A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency
Fauchereau, F., Shalev, S., Chervinsky, E., Beck-Fruchter, R., Legois, B., Fellous, M., Caburet, S., Veitia, R.A.
Published in Clinical genetics (01.05.2016)
Published in Clinical genetics (01.05.2016)
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FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)
Hersmus, R, Kalfa, N, de Leeuw, B, Stoop, H, Oosterhuis, JW, de Krijger, R, Wolffenbuttel, KP, Drop, SLS, Veitia, RA, Fellous, M, Jaubert, F, Looijenga, LHJ
Published in The Journal of pathology (01.05.2008)
Published in The Journal of pathology (01.05.2008)
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A role for SOX9 in post-transcriptional processes: insights from the amphibian oocyte
Penrad-Mobayed, M., Perrin, C., L’Hôte, D., Contremoulins, V., Lepesant, J.-A., Boizet-Bonhoure, B., Poulat, F., Baudin, X., Veitia, R. A.
Published in Scientific reports (08.05.2018)
Published in Scientific reports (08.05.2018)
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Evolution and expression of FOXL2
Cocquet, J, Pailhoux, E, Jaubert, F, Servel, N, Xia, X, Pannetier, M, De Baere, E, Messiaen, L, Cotinot, C, Fellous, M, Veitia, R A
Published in Journal of medical genetics (01.12.2002)
Published in Journal of medical genetics (01.12.2002)
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The genetic make‐up of ovarian development and function: the focus on the transcription factor FOXL2
Elzaiat, M., Todeschini, A.‐L., Caburet, S., Veitia, R.A.
Published in Clinical genetics (01.02.2017)
Published in Clinical genetics (01.02.2017)
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Cytogenetic analyses of premature ovarian failure using karyotyping and interphase fluorescence in situ hybridization (FISH) in a group of 1000 patients
Lakhal, B, Braham, R, Berguigua, R, Bouali, N, Zaouali, M, Chaieb, M, Veitia, RA, Saad, A, Elghezal, H
Published in Clinical genetics (01.08.2010)
Published in Clinical genetics (01.08.2010)
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Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome
Beysen, D., Raes, J., Leroy, B.P., Lucassen, A., Yates, J.R.W., Clayton-Smith, J., Ilyina, H., Brooks, S. Sklower, Christin-Maitre, S., Fellous, M., Fryns, J.P., Kim, J.R., Lapunzina, P., Lemyre, E., Meire, F., Messiaen, L.M., Oley, C., Splitt, M., Thomson, J., Peer, Y. Van de, Veitia, R.A., De Paepe, A., De Baere, E.
Published in American journal of human genetics (01.08.2005)
Published in American journal of human genetics (01.08.2005)
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Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2
Laissue, P, Lakhal, B, Benayoun, B A, Dipietromaria, A, Braham, R, Elghezal, H, Philibert, P, Saâd, A, Sultan, C, Fellous, M, Veitia, R A
Published in Journal of medical genetics (01.07.2009)
Published in Journal of medical genetics (01.07.2009)
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Structure, evolution and expression of the FOXL2 transcription unit
Cocquet, J., De Baere, E., Gareil, M., Pannetier, M., Xia, X., Fellous, M., Veitia, R.A.
Published in Cytogenetic and genome research (01.01.2003)
Published in Cytogenetic and genome research (01.01.2003)
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Conference Proceeding
Adult ovarian granulosa cell tumor transcriptomics: prevalence of FOXL2 target genes misregulation gives insights into the pathogenic mechanism of the p.Cys134Trp somatic mutation
Benayoun, B A, Anttonen, M, L’Hôte, D, Bailly-Bechet, M, Andersson, N, Heikinheimo, M, Veitia, R A
Published in Oncogene (30.05.2013)
Published in Oncogene (30.05.2013)
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Functional evidence implicating FOXL2 in nonsyndromic premature ovarian failure and in the regulation of the transcription factor OSR2
LAISSUE, P, LAKHAL, B, VEITIA, R. A, BENAYOUN, B. A, DIPIETROMARIA, A, BRAHAM, R, ELGHEZAL, H, PHILIBERT, P, SAAD, A, SULTANS, C, FELLOUS, M
Published in Journal of medical genetics (01.07.2009)
Published in Journal of medical genetics (01.07.2009)
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Dosage balance in gene regulation: biological implications
Birchler, James A., Riddle, Nicole C., Auger, Donald L., Veitia, Reiner A.
Published in Trends in genetics (01.04.2005)
Published in Trends in genetics (01.04.2005)
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The mutations and potential targets of the forkhead transcription factor FOXL2
Moumné, L., Batista, F., Benayoun, B.A., Nallathambi, J., Fellous, M., Sundaresan, P., Veitia, R.A.
Published in Molecular and cellular endocrinology (30.01.2008)
Published in Molecular and cellular endocrinology (30.01.2008)
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Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency
BOUHALI, Kamal, DIPIETROMARIA, Aurélie, FONTAINE, Anastasia, CABURET, Sandrine, BARBIERI, Ottavia, BELLESSORT, Brice, FELLOUS, Marc, VEITIA, Reiner A, LEVI, Giovanni
Published in Human molecular genetics (01.07.2011)
Published in Human molecular genetics (01.07.2011)
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Swyer Syndrome and 46,XY Partial Gonadal Dysgenesis Associated with 9p Deletions in the Absence of Monosomy-9p Syndrome
Veitia, R.A., Nunes, M., Quintana-Murci, L., Rappaport, R., Thibaud, E., Jaubert, F., Fellous, M., McElreavey, K., Gonçalves, J., Silva, M., Cidade Rodrigues, J., Caspurro, M., Boieiro, F., Marques, R., Lavinha, J.
Published in American journal of human genetics (01.09.1998)
Published in American journal of human genetics (01.09.1998)
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