Evidence map›Paper›PMID 33931130›Full record

ReviewGenome biology2021

Genetic impacts on DNA methylation: research findings and future perspectives.

Sergio Villicaña, Jordana T Bell

Open access · goldAbstract readReview
In one paragraph

Review in Genome biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 152 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
152citing papers in PubMed, 4 pooled it
24.0field-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

152 citing papers in PubMed, 4 syntheses or guidelines pooled it, 257 citations in OpenAlex.

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92 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

2 authors at 1 institution in 1 country.

Sergio VillicañaDepartment of Twin Research and Genetic Epidemiology, St. Thomas' Hospital, King's College London, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK. sergio.artsc@gmail.com.ORCID 0000-0002-2455-7095
Jordana T BellDepartment of Twin Research and Genetic Epidemiology, St. Thomas' Hospital, King's College London, 3rd Floor, South Wing, Block D, London, SE1 7EH, UK.
St Thomas' Hospital · GB

Funding

Biotechnology and Biological Sciences Research Council BB/S020845/1
6 · The paper itself

Abstract

Multiple recent studies highlight that genetic variants can have strong impacts on a significant proportion of the human DNA methylome. Methylation quantitative trait loci, or meQTLs, allow for the exploration of biological mechanisms that underlie complex human phenotypes, with potential insights for human disease onset and progression. In this review, we summarize recent milestones in characterizing the human genetic basis of DNA methylation variation over the last decade, including heritability findings and genome-wide identification of meQTLs. We also discuss challenges in this field and future areas of research geared to generate insights into molecular processes underlying human complex traits.

Indexed as

DNA MethylationEpigenesis, GeneticGene Expression RegulationAllelesAnimalsCpG IslandsDatabases, GeneticGene-Environment InteractionGenomeGenome-Wide Association StudyGenomicsHumansInheritance PatternsModels, BiologicalOrgan SpecificityQuantitative Trait, HeritableDNA methylationGWASHeritabilitymeQTLMethylation quantitative trait loci

Identifiers

PMID33931130
PMCPMC8086086
OpenAlexW3157163834

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.