Evidence map›Paper›PMID 33981037›Full record

ArticleNature2021

Lineage tracing of human development through somatic mutations.

Michael Spencer Chapman, Anna Maria Ranzoni, Brynelle Myers, Nicholas Williams, Tim H H Coorens, Emily Mitchell, Timothy Butler, Kevin J Dawson, Yvette Hooks, Luiza Moore and 6 more

Abstract 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 102 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 1 pooled it
9.5field-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

102 citing papers in PubMed, 1 synthesis or guideline pooled it, 156 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Clonal selection of somatic mutations shapes NK cell memory.bioRxiv : the preprint server for biology · 2026
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42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 1 country.

Michael Spencer Chapman *Wellcome Trust Sanger Institute, Hinxton, UK.
Anna Maria Ranzoni *Wellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-2573-1382
Brynelle MyersWellcome Trust Sanger Institute, Hinxton, UK.
Nicholas WilliamsWellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0003-3989-9167
Tim H H CoorensWellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-5826-3554
Emily MitchellWellcome Trust Sanger Institute, Hinxton, UK.
Timothy ButlerWellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5803-1035
Kevin J DawsonWellcome Trust Sanger Institute, Hinxton, UK.
Yvette HooksWellcome Trust Sanger Institute, Hinxton, UK.
Luiza MooreWellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0001-5315-516X
Jyoti NangaliaWellcome Trust Sanger Institute, Hinxton, UK.
Philip S RobinsonWellcome Trust Sanger Institute, Hinxton, UK.ORCID http://orcid.org/0000-0002-6237-7159
Kenichi YoshidaWellcome Trust Sanger Institute, Hinxton, UK.
Elizabeth HookDepartment of Histopathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Peter J CampbellWellcome Trust Sanger Institute, Hinxton, UK. pc8@sanger.ac.uk.ORCID http://orcid.org/0000-0002-3921-0510
Ana CvejicWellcome Trust Sanger Institute, Hinxton, UK. as889@cam.ac.uk.ORCID http://orcid.org/0000-0003-3204-9311
Wellcome/MRC Cambridge Stem Cell Institute · GBWellcome Sanger Institute · GBCambridge University Hospitals NHS Foundation Trust · GBImperial College Healthcare NHS Trust · GBUniversity of Cambridge · GB

Funding

Cancer Research UK 23917European Research CouncilMedical Research Council MC_PC_17230Medical Research Council MR/M008975/1Medical Research Council MR/R006237/1Wellcome Trust 203151/Z/16/Z
6 · The paper itself

Abstract

The ontogeny of the human haematopoietic system during fetal development has previously been characterized mainly through careful microscopic observations

Indexed as

MutationBlood CellsCell LineageClone CellsDNA Mutational AnalysisEmbryonic DevelopmentFetusGerm LayersHealthHematopoietic SystemHumansKaryotypingMaleMesodermMutation RateOrgan Specificity

Identifiers

PMID33981037
OpenAlexW3160871525

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.