Evidence map›Paper›PMID 34433963›Full record

ArticleNature2021

Extensive phylogenies of human development inferred from somatic mutations.

Tim H H Coorens, Luiza Moore, Philip S Robinson, Rashesh Sanghvi, Joseph Christopher, James Hewinson, Moritz J Przybilla, Andrew R J Lawson, Michael Spencer Chapman, Alex Cagan and 10 more

Open access · hybridAbstract 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 107 papers.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed
10.7field-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

107 citing papers in PubMed, 160 citations in OpenAlex.

  1. Review
  2. Clonal selection of somatic mutations shapes NK cell memory.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Disease insights from brain somatic mosaicism.Experimental & molecular medicine · 2026
    Review
  9. Review
  10. A distributive germline restricts the spread of new mutations.bioRxiv : the preprint server for biology · 2026
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Polyclonal origins of human premalignant colorectal lesions.bioRxiv : the preprint server for biology · 2025
    Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors at 4 institutions in 1 country.

Tim H H Coorens *Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5826-3554
Luiza Moore *Wellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5315-516X
Philip S RobinsonWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-6237-7159
Rashesh SanghviWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-7703-9216
Joseph ChristopherWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-2059-0154
James HewinsonWellcome Sanger Institute, Hinxton, UK.
Moritz J PrzybillaWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5645-9492
Andrew R J LawsonWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-3592-1005
Michael Spencer ChapmanWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5320-8193
Alex CaganWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-7857-4771
Thomas R W OliverWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-4306-0102
Matthew D C NevilleWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5816-7936
Yvette HooksWellcome Sanger Institute, Hinxton, UK.
Ayesha NooraniWellcome Sanger Institute, Hinxton, UK.
Thomas J MitchellWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-0761-9503
Rebecca C FitzgeraldMRC Cancer Unit, University of Cambridge, Biomedical Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-3434-3568
Peter J CampbellWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-3921-0510
Iñigo MartincorenaWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-1122-4416
Raheleh RahbariWellcome Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-1839-7785
Michael R StrattonWellcome Sanger Institute, Hinxton, UK. mrs@sanger.ac.uk.ORCID http://orcid.org/0000-0001-6035-153X
Wellcome Sanger Institute · GBUniversity of Cambridge · GBCambridge University Hospitals NHS Foundation Trust · GBImperial College Healthcare NHS Trust · GB

Funding

Cancer Research UK 21777Cancer Research UK 27114Cancer Research UK 27176Wellcome TrustWellcome Trust 203943/Z/16/Z
6 · The paper itself

Abstract

Starting from the zygote, all cells in the human body continuously acquire mutations. Mutations shared between different cells imply a common progenitor and are thus naturally occurring markers for lineage tracing

Indexed as

MutationBrainCell LineageChromosomes, Human, YClone CellsEmbryo, MammalianEmbryonic DevelopmentGerm-Line MutationHumansMaleMosaicismOrgan SpecificityPolymorphism, Single Nucleotide

Identifiers

PMID34433963
OpenAlexW3195445434

What OpenQuestion 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 OpenQuestion graph.