Evidence map›Paper›PMID 35916372›Full record

ArticleeLife2022

A paternal bias in germline mutation is widespread in amniotes and can arise independently of cell division numbers.

Marc de Manuel, Felix L Wu, Molly Przeworski

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
22.1field-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

44 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Dynamics of mutators of arbitrary dominance in humans.bioRxiv : the preprint server for biology · 2026
    Article
  4. EstimatingbioRxiv : the preprint server for biology · 2026
    Article
  5. Article
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  8. Evolution of the highest fidelity DNA replication systems.bioRxiv : the preprint server for biology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. What sets the mutation rate of a cell type in an animal species?bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Review
  15. Direct identification ofbioRxiv : the preprint server for biology · 2025
    Article
  16. Article
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  18. Review
  19. Genomic origins and evolution of neo-sex chromosomes in Pacific Island birds.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  20. Article
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

3 authors at 1 institution in 1 country.

Marc de Manuel *Department of Biological Sciences, Columbia University, New York, United States.ORCID 0000-0002-1245-0127
Felix L Wu *Department of Biological Sciences, Columbia University, New York, United States.ORCID 0000-0002-0155-9071
Molly PrzeworskiDepartment of Systems Biology, Columbia University, New York, United States.ORCID 0000-0002-5369-9009
Columbia University · US

Funding

Mutation rate variation in primatesR01GM122975 · NIGMS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI PRZEWORSKI, MOLLY F · 2017 to 2020
$1.6M
NIGMS NIH HHS R01 GM122975
6 · The paper itself

Abstract

In humans and other mammals, germline mutations are more likely to arise in fathers than in mothers. Although this sex bias has long been attributed to DNA replication errors in spermatogenesis, recent evidence from humans points to the importance of mutagenic processes that do not depend on cell division, calling into question our understanding of this basic phenomenon. Here, we infer the ratio of paternal-to-maternal mutations,

Indexed as

Germ-Line MutationHominidaeAnimalsBirdsCell DivisionFathersFemaleHumansMaleMammalsMutationSex Chromosomesamniotesdna damagedna repairevolutionary biologygeneticsgenomicsgermline mutationnonesex differences

Identifiers

PMID35916372
PMCPMC9439683
OpenAlexW4289522729

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.