Evidence map›Paper›PMID 23751783›Full record

ArticleEpigenetics2013

Large offspring syndrome: a bovine model for the human loss-of-imprinting overgrowth syndrome Beckwith-Wiedemann.

Zhiyuan Chen, Katherine Marie Robbins, Kevin Dale Wells, Rocío Melissa Rivera

Open access · hybridAbstract read
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
7.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 151 citations in OpenAlex.

  1. The Maternal Blood Transcriptome Reflects Molecular Signatures Associated With Large Offspring Syndrome and Other Adverse Pregnancy Outcomes in Cattle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Review
  3. Animal reproduction · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Nature does it better: mimickingFrontiers in veterinary science · 2025
    Review
  9. Review
  10. Article
  11. Article
  12. Livestock species as emerging models for genomic imprinting.Frontiers in cell and developmental biology · 2024
    Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Epigenetic Reprogramming and Somatic Cell Nuclear Transfer.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  18. Article
  19. Review
  20. Insights from one thousand cloned dogs.Scientific reports · 2022
    Article

9 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Zhiyuan ChenDivision of Animal Sciences; University of Missouri; Columbia, MO USA.
Katherine Marie Robbins
Kevin Dale Wells
Rocío Melissa Rivera
University of Missouri · USInstitute of Animal Sciences · CN

Funding

Establishment of a phenotypical model of adverse outcomes associated with ARTR21HD062920 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI RIVERA, ROCIO MELISSA, WELLS, KEVIN DALE · 2010 to 2011
$364k
NCI NIH HHS CB000384NICHD NIH HHS 5R21HD062920
6 · The paper itself

Abstract

Beckwith-Wiedemann syndrome (BWS) is a human loss-of-imprinting syndrome primarily characterized by macrosomia, macroglossia, and abdominal wall defects. BWS has been associated with misregulation of two clusters of imprinted genes. Children conceived with the use of assisted reproductive technologies (ART) appear to have an increased incidence of BWS. As in humans, ART can also induce a similar overgrowth syndrome in ruminants which is referred to as large offspring syndrome (LOS). The main goal of our study is to determine if LOS shows similar loss-of-imprinting at loci known to be misregulated in BWS. To test this, Bos taurus indicus × Bos taurus taurus F1 hybrids were generated by artificial insemination (AI; control) or by ART. Seven of the 27 conceptuses in the ART group were in the > 97th percentile body weight when compared with controls. Further, other characteristics reported in BWS were observed in the ART group, such as large tongue, umbilical hernia, and ear malformations. KCNQ1OT1 (the most-often misregulated imprinted gene in BWS) was biallelically-expressed in various organs in two out of seven overgrown conceptuses from the ART group, but shows monoallelic expression in all tissues of the AI conceptuses. Furthermore, biallelic expression of KCNQ1OT1 is associated with loss of methylation at the KvDMR1 on the maternal allele and with downregulation of the maternally-expressed gene CDKN1C. In conclusion, our results show phenotypic and epigenetic similarities between LOS and BWS, and we propose the use of LOS as an animal model to investigate the etiology of BWS.

Indexed as

Disease Models, AnimalGenomic ImprintingAnimalsBeckwith-Wiedemann SyndromeCattleCattle DiseasesCyclin-Dependent Kinase Inhibitor p57DNA MethylationFemaleFertilization in VitroFetusGene Expression Regulation, DevelopmentalGrowth DisordersHumansMaleNuclear ProteinsCDKN1C protein, humanCyclin-Dependent Kinase Inhibitor p57Nuclear ProteinsTSSC3 proteinBWSepigeneticsgenomic imprintingKCNQ1OT1KvDMR1LOS

Identifiers

PMID23751783
PMCPMC3857339
OpenAlexW2034417921

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.