Fazal Rahim
443 Huangshan Road
Hefei, 230027, China
Hefei, 230027, China
Last Updated: 09/26/2026
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Found 16 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
Corrigendum to "Novel bi-allelic variants in DNAH10 lead to multiple morphological abnormalities of sperm flagella and male infertility".
Journal: Asian journal of andrology
Published: August 12, 2025
Novel PNLDC1 mutations underlie nonobstructive azoospermia in humans and mice.
Journal: Human molecular genetics
Published: April 22, 2025
Novel mutations in FSIP2 cause male infertility through multiple morphological abnormalities of the sperm flagella.
Journal: Asian journal of andrology
Published: January 30, 2025
A novel frameshift variant in AXDND1 may cause multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family.
Journal: Asian journal of andrology
Published: December 30, 2024
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 splicing mutation in AK7 causes multiple morphological abnormalities of sperm flagella in patients from consanguineous Pakistani families.
Journal: Asian journal of andrology
Published: April 07, 2024
A novel homozygous missense TTC12 variant identified in an infertile Pakistani man with severe oligoasthenoteratozoospermia and primary ciliary dyskinesia.
Journal: Molecular genetics and genomics : MGG
Published: January 23, 2024
Last Updated: 09/26/2026