Evidence map›Paper›PMID 23381558›Full record

ReviewNature reviews. Rheumatology2013

Genetics and epigenetics of rheumatoid arthritis.

Sebastien Viatte, Darren Plant, Soumya Raychaudhuri

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 7 pooled it
20.5field-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

190 citing papers in PubMed, 7 syntheses or guidelines pooled it, 387 citations in OpenAlex.

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  11. Immune responses in aging adults.The Journal of clinical investigation · 2026
    Review
  12. Review
  13. Review
  14. Hypomethylation of the HumanArchives of Iranian medicine · 2026
    Article
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130 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

3 authors at 3 institutions in 2 countries.

Sebastien ViatteArthritis Research UK Epidemiology Unit, Manchester Academic Health Science Centre, The University of Manchester, Stopford Building, Oxford Road, Manchester M13 9PT, UK.
Darren Plant
Soumya Raychaudhuri
Brigham and Women's Hospital · USManchester Academic Health Science Centre · GBUniversity of Manchester · GB

Funding

Genetic predictors of response to anti-TNF therapy in rheumatoid arthritisU01GM092691 · NIGMS · BRIGHAM AND WOMEN'S HOSPITAL · PI BRENNER, MICHAEL B., RAYCHAUDHURI, SOUMYA · 2010 to 2014
$7.5M
Discovery and Functional Impact of Common and Rare Variants in RAR01AR063759 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Soumya Raychaudhuri · 2013 to 2026
$5.4M
Linking disease-associated variants to transcriptional regulation using ENCODEU01HG007033 · NHGRI · SLOAN-KETTERING INST CAN RESEARCH · PI KLEIN, ROBERT J. · 2012 to 2015
$1.9M
Fine-mapping the MHC associations in rheumatoid arthritis from GWAS dataR01AR062886 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI RAYCHAUDHURI, SOUMYA · 2012 to 2013
$783k
Bioinformatics and Population Genetics to Identify Rheumatoid Arthritis GenesK08AR055688 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI RAYCHAUDHURI, SOUMYA · 2008 to 2012
$724k
Arthritis Research UK 17552NHGRI NIH HHS U01 HG007033NIAMS NIH HHS 1R01AR062886NIAMS NIH HHS 5K08AR055688NIAMS NIH HHS K08 AR055688NIAMS NIH HHS R01 AR062886NIAMS NIH HHS R01 AR063759NIGMS NIH HHS U01 GM092691
6 · The paper itself

Abstract

Investigators have made key advances in rheumatoid arthritis (RA) genetics in the past 10 years. Although genetic studies have had limited influence on clinical practice and drug discovery, they are currently generating testable hypotheses to explain disease pathogenesis. Firstly, we review here the major advances in identifying RA genetic susceptibility markers both within and outside of the MHC. Understanding how genetic variants translate into pathogenic mechanisms and ultimately into phenotypes remains a mystery for most of the polymorphisms that confer susceptibility to RA, but functional data are emerging. Interplay between environmental and genetic factors is poorly understood and in need of further investigation. Secondly, we review current knowledge of the role of epigenetics in RA susceptibility. Differences in the epigenome could represent one of the ways in which environmental exposures translate into phenotypic outcomes. The best understood epigenetic phenomena include post-translational histone modifications and DNA methylation events, both of which have critical roles in gene regulation. Epigenetic studies in RA represent a new area of research with the potential to answer unsolved questions.

Indexed as

Genetic Predisposition to DiseaseAllelesArthritis, RheumatoidDNA MethylationEpigenomicsGenetic LinkageGenetic VariationGenome-Wide Association StudyGenotypeHumansHydrolasesMajor Histocompatibility ComplexPhenotypePolymorphism, Single NucleotideProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4HydrolasesPADI4 protein, humanProtein-Arginine DeiminasesProtein-Arginine Deiminase Type 4Protein Tyrosine Phosphatase, Non-Receptor Type 22PTPN22 protein, human

Identifiers

PMID23381558
PMCPMC3694322
OpenAlexW1968142189

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.