Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

Fertility and sterility - 1 Apr 2011

Knauff Erik A H, Blauw Hylke M, Pearson Peter L, Kok Klaas, Wijmenga Cisca, Veldink Jan H, van den Berg Leonard H, Bouchard Philippe, Fauser Bart C J M, Franke Lude

Abstract excerpt

OBJECTIVE: To investigate whether submicroscopic copy number variants (CNVs) on the X chromosome can be identified in women with primary ovarian insufficiency (POI), defined as spontaneous secondary amenorrhea before 40 years of age accompanied by follicle-stimulating hormone levels above 40 IU/L on at least two occasions. DESIGN: Analysis of intensity data of single nucleotide polymorphism (SNP) probes generated...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Case-Control Studies
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, X

Share to Cohort Studies

Share to DNA Copy Number Variations

Share to Netherlands

Share to Primary Ovarian Insufficiency

Share to Validation Studies as Topic

Source

Identifiers

PMID: 21316664
DOI: 10.1016/j.fertnstert.2011.01.018

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Copy number variants on the X chromosome in women with primary ovarian insufficiency.PMID 21316664Read ↗

Systematic mapping and in silico reevaluation of genomic copy number variations in primary ovarian insufficiency.Semantic proximity Read ↗

X Chromosome Rearrangement Associated with Premature Ovarian Insufficiency as Diagnosed by Molecular Cytogenetic Methods: A Case Reportand review of the literatureSemantic proximity Read ↗

Analysis of X chromosome genomic DNA sequence copy number variation associated with premature ovarian failure (POF).Semantic proximity Read ↗

Array comparative genomic hybridization profiling analysis reveals deoxyribonucleic acid copy number variations associated with premature ovarian failure.Semantic proximity Read ↗

Premature ovarian insufficiency: clinical orientations for genetic testing and genetic counselingSemantic proximity Read ↗

Genetics of primary ovarian insufficiency: new developments and opportunities.Semantic proximity Read ↗

Searching for the 'X' factor: investigating the genetics of primary ovarian insufficiency.Semantic proximity Read ↗

Copy Number Variants in Premature Ovarian Failure and Ovarian DysgenesisSemantic proximity Read ↗

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

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.Semantic proximity Read ↗

Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiencySemantic proximity Read ↗

Primary ovarian insufficiency associated with autosomal abnormalities: from chromosome to genome-wide and beyondSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.