Qinghua Shi

443 Huangshan Road
Hefei, 230027, China

Last Updated: 09/26/2026

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Found 78 publications

Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture.

Loss-of-Function Variants in CCDC189 Cause Human Oligoasthenoteratozoospermia by Disrupting Sperm Flagellar and Acrosomal Architecture.

Journal: Andrology
Published: February 10, 2026

Natural ovulation versus programmed regimens before frozen embryo transfer in ovulatory women: multicentre, randomised clinical trial.

Natural ovulation versus programmed regimens before frozen embryo transfer in ovulatory women: multicentre, randomised clinical trial.

Journal: BMJ (Clinical research ed.)
Published: January 21, 2026

Novel variants in YTHDC2 cause non-obstructive azoospermia by disrupting the mitotic-to-meiotic transition in humans and mice.

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

Bi-allelic mutations of CAMSAP1 result in teratozoospermia with sperm head and flagella defects in humans.

Bi-allelic mutations of CAMSAP1 result in teratozoospermia with sperm head and flagella defects in humans.

Journal: Human reproduction (Oxford, England)
Published: November 25, 2025

A novel flow cytometry approach resolves testicular cell heterogeneity and enables diagnostic profiling in male infertility.

A novel flow cytometry approach resolves testicular cell heterogeneity and enables diagnostic profiling in male infertility.

Journal: Life sciences
Published: August 20, 2025

C2orf74 orchestrates germ-Leydig crosstalk to inhibit white adipose tissue browning in male mice.

C2orf74 orchestrates germ-Leydig crosstalk to inhibit white adipose tissue browning in male mice.

Journal: Nature communications
Published: July 08, 2025

Retraction of Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice.

Retraction of Deficient LRRC8A-dependent volume-regulated anion channel activity is associated with male infertility in mice.

Journal: JCI insight
Published: June 23, 2025

Novel PNLDC1 mutations underlie nonobstructive azoospermia in humans and mice.

Novel PNLDC1 mutations underlie nonobstructive azoospermia in humans and mice.

Journal: Human molecular genetics
Published: April 22, 2025

Fertility test of mice (Mus musculus).

Fertility test of mice (Mus musculus).

Journal: Bio-protocol
Published: April 06, 2025

Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice.

Deficiency in DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice.

Journal: eLife
Published: March 27, 2025

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

A novel mutation in CFAP58 leads to MMAF in humans and mice by disrupting CP assembly.

Journal: Human molecular genetics
Published: January 30, 2025

Follicle-Stimulating Hormone and Testosterone Play a Role in the Regulation of Sertoli Cell Functions Following Germ Cell Depletion In Vitro.

Follicle-Stimulating Hormone and Testosterone Play a Role in the Regulation of Sertoli Cell Functions Following Germ Cell Depletion In Vitro.

Journal: International journal of molecular sciences
Published: December 28, 2024
Showing 1-12 of 78

Last Updated: 09/26/2026