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

[Innovative genetic, clinical and endocrinologic aspects in young females affected by premature ovarian insufficiency].

Minerva ginecologica - 1 Dec 2010

Ciotta L, Pagano I, Stracquadanio M, Pafumi C, Teodoro M C, Giuffrida E

Abstract excerpt

AIM: Heterogeneity premature ovarian insufficiency (POI) is one of the reasons why there are different causes that contribute in determining this type of hormonal disorder. Although the causes have already been established for many types of premature ovarian failure, are still uncertain causes in most cases of idiopathic forms, despite the description of several candidate genes, including BMP-15 gene. The gene...

Read the complete abstract on PubMed

Topics

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

Share to Bone Morphogenetic Protein 15
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Linkage

Share to Genetic Markers

Share to Genome, Human

Share to Polymorphism, Genetic

Share to Primary Ovarian Insufficiency

Share to Transforming Growth Factor beta

Source

Identifiers

PMID: 21079571

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Innovative genetic, clinical and endocrinologic aspects in young females affected by premature ovarian insufficiency].PMID 21079571Read ↗

Cytogenetic & Molecular analysis in Premature Ovarian FailureSemantic proximity Read ↗

Characterization of a Novel Mutation V136L in Bone Morphogenetic Protein 15 Identified in a Woman Affected by POI.Semantic proximity Read ↗

"Evaluation of four genes associated with primary ovarian insufficiency in a cohort of Mexican women".Semantic proximity Read ↗

From Dominant Assumptions to Recessive Trait: Rethinking BMP15 in Ovarian Dysfunction.Semantic proximity Read ↗

Characterization of a novel mutation V136L in bone morphogenetic protein 15 identified in a woman affected by POI.Semantic proximity Read ↗

[Genetic analysis of premature ovarian failure: role of forkhead and TGF-beta genes].Semantic proximity Read ↗

Gene variation and premature ovarian failure: a meta-analysis.Semantic proximity Read ↗

Novel bone morphogenetic protein 15 (BMP15) gene variants implicated in premature ovarian insufficiency.Semantic proximity Read ↗

Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure.Semantic proximity Read ↗

Genes governing premature ovarian failure.Semantic proximity Read ↗

Premature ovarian failure (POF) syndrome: towards the molecular clinical analysis of its genetic complexity.Semantic proximity Read ↗

Hypergonadotropic ovarian failure associated with an inherited mutation of human bone morphogenetic protein-15 (BMP15) gene.Semantic proximity Read ↗

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