| Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies FR Grati, D Molina Gomes, JCPB Ferreira, C Dupont, V Alesi, L Gouas, ... Prenatal diagnosis 35 (8), 801-809, 2015 | 318 | 2015 |
| A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation R Harbuz, R Zouari, V Pierre, MB Khelifa, M Kharouf, C Coutton, ... The American Journal of Human Genetics 88 (3), 351-361, 2011 | 235 | 2011 |
| Expression of the cystathionine β synthase (CBS) gene during mouse development and immunolocalization in adult brain K Robert, F Vialard, E Thiery, K Toyama, PM Sinet, N Janel, J London Journal of Histochemistry & Cytochemistry 51 (3), 363-371, 2003 | 177 | 2003 |
| Large human sperm vacuoles observed in motile spermatozoa under high magnification: nuclear thumbprints linked to failure of chromatin condensation F Boitrelle, F Ferfouri, JM Petit, D Segretain, C Tourain, M Bergere, ... Human Reproduction 26 (7), 1650-1658, 2011 | 159 | 2011 |
| The Aurora Kinase C c. 144delC mutation causes meiosis I arrest in men and is frequent in the North African population K Dieterich, R Zouari, R Harbuz, F Vialard, D Martinez, H Bellayou, ... Human Molecular Genetics 18 (7), 1301-1309, 2009 | 131 | 2009 |
| Genetic polymorphisms influence the ovarian response to rFSH stimulation in patients undergoing in vitro fertilization programs with ICSI R Boudjenah, D Molina-Gomes, A Torre, M Bergere, M Bailly, F Boitrelle, ... PloS one 7 (6), e38700, 2012 | 126 | 2012 |
| Screening for Down syndrome using first-trimester combined screening followed by second-trimester ultrasound examination in an unselected population P Rozenberg, L Bussières, S Chevret, JP Bernard, L Malagrida, H Cuckle, ... American journal of obstetrics and gynecology 195 (5), 1379-1387, 2006 | 113 | 2006 |
| Maternal obesity influences expression and DNA methylation of the adiponectin and leptin systems in human third-trimester placenta P Nogues, E Dos Santos, H Jammes, P Berveiller, L Arnould, F Vialard, ... Clinical epigenetics 11, 1-18, 2019 | 103 | 2019 |
| Array comparative genomic hybridization in prenatal diagnosis: another experience F Vialard, D Molina Gomes, B Leroy, E Quarello, A Escalona, ... Fetal diagnosis and therapy 25 (2), 277-284, 2009 | 102 | 2009 |
| Pregnancy loss: French clinical practice guidelines C Huchon, X Deffieux, G Beucher, P Capmas, X Carcopino, ... European Journal of Obstetrics & Gynecology and Reproductive Biology 201, 18-26, 2016 | 94 | 2016 |
| Prenatal BACs‐on‐Beads™: a new technology for rapid detection of aneuploidies and microdeletions in prenatal diagnosis F Vialard, G Simoni, A Aboura, S De Toffol, D Molina Gomes, L Marcato, ... Prenatal diagnosis 31 (5), 500-508, 2011 | 82 | 2011 |
| 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 I Hammoud, F Boitrelle, F Ferfouri, F Vialard, M Bergere, B Wainer, ... Andrologia 45 (3), 163-170, 2013 | 81 | 2013 |
| MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia C Coutton, R Zouari, F Abada, M Ben Khelifa, G Merdassi, C Triki, ... Human Reproduction 27 (8), 2549-2558, 2012 | 81 | 2012 |
| Cryopreservation of human spermatozoa decreases the number of motile normal spermatozoa, induces nuclear vacuolization and chromatin decondensation F Boitrelle, M Albert, C Theillac, F Ferfouri, M Bergere, F Vialard, R Wainer, ... Journal of andrology 33 (6), 1371-1378, 2012 | 78 | 2012 |
| Karyotype and outcome of fetuses diagnosed with cystic hygroma in the first trimester in relation to nuchal translucency thickness R Kharrat, M Yamamoto, J Roume, S Couderc, F Vialard, Y Hillion, Y Ville Prenatal Diagnosis: Published in Affiliation With the International Society …, 2006 | 75 | 2006 |
| 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 | 72 | 2005 |
| Polymorphisms and endometriosis: a systematic review and meta-analyses L Méar, M Herr, A Fauconnier, C Pineau, F Vialard Human reproduction update 26 (1), 73-103, 2020 | 70 | 2020 |
| Identification of a new recurrent aurora kinase C mutation in both European and African men with macrozoospermia M Ben Khelifa, C Coutton, MGB Blum, F Abada, R Harbuz, R Zouari, ... Human reproduction 27 (11), 3337-3346, 2012 | 69 | 2012 |
| Evidence of a high proportion of premature unbalanced separation of sister chromatids in the first polar bodies of women of advanced age F Vialard, C Petit, M Bergere, DM Gomes, V Martel-Petit, R Lombroso, ... Human Reproduction 21 (5), 1172-1178, 2006 | 68 | 2006 |
| The roles of leptin and adiponectin at the fetal-maternal interface in humans E Dos Santos, F Duval, F Vialard, MN Dieudonné Hormone molecular biology and clinical investigation 24 (1), 47-63, 2015 | 66 | 2015 |
