High-resolution array-CGH analysis on 46,XX patients affected by early onset primary ovarian insufficiency discloses new genes involved in ovarian function

Advances in the Molecular Pathophysiology, Genetics, and Treatment of Primary Ovarian Insufficiency

(2018) Ilpo Huhtaniemi et al.   TRENDS IN ENDOCRINOLOGY AND METABOLISM

Genetics of primary ovarian insufficiency

(2016) R. Rossetti et al.   CLINICAL GENETICS

Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases

(2016) O. Tšuiko et al.   HUMAN REPRODUCTION

Deletion ofCPEB1Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency

(2016) C. Hyon et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

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

(2016) Justine Bouilly et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Array-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology

(2016) Sylvie Jaillard et al.   Journal of Ovarian Research

Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations

(2015) Dora Janeth Fonseca et al.   FERTILITY AND STERILITY

Aetiological coding sequence variants in non-syndromic premature ovarian failure: From genetic linkage analysis to next generation sequencing

(2015) Paul Laissue   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform

(2014) A. Norling et al.   HUMAN REPRODUCTION

Exome Sequencing Reveals SYCE1 Mutation Associated With Autosomal Recessive Primary Ovarian Insufficiency

(2014) Liat de Vries et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Defying DNA Double-Strand Break-Induced Death during Prophase I Meiosis by Temporal TAp63  Phosphorylation Regulation in Developing Mouse Oocytes

(2014) D.-A. Kim et al.   MOLECULAR AND CELLULAR BIOLOGY

Gene dosage as a relevant mechanism contributing to the determination of ovarian function in Turner syndrome

(2013) C. Castronovo et al.   HUMAN REPRODUCTION

TBP Dynamics during Mouse Oocyte Meiotic Maturation and Early Embryo Development

(2013) Shao-Chen Sun et al.   PLoS One

DNA Damage in Oocytes Induces a Switch of the Quality Control Factor TAp63α from Dimer to Tetramer

(2011) Gregor B. Deutsch et al.   CELL

Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure

(2011) Megan M. McGuire et al.   FERTILITY AND STERILITY

Copy number variants on the X chromosome in women with primary ovarian insufficiency

(2011) Erik A.H. Knauff et al.   FERTILITY AND STERILITY

Mapping and analysis of chromatin state dynamics in nine human cell types

(2011) Jason Ernst et al.   NATURE

Array comparative genomic hybridization for the detection of submicroscopic copy number variations of the X chromosome in women with premature ovarian failure

(2010) T. E. Dudding et al.   HUMAN REPRODUCTION

Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF)

(2010) C. R. Quilter et al.   HUMAN REPRODUCTION

Copy Number Variants in Premature Ovarian Failure and Ovarian Dysgenesis

(2010) S. Ledig et al.   Sexual Development

Array Comparative Genomic Hybridization Profiling Analysis Reveals Deoxyribonucleic Acid Copy Number Variations Associated with Premature Ovarian Failure

(2009) Azzedine Aboura et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mutation of the Mouse Syce1 Gene Disrupts Synapsis and Suggests a Link between Synaptonemal Complex Structural Components and DNA Repair

(2009) Ewelina Bolcun-Filas et al.   PLoS Genetics