Evidence map›Paper›PMID 26242864›Full record

SynthesisNature communications2015

Multicohort analysis of the maternal age effect on recombination.

Hilary C Martin, Ryan Christ, Julie G Hussin, Jared O'Connell, Scott Gordon, Hamdi Mbarek, Jouke-Jan Hottenga, Kerrie McAloney, Gonnecke Willemsen, Paolo Gasparini and 11 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
–field-weighted citation impact
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

20 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Levels of Heterochiasmy DuringG3 (Bethesda, Md.) · 2020
    Article
  12. Article
  13. Variation in recombination frequency and distribution across eukaryotes: patterns and processes.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  14. The impact of recombination on human mutation load and disease.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Hilary C MartinWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX17BN, UK.
Ryan ChristWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX17BN, UK.
Julie G HussinWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX17BN, UK.
Jared O'ConnellIllumina, Inc., Chesterford Research Park, Little Chesterford CB10 1XL, UK.
Scott GordonQIMR Berghofer Medical Research Institute, Brisbane, Queensland 4006, Australia.
Hamdi MbarekDepartment for Biological Psychiatry, Vrije Universiteit, Amsterdam 1081, The Netherlands.
Jouke-Jan HottengaDepartment for Biological Psychiatry, Vrije Universiteit, Amsterdam 1081, The Netherlands.
Kerrie McAloneyQIMR Berghofer Medical Research Institute, Brisbane, Queensland 4006, Australia.
Gonnecke WillemsenDepartment for Biological Psychiatry, Vrije Universiteit, Amsterdam 1081, The Netherlands.
Paolo GaspariniInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, University of Trieste, Trieste 34137, Italy.
Nicola PirastuInstitute for Maternal and Child Health-IRCCS Burlo Garofolo, University of Trieste, Trieste 34137, Italy.
Grant W MontgomeryQIMR Berghofer Medical Research Institute, Brisbane, Queensland 4006, Australia.
Pau NavarroMRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, UK.
Nicole SoranzoWellcome Trust Sanger Institute, Hinxton CB10 1HH, UK.ORCID http://orcid.org/0000-0003-1095-3852
Daniela TonioloDivision of Genetics and Cell Biology, San Raffaele Scientific Institute, Milan 20132, Italy.
Veronique VitartMRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, UK.
James F WilsonMRC Human Genetics Unit, MRC Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh EH4 2XU, UK.
Jonathan MarchiniWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX17BN, UK.ORCID http://orcid.org/0000-0003-0610-8322
Dorret I BoomsmaDepartment for Biological Psychiatry, Vrije Universiteit, Amsterdam 1081, The Netherlands.
Nicholas G MartinQIMR Berghofer Medical Research Institute, Brisbane, Queensland 4006, Australia.
Peter DonnellyWellcome Trust Centre for Human Genetics, University of Oxford, Oxford OX17BN, UK.

Funding

Medical Research Council MC_PC_U127592696Wellcome Trust 090532Wellcome Trust 095552
6 · The paper itself

Abstract

Several studies have reported that the number of crossovers increases with maternal age in humans, but others have found the opposite. Resolving the true effect has implications for understanding the maternal age effect on aneuploidies. Here, we revisit this question in the largest sample to date using single nucleotide polymorphism (SNP)-chip data, comprising over 6,000 meioses from nine cohorts. We develop and fit a hierarchical model to allow for differences between cohorts and between mothers. We estimate that over 10 years, the expected number of maternal crossovers increases by 2.1% (95% credible interval (0.98%, 3.3%)). Our results are not consistent with the larger positive and negative effects previously reported in smaller cohorts. We see heterogeneity between cohorts that is likely due to chance effects in smaller samples, or possibly to confounders, emphasizing that care should be taken when interpreting results from any specific cohort about the effect of maternal age on recombination.

Indexed as

Crossing Over, GeneticMaternal AgeRecombination, GeneticAneuploidyBayes TheoremCohort StudiesHumansLinear ModelsModels, Genetic

Identifiers

PMID26242864
PMCPMC4580993

What OpenQuestion holds

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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.