Evidence map›Paper›PMID 30238782›Full record

ArticleEpigenomics2018

Allele-specific methylation of imprinted genes in fetal cord blood is influenced by cis-acting genetic variants and parental factors.

Ramya Potabattula, Marcus Dittrich, Julia Böck, Larissa Haertle, Tobias Müller, Thomas Hahn, Martin Schorsch, Nady El Hajj, Thomas Haaf

Open access · hybridAbstract read
In one paragraph

Article in Epigenomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. rDNA Copy Number Variation and Methylation in Human and Mouse Sperm.International journal of molecular sciences · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. The methylation profile ofFrontiers in immunology · 2023
    Article
  9. Epigenetic Risks of Medically Assisted Reproduction.Journal of clinical medicine · 2022
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
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

9 authors at 2 institutions in 2 countries.

Ramya PotabattulaInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
Marcus DittrichInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
Julia BöckInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
Larissa HaertleInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
Tobias MüllerDepartment of Bioinformatics, Julius Maximilians University, 97074 Würzburg, Germany.
Thomas HahnFertility Center; 65189 Wiesbaden, Germany.
Martin SchorschFertility Center; 65189 Wiesbaden, Germany.
Nady El HajjInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
Thomas HaafInstitute of Human Genetics, Julius Maximilians University, 97074 Würzburg, Germany.
GTx (United States) · USUniversity of Würzburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo examine the effects of genetic variation, parental age and BMI on parental allele-specific methylation of imprinted genes in fetal cord blood samples. METHODOLOGY: We have developed SNP genotyping and deep bisulphite sequencing assays for six imprinted genes to determine parental allele-specific methylation patterns in diploid somatic tissues.

resultsMultivariate linear regression analyses revealed a negative correlation of paternal age with paternal MEG3 allele methylation in fetal cord blood. Methylation of the maternal PEG3 allele showed a positive correlation with maternal age. Paternal BMI was positively correlated with paternal MEST allele methylation. In addition to parental origin, allele-specific methylation of most imprinted genes was largely dependent on the underlying SNP haplotype.

conclusionOur study supports the idea that parental factors can have an impact, although of small effect size, on the epigenome of the next generation, providing an additional layer of complexity to phenotypic diversity.

Indexed as

AllelesDNA MethylationGenomic ImprintingAdultFemaleFetal BloodHumansMaleMaternal AgeMiddle AgedPaternal AgePolymorphism, Single Nucleotideallele-specific methylationdeep bisulphite sequencingepimutation ratesfetal cord blood samplesgenotypingimprinted genesparental age and BMI effectssingle nucleotide polymorphism haplotypesunmethylated and methylated alleles

Identifiers

PMID30238782
PMCPMC6240887
OpenAlexW2890323033

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.