Pierre F. Ray

Grenoble, France

Last Updated: 09/26/2026

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Found 114 publications

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

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

Journal: Clinical genetics

Published: May 15, 2026

Sperm motility in mice with oligo-astheno-teratozoospermia restored by in vivo injection and electroporation of naked mRNA.

Sperm motility in mice with oligo-astheno-teratozoospermia restored by in vivo injection and electroporation of naked mRNA.

Journal: eLife

Published: March 03, 2026

ARMC2 loss impairs cilia structure and leads to primary ciliary dyskinesia symptoms in mouse organs.

ARMC2 loss impairs cilia structure and leads to primary ciliary dyskinesia symptoms in mouse organs.

Journal: Frontiers in cell and developmental biology

Published: August 29, 2025

CNN-based approach for 3D artifact correction of intensity diffraction tomography images.

CNN-based approach for 3D artifact correction of intensity diffraction tomography images.

Journal: Optics express

Published: June 14, 2025

Administration of ethiodized poppy seed oil-based contrast agent into the uterus enhances fertilization rate in mice inseminated with low sperm numbers.

Administration of ethiodized poppy seed oil-based contrast agent into the uterus enhances fertilization rate in mice inseminated with low sperm numbers.

Journal: Human reproduction (Oxford, England)

Published: December 20, 2024

A recurrent loss-of-function variant in DRC1 causes non-syndromic severe asthenozoospermia with favorable intracytoplasmic sperm injection and pregnancy outcomes.

A recurrent loss-of-function variant in DRC1 causes non-syndromic severe asthenozoospermia with favorable intracytoplasmic sperm injection and pregnancy outcomes.

Journal: Andrology

Published: October 21, 2024

A comprehensive study of the sperm head defects in MMAF condition and their impact on embryo development in mice.

A comprehensive study of the sperm head defects in MMAF condition and their impact on embryo development in mice.

Journal: Molecular human reproduction

Published: September 16, 2024

Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1.

Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1.

Journal: Journal of assisted reproduction and genetics

Published: September 12, 2024

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Homozygous deleterious variants in MYCBPAP induce asthenoteratozoospermia involving abnormal acrosome biogenesis, manchette structure and sperm tail assembly in humans and mice.

Journal: Science China. Life sciences

Published: August 15, 2024

Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non-obstructive azoospermia in an Iranian family.

Whole genome sequencing identifies a homozygous splicing variant in TDRKH segregating with non-obstructive azoospermia in an Iranian family.

Journal: Clinical genetics

Published: May 21, 2024

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse.

Lack of CCDC146, a ubiquitous centriole and microtubule-associated protein, leads to non-syndromic male infertility in human and mouse.

Journal: eLife

Published: March 05, 2024

Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.

Phenotypic continuum and poor intracytoplasmic sperm injection intracytoplasmic sperm injection prognosis in patients harboring HENMT1 variants.

Journal: Andrology

Published: February 21, 2024

Showing 1-12 of 114

Last Updated: 09/26/2026