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Meta-analysis of muscle transcriptome data using the MADMuscle database reveals biologically relevant gene patterns.

Daniel Baron , Emeric Dubois , Audrey Bihouée , Raluca Teusan , Marja Steenman et al.
BMC Genomics, 2011, 12 (1), pp.113. ⟨10.1186/1471-2164-12-113⟩
Journal articles inserm-00663672v1
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The Transcription Factor Encyclopedia.

Dimas Yusuf , Stefanie Butland , Magdalena Swanson , Eugene Bolotin , Amy Ticoll et al.
Genome Biology, 2012, 13 (3), pp.R24. ⟨10.1186/gb-2012-13-3-r24⟩
Journal articles inserm-00716041v1
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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
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Functional evidence implicating FOXL2 in non syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.

Paul Laissue , Besma Lakhal , Bérénice A Benayoun , Aurélie Dipietromaria , Rim Braham et al.
Journal of Medical Genetics, 2009, 46 (7), pp.455. ⟨10.1136/jmg.2008.065086⟩
Journal articles istex hal-00552682v1
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Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

Bérénice Benayoun , Sandrine Caburet , Aurélie Dipietromaria , Adrien Georges , Barbara d'Haene et al.
PLoS ONE, 2010, 5 (1), pp.e8789. ⟨10.1371/journal.pone.0008789⟩
Journal articles hal-02116167v1
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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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Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5′UTR Mutations and Copy-Number Variations of NMNAT1

Frauke Coppieters , Anne Laure Todeschini , Takuro Fujimaki , Annelot Baert , Marieke de Bruyne et al.
Human Mutation, 2015, 36 (12), pp.1188-1196. ⟨10.1002/humu.22899⟩
Journal articles hal-02119195v1

Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency

Justine Bouilly , Isabelle Beau , Sara Barraud , Valérie Bernard , Kemal Azibi et al.
Journal of Clinical Endocrinology and Metabolism, 2016, 101 (12), pp.4541-4550. ⟨10.1210/jc.2016-2152⟩
Journal articles hal-02896004v1
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Combined comparative genomic hybridization and transcriptomic analyses of ovarian granulosa cell tumors point to novel candidate driver genes

Sandrine Caburet , Mikko Anttonen , Anne-Laure Todeschini , Leila Unkila-Kallio , Denis Mestivier et al.
BMC Cancer, 2015, 15 (1), ⟨10.1186/s12885-015-1283-0⟩
Journal articles hal-02119186v1