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Association of FMR1 repeat size with ovarian dysfunction
Human Reproduction · 2004 · Vol. 20(2) · pp. 402–412
Amy K. Sullivan(Emory University)Michele Marcus(Emory University)Michael P. Epstein(Emory University)Emily G. Allen(Emory University)Aimee Anido(Emory University)Jasmine Paquin(Emory University)Maneesha Yadav-Shah(Emory University)Stephanie L. Sherman✉(Emory University)
Abstract
We found a significant positive association of repeat size with ovarian dysfunction, but have preliminary evidence that this relationship is non-linear. We suggest that FMR1 repeat size in the lower range (<80 repeats) contributes to the variation in age at menopause; thus, FMR1 could be considered a quantitative trait locus. More importantly, when repeat size exceeds this threshold, the increase in risk for ovarian dysfunction is clinically significant. Intriguingly, this risk appears to plateau, or perhaps decrease, among women with very high repeats (> or =100 repeats).
Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder ResearchGenomic variations and chromosomal abnormalitiesFMR1MenopauseAlleleBiologyTrinucleotide repeat expansionGeneticsPremature ovarian failureLocus (genetics)Internal medicineMedicine
MeSH terms
AdolescentAdultAgedDosage Compensation, GeneticFemaleFollicle Stimulating HormoneHumansMenopause, PrematureMiddle AgedNerve Tissue ProteinsRepetitive Sequences, Nucleic AcidRisk FactorsPrevalenceRNA-Binding ProteinsPrimary Ovarian Insufficiency
Funding
- Emory University
- National Institutes of Health
Citations
497
FWCI
7.40
field-weighted impact
References
27
Percentile
98%
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Citations per year
Cited by
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References
Longitudinal Data Analysis for Discrete and Continuous Outcomes
Biometrics · 1986 · 7,806 citations
DNA methylation represses <i>FMR-1</i> transcription in fragile X syndrome
Human Molecular Genetics · 1992 · 680 citations
Estimation of Relationships for Limited Dependent Variables
Econometrica · 1958 · 6,884 citations
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