Guanxiong Wang
No 81 Meishan Road
Hefei, 230032, China
Hefei, 230032, China
Last Updated: 09/26/2026
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Found 23 publications
Tetrachloro-1,4-benzoquinone disrupts oocyte quality through mitochondrial dysfunction and oxidative stress.
Journal: Ecotoxicology and environmental safety
Published: May 08, 2026
CFAP251 Deficiency Induces Male Infertility and PCD-like Ciliary Defects by Disrupting TUBB4B and SLC25A4 Recruitment in Humans and Mice.
Journal: International journal of biological sciences
Published: November 22, 2025
Mapping the Non-Canonical Splicing Variants: Decrypting the Hidden Genetic Architecture of Idiopathic Male Infertility.
Journal: Advanced science (Weinheim, Baden-Wurttemberg, Germany)
Published: August 12, 2025
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 homozygous variants in piRNA pathway factors lead to male infertility in humans.
Journal: Reproductive biomedicine online
Published: June 17, 2024
Aberrant acetylation caused by a CDYL splicing mutation contributes to thin mid-piece related asthenoteratozoospermia and male infertility.
Journal: Andrology
Published: May 30, 2024
Adenylate kinase phosphate energy shuttle underlies energetic communication in flagellar axonemes.
Journal: Science China. Life sciences
Published: November 21, 2023
Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans.
Journal: Journal of medical genetics
Published: November 16, 2023
Genetic analysis of a patient with familial hypercholesterolemia due to variant of LDLR gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: March 27, 2023
A homozygous frameshift mutation in ADAD2 causes male infertility with spermatogenic impairments.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: August 26, 2022
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
Last Updated: 09/26/2026