.
American Journal of Human Genetics|October 9, 2021
Comparative single-cell analysis of biopsies clarifies pathogenic mechanisms in Klinefelter syndromeEisa Mahyari, Jingtao Guo, Ana C Lima, et al.
Biorxiv : the Preprint Server for Biology|November 28, 2023
AXDND1 is required to balance spermatogonial commitment and for sperm tail formation in mice and humansBrendan J Houston, Joseph Nguyen, D Jo Merriner, et al.
Cell Death & Disease|July 12, 2024
AXDND1 is required to balance spermatogonial commitment and for sperm tail formation in mice and humansBrendan J Houston, Joseph Nguyen, D Jo Merriner, et al.
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