Xiaomin Zha

Hefei, 230022, China

Last Updated: 09/26/2026

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Found 16 publications

A missense mutation in TCFL5 is associated with male infertility due to oligoasthenoteratozoospermia.

A missense mutation in TCFL5 is associated with male infertility due to oligoasthenoteratozoospermia.

Journal: Molecular genetics and genomics : MGG

Published: April 29, 2025

Novel CCDC188 variants cause acephalic spermatozoa syndrome with poor intracytoplasmic sperm injection outcome.

Novel CCDC188 variants cause acephalic spermatozoa syndrome with poor intracytoplasmic sperm injection outcome.

Journal: Journal of assisted reproduction and genetics

Published: March 17, 2025

Association of lifestyle and occupational exposure factors with human semen quality: a cross-sectional study of 1060 participants.

Association of lifestyle and occupational exposure factors with human semen quality: a cross-sectional study of 1060 participants.

Journal: Systems biology in reproductive medicine

Published: June 19, 2024

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Novel and recurrent hemizygous variants in BCORL1 cause oligoasthenoteratozoospermia by interfering transcription.

Journal: Andrology

Published: April 19, 2024

A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

A homozygous loss-of-function mutation in CEP250 is associated with acephalic spermatozoa syndrome in humans.

Journal: Andrology

Published: April 18, 2024

Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice.

Unraveling the Impact of the PROCA1 Mutation in Male Infertility: Incorporating Whole Exome Sequencing in Teratozoospermia Patients and Analyzing Proca1 Knockout Mice.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: December 26, 2023

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.

Journal: Science China. Life sciences

Published: November 21, 2023

Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

Biallelic loss-of-function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

Journal: Human mutation

Published: July 18, 2022

A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia.

A novel homozygous missense mutation in AK7 causes multiple morphological anomalies of the flagella and oligoasthenoteratozoospermia.

Journal: Journal of assisted reproduction and genetics

Published: August 31, 2021

Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.

Pathogenesis of acephalic spermatozoa syndrome caused by splicing mutation and de novo deletion in TSGA10.

Journal: Journal of assisted reproduction and genetics

Published: June 10, 2021

Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome.

Novel Mutation and Deletion in SUN5 Cause Male Infertility with Acephalic Spermatozoa Syndrome.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: March 25, 2021

A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.

A novel homozygous missense mutation of PMFBP1 causes acephalic spermatozoa syndrome.

Journal: Journal of assisted reproduction and genetics

Published: December 01, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026