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Aneuploidy: the impact of chromosome imbalance on nuclear organization and overall genome expression.
Published in:
Clinical Genetics, 2016, v. 90, n. 1, p. 35, doi. 10.1111/cge.12731
By:
- Hervé, B.;
- Coussement, A.;
- Gilbert, T.;
- Dumont, F.;
- Jacques, S.;
- Cuisset, L.;
- Chicard, M.;
- Hizem, S.;
- Bourdoncle, P.;
- Letourneur, F.;
- Dupont, C.;
- Vialard, F.;
- Choiset, A.;
- Dupont, J.‐M.
Publication type:
Article
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.
Published in:
Clinical Genetics, 2014, v. 85, n. 3, p. 233, doi. 10.1111/cge.12138
By:
- Marle, N.;
- Martinet, D.;
- Aboura, A.;
- Joly‐Helas, G.;
- Andrieux, J.;
- Flori, E.;
- Puechberty, J.;
- Vialard, F.;
- Sanlaville, D.;
- Fert Ferrer, S.;
- Bourrouillou, G.;
- Tabet, A.C.;
- Quilichini, B.;
- Simon‐Bouy, B.;
- Bazin, A.;
- Becker, M.;
- Stora, H.;
- Amblard, S.;
- Doco‐Fenzy, M.;
- Molina Gomes, D.
Publication type:
Article
A genome-wide DNA methylation study in azoospermia.
Published in:
Andrology, 2013, v. 1, n. 6, p. 815, doi. 10.1111/j.2047-2927.2013.00117.x
By:
- Ferfouri, F.;
- Boitrelle, F.;
- Ghout, I.;
- Albert, M.;
- Molina Gomes, D.;
- Wainer, R.;
- Bailly, M.;
- Selva, J.;
- Vialard, F.
Publication type:
Article
DNA fragmentation is higher in spermatozoa with chromosomally unbalanced content in men with a structural chromosomal rearrangement.
Published in:
Andrology, 2013, v. 1, n. 4, p. 632, doi. 10.1111/j.2047-2927.2013.00100.x
By:
- Perrin, A.;
- Nguyen, M. H.;
- Bujan, L.;
- Vialard, F.;
- Amice, V.;
- Guéganic, N.;
- Douet‐Guilbert, N.;
- Braekeleer, M.;
- Morel, F.
Publication type:
Article
EP18.17: Whole exome sequencing in prenatal diagnosis: anomaly of low diagnostic yield and incidental findings management.
Published in:
Ultrasound in Obstetrics & Gynecology, 2024, v. 64, p. 286, doi. 10.1002/uog.28753
By:
- Abdallah, W.;
- Koraichi, F.;
- Cohen, C.;
- Vialard, F.;
- Quibel, T.;
- Dard, R.
Publication type:
Article
Non‐invasive cell‐free DNA prenatal screening for trisomy 21 as part of primary screening strategy in twin pregnancy.
Published in:
Ultrasound in Obstetrics & Gynecology, 2024, v. 63, n. 6, p. 807, doi. 10.1002/uog.26311
By:
- Claudel, N.;
- Barrois, M.;
- Vivanti, A. J.;
- Rosenblatt, J.;
- Salomon, L. J.;
- Jouannic, J.‐M.;
- Picone, O.;
- Carbillon, L.;
- Vialard, F.;
- Launay, E.;
- Tsatsaris, V.;
- Curis, E.;
- El Khattabi, L.;
- Rosefort, Audrey;
- Dommergues, Marc;
- Valentin, Morgane;
- Bouchghoul, Hanane;
- François Ceccaldi, Pierre;
- Sroussi, Jeremy;
- Brayet, Jocelyn
Publication type:
Article
Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016.
Published in:
2016
By:
- Benchimol, G.;
- Bouhanna, P.;
- Roume, J.;
- Vialard, F.;
- Thibaud, Q.
Publication type:
journal article
A human morphologically normal spermatozoon may have noncondensed chromatin.
Published in:
Andrologia, 2015, v. 47, n. 8, p. 879, doi. 10.1111/and.12341
By:
- Boitrelle, F.;
- Pagnier, M.;
- Athiel, Y.;
- Swierkowski‐Blanchard, N.;
- Torre, A.;
- Alter, L.;
- Muratorio, C.;
- Vialard, F.;
- Albert, M.;
- Selva, J.
