Evidence map›Paper›PMID 35831506›Full record

ArticleNature2022

Nuclear chromosome locations dictate segregation error frequencies.

Sjoerd J Klaasen, My Anh Truong, Richard H van Jaarsveld, Isabella Koprivec, Valentina Štimac, Sippe G de Vries, Patrik Risteski, Snježana Kodba, Kruno Vukušić, Kim L de Luca and 8 more

Open access · hybridAbstract read
In one paragraph

Article in Nature, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
13.8field-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

77 citing papers in PubMed, 126 citations in OpenAlex.

  1. Genetic mechanisms of mitotic error in 840,853 blood genomes.medRxiv : the preprint server for health sciences · 2026
    Article
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  5. Article
  6. Micronuclei: origins, assays, mechanisms, diseases and treatments.Signal transduction and targeted therapy · 2026
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. The Hallmarks of Aneuploidy in Cancer and Congenital Syndromes.Annual review of genomics and human genetics · 2025
    Review
  18. Article
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 2 countries.

Sjoerd J KlaasenOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
My Anh Truong *Oncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-9450-1978
Richard H van Jaarsveld *Oncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Isabella KoprivecRuđer Bošković Institute, Zagreb, Croatia.
Valentina ŠtimacRuđer Bošković Institute, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-0398-5493
Sippe G de VriesOncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-4803-4288
Patrik RisteskiRuđer Bošković Institute, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-2137-7491
Snježana KodbaRuđer Bošković Institute, Zagreb, Croatia.
Kruno VukušićRuđer Bošković Institute, Zagreb, Croatia.
Kim L de LucaOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0002-5900-5100
Joana F MarquesOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Elianne M GerritsOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.
Bjorn BakkerDepartment of Ageing Biology/ERIBA, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Floris FoijerDepartment of Ageing Biology/ERIBA, University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.ORCID http://orcid.org/0000-0003-0989-3127
Jop KindOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands.ORCID http://orcid.org/0000-0001-7538-2638
Iva M TolićRuđer Bošković Institute, Zagreb, Croatia.ORCID http://orcid.org/0000-0003-1305-7922
Susanne M A LensOncode Institute, Centre for Molecular Medicine, University Medical Centre Utrecht, Utrecht University, Utrecht, The Netherlands.
Geert J P L KopsOncode Institute, Hubrecht Institute-KNAW (Royal Academy of Arts and Sciences) and University Medical Centre Utrecht, Utrecht, the Netherlands. g.kops@hubrecht.eu.ORCID http://orcid.org/0000-0003-3555-5295
Royal Netherlands Academy of Arts and Sciences · NLRuđer Bošković Institute · HRUtrecht University · NLUniversity Medical Center Groningen · NL

Funding

European Research Council 855158
6 · The paper itself

Abstract

Chromosome segregation errors during cell divisions generate aneuploidies and micronuclei, which can undergo extensive chromosomal rearrangements such as chromothripsis

Indexed as

AneuploidyChromosome PositioningChromosomesChromosome SegregationCell LineCell Line, TumorChromothripsisCRISPR-Associated Protein 9Growth and DevelopmentHumansInterphaseMicronuclei, Chromosome-DefectiveMitosisNeoplasmsOrganoidsSequence Analysis, DNACRISPR-Associated Protein 9

Identifiers

PMID35831506
PMCPMC9300461
OpenAlexW4285087726

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.