Evidence map›Paper›PMID 30872577›Full record

ArticleNature communications2019

Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.

Fiona Allum, Åsa K Hedman, Xiaojian Shao, Warren A Cheung, Jinchu Vijay, Frédéric Guénard, Tony Kwan, Marie-Michelle Simon, Bing Ge, Cristiano Moura and 10 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

15 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Metaboepigenetic regulation of gene expression in obesity and insulin resistance.Metabolomics : Official journal of the Metabolomic Society · 2024
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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

20 authors at 8 institutions in 4 countries.

Fiona AllumDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.ORCID http://orcid.org/0000-0002-1205-4685
Åsa K HedmanDepartment of Medicine Solna, Cardiovascular Medicine Unit, Karolinska Institute, Stockholm, 171 76, Sweden.
Xiaojian ShaoDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Warren A CheungDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Jinchu VijayDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.ORCID http://orcid.org/0000-0002-7311-475X
Frédéric GuénardInstitute of Nutrition and Functional Foods (INAF), Université Laval, Québec, QC, G1V 0A6, Canada.
Tony KwanDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.ORCID http://orcid.org/0000-0001-8929-2334
Marie-Michelle SimonDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Bing GeDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Cristiano MouraDepartment of Epidemiology, McGill University, Montréal, QC, H3A 1A2, Canada.
Elodie BoulierDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Lars RönnblomDepartment of Medical Sciences, Uppsala University, Uppsala, 751 85, Sweden.
Sasha BernatskyDepartment of Epidemiology, McGill University, Montréal, QC, H3A 1A2, Canada.
Mark LathropDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Mark I McCarthyOxford Centre for Diabetes, Endocrinology and Metabolism, Churchill Hospital, University of Oxford, Old Road, Headington, Oxford, OX3 7LJ, UK.ORCID http://orcid.org/0000-0002-4393-0510
Panos DeloukasWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Charterhouse Square, London, EC1M 6BQ, UK.ORCID http://orcid.org/0000-0001-9251-070X
André TchernofQuébec Heart and Lung Institute, Université Laval, Québec, QC, G1V 0A6, Canada.
Tomi PastinenDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada.
Marie-Claude VohlInstitute of Nutrition and Functional Foods (INAF), Université Laval, Québec, QC, G1V 0A6, Canada.
Elin GrundbergDepartment of Human Genetics, McGill University, Montréal, QC, H3A 0C7, Canada. egrundberg@cmh.edu.
McGill University and Génome Québec Innovation Centre · CAChildren's Mercy Hospital · USUniversité Laval · CAMcGill University · CACentre for Human Genetics · GBKarolinska Institutet · SEQueen Mary University of London · GBUppsala University · SE

Funding

British Heart Foundation RG/14/5/30893Wellcome Trust
6 · The paper itself

Abstract

Sparse profiling of CpG methylation in blood by microarrays has identified epigenetic links to common diseases. Here we apply methylC-capture sequencing (MCC-Seq) in a clinical population of ~200 adipose tissue and matched blood samples (N

Indexed as

Epigenesis, GeneticAdipose TissueAdultAgedCardiovascular DiseasesCpG IslandsDNA MethylationEpigenomicsFemaleGene Expression ProfilingGenome, HumanGenome-Wide Association StudyHigh-Throughput Nucleotide SequencingHumansLipidsMaleLipids

Identifiers

PMID30872577
PMCPMC6418220
OpenAlexW2921281224

What OpenQuestion 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 OpenQuestion graph.