Vialard F - Search Results

1

A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.

Ben Khelifa M, Ghieh F, Boudjenah R, Hue C, Fauvert D, Dard R, Garchon HJ, Vialard F. Ben Khelifa M, et al. Among authors: vialard f. Hum Reprod. 2018 Jun 1;33(6):1034-1037. doi: 10.1093/humrep/dey073. Hum Reprod. 2018. PMID: 29659827

2

MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.

Coutton C, Zouari R, Abada F, Ben Khelifa M, Merdassi G, Triki C, Escalier D, Hesters L, Mitchell V, Levy R, Sermondade N, Boitrelle F, Vialard F, Satre V, Hennebicq S, Jouk PS, Arnoult C, Lunardi J, Ray PF. Coutton C, et al. Among authors: vialard f. Hum Reprod. 2012 Aug;27(8):2549-58. doi: 10.1093/humrep/des160. Epub 2012 May 24. Hum Reprod. 2012. PMID: 22627659

3

Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia.

Ben Khelifa M, Coutton C, Blum MG, Abada F, Harbuz R, Zouari R, Guichet A, May-Panloup P, Mitchell V, Rollet J, Triki C, Merdassi G, Vialard F, Koscinski I, Viville S, Keskes L, Soulie JP, Rives N, Dorphin B, Lestrade F, Hesters L, Poirot C, Benzacken B, Jouk PS, Satre V, Hennebicq S, Arnoult C, Lunardi J, Ray PF. Ben Khelifa M, et al. Among authors: vialard f. Hum Reprod. 2012 Nov;27(11):3337-46. doi: 10.1093/humrep/des296. Epub 2012 Aug 11. Hum Reprod. 2012. PMID: 22888167

4

Can one translocation impact the meiotic segregation of another translocation? A sperm-FISH analysis of a 46,XY,t(1;16)(q21;p11.2),t(8;9) (q24.3;p24) patient and his 46,XY,t(8;9)(q24.3;p24) brother and cousin.

Ferfouri F, Boitrelle F, Clément P, Molina Gomes D, Selva J, Vialard F. Ferfouri F, et al. Among authors: vialard f. Mol Hum Reprod. 2013 Feb;19(2):109-17. doi: 10.1093/molehr/gas048. Epub 2012 Oct 25. Mol Hum Reprod. 2013. PMID: 23100463

5

The vascular endothelial growth factor (VEGF) +405 G/C polymorphism and its relationship with recurrent implantation failure in women in an IVF programme with ICSI.

Boudjenah R, Molina-Gomes D, Wainer R, de Mazancourt P, Selva J, Vialard F. Boudjenah R, et al. Among authors: vialard f. J Assist Reprod Genet. 2012 Dec;29(12):1415-20. doi: 10.1007/s10815-012-9878-8. Epub 2012 Oct 27. J Assist Reprod Genet. 2012. PMID: 23104639 Free PMC article.

6

Tumor necrosis factor-308 polymorphism increases the embryo implantation rate in women undergoing in vitro fertilization.

Vialard F, El Sirkasi M, Tronchon V, Boudjenah R, Molina-Gomes D, Bergere M, Mauduit C, Wainer R, Selva J, Benahmed M. Vialard F, et al. Hum Reprod. 2013 Oct;28(10):2774-83. doi: 10.1093/humrep/det264. Epub 2013 Aug 1. Hum Reprod. 2013. PMID: 23906902

7

Associations between Individual and Combined Polymorphisms of the TNF and VEGF Genes and the Embryo Implantation Rate in Patients Undergoing In Vitro Fertilization (IVF) Programs.

Boudjenah R, Molina-Gomes D, Torre A, Boitrelle F, Taieb S, Dos Santos E, Wainer R, de Mazancourt P, Selva J, Vialard F. Boudjenah R, et al. Among authors: vialard f. PLoS One. 2014 Sep 23;9(9):e108287. doi: 10.1371/journal.pone.0108287. eCollection 2014. PLoS One. 2014. PMID: 25247819 Free PMC article.

8

Birth of a boy with isolated short stature after prenatal diagnosis of a Xp22.3 nullosomy due to an inherited t(X;15) (p22.3;p10) translocation.

Blondeel E, Molina-Gomes D, Bouhanna P, Fauvert D, Crosnier H, Dessuant H, Vialard F. Blondeel E, et al. Among authors: vialard f. Clin Case Rep. 2014 Jun;2(3):98-102. doi: 10.1002/ccr3.71. Epub 2014 May 5. Clin Case Rep. 2014. PMID: 25356259 Free PMC article.

9

Low-level mosaicism of a de novo derivative chromosome 9 from a t(5;9)(q35.1;q34.3) has a major phenotypic impact.

Hervé B, Roume J, Cognard S, Fauvert D, Molina-Gomes D, Vialard F. Hervé B, et al. Among authors: vialard f. Eur J Med Genet. 2015 Jun-Jul;58(6-7):346-50. doi: 10.1016/j.ejmg.2015.04.005. Epub 2015 May 8. Eur J Med Genet. 2015. PMID: 25963108

10

The emerging microduplication 3q13.31: Expanding the genotype-phenotype correlations of the reciprocal microdeletion 3q13.31 syndrome.

Hervé B, Fauvert D, Dard R, Roume J, Cognard S, Goidin D, Lozach F, Molina-Gomes D, Vialard F. Hervé B, et al. Among authors: vialard f. Eur J Med Genet. 2016 Sep;59(9):463-9. doi: 10.1016/j.ejmg.2016.08.010. Epub 2016 Aug 26. Eur J Med Genet. 2016. PMID: 27568866

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