Evidence map›Paper›PMID 40992378›Full record

ArticleAmerican journal of human genetics2025

The Indian Ocean slave trade and colonial expansion resulted in strong sex-biased admixture in South Africa.

Austin W Reynolds, Haiko Schurz, Gillian Meeks, Simon Gravel, Justin W Myrick, Stacy Edington, Fernando L Mendez, Cedric J Werely, Paul D van Helden, Eileen G Hoal and 6 more

Abstract read
In one paragraph

Article in American journal of human genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

16 authors.

Austin W ReynoldsDepartment of Microbiology, Immunology, and Genetics, School of Biomedical Sciences, University of North Texas Health Science Center, Fort Worth, TX 76107, USA; Department of Anthropology, University of California, Davis, Davis, CA 95694, USA.
Haiko SchurzDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa.
Gillian MeeksProgram in Integrative Genetics and Genomics, University of California, Davis, Davis, CA 95694, USA.
Simon GravelDepartment of Human Genetics, McGill University, Montreal, QC, Canada.
Justin W MyrickUC Davis Genome Center, University of California, Davis, Davis, CA 95694, USA.
Stacy EdingtonDepartment of Biology, Baylor University, Waco, TX 76706, USA.
Fernando L MendezDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Cedric J WerelyDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa.
Paul D van HeldenDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa.
Eileen G HoalDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa.
G David PoznikDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Minju KimDepartment of Ecology and Evolution, Stony Brook University, Stony Brook, NY 11794, USA.
Caitlin UrenDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa; Centre for Bioinformatics and Computational Biology, Stellenbosch University, Stellenbosch, 7602, South Africa.
Peter A UnderhillDepartment of Genetics, Stanford University, Stanford, CA 94305, USA.
Marlo MöllerDSI-NRF Centre of Excellence for Biomedical Tuberculosis Research; South African Medical Research Council Centre for Tuberculosis Research; Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, 8000, South Africa; Centre for Bioinformatics and Computational Biology, Stellenbosch University, Stellenbosch, 7602, South Africa.
Brenna M HennDepartment of Anthropology, University of California, Davis, Davis, CA 95694, USA; UC Davis Genome Center, University of California, Davis, Davis, CA 95694, USA. Electronic address: bmhenn@ucdavis.edu.

Funding

Supplement: Improving Inference of Genetic Architecture and Selection with African GenomesR35GM133531 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HENN, BRENNA M · 2019 to 2023
$2.3M
NIGMS NIH HHS R35 GM133531
6 · The paper itself

Abstract

The colonial-period arrival of Europeans in southern Africa is associated with strong sex-biased migration by which male settlers displaced Indigenous Khoekhoe and San men. Concurrently, the importation of enslaved individuals from South Asia, Indonesia, and eastern Africa likely contributed to female-biased migration. Using genetic data from over 1,400 individuals, we examine the spatial and temporal spread of sex-biased migration from the Cape to the northern edges of the historic colonial frontier. In all regions, admixture patterns were sex biased, with evidence of a greater male contribution of European ancestry and greater female contribution of Khoe-San ancestry. While admixture among Khoe-San, European, equatorial African, and Asian groups has likely been continuous from the founding of Cape Town to the present day, we find that Khoe-San groups further north experienced a single pulse of European admixture 6-8 generations ago. European admixture was followed by additional Khoe-San gene flow, potentially reflecting an aggregation of Indigenous groups due to disruption by colonial interlopers. Male migration into the northern frontier territories was not a homogenous group of expanding Afrikaners and slaves. The Nama exhibit distinct founder effects and derive 15% of their Y chromosome haplogroups from Asian lineages, a pattern absent in the ≠Khomani San. Khoe-San ancestry from the paternal line is greatly diminished in populations from Cape Town, the Cederberg Mountains, and Upington but remains more frequent in self-identified Indigenous ethnic groups. Strikingly, we estimate that Khoe-San Y chromosomes were experiencing unprecedented population growth at the time of European arrival. Our findings shed light on the patterns of admixture and population history of South Africa as the colonial frontier expanded.

Indexed as

African PeopleBlack PeopleColonialismEnslavementHuman MigrationWhite PeopleChromosomes, Human, YEnslaved PersonsFemaleGene FlowGenetics, PopulationHumansIndian OceanMaleSouth AfricaadmixtureancestrycolonialismKhoe-Sanpopulation geneticssex biasSouth AfricaY chromosome

Identifiers

PMID40992378
PMCPMC12696499

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.