| -308 TNF alpha polymorphism: a new pharmacogenetic marker for selecting patients during in vitro fertilization for single embryo transfer M Benahmed, V Tronchon, F Vialard, M El Sirkasi, DM Gomes, M Bergere, ... HUMAN REPRODUCTION 22, I213-I213, 2007 | | 2007 |
| «Test ADNlc T21» ou test génétique non invasif de dépistage de la trisomie 21 fœtale: à propos d’un consortium d’utilisateurs L Gouas, P Callier, N Chelloug, H Copin, C Le Caignec, M Doco-Fenzy, ... Morphologie 102 (338), 140-141, 2018 | | 2018 |
| [9h30-9h50] PreImplantation Factor implications in maternal-fetal interface H Moindjie, E Dos Santos, K Fathallah, ER Barnea, F Vialard, ... Journal of Reproductive Immunology 158, 103521, 2023 | | 2023 |
| 11 Diffeomorphisms groups generated by Gaussian vector fields FX Vialard Math in the Cabin-Shape Analysis Workshop in Bad Gastein, 23, 0 | | |
| 119 Transplacental transfer of alectinib and osimertinib using an ex vivo human placental perfusion model L Benoit, D Combarel, MN Dieudonné, O Mir, S Grassin-Delyle, A Paci, ... American Journal of Obstetrics & Gynecology 230 (1), S81, 2024 | | 2024 |
| 1p36 deletion syndrome: Review and mapping with further characterization of the phenotype, a new cohort of 86 patients C Jacquin, E Landais, C Poirsier, A Afenjar, A Akhavi, N Bednarek, ... American Journal of Medical Genetics Part A 191 (2), 445-458, 2023 | 8 | 2023 |
| 2p25.3 microduplications involving MYT1L: further phenotypic characterization through an assessment of 16 new cases and a literature review M Bouassida, M Egloff, J Levy, N Chatron, L Bernardini, G Le Guyader, ... European Journal of Human Genetics 31 (8), 895-904, 2023 | 2 | 2023 |
| 36 Evaluation of transplacental transfer of cancer therapies in melanoma via the perfused human placental model E Heggarty, D Combarel, F Vialard, S Grassin-Delyle, O Mir, A Paci, ... American Journal of Obstetrics & Gynecology 230 (1), S28-S29, 2024 | | 2024 |
| 6 fold increase of spermatozoa aneuploidy from meiotic origin in patients with non obstructive azoospermia compared to patients with obstructive azoospermia J Selva, H Bouazzi, M Bailly, JC Pont, M Albert, F Vialard Fertility and Sterility 90, S319, 2008 | | 2008 |
| A 32 year retrospective prenatal study of 47, XXX and 47, XYY dysgonosomies: P1-8 E Blondeel, N Gruchy, F Prieur, P Vago, A Vigouroux-Castera, F Amblard, ... Prenatal Diagnosis 33, 2013 | | 2013 |
| A French collaborative survey of 272 fetuses with 22q11. 2 deletion: ultrasound findings, fetal autopsies and pregnancy outcomes J Besseau‐Ayasse, C Violle‐Poirsier, A Bazin, N Gruchy, A Moncla, ... Prenatal Diagnosis 34 (5), 424-430, 2014 | 58 | 2014 |
| A French multicenter study of over 700 patients with 22q11 deletions diagnosed using FISH or aCGH C Poirsier, J Besseau-Ayasse, C Schluth-Bolard, J Toutain, C Missirian, ... European Journal of Human Genetics 24 (6), 844-851, 2016 | 61 | 2016 |
| A genome‐wide DNA methylation study in azoospermia F Ferfouri, F Boitrelle, I Ghout, M Albert, D Molina Gomes, R Wainer, ... Andrology 1 (6), 815-821, 2013 | 39 | 2013 |
| A geometric Laplace expansion F Léger, FX Vialard | | 2022 |
| A geometric Laplace method F Léger, FX Vialard Pure and Applied Analysis 5 (4), 1041-1080, 2023 | | 2023 |
| A high level of tetrasomy 9p mosaicism but no clinical manifestations other than moderate oligozoospermia with chromosomally balanced sperm: A case report H Bellil, B Herve, E Herzog, JM Ayoubi, F Vialard, M Poulain Journal of Assisted Reproduction and Genetics 37, 573-577, 2020 | 6 | 2020 |
| A histomorphometric and cytogenetic study of testis from men 29–102 years old M Dakouane, L Bicchieray, M Bergere, M Albert, F Vialard, J Selva Fertility and sterility 83 (4), 923-928, 2005 | 73 | 2005 |
| A human morphologically normal spermatozoon may have noncondensed chromatin F Boitrelle, M Pagnier, Y Athiel, N Swierkowski‐Blanchard, A Torre, L Alter, ... Andrologia 47 (8), 879-886, 2015 | 19 | 2015 |
| A MEI1 homozygous missense mutation associated with meiotic arrest in a consanguineous family M Ben Khelifa, F Ghieh, R Boudjenah, C Hue, D Fauvert, R Dard, ... Human Reproduction 33 (6), 1034-1037, 2018 | 54 | 2018 |
| A Rare Chromosome Rearrangement Leading to de la Chapelle Syndrome with a Mosaic 45, X Cell Line:(46, X, psu dic (X; Y)(p22. 13; q11. 221)/45, X/45, psu dic (X; Y)(p22. 13; q11 … A Clement, T Dominot, J Chammas, M Montagnon, M Delcroix, J Pfeffer, ... Genes 14 (1), 81, 2022 | | 2022 |
