Evidence map›Paper›PMID 35466858›Full record

ArticleEpigenetics2022

Spontaneous and ART-induced large offspring syndrome: similarities and differences in DNA methylome.

Yahan Li, Jordana Sena Lopes, Pilar Coy-Fuster, Rocío Melissa Rivera

Open access · hybridAbstract read
In one paragraph

Article in Epigenetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Emerging opportunities for DNA methylation biomarkers in cattle improvement.The Journal of reproduction and development · 2026
    Review
  2. Review
  3. Article
  4. Nature does it better: mimickingFrontiers in veterinary science · 2025
    Review
  5. Article
  6. Bovine embryo productionAnimal reproduction · 2024
    Review
  7. Review
  8. Article
  9. Review
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 3 institutions in 3 countries.

Yahan LiDivision of Animal Sciences, University of Missouri, Columbia, Missouri, USA.ORCID 0000-0003-3062-4626
Jordana Sena LopesPhysiology Department. International Excellence Campus for Higher Education and Research (Campus Mare Nostrum), Universidad de Murcia, Murcia, Spain.ORCID 0000-0002-8419-7845
Pilar Coy-FusterPhysiology Department. International Excellence Campus for Higher Education and Research (Campus Mare Nostrum), Universidad de Murcia, Murcia, Spain.ORCID 0000-0002-3943-1890
Rocío Melissa RiveraDivision of Animal Sciences, University of Missouri, Columbia, Missouri, USA.ORCID 0000-0002-9832-9618
University of Missouri · USInstituto Murciano de Investigación Biosanitaria · ESUniversity of Évora · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Large/abnormal offspring syndrome (LOS/AOS) is a congenital overgrowth syndrome reported in ruminants produced by assisted reproduction (ART-LOS) which exhibit global disruption of the epigenome and transcriptome. LOS/AOS shares phenotypes and epigenotypes with the human congenital overgrowth condition Beckwith-Wiedemann syndrome. We have reported that LOS occurs spontaneously (SLOS); however, to date, no study has been conducted to determine if SLOS has the same methylome epimutations as ART-LOS. In this study, we performed whole-genome bisulphite sequencing to examine global DNA methylation in bovine SLOS and ART-LOS tissues. We observed unique patterns of global distribution of differentially methylated regions (DMRs) over different genomic contexts, such as promoters, CpG Islands, shores and shelves, as well as at repetitive sequences. In addition, we included data from two previous LOS studies to identify shared vulnerable genomic loci in LOS. Overall, we identified 320 genomic loci in LOS that have alterations in DNA methylation when compared to controls. Specifically, there are 25 highly vulnerable loci that could potentially serve as molecular markers for the diagnosis of LOS, including at the promoters of

Indexed as

Beckwith-Wiedemann SyndromeGenomic ImprintingAbnormalities, MultipleAnimalsCattleDNA MethylationEpigenomeGenetic Diseases, X-LinkedHumansIchthyosiform Erythroderma, CongenitalLimb Deformities, CongenitalReproductive Techniques, Assistedabnormal offspring syndromeassisted reproductive technologiesbovineDNA methylationgenomic imprintingIGF2Rreproductive fluidsSpontaneous large offspring syndrome

Identifiers

PMID35466858
PMCPMC9586674
OpenAlexW4225391744

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.