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authFullName_s : Bérangère Legois

A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations

Françoise Paris , Delphine Flatters , Sandrine Caburet , Bérangère Legois , Nadège Servant et al.
Clinical Endocrinology, 2017, 87 (5), pp.539 - 544. ⟨10.1111/cen.13420⟩
Journal articles hal-01758673v1
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A homozygous $FANCM$ mutation underlies a familial case of non-syndromic primary ovarian insufficiency

Baptiste Fouquet , Patrycja Pawlikowska , Sandrine Caburet , Céline Guigon , Marika Mäkinen et al.
eLife, 2017, 6, pp.e30490. ⟨10.7554/eLife.30490⟩
Journal articles hal-02391886v1
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The transcription factor FOXL2 mobilizes estrogen signaling to maintain the identity of ovarian granulosa cells

Adrien Georges , David L'Hôte , Anne Laure Todeschini , Aurelie A. Auguste , Bérangère Legois et al.
Journal articles hal-02118875v1
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A Hot-spot of In-frame Duplications Activates the Oncoprotein AKT1 in Juvenile Granulosa Cell Tumors

Laurianne Bessière , Anne-Laure Todeschini , Aurelie A. Auguste , Sabine Sarnacki , Delphine Flatters et al.
EBioMedicine, 2015, 2 (5), pp.421-431. ⟨10.1016/j.ebiom.2015.03.002⟩
Journal articles hal-02118885v1

Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.

Aurélie Auguste , Laurianne Bessière , Anne-Laure Todeschini , Sandrine Caburet , Sabine Sarnacki et al.
Human Molecular Genetics, 2015, 24 (23), pp.6687-98. ⟨10.1093/hmg/ddv373⟩
Journal articles hal-01266741v1