Xiaopei Zhou

Key Laboratory Of Molecular Biophysics Of The Ministry Of Education
Wuhan, China

Last Updated: 09/26/2026

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Found 16 publications

GBF1 deficiency causes cataracts in human and mouse.

GBF1 deficiency causes cataracts in human and mouse.

Journal: Human genetics

Published: April 26, 2024

Loss of function variant in CIP2A associated with female infertility with early embryonic arrest and fragmentation.

Loss of function variant in CIP2A associated with female infertility with early embryonic arrest and fragmentation.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: October 11, 2023

A novel homozygous mutation in ACTL7A leads to male infertility.

A novel homozygous mutation in ACTL7A leads to male infertility.

Journal: Molecular genetics and genomics : MGG

Published: September 13, 2022

Actl7a deficiency in mice leads to male infertility and fertilization failure.

Actl7a deficiency in mice leads to male infertility and fertilization failure.

Journal: Biochemical and biophysical research communications

Published: June 26, 2022

Two novel STAT1 mutations cause Mendelian susceptibility to mycobacterial disease.

Two novel STAT1 mutations cause Mendelian susceptibility to mycobacterial disease.

Journal: Biochemical and biophysical research communications

Published: September 30, 2021

Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.

Novel Heterozygous Mutations in ZP2 Cause Abnormal Zona Pellucida and Female Infertility.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: August 20, 2021

Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility.

Novel Compound Heterozygous Mutation in FSIP2 Causes Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) and Male Infertility.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: August 16, 2021

TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure.

TUBB8 Mutations Cause Female Infertility with Large Polar Body Oocyte and Fertilization Failure.

Journal: Reproductive sciences (Thousand Oaks, Calif.)

Published: December 22, 2020

A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.

A novel microdeletion upstream of HOXD13 in a Chinese family with synpolydactyly.

Journal: American journal of medical genetics. Part A

Published: December 09, 2020

A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.

A novel mutation in ZP3 causes empty follicle syndrome and abnormal zona pellucida formation.

Journal: Journal of assisted reproduction and genetics

Published: March 19, 2020

Tsga10 is essential for arrangement of mitochondrial sheath and male fertility in mice.

Tsga10 is essential for arrangement of mitochondrial sheath and male fertility in mice.

Journal: Andrology

Published: February 01, 2020

Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.

Deficiency of SCAMP5 leads to pediatric epilepsy and dysregulation of neurotransmitter release in the brain.

Journal: Human genetics

Published: November 20, 2019

Showing 1-12 of 16

Last Updated: 09/26/2026