Evidence map›Paper›PMID 31604276›Full record

ArticleScience (New York, N.Y.)2019

Chromosome errors in human eggs shape natural fertility over reproductive life span.

Jennifer R Gruhn, Agata P Zielinska, Vallari Shukla, Robert Blanshard, Antonio Capalbo, Danilo Cimadomo, Dmitry Nikiforov, Andrew Chi-Ho Chan, Louise J Newnham, Ivan Vogel and 20 more

Open access · goldAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 257 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
257citing papers in PubMed, 1 pooled it
62.0field-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

257 citing papers in PubMed, 1 synthesis or guideline pooled it, 453 citations in OpenAlex.

  1. Pooled it
  2. Declining ribosome function limits oocyte longevity.bioRxiv : the preprint server for biology · 2026
    Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. From Cytoskeletal Remodeling to Oocyte Quality: The Emerging Role of Mechanics.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. A cohesion optimum underlies chromosome segregation fidelity in oocytes.bioRxiv : the preprint server for biology · 2026
    Article
  16. Probing Proteoform Heterogeneity From Single Human Oocytes.Molecular & cellular proteomics : MCP · 2026
    Article
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

30 authors at 15 institutions in 6 countries.

Jennifer R Gruhn *DNRF Center for Chromosome Stability, Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.ORCID 0000-0002-4093-142X
Agata P Zielinska *Max Planck Institute for Biophysical Chemistry, Department of Meiosis, Göttingen, Germany.ORCID 0000-0003-4208-0072
Vallari Shukla *DNRF Center for Chromosome Stability, Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.ORCID 0000-0003-3329-5418
Robert Blanshard *Genome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, UK.ORCID 0000-0002-8280-3733
Antonio CapalboIgenomix, Marostica, Italy.
Danilo CimadomoG.en.e.r.a., Centers for Reproductive Medicine, Clinica Valle Giulia, via de notaris 2b, 00197 Rome, Italy.
Dmitry NikiforovLaboratory of Reproductive Biology, The Juliane Marie Centre for Women, Children and Reproduction, Copenhagen University Hospital and Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.ORCID 0000-0002-8523-3035
Andrew Chi-Ho ChanDNRF Center for Chromosome Stability, Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Louise J NewnhamGenome Damage and Stability Centre, School of Life Sciences, University of Sussex, Brighton, UK.
Ivan VogelDNRF Center for Chromosome Stability, Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Catello ScaricaDAHFMO, Unit of Histology and Medical Embryology, Sapienza, University of Rome, Italy.
Marta KrapchevINVICTA Fertility and Reproductive Center, Gdańsk, Poland.ORCID 0000-0002-4419-1481
Deborah TaylorWarwick Medical School, University of Warwick and Centre for Reproductive Medicine, University Hospital Coventry, UK.ORCID 0000-0001-7334-5411
Stine Gry KristensenLaboratory of Reproductive Biology, The Juliane Marie Centre for Women, Children and Reproduction, Copenhagen University Hospital and Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.ORCID 0000-0003-1194-8393
Junping ChengLaboratory of Reproductive Biology, The Juliane Marie Centre for Women, Children and Reproduction, Copenhagen University Hospital and Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Erik ErnstDepartment of Obstetrics and Gynaecology, University Hospital of Aarhus, Skejby Sygehus, Aarhus, Denmark.
Anne-Mette Bay BjørnDepartment of Obstetrics and Gynaecology, University Hospital of Aarhus, Skejby Sygehus, Aarhus, Denmark.
Lotte Berdiin ColmornThe Fertility Clinic, The Juliane Marie Centre for Women, Children and Reproduction, Copenhagen University Rigshospitalet, Denmark.
Martyn BlayneyBourn Hall Clinic, Cambridge, UK.
Kay ElderBourn Hall Clinic, Cambridge, UK.ORCID 0000-0003-3510-8268
Joanna LissINVICTA Fertility and Reproductive Center, Gdańsk, Poland.ORCID 0000-0002-9199-5212
Geraldine HartshorneWarwick Medical School, University of Warwick and Centre for Reproductive Medicine, University Hospital Coventry, UK.ORCID 0000-0003-2070-8471
Marie Louise GrøndahlDepartment of Obstetrics and Gynaecology, Department of Reproductive Medicine, Copenhagen University Hospital Herlev, Denmark.
Laura RienziG.en.e.r.a., Centers for Reproductive Medicine, Clinica Valle Giulia, via de notaris 2b, 00197 Rome, Italy.
Filippo UbaldiG.en.e.r.a., Centers for Reproductive Medicine, Clinica Valle Giulia, via de notaris 2b, 00197 Rome, Italy.
Rajiv McCoyDepartment of Biology, Johns Hopkins University, Baltimore, MD, USA.ORCID 0000-0003-0615-146X
Krzysztof LukaszukINVICTA Fertility and Reproductive Center, Gdańsk, Poland.ORCID 0000-0001-5996-6991
Claus Yding AndersenLaboratory of Reproductive Biology, The Juliane Marie Centre for Women, Children and Reproduction, Copenhagen University Hospital and Faculty of Health and Medical Sciences, University of Copenhagen, Denmark.
Melina SchuhMax Planck Institute for Biophysical Chemistry, Department of Meiosis, Göttingen, Germany.ORCID 0000-0003-0025-8952
Eva R HoffmannDNRF Center for Chromosome Stability, Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Denmark. eva@sund.ku.dk.ORCID 0000-0002-2588-0652
University of Copenhagen · DKCopenhagen University Hospital · DKClinica Valle Giulia · ITAarhus University Hospital · DKBourn Hall Clinic · GBMax Planck Institute for Biophysical Chemistry · DEUniversity Hospital Coventry · GBUniversity of Sussex · GBGdańsk Medical University · PLIgenomix · ITJohns Hopkins University · USMedical University of Warsaw · PLRigshospitalet · DKSapienza University of Rome · ITUniversity of Teramo · IT

Funding

Function and fitness consequences of human genetic variationR35GM133747 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI Rajiv Champion McCoy · 2019 to 2026
$3.3M
European Research Council 337415European Research Council 724718Medical Research Council MR/M000664/1NIGMS NIH HHS R35 GM133747
6 · The paper itself

Abstract

Chromosome errors, or aneuploidy, affect an exceptionally high number of human conceptions, causing pregnancy loss and congenital disorders. Here, we have followed chromosome segregation in human oocytes from females aged 9 to 43 years and report that aneuploidy follows a U-curve. Specific segregation error types show different age dependencies, providing a quantitative explanation for the U-curve. Whole-chromosome nondisjunction events are preferentially associated with increased aneuploidy in young girls, whereas centromeric and more extensive cohesion loss limit fertility as women age. Our findings suggest that chromosomal errors originating in oocytes determine the curve of natural fertility in humans.

Indexed as

AgingAneuploidyChromosome SegregationFertilityAdolescentAdultChildFemaleHumansMeiosisNondisjunction, GeneticOocytesYoung Adult

Identifiers

PMID31604276
PMCPMC7212007
OpenAlexW2975979611

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.