Marjorie Whitfield

Grenoble, 38000, France

Last Updated: 09/26/2026

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Found 22 publications

The annulus: composition, role and importance in sperm flagellum biogenesis and male fertility.

The annulus: composition, role and importance in sperm flagellum biogenesis and male fertility.

Journal: Basic and clinical andrology
Published: September 01, 2024

Human asthenozoospermia: Update on genetic causes, patient management, and clinical strategies.

Human asthenozoospermia: Update on genetic causes, patient management, and clinical strategies.

Journal: Andrology
Published: August 19, 2024

CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.

CCDC65, encoding a component of the axonemal Nexin-Dynein regulatory complex, is required for sperm flagellum structure in humans.

Journal: Clinical genetics
Published: September 11, 2023

Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy.

Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy.

Journal: Reproductive biomedicine online
Published: April 13, 2023

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.

Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans.

Journal: iScience
Published: April 04, 2023

Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives.

Sperm Ion Transporters and Channels in Human Asthenozoospermia: Genetic Etiology, Lessons from Animal Models, and Clinical Perspectives.

Journal: International journal of molecular sciences
Published: February 28, 2022

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse.

Journal: Human genetics
Published: April 16, 2021

Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Correction to: A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Journal: Human genetics
Published: March 26, 2021

Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.

Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa.

Journal: International journal of molecular sciences
Published: January 29, 2021

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet-Biedl syndrome.

Journal: Human genetics
Published: January 09, 2021

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.

The sodium/proton exchanger SLC9C1 (sNHE) is essential for human sperm motility and fertility.

Journal: Clinical genetics
Published: October 29, 2020

Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility.

Tubulin glycylation controls axonemal dynein activity, flagellar beat, and male fertility.

Journal: Science (New York, N.Y.)
Published: June 26, 2020
Showing 1-12 of 22

Last Updated: 09/26/2026