Publication type:
Article
Sperm FISH analysis of a 44,X,der(Y),t(Y;15)(q12;q10)pat,rob(13;14)(q10;q10)mat complex chromosome rearrangement.
Published in:
Andrologia, 2014, v. 46, n. 5, p. 576, doi. 10.1111/and.12112
By:
- Ferfouri, F.;
- Boitrelle, F.;
- Clement, P.;
- Molina Gomes, D.;
- Selva, J.;
- Vialard, F.
Publication type:
Article
Selection of normal spermatozoa with a vacuole-free head (x6300) improves selection of spermatozoa with intact DNA in patients with high sperm DNA fragmentation rates.
Published in:
Andrologia, 2013, v. 45, n. 3, p. 163, doi. 10.1111/j.1439-0272.2012.01328.x
By:
- Hammoud, I.;
- Boitrelle, F.;
- Ferfouri, F.;
- Vialard, F.;
- Bergere, M.;
- Wainer, B.;
- Bailly, M.;
- Albert, M.;
- Selva, J.
Publication type:
Article
A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family.
Published in:
2018
By:
- Ben Khelifa, M.;
- Ghieh, F.;
- Boudjenah, R.;
- Hue, C.;
- Fauvert, D.;
- Dard, R.;
- Garchon, H. J.;
- Vialard, F.
Publication type:
journal article
Tumor necrosis factor-308 polymorphism increases the embryo implantation rate in women undergoing in vitro fertilization.
Published in:
2013
By:
- Vialard, F;
- El Sirkasi, M;
- Tronchon, V;
- Boudjenah, R;
- Molina-Gomes, D;
- Bergere, M;
- Mauduit, C;
- Wainer, R;
- Selva, J;
- Benahmed, M
Publication type:
Journal Article
Tumor necrosis factor-308 polymorphism increases the embryo implantation rate in women undergoing in vitro fertilization.
Published in:
Human Reproduction, 2013, v. 28, n. 10, p. 2774, doi. 10.1093/humrep/det264
By:
- Vialard, F.;
- El Sirkasi, M.;
- Tronchon, V.;
- Boudjenah, R.;
- Molina-gomes, D.;
- Bergere, M.;
- Mauduit, C.;
- Wainer, R.;
- Selva, J.;
- Benahmed, M.
Publication type:
Article
Identification of a new recurrent Aurora kinase C mutation in both European and African men with macrozoospermia.
Published in:
2012
By:
- 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
Publication type:
Journal Article
MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia.
Published in:
2012
By:
- 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
Publication type:
Journal Article
Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case report.
Published in:
BMC Cardiovascular Disorders, 2023, v. 23, n. 1, p. 1, doi. 10.1186/s12872-023-03169-z
By:
- Najib, B.;
- Quibel, T.;
- Tessier, A.;
- Mortreux, J.;
- Bouvagnet, P.;
- Cohen, C.;
- Vialard, F.;
- Dard, R.
Publication type:
Article
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.
Published in:
Clinical Case Reports, 2014, v. 2, n. 3, p. 98, doi. 10.1002/ccr3.71
By:
- Blondeel, E.;
- Molina‐Gomes, D.;
- Bouhanna, P.;
- Fauvert, D.;
- Crosnier, H.;
- Dessuant, H.;
- Vialard, F.
Publication type:
Article
OC28.02: BACs on beads: a clue to ultrasound findings.
Published in:
Ultrasound in Obstetrics & Gynecology, 2011, v. 38, p. 50, doi. 10.1002/uog.9243
By:
- Sonnier, L.;
- Popowski, T.;
- Bouhanna, P.;
- Loeuillet, L.;
- Leroy, B.;
- Vialard, F.;
- Molina-Gomes, D.;
- Roume, J.;
- Bault, J.
Publication type:
Article
P02.05: Aneuploidy recurrence: new data.
Published in:
Ultrasound in Obstetrics & Gynecology, 2009, v. 34, n. S1, p. 183, doi. 10.1002/uog.7029
By:
- Bouhanna, P.;
- Quebel, T.;
- Molina Gomes, D.;
- Jacquemard, F.;
- Bault, J.;
- Lacam, C.;
- Selva, J.;
- Rozenberg, P.;
- Vialard, F.
Publication type:
Article
OP22.09: Fetal karyotype in twin to twin transfusion syndrome: A seven-year study.
