Publications et travaux

L'enseignement, les publications, la diffusion des savoirs et des résultats des études menées par notre équipe,font partie de la dynamique soutenue par notre Institut de recherche en santé de la femme.

GENETIQUE ET BIOLOGIE DE LA REPRODUCTION

A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.
Besseau-Ayasse J, et al. Prenat Diagn. 2014 May;34(5):424-30.
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Tumor necrosis factor-308 polymorphism increases the embryo implantation rate in women undergoing in vitro fertilization.
Vialard F et al.. Hum Reprod. 2013 Oct;28(10):2774-83.
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A genome-wide DNA methylation study in azoospermia.
Ferfouri F et al. Andrology. 2013 Nov;1(6):815-21.
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Small human sperm vacuoles observed under high magnification are pocket-like nuclear concavities linked to chromatin condensation failure.
Boitrelle F, et al. Reprod Biomed Online. 2013 Aug;27(2):201-11.
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High-magnification sperm selection does not decrease the aneuploidy rate in patients who are heterozygous for reciprocal translocations.
Chelli MH, et al. J Assist Reprod Genet. 2013 Apr;30(4):525-30.
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Application of a new molecular technique for the genetic evaluation of products of conception.
Grati FR, et al. Prenat Diagn. 2013 Jan;33(1):32-41.
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The high frequency of sperm aneuploidy in klinefelter patients and in nonobstructive azoospermia is due to meiotic errors in euploid spermatocytes.
Vialard F et al. J Androl. 2012 Nov-Dec;33(6):1352-9.
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The chromosomal risk in sperm from heterozygous Robertsonian translocation carriers is related to the sperm count and the translocation type.
Ferfouri F, et al. Fertil Steril. 2011 Dec;96(6):1337-43
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Prenatal BACs-on-Beads™ : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.
Vialard F, et al. Prenat Diagn. 2011 May;31(5):500-8.
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Could Digital PCR Be an Alternative as a Non-Invasive
Prenatal Test for Trisomy 21: A Proof of Concept Study.
El Khattabi LA, Rouillac-Le Sciellour C, Le Tessier D, Luscan A, Coustier A, Porcher R, Bhouri R, Nectoux J, Sérazin V, Quibel T, Mandelbrot L, Tsatsaris V, Vialard F, Dupont JM.
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Adiponectin Inhibits Nutrient Transporters and Promotes Apoptosis in Human Villous Cytotrophoblasts: Involvement in the Control of Fetal Growth.
Duval F, Santos ED, Poidatz D, Sérazin V, Gronier H, Vialard F, Dieudonné MN.
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Pregnancy outcomes in prenatally diagnosed 47, XXX and 47, XYY syndromes: a 30-year French, retrospective, multicentre study.
Gruchy N, Blondeel E, Le Meur N, Joly-Hélas G, Chambon P, Till M, Herbaux M, Vigouroux-Castera A, Coussement A, Lespinasse J, Amblard F, Jimenez Pocquet M, Lebel-Roy C, Carré-Pigeon F, Flori E, Mugneret F,Jaillard S, Yardin C, Harbuz R, Collonge-Rame MA, Vago P, Valduga M, Leporrier N, Vialard F.
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PreImplantation Factor (PIF*) endogenously prevents preeclampsia: Promotes trophoblast invasion and reduces oxidative stress.
Barnea ER, Vialard F, Moindjie H, Ornaghi S, Dieudonne MN, Paidas MJ.
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Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Grati FR, Molina Gomes D, Ferreira JC, Dupont C, Alesi V, Gouas L, Horelli-Kuitunen N, Choy KW, García-Herrero S, de la Vega AG, Piotrowski K, enesio R, Queipo G, Malvestiti B, Hervé B, Benzacken B, Novelli A, Vago P, iippo K, Leung TY, Maggi F, Quibel T, Tabet AC, Simoni G, Vialard F.
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A human morphologically normal spermatozoon may have noncondensed chromatin.
Boitrelle F, Pagnier M, Athiel Y, Swierkowski-Blanchard N, Torre A, Alter L,Muratorio C, Vialard F, Albert M, Selva J.
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Prenatal diagnosis of 24 cases of microduplication 22q11.2: an investigation of phenotype-genotype correlations.
Dupont C, Grati FR, Choy KW, Jaillard S, Toutain J, Maurin ML,
Martínez-Conejero JA, Beneteau C, Coussement A, Molina-Gomes D, Horelli-Kuitunen N, Aboura A, Tabet AC, Besseau-Ayasse J, Bessieres-Grattagliano B, Simoni G,Ayala G, Benzacken B, Vialard F.
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A French collaborative survey of 272 fetuses with 22q11.2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes.
Besseau-Ayasse J, Violle-Poirsier C, Bazin A, Gruchy N, Moncla A, Girard F,Till M, , Receveur A, Douet Guilbert N, Lallaoui H, Bouquillon S, GatinoisV, Joly-Helas G, Prieur F, Cartault F, Martin D, Kleinfinger P, Molina Gomes D,Doco-Fenzy M, Vialard F.
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RHOXF2 gene, a new candidate gene for spermatogenesis failure.
Frainais C, Kannengiesser C, Albert M, Molina-Gomes D, Boitrelle F, Bailly M,Grandchamp B, Selva J, Vialard F.
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High-magnification selection of spermatozoa prior to oocyte injection: confirmed and potential indications.
Boitrelle F, Guthauser B, Alter L, Bailly M, Bergere M, Wainer R, Vialard F, Albert M, Selva J.
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A genome-wide DNA methylation study in azoospermia.
Ferfouri F, Boitrelle F, Ghout I, Albert M, Molina Gomes D, Wainer R, Bailly M, Selva J, Vialard F.
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