Evidence map›Paper›PMID 34646017›Full record

ArticleNature2021

Convergent somatic mutations in metabolism genes in chronic liver disease.

Stanley W K Ng, Foad J Rouhani, Simon F Brunner, Natalia Brzozowska, Sarah J Aitken, Ming Yang, Federico Abascal, Luiza Moore, Efterpi Nikitopoulou, Lia Chappell and 21 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Nature, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 122 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
122citing papers in PubMed, 1 pooled it
22.0field-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

122 citing papers in PubMed, 1 synthesis or guideline pooled it, 187 citations in OpenAlex.

  1. Pooled it
  2. Inhibition of Acetylation Activity of p300/CBP Ameliorates Hepatic Steatosis Through Downregulation of ACSL4.Liver international : official journal of the International Association for the Study of the Liver · 2026
    Article
  3. Review
  4. Review
  5. Review
  6. Genetic testing in liver diseases: Clinical applications.JHEP reports : innovation in hepatology · 2026
    Review
  7. [Proportion and clinical characteristics of probable metabolic-associated fatty liver disease-related cirrhosis in cryptogenic cirrhosis].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2026
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

62 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

31 authors at 5 institutions in 2 countries.

Stanley W K NgCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Foad J RouhaniCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Simon F BrunnerCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5935-6189
Natalia BrzozowskaCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Sarah J AitkenCRUK Cambridge Institute, Cambridge, UK.ORCID http://orcid.org/0000-0002-1897-4140
Ming YangMRC Cancer Unit, University of Cambridge, Cambridge, UK.
Federico AbascalCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-6201-1587
Luiza MooreCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5315-516X
Efterpi NikitopoulouMRC Cancer Unit, University of Cambridge, Cambridge, UK.
Lia ChappellCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Daniel LeongamornlertCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-3486-3168
Aleksandra IvovicCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Philip RobinsonCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-6237-7159
Timothy ButlerCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5803-1035
Mathijs A SandersCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Nicholas WilliamsCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-3989-9167
Tim H H CoorensCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5826-3554
Jon TeagueCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Keiran RaineCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5634-1539
Adam P ButlerCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Yvette HooksCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Beverley WilsonCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Natalie BirtchnellCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.
Huw NaylorDepartment of Surgery, Addenbrooke's Hospital, Cambridge, UK.ORCID http://orcid.org/0000-0001-8264-8596
Susan E DaviesDepartment of Pathology, Addenbrooke's Hospital, Cambridge, UK.
Michael R StrattonCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-6035-153X
Iñigo MartincorenaCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-1122-4416
Raheleh RahbariCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-1839-7785
Christian FrezzaMRC Cancer Unit, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-3293-7397
Matthew HoareCRUK Cambridge Institute, Cambridge, UK. Matthew.Hoare@cruk.cam.ac.uk.ORCID http://orcid.org/0000-0001-5990-9604
Peter J CampbellCancer Genome Project, Wellcome Sanger Institute, Hinxton, UK. pc8@sanger.ac.uk.ORCID http://orcid.org/0000-0002-3921-0510
Wellcome Sanger Institute · GBUniversity of Cambridge · GBAddenbrooke's Hospital · GBErasmus MC · NLWellcome/MRC Cambridge Stem Cell Institute · GB

Funding

Cancer Research UK 19924Cancer Research UK 21777Cancer Research UK 26813Cancer Research UK 27114Cancer Research UK 29681Medical Research Council MC_UP_1101/3Medical Research Council MC_UU_12022/6Wellcome Trust
6 · The paper itself

Abstract

The progression of chronic liver disease to hepatocellular carcinoma is caused by the acquisition of somatic mutations that affect 20-30 cancer genes

Indexed as

Active Transport, Cell NucleusApoptosis Regulatory ProteinsCell Line, TumorChronic DiseaseCohort StudiesFatty Acids, NonesterifiedFemaleForkhead Box Protein O1HumansInsulin ResistanceLiverLiver DiseasesLiver Diseases, AlcoholicMaleMutationNon-alcoholic Fatty Liver DiseaseApoptosis Regulatory ProteinsCIDEB protein, humanFatty Acids, NonesterifiedForkhead Box Protein O1FOXO1 protein, humanTriglycerides

Identifiers

PMID34646017
OpenAlexW3206615564

What Socratic holds

Textmetadata
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.