Ihsan Khan
Hefei, China
Last Updated: 09/26/2026
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Found 22 publications
Novel homozygous SPAG17 variants cause human male infertility through multiple morphological abnormalities of spermatozoal flagella related to axonemal microtubule doublets.
Journal: Asian journal of andrology
Published: May 28, 2024
Novel biallelic ADCY10 variants cause asthenozoospermia with excessive residual cytoplasm and hydronephrosis in humans.
Journal: Reproductive biomedicine online
Published: May 17, 2024
A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family.
Journal: Basic and clinical andrology
Published: October 07, 2023
A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans.
Journal: Frontiers in endocrinology
Published: December 20, 2022
M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination.
Journal: EMBO reports
Published: July 12, 2022
Cornichon protein CNIH4 is not essential for mice gametogenesis and fertility.
Journal: Developmental biology
Published: June 13, 2022
A novel homozygous variant in homologous recombination repair gene ZSWIM7 causes azoospermia in males and primary ovarian insufficiency in females.
Journal: European journal of medical genetics
Published: May 04, 2022
A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms.
Journal: Asian journal of andrology
Published: March 09, 2022
Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility.
Journal: Frontiers in cell and developmental biology
Published: October 28, 2021
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
Last Updated: 09/26/2026