Published in:
Ultrasound in Obstetrics & Gynecology, 2008, v. 32, n. 3, p. 387, doi. 10.1002/uog.5863
By:
- Salomon, L. J.;
- Vialard, F.;
- Nasr, B.;
- Essaoui, M.;
- Molina-Gomes, D.;
- Bussières, L.;
- Ville, Y.
Publication type:
Article
Fetal gender: antenatal discrepancy between phenotype and genotype.
Published in:
Ultrasound in Obstetrics & Gynecology, 2002, v. 20, n. 3, p. 286, doi. 10.1046/j.1469-0705.2002.00778.x
By:
- Bretelle, F.;
- Salomon, L.;
- Senat, M.-V.;
- Vialard, F.;
- Albert, M.;
- Roume, J.;
- Ville, Y.
Publication type:
Article
Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndrome.
Published in:
Human Reproduction, 2011, v. 26, n. 9, p. 2570, doi. 10.1093/humrep/der193
By:
- Gruchy, N.;
- Vialard, F.;
- Decamp, M.;
- Choiset, A.;
- Rossi, A.;
- Le Meur, N.;
- Moirot, H.;
- Yardin, C.;
- Bonnet-Dupeyron, M.N.;
- Lespinasse, J.;
- Herbaut-Graux, M.;
- Till, M.;
- Layet, V.;
- Leporrier, N.
Publication type:
Article
Large human sperm vacuoles observed in motile spermatozoa under high magnification: nuclear thumbprints linked to failure of chromatin condensation.
Published in:
Human Reproduction, 2011, v. 26, n. 7, p. 1650, doi. 10.1093/humrep/der129
By:
- Boitrelle, F.;
- Ferfouri, F.;
- Petit, J.M.;
- Segretain, D.;
- Tourain, C.;
- Bergere, M.;
- Bailly, M.;
- Vialard, F.;
- Albert, M.;
- Selva, J.
Publication type:
Article
Tumor necrosis factor-alpha -308 polymorphism in infertile men with altered sperm production or motility.
Published in:
Human Reproduction, 2008, v. 23, n. 12, p. 2858, doi. 10.1093/humrep/den277
By:
- V. Tronchon;
- F. Vialard;
- M. El Sirkasi;
- H. Dechaud;
- J. Rollet;
- M. Albert;
- M. Bailly;
- P. Roy;
- C. Mauduit;
- P. Fenichel;
- J. Selva;
- M. Benahmed
Publication type:
Article
Evidence of a high proportion of premature unbalanced separation of sister chromatids in the first polar bodies of women of advanced age.
Published in:
Human Reproduction, 2006, v. 21, n. 5, p. 1172, doi. 10.1093/humrep/dei484
By:
- F. Vialard;
- C. Petit;
- M. Bergere;
- D. Molina Gomes;
- V. Martel-Petit;
- R. Lombroso;
- Y. Ville;
- H. Gerard;
- J. Selva
Publication type:
Article
Inverse correlation between chromatin condensation and sperm head size in a case of enlarged sperm heads.
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2011, v. 23, n. 6, p. 711, doi. 10.1016/j.rbmo.2011.07.011
By:
- Guthauser, B.;
- Albert, M.;
- Ferfouri, F.;
- Ray, P. F.;
- Rabiey, G.;
- Selva, J.;
- Vialard, F.
Publication type:
Article
Meiotic segregation in spermatozoa of a 46,X,t(Y;10)(q11.2;p15.2) fertile translocation carrier.
Published in:
2009
By:
- Vialard, F.;
- Molina-Gomes, D.;
- Roume, J.;
- Podbiol, A.;
- Hirel, C.;
- Bailly, M.;
- Hammoud, I.;
- Dupont, J. M.;
- De Mazancourt, P.;
- Selva, J.
Publication type:
Case Study
Pronuclear morphology differs between women more than 38 and women less than 30 years of age.
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2009, v. 18, n. 3, p. 367, doi. 10.1016/S1472-6483(10)60095-8
By:
- Maille, L.;
- Bergere, M.;
- Lemoine, E.;
- Camier, B.;
- Prevost, J. F.;
- Bourdrel, J. M.;
- Hammoud, I.;
- Selva, J.;
- Vialard, F.
Publication type:
Article
Stability of aneuploidy rate in polar bodies in two cohorts from the same patient.
