Evidence map›Paper›PMID 33833454›Full record

ArticleNature genetics2021

Single-cell transcriptomics of human embryos identifies multiple sympathoblast lineages with potential implications for neuroblastoma origin.

Polina Kameneva, Artem V Artemov, Maria Eleni Kastriti, Louis Faure, Thale K Olsen, Jörg Otte, Alek Erickson, Bettina Semsch, Emma R Andersson, Michael Ratz and 14 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
16.4field-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

119 citing papers in PubMed, 190 citations in OpenAlex.

  1. Review
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  8. Review
  9. Modern Mining: The Role of Single-cell RNA Sequencing in Advancing Neuroscience Research.BioEssays : news and reviews in molecular, cellular and developmental biology · 2026
    Review
  10. Article
  11. Article
  12. Article
  13. Epigenetic crosstalk in neuroblastoma development and progression.Frontiers in cell and developmental biology · 2026
    Review
  14. Review
  15. Review
  16. Article
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  18. Article
  19. HIF2α negatively regulates MYCN protein levels and promotes a low-risk noradrenergic phenotype in neuroblastoma.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 5 countries.

Polina Kameneva *Department of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Artem V Artemov *Department of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.
Maria Eleni KastritiDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.ORCID http://orcid.org/0000-0002-0563-7399
Louis FaureDepartment of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0003-4621-586X
Thale K OlsenChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Jörg OtteChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Alek EricksonDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Bettina SemschDepartment of Comparative Medicine, Karolinska Institutet, Solna, Sweden.
Emma R AnderssonDepartment of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.ORCID http://orcid.org/0000-0002-8608-625X
Michael RatzDepartment of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
Jonas FrisénDepartment of Cell and Molecular Biology, Karolinska Institutet, Solna, Sweden.
Arthur S TischlerDepartment of Pathology and Laboratory Medicine, Tufts Medical Center, Boston, MA, USA.
Ronald R de KrijgerPrincess Máxima Center for Pediatric Oncology CS, Utrecht, the Netherlands.
Thibault BouderliqueDepartment of Neuroimmunology, Center for Brain Research, Medical University of Vienna, Vienna, Austria.ORCID http://orcid.org/0000-0002-3926-990X
Natalia AkkuratovaDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden.
Maria VorontsovaEndocrinology Research Centre, Moscow, Russian Federation.
Oleg GusevInstitute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russian Federation.
Kaj FriedDepartment of Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Erik SundströmDepartment of Neurobiology, Care Sciences and Society, Karolinska Institutet, Solna, Sweden.
Shenglin MeiDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA.
Per KognerChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-2202-9694
Ninib BaryawnoChildhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Peter V KharchenkoDepartment of Biomedical Informatics, Harvard Medical School, Boston, MA, USA. peter_kharchenko@hms.harvard.edu.ORCID http://orcid.org/0000-0002-6036-5875
Igor AdameykoDepartment of Physiology and Pharmacology, Karolinska Institutet, Solna, Sweden. igor.adameyko@meduniwien.ac.at.ORCID http://orcid.org/0000-0001-5471-0356
Karolinska Institutet · SEMedical University of Vienna · ATHarvard University · USKazan Federal University · RUMoscow Institute of Physics and Technology · RUSt Petersburg University · RUTufts Medical Center · USUtrecht University · NL

Funding

Statistical methods for analysis of single-cell variabilityR01HL131768 · NHLBI · HARVARD MEDICAL SCHOOL · PI KHARCHENKO, PETER V · 2015 to 2019
$2.4M
Austrian Science Fund FWF DOC 33Austrian Science Fund FWF I 3733European Research Council 647844NHLBI NIH HHS R01 HL131768
6 · The paper itself

Abstract

Characterization of the progression of cellular states during human embryogenesis can provide insights into the origin of pediatric diseases. We examined the transcriptional states of neural crest- and mesoderm-derived lineages differentiating into adrenal glands, kidneys, endothelium and hematopoietic tissue between post-conception weeks 6 and 14 of human development. Our results reveal transitions connecting the intermediate mesoderm and progenitors of organ primordia, the hematopoietic system and endothelial subtypes. Unexpectedly, by using a combination of single-cell transcriptomics and lineage tracing, we found that intra-adrenal sympathoblasts at that stage are directly derived from nerve-associated Schwann cell precursors, similarly to local chromaffin cells, whereas the majority of extra-adrenal sympathoblasts arise from the migratory neural crest. In humans, this process persists during several weeks of development within the large intra-adrenal ganglia-like structures, which may also serve as reservoirs of originating cells in neuroblastoma.

Indexed as

Cell LineageSingle-Cell AnalysisAnimalsChromaffin CellsCluster AnalysisEmbryo, MammalianEmbryonic DevelopmentGene Expression Regulation, DevelopmentalGene Expression Regulation, NeoplasticHumansInfantMiceNeural Stem CellsNeuroblastomaSchwann CellsSympathoadrenal System

Identifiers

PMID33833454
PMCPMC7610777
OpenAlexW3143387950

What OpenQuestion holds

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Registered trials

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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.