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Paul Laissue
Paul Laissue
LATAM Medical Director. Orphan Diseases Unit. Biopas Laboratoires. BIOPAS Group. Inserm U1016, CNRS
Bestätigte E-Mail-Adresse bei biopasgroup.com
Titel
Zitiert von
Zitiert von
Jahr
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
6292003
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
3412006
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
1682007
The forkhead-box family of transcription factors: key molecular players in colorectal cancer pathogenesis
P Laissue
Molecular cancer 18 (1), 5, 2019
1192019
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
1042008
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
1002012
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
862009
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
802017
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
802017
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
782015
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
742017
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
722015
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
702019
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
632017
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
632015
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
612016
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
592008
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
562007
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
522012
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
502015
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