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Article

Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.

Genetic epidemiology - 1 Sept 2008

Hunter Jessica Ezzell, Epstein Michael P, Tinker Stuart W, Charen Krista H, Sherman Stephanie L

Abstract excerpt

The fragile X mental retardation gene (FMR1) contains a CGG repeat sequence in its 5' untranslated region that can become unstable and expand in length from generation to generation. Alleles with expanded repeats in the range of approximately 55-199, termed premutation alleles, are associated wit...

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Share to Age of Onset
Share to Fragile X Mental Retardation Protein
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Proportional Hazards Models

Share to Quantitative Trait, Heritable

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Source

Open in PubMed Open full text

Identifiers

PMID: 18357616
DOI: 10.1002/gepi.20329
PMCID: PMC2881575

Genes

FMR1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-18357616-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

Related research

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Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.PMID 18357616Read ↗

Predictors and risk model development for menopausal age in fragile X premutation carriers.Semantic proximity Read ↗

FMR1 and the continuum of primary ovarian insufficiency.Semantic proximity Read ↗

Fragile X premutation in women: recognizing the health challenges beyond primary ovarian insufficiency.Semantic proximity Read ↗

PGT-M for Premature Ovarian Failure Related to CGG Repeat Expansion of the FMR1 Gene.Semantic proximity Read ↗

Reproductive and gynecologic care of women with fragile X primary ovarian insufficiency (FXPOI).Semantic proximity Read ↗

Large-scale analysis of FMR1 CGG repeat length and risk of premature ovarian insufficiency in over 92 000 women.Semantic proximity Read ↗

FMR1 allelic complexity in premutation carriers provides no evidence for a correlation with age at amenorrhea.Semantic proximity Read ↗

Identifying susceptibility genes for primary ovarian insufficiency on the high-risk genetic background of a fragile X premutation.Semantic proximity Read ↗

Premature ovarian failure in the fragile X syndrome.Semantic proximity Read ↗

Clustering of comorbid conditions among women who carry an FMR1 premutation.Semantic proximity Read ↗

Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency.Semantic proximity Read ↗

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

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