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

Next-Generation Sequencing of Duplication CNVs Reveals that Most Are Tandem and Some Create Fusion Genes at Breakpoints

(2015) Scott Newman et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The prevalence and phenotypic characteristics of spontaneous premature ovarian failure: a general population registry-based study

(2015) K. Haller-Kikkatalo et al.   HUMAN REPRODUCTION

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

Mutant Cohesin in Premature Ovarian Failure

(2014) Sandrine Caburet et al.   NEW ENGLAND JOURNAL OF MEDICINE

Androgens regulate ovarian follicular development by increasing follicle stimulating hormone receptor and microRNA-125b expression

(2014) A. Sen et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Spire and Formin 2 Synergize and Antagonize in Regulating Actin Assembly in Meiosis by a Ping-Pong Mechanism

(2014) Pierre Montaville et al.   PLOS BIOLOGY

Clinical Significance of De Novo and Inherited Copy-Number Variation

(2013) Anneke T. Vulto-van Silfhout et al.   HUMAN MUTATION

Gene Expression of Catalytic Proteasome Subunits and Resistance Toward Proteasome Inhibition of B Lymphocytes from Patients with Primary Sjogren Syndrome

(2013) L. Martinez-Gamboa et al.   JOURNAL OF RHEUMATOLOGY

The Database of Genomic Variants: a curated collection of structural variation in the human genome

(2013) Jeffrey R. MacDonald et al.   NUCLEIC ACIDS RESEARCH

TBP Dynamics during Mouse Oocyte Meiotic Maturation and Early Embryo Development

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

Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure

(2013) Artur Beke et al.   Molecular Cytogenetics

Primer3—new capabilities and interfaces

(2012) Andreas Untergasser et al.   NUCLEIC ACIDS RESEARCH

XX Ovarian Dysgenesis Is Caused by a PSMC3IP/HOP2 Mutation that Abolishes Coactivation of Estrogen-Driven Transcription

(2011) David Zangen et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Review on Autoimmune Reactions in Female Infertility: Antibodies to Follicle Stimulating Hormone

(2011) Kadri Haller-Kikkatalo et al.   Clinical & Developmental Immunology

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

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants

(2011) Hutton M Kearney et al.   GENETICS IN MEDICINE

g:Profiler—a web server for functional interpretation of gene lists (2011 update)

(2011) Jüri Reimand et al.   NUCLEIC ACIDS RESEARCH

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

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

Genes involved in human premature ovarian failure

(2010) Luca Persani et al.   JOURNAL OF MOLECULAR ENDOCRINOLOGY

Premature ovarian failure

(2010) Andrew N Shelling   REPRODUCTION

Copy Number Variants in Premature Ovarian Failure and Ovarian Dysgenesis

(2010) S. Ledig et al.   Sexual Development

Predicting Meiotic Pathways in Human Fetal Oogenesis1

(2009) Ping Zheng et al.   BIOLOGY OF REPRODUCTION

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

Premature menopause or early menopause: Long-term health consequences

(2009) Lynne T. Shuster et al.   MATURITAS

The differential transcriptome and ontology profiles of floating and cumulus granulosa cells in stimulated human antral follicles

(2009) S. Kõks et al.   MOLECULAR HUMAN REPRODUCTION

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

The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report

(2008) Ricardo Azziz et al.   FERTILITY AND STERILITY

Shugoshin-2 is essential for the completion of meiosis but not for mitotic cell division in mice

(2008) E. Llano et al.   GENES & DEVELOPMENT

Cellular and molecular aspects of ovarian follicle ageing

(2008) Carla Tatone et al.   HUMAN REPRODUCTION UPDATE

Menopause and the Menopausal Transition

(2008) Kirsten J. Lund   MEDICAL CLINICS OF NORTH AMERICA

Systematic assessment of copy number variant detection via genome-wide SNP genotyping

(2008) Gregory M Cooper et al.   NATURE GENETICS