Skip to content

Author

G. Martinez

We have 2 of 77 papers

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Sep 2026

A CCNA1 Missense Variant Associated With Chromatid Non-Disjunction in Abnormal-Headed Sperm and Male Infertility.

This study establishes the first clinical association between CCNA1 mutations and chromatid non-disjunction in human spermatogenesis, highlighting the limitations of current morphology-based diagnostic thresholds and supports cytogenetic and genomic assessment for severe teratozoospermia (especially head abnormalities)...

A. Perrin, Frédéric Morel, Zeinab Wehbe et al. · 0 citations
Open access Jul 2026

Biallelic Truncating Variant in LRGUK Is Associated With Severe Multiple Morphological Abnormalities of the Sperm Flagella and Sperm Nuclear Defects in Humans.

Findings identify LRGUK as a novel gene involved in male infertility, essential for spermatid morphogenesis and flagellum assembly, essential for spermatid morphogenesis and flagellum assembly.

Wiâme Mokkedem, Zeinab Wehbe, A. Barbotin et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.