Fuxi Zhu

No 81 Meishan Road
Hefei, 230032, China

Last Updated: 09/26/2026

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Found 30 publications

Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice.

Biallelic mutations in ANAPC13 cause female infertility characterized by oocyte maturation arrest both in humans and mice.

Journal: American journal of obstetrics and gynecology

Published: December 04, 2025

Healthy live birth after microsurgical enucleation of tripronuclear human zygote derived from ICSI: a case report.

Healthy live birth after microsurgical enucleation of tripronuclear human zygote derived from ICSI: a case report.

Journal: Journal of ovarian research

Published: June 09, 2025

Novel Variants in MDC1 are Associated With Severe Oligoasthenoteratozoospermia.

Novel Variants in MDC1 are Associated With Severe Oligoasthenoteratozoospermia.

Journal: Clinical genetics

Published: June 06, 2025

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 CYLC1 variants are associated with male infertility due to sperm head deformity.

Novel CYLC1 variants are associated with male infertility due to sperm head deformity.

Journal: Journal of assisted reproduction and genetics

Published: March 22, 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

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

TMEM232 is required for the formation of sperm flagellum and male fertility in mice.

TMEM232 is required for the formation of sperm flagellum and male fertility in mice.

Journal: Cell death & disease

Published: January 29, 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

Genotype-phenotype correlation study of structural abnormalities in a fetal brain caused by a novel KDM4B variant.

Genotype-phenotype correlation study of structural abnormalities in a fetal brain caused by a novel KDM4B variant.

Journal: Molecular biology reports

Published: November 03, 2023

Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression.

Loss of PMFBP1 Disturbs Mouse Spermatogenesis by Downregulating HDAC3 Expression.

Journal: Journal of assisted reproduction and genetics

Published: February 27, 2023

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Last Updated: 09/26/2026