Evidence map›Paper›PMID 41006719›Full record

ArticleCommunications biology2025

Archaic adaptive introgression in modern human reproductive genes.

Christopher Kendall, Amin Nooranikhojasteh, Esteban J Parra, Michael A Schillaci, Bence Viola

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

5 authors.

Christopher KendallNeurosciences and Mental Health Department, The Hospital for Sick Children, Toronto, ON, Canada. chris.kendall@sickkids.ca.ORCID http://orcid.org/0000-0003-2252-0106
Amin NooranikhojastehEpigenome Lab, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0009-0009-4265-2406
Esteban J ParraDepartment of Anthropology, University of Toronto Mississauga, Mississauga, ON, Canada.ORCID http://orcid.org/0000-0002-2057-8577
Michael A SchillaciDepartment of Anthropology, University of Toronto Scarborough, Scarborough, ON, Canada.
Bence ViolaDepartment of Anthropology, University of Toronto, Toronto, ON, Canada.ORCID http://orcid.org/0000-0001-8052-707X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modern humans and archaic hominins, namely Denisovans and Neanderthals, have a long history of admixture. Some of these admixture events have allowed modern humans to adapt to new environments outside of Africa. Little research has been done on the impact of archaic introgression on genes associated with reproduction. In this study we report evidence of adaptive introgression of 118 genes within modern humans that have been previously associated with reproduction in mice or modern humans. We identified 11 archaic core haplotypes, three that have been positively selected, with 327 archaic alleles being genome-wide significant for a variety of traits. Over 300 of these variants were discovered to be eQTLs regulating 176 genes with 81% of the archaic eQTLs overlapping a core haplotype region regulating genes expressed in reproductive tissues. Several of the adaptively introgressed genes in our results are enriched in developmental and cancer pathways, while some have been associated with embryo development and reproductive-inhibiting phenotypes like endometriosis and preeclampsia. Lastly, we find that archaic alleles overlapping an introgressed segment on chromosome 2 are protective against prostate cancer. Our results highlight that archaic alleles show connections with important developmental pathways throughout the lifespan and may help regulate these critical processes.

Indexed as

Genetic IntrogressionHominidaeReproductionAllelesAnimalsFemaleHaplotypesHumansMaleNeanderthalsPolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID41006719
PMCPMC12474892

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.