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[Premature ovarian failure].
Christin-Maitre S, Pasquier M, Donadille B, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Ann Endocrinol (Paris). 2006 Dec;67(6):557-66. doi: 10.1016/s0003-4266(06)73007-4. Ann Endocrinol (Paris). 2006. PMID: 17194965 Review. French.
Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
Beysen D, De Jaegere S, Amor D, Bouchard P, Christin-Maitre S, Fellous M, Touraine P, Grix AW, Hennekam R, Meire F, Oyen N, Wilson LC, Barel D, Clayton-Smith J, de Ravel T, Decock C, Delbeke P, Ensenauer R, Ebinger F, Gillessen-Kaesbach G, Hendriks Y, Kimonis V, Laframboise R, Laissue P, Leppig K, Leroy BP, Miller DT, Mowat D, Neumann L, Plomp A, Van Regemorter N, Wieczorek D, Veitia RA, De Paepe A, De Baere E. Beysen D, et al. Among authors: bouchard p. Hum Mutat. 2008 Nov;29(11):E205-19. doi: 10.1002/humu.20819. Hum Mutat. 2008. PMID: 18642388 Free article.
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.
D'haene B, Attanasio C, Beysen D, Dostie J, Lemire E, Bouchard P, Field M, Jones K, Lorenz B, Menten B, Buysse K, Pattyn F, Friedli M, Ucla C, Rossier C, Wyss C, Speleman F, De Paepe A, Dekker J, Antonarakis SE, De Baere E. D'haene B, et al. Among authors: bouchard p. PLoS Genet. 2009 Jun;5(6):e1000522. doi: 10.1371/journal.pgen.1000522. Epub 2009 Jun 19. PLoS Genet. 2009. PMID: 19543368 Free PMC article.
FOXO3a variants in patients with premature ovarian failure.
Vinci G, Christin-Maitre S, Pasquier M, Bouchard P, Fellous M, Veitia RA. Vinci G, et al. Among authors: bouchard p. Clin Endocrinol (Oxf). 2008 Mar;68(3):495-7. doi: 10.1111/j.1365-2265.2007.03052.x. Epub 2007 Sep 19. Clin Endocrinol (Oxf). 2008. PMID: 17888023 No abstract available.
Mutations and sequence variants in GDF9 and BMP15 in patients with premature ovarian failure.
Laissue P, Christin-Maitre S, Touraine P, Kuttenn F, Ritvos O, Aittomaki K, Bourcigaux N, Jacquesson L, Bouchard P, Frydman R, Dewailly D, Reyss AC, Jeffery L, Bachelot A, Massin N, Fellous M, Veitia RA. Laissue P, et al. Among authors: bouchard p. Eur J Endocrinol. 2006 May;154(5):739-44. doi: 10.1530/eje.1.02135. Eur J Endocrinol. 2006. PMID: 16645022
Genes and premature ovarian failure.
Christin-Maitre S, Vasseur C, Portnoï MF, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Mol Cell Endocrinol. 1998 Oct 25;145(1-2):75-80. doi: 10.1016/s0303-7207(98)00172-5. Mol Cell Endocrinol. 1998. PMID: 9922102 Review.
[Genes and ovarian insufficiency].
Christin-Maitre S, Bouchard P. Christin-Maitre S, et al. Among authors: bouchard p. Ann Endocrinol (Paris). 1999 Jul;60(2):118-22. Ann Endocrinol (Paris). 1999. PMID: 10456183 Review. French.
Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.
Aboura A, Dupas C, Tachdjian G, Portnoï MF, Bourcigaux N, Dewailly D, Frydman R, Fauser B, Ronci-Chaix N, Donadille B, Bouchard P, Christin-Maitre S. Aboura A, et al. Among authors: bouchard p. J Clin Endocrinol Metab. 2009 Nov;94(11):4540-6. doi: 10.1210/jc.2009-0186. Epub 2009 Oct 16. J Clin Endocrinol Metab. 2009. PMID: 19837940
556 results