Evidence map›Paper›PMID 35922514›Full record

ArticleNature2022

RNA editing underlies genetic risk of common inflammatory diseases.

Qin Li, Michael J Gloudemans, Jonathan M Geisinger, Boming Fan, François Aguet, Tao Sun, Gokul Ramaswami, Yang I Li, Jin-Biao Ma, Jonathan K Pritchard and 2 more

Open access · greenAbstract read
In one paragraph

Article in Nature, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 130 papers.

0numbers the graph read from it
0cells of the map it votes in
130citing papers in PubMed
17.3field-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

130 citing papers in PubMed, 191 citations in OpenAlex.

  1. Article
  2. Article
  3. Atlas of glomerular disease-specific genetic effects on blood transcriptome.medRxiv : the preprint server for health sciences · 2026
    Article
  4. Article
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  12. Review
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  14. Article
  15. Article
  16. ADAR-GPT: Learning the language of the epitranscriptome.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  17. Article
  18. Multi-Tissue Genetic Regulation of RNA Editing in Pigs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  19. Review
  20. Two codes of RNA editing by deamination in human diseases.Experimental & molecular medicine · 2026
    Review

70 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 4 institutions in 2 countries.

Qin LiDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-8948-2717
Michael J GloudemansDepartment of Pathology, Stanford University, Stanford, CA, USA.
Jonathan M GeisingerDepartment of Genetics, Stanford University, Stanford, CA, USA.
Boming FanState Key Laboratory of Genetic Engineering, Department of Biochemistry and Biophysics, School of Life Sciences, Fudan University, Shanghai, China.
François AguetBroad Institute of MIT and Harvard, Cambridge, MA, USA.ORCID http://orcid.org/0000-0001-9414-300X
Tao SunDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-2800-0921
Gokul RamaswamiDepartment of Genetics, Stanford University, Stanford, CA, USA.
Yang I LiDepartment of Genetics, Stanford University, Stanford, CA, USA.
Jin-Biao MaState Key Laboratory of Genetic Engineering, Department of Biochemistry and Biophysics, School of Life Sciences, Fudan University, Shanghai, China.
Jonathan K PritchardDepartment of Genetics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-8828-5236
Stephen B Montgomery *Department of Genetics, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-5200-3903
Jin Billy Li *Department of Genetics, Stanford University, Stanford, CA, USA. jin.billy.li@stanford.edu.ORCID http://orcid.org/0000-0003-0713-1399
Stanford University · USFudan University · CNBroad Institute · USUniversity of Chicago · US

Funding

POSTDOCTORAL TRAINING IN MEDICAL INFORMATION SCIENCEST15LM007033 · NLM · STANFORD UNIVERSITY · PI SYLVIA KATINA PLEVRITIS · 1985 to 2026
$25.5M
Integration of genetic association mapping and functional data to elucidate genetic mechanisms of diseaseR01HG008140 · NHGRI · STANFORD UNIVERSITY · PI JONATHAN K PRITCHARD · 2016 to 2026
$7.3M
Mapping Molecular and Phenotypic Interactions in Alzheimers DiseaseR01AG066490 · NIA · STANFORD UNIVERSITY · PI MONTGOMERY, STEPHEN · 2020 to 2024
$3.6M
Decoding the regulatory architecture of the human genome across cell types, individuals and diseaseU01HG009431 · NHGRI · STANFORD UNIVERSITY · PI PRITCHARD, JONATHAN K · 2017 to 2021
$3.5M
Regulatory and Mechanistic Understanding of ADAR-Mediated RNA EditingR35GM144100 · NIGMS · STANFORD UNIVERSITY · PI Jin Billy Li · 2022 to 2026
$3.2M
Profiling and Dissecting the Dynamic Regulation of RNA EditingR01GM102484 · NIGMS · STANFORD UNIVERSITY · PI LI, JIN BILLY · 2013 to 2021
$3.1M
Identifying causal genetic variants and molecular mechanisms impacting mental healthR01MH125244 · NIMH · STANFORD UNIVERSITY · PI KUNDAJE, ANSHUL, MONTGOMERY, STEPHEN · 2021 to 2025
$3.0M
Systematic characterization of trans regulation of A-to-I RNA editing in neuronsR01MH115080 · NIMH · STANFORD UNIVERSITY · PI LI, JIN BILLY · 2017 to 2021
$2.3M
Systematic identification and characterization of immunogenic double-stranded RNAsR01AI182437 · NIAID · STANFORD UNIVERSITY · PI Jin Billy Li · 2024 to 2026
$2.1M
Systematic approaches to deciphering cis regulation of A-to-I RNA editingR01GM124215 · NIGMS · STANFORD UNIVERSITY · PI LI, JIN BILLY · 2017 to 2020
$1.7M
HIGH RESOLUTION ALLELE SPECIFIC EXPRESSION ASSAYSU01HG007593 · NHGRI · STANFORD UNIVERSITY · PI LI, JIN BILLY · 2014 to 2016
$1.3M
American Heart Association-American Stroke Association 17IFUNP33820059NHGRI NIH HHS R01 HG008140NHGRI NIH HHS U01 HG007593NHGRI NIH HHS U01 HG009431NIAID NIH HHS R01 AI182437NIA NIH HHS R01 AG066490NIGMS NIH HHS R01 GM102484NIGMS NIH HHS R01 GM124215NIGMS NIH HHS R35 GM144100NIMH NIH HHS R01 MH115080NIMH NIH HHS R01 MH125244
6 · The paper itself

Abstract

A major challenge in human genetics is to identify the molecular mechanisms of trait-associated and disease-associated variants. To achieve this, quantitative trait locus (QTL) mapping of genetic variants with intermediate molecular phenotypes such as gene expression and splicing have been widely adopted

Indexed as

Adenosine DeaminaseGenetic Predisposition to DiseaseImmune System DiseasesInflammationRNA, Double-StrandedRNA EditingAdenosineAlu ElementsAutoimmune DiseasesGenome-Wide Association StudyHumansImmunity, InnateInosineInterferon-Induced Helicase, IFIH1InterferonsQuantitative Trait LociADAR protein, humanAdenosineAdenosine DeaminaseIFIH1 protein, humanInosineInterferon-Induced Helicase, IFIH1InterferonsRNA-Binding ProteinsRNA, Double-Stranded

Identifiers

PMID35922514
PMCPMC9790998
OpenAlexW4289637911

What OpenQuestion holds

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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.