Evidence map›Paper›PMID 32971526›Full record

ArticleNature2020

Cells of the adult human heart.

Monika Litviňuková, Carlos Talavera-López, Henrike Maatz, Daniel Reichart, Catherine L Worth, Eric L Lindberg, Masatoshi Kanda, Krzysztof Polanski, Matthias Heinig, Michael Lee and 23 more

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,138 papers.

0numbers the graph read from it
0cells of the map it votes in
1,138citing papers in PubMed
71.4field-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

1,138 citing papers in PubMed, 1,693 citations in OpenAlex.

  1. Review
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  13. A practical toolbox for modelling fibrosis in vitro.Nature biomedical engineering · 2026
    Review
  14. Optimized cardiac leukocyte isolation for flow cytometry enumeration and sorting.American journal of physiology. Heart and circulatory physiology · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. celltypeEnrich: a consensus-based scRNA-seq cluster annotation tool.bioRxiv : the preprint server for biology · 2026
    Article
  20. Article

1,078 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 11 institutions in 7 countries.

Monika Litviňuková *Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Carlos Talavera-López *Cellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Henrike Maatz *Cardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Daniel Reichart *Department of Genetics, Harvard Medical School, Boston, MA, USA.
Catherine L WorthCardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID http://orcid.org/0000-0002-1796-9606
Eric L LindbergCardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.
Masatoshi KandaCardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID http://orcid.org/0000-0003-3468-3586
Krzysztof PolanskiCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0002-2586-9576
Matthias HeinigInstitute of Computational Biology (ICB), HMGU, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-5612-1720
Michael LeeNational Heart and Lung Institute, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-0186-4439
Emily R NadelmannDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Kenny RobertsCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0001-6155-0821
Liz TuckCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Eirini S FasouliCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Daniel M DeLaughterDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Barbara McDonoughDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Hiroko WakimotoDepartment of Genetics, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0225-6424
Joshua M GorhamDepartment of Genetics, Harvard Medical School, Boston, MA, USA.
Sara SamariNational Heart and Lung Institute, Imperial College London, London, UK.
Krishnaa T MahbubaniDepartment of Surgery, University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0002-1327-2334
Kourosh Saeb-ParsyDepartment of Surgery, University of Cambridge, NIHR Cambridge Biomedical Centre, Cambridge Biorepository for Translational Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0002-0633-3696
Giannino PatoneCardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany.ORCID http://orcid.org/0000-0002-7242-0341
Joseph J BoyleNational Heart and Lung Institute, Imperial College London, London, UK.ORCID http://orcid.org/0000-0002-4337-3320
Hongbo ZhangCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.
Hao ZhangDivision of Cardiology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Anissa ViveirosDivision of Cardiology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Gavin Y OuditDivision of Cardiology, Department of Medicine, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Omer Ali BayraktarCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK.ORCID http://orcid.org/0000-0001-6055-277X
J G SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, USA. seidman@genetics.med.harvard.edu.
Christine E SeidmanDepartment of Genetics, Harvard Medical School, Boston, MA, USA. cseidman@genetics.med.harvard.edu.ORCID http://orcid.org/0000-0001-6380-1209
Michela NosedaNational Heart and Lung Institute, Imperial College London, London, UK. m.noseda@imperial.ac.uk.ORCID http://orcid.org/0000-0002-9553-5029
Norbert HubnerCardiovascular and Metabolic Sciences, Max Delbrück Center for Molecular Medicine in the Helmholtz Association (MDC), Berlin, Germany. nhuebner@mdc-berlin.de.ORCID http://orcid.org/0000-0002-1218-6223
Sarah A TeichmannCellular Genetics Programme, Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, UK. st9@sanger.ac.uk.ORCID http://orcid.org/0000-0002-6294-6366
Harvard University · USMax Delbrück Center · DEWellcome Sanger Institute · GBUniversity of Alberta · CAImperial College London · GBUniversity of Cambridge · GBBrigham and Women's Hospital · USBritish Heart Foundation · GBEuropean Bioinformatics Institute · GBSapporo Medical University · JPTechnical University of Munich · DE

Funding

Defining Pathways from Gene Mutation to Heart FailureR01HL080494 · NHLBI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI CHEN, CHRISTOPHER S, SEIDMAN, CHRISTINE E · 2005 to 2024
$9.4M
Regulation of Cardiac Development in Health and DiseaseUM1HL098166 · NHLBI · HARVARD MEDICAL SCHOOL · PI PENNACCHIO, LEN ALEXANDER, PU, WILLIAM TSWENCHING · 2015 to 2019
$4.4M
NHLBI NIH HHS R01 HL080494NHLBI NIH HHS UM1 HL098166Wellcome Trust
6 · The paper itself

Abstract

Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies.

Indexed as

Single-Cell AnalysisTranscriptomeAdipocytesAdultAngiotensin-Converting Enzyme 2Epithelial CellsEpitheliumFemaleFibroblastsGene Expression ProfilingGenome-Wide Association StudyHeart AtriaHeart VentriclesHomeostasisHumansMacrophagesACE2 protein, humanAngiotensin-Converting Enzyme 2Receptors, Coronavirus

Identifiers

PMID32971526
PMCPMC7681775
OpenAlexW3088401235

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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.