Search for Genetic Defects in the Transcription Factor Genes FOXL2, FOXE1, BMP15, NOBOX, and GDF9 in Children, Adolescents and Young Adults With Premature Ovarian Insufficiency POI — Nikolaos Settas (2014) | RDL Network

Home
Publications
Search for Genetic Defects in the Transcription Factor Genes FOXL2, FOXE1, BMP15, NOBOX, and GDF9 in Children, Adolescents and Young Adults With Premature Ovarian Insufficiency POI

Shared by

George Chrousos

National Technical University of Athens

Search for Genetic Defects in the Transcription Factor Genes FOXL2, FOXE1, BMP15, NOBOX, and GDF9 in Children, Adolescents and Young Adults With Premature Ovarian Insufficiency POI

Article 2014 en

Authors

NS
Nikolaos Settas
MA
Margarita Anapliotou
ED
Euthimios Deligeoroglou

Discussion(0)

No comments yet. Be the first to comment.

Publication Info

Year: 2014
Published: —
Language: en

Article Details

Volume: 82
Link Of The Paper: https://abstracts.eurospe.org/hrp/0082/hrp0082FC6.1

Timeline

Created:June 19, 2026

Related publications

Article2015

Co-Existing Variants of FOXE1 and BMP15 Genes in Young Females with Primary Ovarian Insufficiency: Evidence of Digenic Inheritance

Nikolaos Settas, Lina Michala, Efthimios Deligeoroglou, Dionisios Chrysis, Ανδρέας Παμπάνος, Eleni Theochari, Olympia Valla, Christalena Sofocleous, Kitsiou Sofia, Helen Fryssira, Emmanuel Kanavakis, Catherine Dacou‐Voutetakis, George Chrousos, Antonis Voutetakis

Article2015

Co-Existing Variants of FOXE1 and BMP15 Genes in Young Females with Primary Ovarian Insufficiency: Evidence of Digenic Inheritance

Article2015

A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis–ptosis–epicanthus inversus syndrome

Nikolaos Settas, Margarita Anapliotou, Emmanuel Kanavakis, Helen Fryssira, Christalena Sofocleous, Catherine Dacou‐Voutetakis, George Chrousos, Antonis Voutetakis

Article2021

Effectiveness of enhancing cognitive reserve in children, adolescents and young adults at genetic risk for psychosis: Study protocol for a randomized controlled trial

Elena de la Serna, Laura Montejo, Brisa Solé, Josefina Castro‐Fornieles, Patricia Camprodon‐Boadas, Gisela Sugranyes, Mireia Rosa-Justícia, Anabel Martínez‐Arán, Eduard Vieta, Muriel Vicent-Gil, Maria Serra-Blasco, Narcı́s Cardoner, Carla Torrent

Article2023

Transition readiness among adolescents and young adults with haemophilia in the Netherlands: Nationwide questionnaire study

Martijn R Brands, E Janssen, Marjon H. Cnossen, Cees Smit, Lize F. D. van Vulpen, Paul van der Valk, Jeroen Eikenboom, Floor Heubel-Moenen, Louise Hooimeijer, Paula F. Ypma, Laurens Nieuwenhuizen, Michiel Coppens, Saskia E.M. Schols, Britta A. P. Laros‐van Gorkom, Frank W.G. Leebeek, M.H.E. Driessens, Frits R. Rosendaal, Johanna G. van der Bom, Karin Fijnvandraat, Samantha C. Gouw

Haemophilia