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European Journal of Human Genetics (2)
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Showing 1–8 of 8 results

Advanced filters: Author: Sandrine Barbaux Clear advanced filters

Donor splice-site mutations in WT1 are responsible for Frasier syndrome

Sandrine Barbaux
Patrick Niaudet
Ken McElreavey
Research01 Dec 1997
Nature Genetics

Volume: 17, P: 467-470
Spermatozoa lacking TEX51 display hypofertility and defects in morphology

TEX51 is a proposed IST superfamily member associated with mammalian fertilization. Tex51 knockout mice show hypofertility and sperm defects, suggesting a broader role for IST proteins in sperm development and reproductive function.

Sophie Dupuis
Morgane Le Beulze
Sandrine Barbaux
ResearchOpen Access13 Nov 2025
Communications Biology

Volume: 8, P: 1-11
The genetic basis of murine and human sex determination: a review

Ken McElreavey
Sandrine Barbaux
Marc Fellous
Research01 Dec 1995
Heredity

Volume: 75, P: 599-611
Differential haplotypic expression of the interleukin-18 gene

Sandrine Barbaux
Odette Poirier
Laurence Tiret
Research09 May 2007
European Journal of Human Genetics

Volume: 15, P: 856-863
A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21

Laïla Allach El Khattabi
Stéphanie Backer
Sandrine Barbaux
Research11 Sept 2018
European Journal of Human Genetics

Volume: 27, P: 49-60
Transcriptomic analysis of human placenta in intrauterine growth restriction

Doriane Madeleneau
Christophe Buffat
Géraldine Gascoin
Research03 Mar 2015
Pediatric Research

Volume: 77, P: 799-807
Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion

Sandrine Barbaux
Côme Ialy-Radio
Ahmed Ziyyat
ResearchOpen Access24 Mar 2020
Scientific Reports

Volume: 10, P: 1-15
Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

Aurélien Ducat
Ludivine Doridot
Daniel Vaiman
ResearchOpen Access13 Jan 2016
Scientific Reports

Volume: 6, P: 1-9