Anne L. Todeschini
Paris, France
Last Updated: 09/26/2026
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Found 8 publications
The Oncogenic FOXL2 C134W Mutation Is a Key Driver of Granulosa Cell Tumors.
Journal: Cancer research
Published: June 09, 2022
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency.
Journal: The Journal of clinical endocrinology and metabolism
Published: September 08, 2016
Hidden Genetic Variation in LCA9-Associated Congenital Blindness Explained by 5'UTR Mutations and Copy-Number Variations of NMNAT1.
Journal: Human mutation
Published: April 15, 2015
Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles.
Journal: Human molecular genetics
Published: May 01, 2012
Homology-dependent silencing by an exogenous sequence in the Drosophila germline.
Journal: G3 (Bethesda, Md.)
Published: November 24, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026