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Association of FMR1 repeat size with ovarian dysfunction

Human Reproduction · 2004 · Vol. 20(2) · pp. 402–412
Amy K. SullivanMichele MarcusMichael P. EpsteinEmily G. AllenAimee AnidoJasmine PaquinManeesha Yadav-ShahStephanie L. Sherman

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
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