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 17, n. 2, p. 213, doi. 10.1016/S1472-6483(10)60197-6
By:
- Vialard, F.;
- Gomes, D. Molina;
- Hammoud, I.;
- Bergere, M.;
- Wainer, R.;
- Bailly, M.;
- Lombroso, R.;
- Selva, J.
Publication type:
Article
Can high magnification morphological selection of spermatozoa be effective reducing chromosomal risk for patients carrying translocations?
Published in:
Reproductive BioMedicine Online (Reproductive Healthcare Limited), 2008, v. 16, p. S-27, doi. 10.1016/S1472-6483(10)61362-4
By:
- F., Vialard;
- M. H., Chelli;
- M., Albert;
- L., Hammoud;
- M. I., Bailly;
- M., Bergere;
- Gomes D., Molina;
- J., Selva
Publication type:
Article
Follicular fluid protein content (FSH, LH, PG4, E2 and AMH) and polar body aneuploidy.
Published in:
Journal of Assisted Reproduction & Genetics, 2012, v. 29, n. 10, p. 1123, doi. 10.1007/s10815-012-9841-8
By:
- Hammoud, I.;
- Vialard, F.;
- Bergere, M.;
- Albert, M.;
- Gomes, D.;
- Adler, M.;
- Malagrida, L.;
- Bailly, M.;
- Wainer, R.;
- Selva, J.
Publication type:
Article
Preconceptional diagnosis for Robertsonian translocation as an alternative to preimplantation genetic diagnosis in two situations: a pilot study.
Published in:
Journal of Assisted Reproduction & Genetics, 2009, v. 26, n. 2/3, p. 113, doi. 10.1007/s10815-009-9293-y
By:
- Gomes, D. Molina;
- Hammoud, I.;
- Bailly, M.;
- Bergere, M.;
- Wainer, R.;
- Selva, J.;
- Vialard, F.
Publication type:
Article
Gamete cytogenetic study in couples with implantation failure: aneuploidy rate is increased in both couple members.
Published in:
Journal of Assisted Reproduction & Genetics, 2008, v. 25, n. 11/12, p. 539, doi. 10.1007/s10815-008-9258-6
By:
- Vialard, F.;
- Hammoud, I.;
- Molina-Gomes, D.;
- Wainer, R.;
- Bergere, M.;
- Albert, M.;
- Bailly, M.;
- de Mazancourt, P.;
- Selva, J.
Publication type:
Article
Non-invasive prenatal testing for trisomy 21 based on analysis of cell-free fetal DNA circulating in the maternal plasma.
Published in:
Prenatal Diagnosis, 2015, v. 35, n. 5, p. 471, doi. 10.1002/pd.4561
By:
- Alberti, A.;
- Salomon, L. J.;
- Le Lorc'h, M.;
- Couloux, A.;
- Bussières, L.;
- Goupil, S.;
- Malan, V.;
- Pelletier, E.;
- Hyon, C.;
- Vialard, F.;
- Rozenberg, P.;
- Bouhanna, P.;
- Oury, J. F.;
- Schmitz, T.;
- Romana, S.;
- Weissenbach, J.;
- Vekemans, M.;
- Ville, Y.
Publication type:
Article
Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases.
Published in:
Prenatal Diagnosis, 2014, v. 34, n. 12, p. 1133, doi. 10.1002/pd.4439
By:
- Gruchy, N.;
- Vialard, F.;
- Blondeel, E.;
- Le Meur, N.;
- Joly‐Hélas, G.;
- Chambon, P.;
- Till, M.;
- Herbaut‐Graux, M.;
- Vigouroux‐Castera, A.;
- Coussement, A.;
- Lespinasse, J.;
- Amblard, F.;
- Jimenez, M.;
- Lebel Roy Camille, L.;
- Carré‐Pigeon, F.;
- Flori, E.;
- Mugneret, F.;
- Jaillard, S.;
- Yardin, C.;
- Harbuz, R.
Publication type:
Article
Prenatal BACs-on-Beads(TM) : the prospective experience of five prenatal diagnosis laboratories.
Published in:
2012
By:
- Vialard F;
- Simoni G;
- Gomes DM;
- Abourra A;
- Toffol SD;
- Bru F;
- Romero MC;
- Nitsch L;
- Bouhanna P;
- Marcato L;
- Popowski T;
- Grimi B;
- Martínez-Conejero JA;
- Benzacken B;
- Genesio R;
- Grati FR
Publication type:
Journal Article
Prenatal BACs-on-Beads([TM]) : a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis.
