Associated Papers
Genetic and epigenetic insights into non-obstructive azoospermia: mechanisms, biomarkers, and clinical perspectives.
Wang X et al.
Reproductive Biology and Endocrinology : Rb&e, 2025
Summarizing the human genes and their variants causative of non-obstructive azoospermia uncovered using whole genome/exome sequencing.
Ibrahim R et al.
Reproductive Biology, 2025
Genetic variants underlying spermatogenic arrests in men with non-obstructive azoospermia.
Ozturk S
Cell Cycle (georgetown, Tex.), 2023
Sertoli cell-only syndrome: advances, challenges, and perspectives in genetics and mechanisms.
Wang X et al.
Cellular and Molecular Life Sciences : Cmls, 2023
Identification of pathogenic mutations from nonobstructive azoospermia patients†.
Jiang H et al.
Biology of Reproduction, 2022
Fanconi Anemia Gene Variants in Patients with Gonadal Dysfunction.
Daum H et al.
Reproductive Sciences (thousand Oaks, Calif.), 2022
Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia.
Zhang Y et al.
Frontiers in Genetics, 2021
A homozygous FANCM frameshift pathogenic variant causes male infertility.
Yin H et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
Genotype-phenotype correlations in biallelic carriers of FANCM protein truncating variants: A systematic literature review.
Figlioli G et al.
Mutation Research. Reviews in Mutation Research, 0
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