Berangere Legois
Paris, France
Last Updated: 09/26/2026
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Found 12 publications
Deciphering the Impact of AKT1 Pathogenic Variants in Juvenile Granulosa Cell Tumors Using a Drosophila Model.
Journal: Molecular & cellular proteomics : MCP
Published: February 12, 2025
A cellular model provides insights into the pathogenicity of the oncogenic FOXL2 somatic variant p.Cys134Trp.
Journal: British journal of cancer
Published: May 15, 2023
DHH pathogenic variants involved in 46,XY disorders of sex development differentially impact protein self-cleavage and structural conformation.
Journal: Human genetics
Published: April 21, 2020
High-throughput Exploration of the Network Dependent on AKT1 in Mouse Ovarian Granulosa Cells.
Journal: Molecular & cellular proteomics : MCP
Published: March 21, 2019
A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks.
Journal: EBioMedicine
Published: February 28, 2019
A novel variant of DHH in a familial case of 46,XY disorder of sex development: Insights from molecular dynamics simulations.
Journal: Clinical endocrinology
Published: April 24, 2017
A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome.
Journal: European journal of endocrinology
Published: November 24, 2016
A non-sense MCM9 mutation in a familial case of primary ovarian insufficiency.
Journal: Clinical genetics
Published: December 02, 2015
Molecular analyses of juvenile granulosa cell tumors bearing AKT1 mutations provide insights into tumor biology and therapeutic leads.
Journal: Human molecular genetics
Published: July 24, 2015
Showing 1-12 of 12
Last Updated: 09/26/2026