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List of works by Sandrine Barbaux

46,XX karyotype males, based on a specific case

scientific article published in May 1996

A genome-wide approach reveals novel imprinted genes expressed in the human placenta

scientific article published on 16 August 2012

A genome-wide search for new imprinted genes in the human placenta identifies DSCAM as the first imprinted gene on chromosome 21

scientific article published in January 2019

A high frequency of Y chromosome deletions in males with nonidiopathic infertility

scientific article published on 01 October 1999

Accurate and rapid "multiplex heteroduplexing" method for genotyping key enzymes involved in folate/homocysteine metabolism

scientific article published on 01 July 2000

Adhesion molecules and atherosclerosis

scientific article published on October 2003

Association Between P-Selectin Gene Polymorphisms and Soluble P-Selectin Levels and Their Relation to Coronary Artery Disease

article

Combination of promoter hypomethylation and PDX1 overexpression leads to TBX15 decrease in vascular IUGR placentas.

scientific article published on February 2011

Could male infertility become hereditary?

scientific article published in March 1997

Cullins in human intra-uterine growth restriction: expressional and epigenetic alterations

scientific article published on 14 December 2009

Differential haplotypic expression of the interleukin-18 gene.

scientific article published on 9 May 2007

EG-VEGF controls placental growth and survival in normal and pathological pregnancies: case of fetal growth restriction (FGR)

scientific article published on 2 September 2012

Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia

scientific article

Gene polymorphisms of the renin-angiotensin system and early development of hypertension.

scientific article published in August 2006

Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular disease

scientific article published on 25 July 2005

Genetic and epigenetic mechanisms collaborate to control SERPINA3 expression and its association with placental diseases

scientific article published on 13 January 2012

Haplotypes of the caspase-1 gene, plasma caspase-1 levels, and cardiovascular risk

scientific article published on 15 June 2006

Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases

article

High frequency of well-defined Y-chromosome deletions in idiopathic Sertoli cell-only syndrome

scientific article published in February 1998

IFPA meeting 2014 workshop report: Animal models to study pregnancy pathologies; new approaches to study human placental exposure to xenobiotics; biomarkers of pregnancy pathologies; placental genetics and epigenetics; the placenta and stillbirth an

scientific article

Identification of a novel member of the pentrax in family inXenopus laevis

scientific article published on 22 September 1993

In vitro fertilization and embryo culture strongly impact the placental transcriptome in the mouse model

scientific article

Loss of sequences 3' to the testis-determining gene, SRY, including the Y pseudoautosomal boundary associated with partial testicular determination.

scientific article published on August 1996

Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida

scientific article published in November 2002

Mutations and sequence variants in the testis-determining region of the Y chromosome in individuals with a 46,XY female phenotype.

scientific article published on May 1997

Nitroso-redox balance and mitochondrial homeostasis are regulated by STOX1, a pre-eclampsia-associated gene

scientific article

Placental BDNF/TrkB signaling system is modulated by fetal growth disturbances in rat and human.

scientific article published on 7 July 2010

Placental expression of the obesity-associated gene FTO is reduced by fetal growth restriction but not by macrosomia in rats and humans

scientific article published in April 2013

Polymorphisms in 33 inflammatory genes and risk of myocardial infarction--a system genetics approach

scientific article published on 19 July 2007

Polymorphisms of genes controlling homocysteine/folate metabolism and cognitive function

article

Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study

scientific article

Preeclampsia-like symptoms induced in mice by fetoplacental expression of STOX1 are reversed by aspirin treatment

scientific article

Proximal deletions of the long arm of the Y chromosome suggest a critical region associated with a specific subset of characteristic Turner stigmata

scientific article published in 1995

Re-evaluation of the role of STOX1 transcription factor in placental development and preeclampsia

scientific article published on 03 July 2009

Research resource: genome-wide profiling of methylated promoters in endometriosis reveals a subtelomeric location of hypermethylation

scientific article published on 4 August 2010

SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease.

scientific article published in November 2003

STOX1 overexpression in choriocarcinoma cells mimics transcriptional alterations observed in preeclamptic placentas

scientific article

Sex chromosome mosaicism in males carrying Y chromosome long arm deletions

scientific article published on 01 December 2000

Specific haplotypes of the P-selectin gene are associated with myocardial infarction.

scientific article published in August 2002

Sperm SPACA6 protein is required for mammalian Sperm-Egg Adhesion/Fusion

scientific article published on 24 March 2020

Testicular development in an SRY-negative 46,XX individual harboring a distal Xp deletion

scientific article published in October 1995

The Gpr1/Zdbf2 locus provides new paradigms for transient and dynamic genomic imprinting in mammals

scientific article published on March 2014

The Xenopus laevis homologue of the 64-kDa subunit of cleavage stimulation factor.

scientific article published in July 1996

The activity of the highly inducible mouse phenylalanine hydroxylase gene promoter is dependent upon a tissue-specific, hormone-inducible enhancer

scientific article published on June 1996

The adhesion mediated by the P-selectin P-selectin glycoprotein ligand-1 (PSGL-1) couple is stronger for shorter PSGL-1 variants

scientific article published on 5 January 2010

The genetic basis of murine and human sex determination: a review.

scientific article

The human SRY protein is present in fetal and adult Sertoli cells and germ cells

scientific article published on 01 March 1999

The human T locus and spina bifida risk

scientific article published on 24 September 2004

The intensity of IUGR-induced transcriptome deregulations is inversely correlated with the onset of organ function in a rat model

scientific article (publication date: 2011)

The methionine synthase reductase (MTRR) A66G polymorphism is a novel genetic determinant of plasma homocysteine concentrations

scientific journal article

The single nucleotide polymorphism story

scientific article published in August 2003

Transcriptomic analysis of human placenta in intrauterine growth restriction

scientific article published on 03 March 2015

Trophoblasts, invasion, and microRNA.

scientific article published on 21 November 2013

True hermaphroditism: clinical aspects and molecular studies in 16 cases

scientific article published on February 1997

Ullrich-Turner Syndrome: Relevance of Searching for Y Chromosome Fragments

scientific article published in January 1999

Use of degenerate oligonucleotide primed PCR (DOP-PCR) for the genotyping of low-concentration DNA samples

scientific article published on 7 April 2001

ZP2 heterozygous mutation in an infertile woman.

scientific article

[Genetics and nephrotic syndrome]

scientific article published on 01 January 1998

miR-34a expression, epigenetic regulation, and function in human placental diseases

scientific article published on 30 September 2013

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