Published in:
2011
By:
- Vialard F;
- Simoni G;
- Aboura A;
- De Toffol S;
- Molina Gomes D;
- Marcato L;
- Serero S;
- Clement P;
- Bouhanna P;
- Rouleau E;
- Grimi B;
- Selva J;
- Gaetani E;
- Maggi F;
- Joseph A;
- Benzacken B;
- Grati FR
Publication type:
Journal Article
Prenatal BACs-on-Beads.
Published in:
Prenatal Diagnosis, 2011, v. 31, n. 5, p. 500, doi. 10.1002/pd.2727
By:
- Vialard, F.;
- Simoni, G.;
- Aboura, A.;
- De Toffol, S.;
- Molina Gomes, D.;
- Marcato, L.;
- Serero, S.;
- Clement, P.;
- Bouhanna, P.;
- Rouleau, E.;
- Grimi, B.;
- Selva, J.;
- Gaetani, E.;
- Maggi, F.;
- Joseph, A.;
- Benzacken, B.;
- Grati, F. R.
Publication type:
Article
Fetal karyotype in feto-fetal transfusion syndrome: a 7-year experience.
Published in:
Prenatal Diagnosis, 2009, v. 29, n. 8, p. 804, doi. 10.1002/pd.2272
By:
- Vialard, F.;
- Salomon, L.J.;
- Winer, N.;
- Bussières, L.;
- Molina Gomes, D.;
- Ville, Y.
Publication type:
Article
Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus sampling.
Published in:
Prenatal Diagnosis, 2006, v. 26, n. 3, p. 239, doi. 10.1002/pd.1389
By:
- Molina-Gomes, D.;
- Nebout, V.;
- Daikha-Dahmane, F.;
- Vialard, F.;
- Ville, Y.;
- Selva, J.
Publication type:
Article
Dandy - Walker syndrome and corpus callosum agenesis in 5p deletion.
Published in:
Prenatal Diagnosis, 2005, v. 25, n. 4, p. 311, doi. 10.1002/pd.1130
By:
- Vialard, F.;
- Robyr, R.;
- Hillion, Y.;
- Gomes, D. Molina;
- Selva, J.;
- Ville, Y.
Publication type:
Article
Possible human chimera detected prenatally after in vitro fertilization: a case report.
Published in:
Prenatal Diagnosis, 2003, v. 23, n. 11, p. 935, doi. 10.1002/pd.733
By:
- Simon-Bouy, B.;
- Plachot, M.;
- Mokdad, A.;
- Lavaud, N.;
- Muti, C.;
- Bazin, A.;
- Vialard, F.;
- Belaisch-Allart, J.
Publication type:
Article
Array Comparative Genomic Hybridization in Prenatal Diagnosis: Another Experience.
Published in:
Fetal Diagnosis & Therapy, 2009, v. 25, n. 2, p. 277, doi. 10.1159/000224112
By:
- Vialard, F.;
- Gomes, D. Molina;
- Leroy, B.;
- Quarello, E.;
- Escalona, A.;
- Le Sciellour, C.;
- Serazin, V.;
- Roume, J.;
- Ville, Y.;
- de Mazancourt, P.;
- Selva, J.
Publication type:
Article
Partial Chromosome Deletion: A New Trisomy Rescue Mechanism?
Published in:
Fetal Diagnosis & Therapy, 2009, v. 25, n. 1, p. 111, doi. 10.1159/000203400
By:
- Vialard, F.;
- Molina-Gomes, D.;
- Quarello, E.;
- Leroy, B.;
- Ville, Y.;
- Selva, J.
Publication type:
Article
Predisposition to Aneuploidy in the Oocyte.
Published in:
Cytogenetic & Genome Research, 2011, v. 133, n. 2-4, p. 127, doi. 10.1159/000324231
By:
- Vialard, F.;
- Boitrelle, F.;
- Molina-Gomes, D.;
- Selva, J.
Publication type:
Article
The X chromosome and ovarian function.
Published in:
Cytogenetic & Genome Research, 2002, v. 99, n. 1-4, p. 218, doi. 10.1159/000071596
By:
- Vialard, F.;
- Cocquet, J.;
- Christin-Maitre, S.;
- Veita, R.;
- Fellous, M.
Publication type:
Article

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