Paul Laissue
Paul Laissue
Medical Manager. Biopas Laboratories. BIOPAS Group. Inserm U1016, CNRS UMR8104. Institut Cochin
Η διεύθυνση ηλεκτρονικού ταχυδρομείου έχει επαληθευτεί στον τομέα urosario.edu.co
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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
5612003
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
2852006
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
1332007
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
892008
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
762009
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
732012
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
572008
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
552015
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
532007
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
512015
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, 19196, 2016
432016
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
422012
Success stories in genomic medicine from resource-limited countries
K Mitropoulos, H Al Jaibeji, DA Forero, P Laissue, A Wonkam, ...
Human Genomics 9 (1), 1-7, 2015
412015
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis
P Laissue
Molecular cancer 18 (1), 1-13, 2019
402019
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
402017
Whole-exome sequencing enables rapid determination of xeroderma pigmentosum molecular etiology
O Ortega-Recalde, JI Vergara, DJ Fonseca, X Ríos, H Mosquera, ...
PLoS One 8 (6), e64692, 2013
362013
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
322017
Exome sequencing is an efficient tool for variant late-infantile neuronal ceroid lipofuscinosis molecular diagnosis
LC Patiño, R Battu, O Ortega-Recalde, J Nallathambi, VR Anandula, ...
PLoS One 9 (10), e109576, 2014
322014
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
312017
BMP15 c.-9C> G promoter sequence variant may contribute to the cause of non-syndromic premature ovarian failure
DJ Fonseca, O Ortega-Recalde, C Esteban-Perez, H Moreno-Ortiz, ...
Reproductive biomedicine online 29 (5), 627-633, 2014
302014
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