No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers.

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

Who cites it

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 53 citations in OpenAlex.

1. ACMG Standards and Guidelines for fragile X testing: a revision to the disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics and Genomics.Genetics in medicine : official journal of the American College of Medical Genetics · 2013
   Guideline
2. Genetic counseling for fragile x syndrome: updated recommendations of the national society of genetic counselors.Journal of genetic counseling · 2005
   Guideline
3. Native functions of short tandem repeats.eLife · 2023
   Article
4. Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).Genetics in medicine : official journal of the American College of Medical Genetics · 2021
   Article
5. Fragile X-Associated Diminished Ovarian Reserve and Primary Ovarian Insufficiency from Molecular Mechanisms to Clinical Manifestations.Frontiers in molecular neuroscience · 2017
   Review
6. Early menopause: A hazard to a woman's health.The Indian journal of medical research · 2016
   Review
7. Repeat-mediated genetic and epigenetic changes at the FMR1 locus in the Fragile X-related disorders.Frontiers in genetics · 2014
   Review
8. Pathogenesis and causes of premature ovarian failure: an update.International journal of fertility & sterility · 2011
   Review
9. FMR1: a gene with three faces.Biochimica et biophysica acta · 2009
   Review
10. Expanded clinical phenotype of women with the FMR1 premutation.American journal of medical genetics. Part A · 2008
    Article
11. An enhanced polymerase chain reaction assay to detect pre- and full mutation alleles of the fragile X mental retardation 1 gene.The Journal of molecular diagnostics : JMD · 2005
    Article
12. Premature ovarian failure among fragile X premutation carriers: parent-of-origin effect?American journal of human genetics · 2000
    Article

Corrections and comments

• Commented on by
  Premature ovarian failure among fragile X premutation carriers: parent-of-origin effect?2000
• Comment on
  Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations.2000

Authors and funding

3 authors at 1 institution in 1 country.

Funding

No grant is acknowledged in the PubMed record.

Abstract

PubMed holds no abstract for this paper.

Indexed as