Guang-xiu P. Lu

Changsha, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 68 publications

SPEM2 deficiency disrupts spermiation leading to oligoasthenoteratozoospermia and male infertility†.

SPEM2 deficiency disrupts spermiation leading to oligoasthenoteratozoospermia and male infertility†.

Journal: Biology of reproduction

Published: January 23, 2026

Identification of novel JAK3 variants in a suspected SCID patient and two couples undergoing carrier screening.

Identification of novel JAK3 variants in a suspected SCID patient and two couples undergoing carrier screening.

Journal: Frontiers in genetics

Published: May 07, 2025

Genetic analysis and reproductive interventions in families affected by congenital cataracts: a study of 107 cases.

Genetic analysis and reproductive interventions in families affected by congenital cataracts: a study of 107 cases.

Journal: Journal of applied genetics

Published: March 28, 2025

Biallelic variants in TBC1D8 are potentially associated with male infertility due to non-obstructive azoospermia or cryptozoospermia.

Biallelic variants in TBC1D8 are potentially associated with male infertility due to non-obstructive azoospermia or cryptozoospermia.

Journal: Asian journal of andrology

Published: February 20, 2025

Genetic Study and Prenatal Diagnosis of Inherited Glycosylphosphatidylinositol Disorders due to Novel Variants in Phosphatidylinositol Glycan Genes.

Genetic Study and Prenatal Diagnosis of Inherited Glycosylphosphatidylinositol Disorders due to Novel Variants in Phosphatidylinositol Glycan Genes.

Journal: Clinical genetics

Published: December 12, 2024

Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturation.

Women with FSHR-inactivating mutations causing resistant ovarian syndrome benefit from oocyte in-vitro maturation.

Journal: Reproductive biomedicine online

Published: July 04, 2024

Two missense STK11 gene variations impaired LKB1/adenosine monophosphate-activated protein kinase signaling in Peutz-Jeghers syndrome.

Two missense STK11 gene variations impaired LKB1/adenosine monophosphate-activated protein kinase signaling in Peutz-Jeghers syndrome.

Journal: World journal of gastrointestinal oncology

Published: December 05, 2023

A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.

A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.

Journal: Clinical genetics

Published: November 30, 2023

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination.

A case report of a normal fertile woman with 46,XX/46,XY somatic chimerism reveals a critical role for germ cells in sex determination.

Journal: Human reproduction (Oxford, England)

Published: October 23, 2023

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192.

Mosaic variegated aneuploidy syndrome with tetraploid, and predisposition to male infertility triggered by mutant CEP192.

Journal: HGG advances

Published: August 03, 2023

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Bi-allelic variants in DNAH3 cause male infertility with asthenoteratozoospermia in humans and mice.

Journal: Human reproduction open

Published: July 19, 2023

A DMD case caused by X chromosome rearrangement.

A DMD case caused by X chromosome rearrangement.

Journal: Yi chuan = Hereditas

Published: March 17, 2023

Showing 1-12 of 68

Last Updated: 09/26/2026