Evidence map›Paper›PMID 26135290›Full record

ReviewSeminars in cell & developmental biology2015

Intergenerational epigenetic inheritance in models of developmental programming of adult disease.

Denise S Fernandez-Twinn, Miguel Constância, Susan E Ozanne

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
21.8field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 97 citations in OpenAlex.

  1. Review
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  5. How Early-Life Programming During Embryogenesis Imprints Cellular Memory.International journal of molecular sciences · 2025
    Review
  6. Article
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  8. Antioxidants: powering the fight against fetal hypoxia.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
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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

3 authors at 2 institutions in 1 country.

Denise S Fernandez-TwinnUniversity of Cambridge Metabolic Research Laboratories, MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Box 289, Addenbrookes Treatment Centre, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom.
Miguel ConstânciaUniversity of Cambridge Metabolic Research Laboratories, MRC Metabolic Diseases Unit, Department of Obstetrics and Gynaecology, United Kingdom; National Institute for Health Research Cambridge Biomedical Research Centre, University of Cambridge, United Kingdom; Centre for Trophoblast Research, University of Cambridge, United Kingdom.
Susan E OzanneUniversity of Cambridge Metabolic Research Laboratories, MRC Metabolic Diseases Unit, Wellcome Trust-MRC Institute of Metabolic Science, Level 4, Box 289, Addenbrookes Treatment Centre, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom. Electronic address: seo10@cam.ac.uk.
University of Cambridge · GBAddenbrooke's Hospital · GB

Funding

Biotechnology and Biological Sciences Research Council BB/D01235X/1Biotechnology and Biological Sciences Research Council BB/D01235X/2British Heart Foundation FS/09/029/27902Medical Research Council MC UU 12012/4Medical Research Council MC_UU_12012/4Medical Research Council MC_UU_12012/5Medical Research Council MR/J001562/1
6 · The paper itself

Abstract

It is now well established that the environment to which we are exposed during fetal and neonatal life can have a long-term impact on our health. This has been termed the developmental origins of health and disease. Factors known to have such programming effects include intrauterine nutrient availability (determined by maternal nutrition and placental function), endocrine disruptors, toxins and infectious agents. Epigenetic processes have emerged as a key mechanism by which the early environment can permanently influence cell function and metabolism after multiple rounds of cell division. More recently it has been suggested that programmed effects can be observed beyond the first generation and that therefore epigenetic mechanisms could form the basis of transmission of phenotype from parent to child to grandchild and beyond. Here we review the evidence for such processes.

Indexed as

Cell DivisionChromatinDNA MethylationEnvironmental ExposureEpigenesis, GeneticFemaleHistonesHumansInheritance PatternsMaternal Nutritional Physiological PhenomenaMicroRNAsModels, GeneticChromatinHistonesMicroRNAsChromatinDevelopmental programmingGlobal nutrient restrictionHistone modificationsIntergenerational epigenetic inheritanceIntrauterine growth restrictionMaternal obesityMaternal protein restrictionMethylationMicroRNAspiRNAs

Identifiers

PMID26135290
PMCPMC5844462
OpenAlexW805964733

What OpenQuestion holds

Textmetadata
LicenceTDM
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.