| Undertreatment strongly decreases prognosis of breast cancer in elderly women C Bouchardy, E Rapiti, G Fioretta, P Laissue, I Neyroud-Caspar, ... Journal of clinical oncology 21 (19), 3580-3587, 2003 | 633 | 2003 |
| Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure P Laissue, S Christin-Maitre, P Touraine, F Kuttenn, O Ritvos, K Aittomaki, ... European Journal of Endocrinology 154 (5), 739-744, 2006 | 346 | 2006 |
| Expressional and Epigenetic Alterations of Placental Serine Protease Inhibitors: SERPINA3 Is a Potential Marker of Preeclampsia ST Chelbi, F Mondon, H Jammes, C Buffat, TM Mignot, J Tost, F Busato, ... Hypertension 49 (1), 76-83, 2007 | 169 | 2007 |
| The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis P Laissue Molecular cancer 18 (1), 5, 2019 | 124 | 2019 |
| Recent advances in the study of genes involved in non-syndromic premature ovarian failure P Laissue, G Vinci, RA Veitia, M Fellous Molecular and Cellular Endocrinology 282 (1-2), 101-111, 2008 | 104 | 2008 |
| Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis CP Diggle, DA Parry, CV Logan, P Laissue, C Rivera, CM Restrepo, ... Human mutation 33 (8), 1175-1181, 2012 | 103 | 2012 |
| Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2 P Laissue, B Lakhal, BA Benayoun, A Dipietromaria, R Braham, ... Journal of medical genetics 46 (7), 455-457, 2009 | 87 | 2009 |
| Novel genes and mutations in patients affected by recurrent pregnancy loss P Quintero-Ronderos, E Mercier, M Fukuda, R González, CF Suárez, ... PloS one 12 (10), e0186149, 2017 | 81 | 2017 |
| New mutations in non-syndromic primary ovarian insufficiency patients identified via whole-exome sequencing LC Patiño, I Beau, C Carlosama, JC Buitrago, R González, CF Suárez, ... Human reproduction 32 (7), 1512-1520, 2017 | 81 | 2017 |
| Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations DJ Fonseca, LC Patiño, YC Suárez, A de Jesús Rodríguez, HE Mateus, ... Fertility and sterility 104 (1), 154-162. e2, 2015 | 81 | 2015 |
| A homozygous donor splice-site mutation in the meiotic gene MSH4 causes primary ovarian insufficiency C Carlosama, M Elzaiat, LC Patiño, HE Mateus, RA Veitia, P Laissue Human molecular genetics 26 (16), 3161-3166, 2017 | 78 | 2017 |
| Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing P Laissue Molecular and cellular endocrinology 411, 243-257, 2015 | 73 | 2015 |
| ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure C Delcour, L Amazit, LC Patino, F Magnin, J Fagart, B Delemer, J Young, ... Genetics in Medicine 21 (4), 930-938, 2019 | 72 | 2019 |
| Success stories in genomic medicine from resource-limited countries K Mitropoulos, H Al Jaibeji, DA Forero, P Laissue, A Wonkam, ... Human genomics 9, 1-7, 2015 | 65 | 2015 |
| Endothelial cell dysfunction and cardiac hypertrophy in the STOX1 model of preeclampsia A Ducat, L Doridot, R Calicchio, C Méhats, JL Vilotte, J Castille, ... Scientific reports 6 (1), 19196, 2016 | 64 | 2016 |
| BMP15 mutations associated with primary ovarian insufficiency reduce expression, activity, or synergy with GDF9 LC Patiño, KL Walton, TD Mueller, KE Johnson, W Stocker, D Richani, ... The Journal of Clinical Endocrinology & Metabolism 102 (3), 1009-1019, 2017 | 63 | 2017 |
| Identification of 34 novel and 56 known FOXL2 mutations in patients with blepharophimosis syndrome D Beysen, S De Jaegere, D Amor, P Bouchard, S Christin‐Maitre, ... Human mutation 29 (11), E205-E219, 2008 | 60 | 2008 |
| Centimorgan-range one-step mapping of fertility traits using interspecific recombinant congenic mice D L'Hôte, C Serres, P Laissue, A Oulmouden, C Rogel-Gaillard, ... Genetics 176 (3), 1907-1921, 2007 | 57 | 2007 |
| Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial premature ovarian failure S Caburet, P Zavadakova, Z Ben-Neriah, K Bouhali, A Dipietromaria, ... PLoS one 7 (3), e33412, 2012 | 52 | 2012 |
| Biallelic HERC1 mutations in a syndromic form of overgrowth and intellectual disability O Ortega‐Recalde, OI Beltrán, JM Gálvez, A Palma‐Montero, ... Clinical genetics 88 (4), e1-e3, 2015 | 51 | 2015 |
Vaiman DanielDepartment Genetics and Development, Cochin Institute, Paris在 inserm.fr 的电子邮件经过验证
