Evidence map›Paper›PMID 41493817›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Sudan's complex genetic admixture history drives adaptation to malaria in Sudanese Copts.

Laura Vilà-Valls, Jorge Garcia-Calleja, Javier Prado-Martinez, Elena Bosch, Aida M Andrés, Mihai G Netea, David Comas, Hisham Y Hassan

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Laura Vilà-VallsInstitute of Evolutionary Biology (Consejo Superior de Investigaciones Científicas - Universitat Pompeu Fabra), Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.ORCID 0000-0002-9027-304X
Jorge Garcia-CallejaInstitute of Evolutionary Biology (Consejo Superior de Investigaciones Científicas - Universitat Pompeu Fabra), Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.ORCID 0000-0002-4614-4574
Javier Prado-MartinezInstitute of Evolutionary Biology (Consejo Superior de Investigaciones Científicas - Universitat Pompeu Fabra), Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.ORCID 0000-0001-5402-2721
Elena BoschInstitute of Evolutionary Biology (Consejo Superior de Investigaciones Científicas - Universitat Pompeu Fabra), Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.ORCID 0000-0003-2848-103X
Aida M AndrésDivision of Biosciences, University College London, London WC1E 6BT, United Kingdom.
Mihai G NeteaDepartment of Internal Medicine, Radboud University Medical Center, Nijmegen 6525 GA, Netherlands.
David ComasInstitute of Evolutionary Biology (Consejo Superior de Investigaciones Científicas - Universitat Pompeu Fabra), Department of Medicine and Life Sciences, Universitat Pompeu Fabra, Barcelona 08003, Spain.ORCID 0000-0002-5075-0956
Hisham Y HassanBanoon Assisted Reproductive Technology and Cytogenetics Centre, Military Hospital, Royal Medical Services, Riffa 28743, Kingdom of Bahrain.

Funding

MEC | Agencia Estatal de Investigación (AEI) PID2022-138755NB-I00MEC | Agencia Estatal de Investigación (AEI) PID2023-147621NB-I00
6 · The paper itself

Abstract

Sudan lies at the crossroads of Africa and the Middle East, with rich cultural, linguistic, and ecological diversity shaped by a complex demographic history. We present a whole-genome sequencing (WGS) study of Sudanese populations, analyzing high-coverage genomes (~30×) from 125 individuals representing five ethnolinguistic groups across three language families. Our results reveal deep population structure, involving Nilo-Saharan, West Eurasian, Northern African, and Western African ancestral components, as well as signatures of the Arab expansion. We report over one million novel variants, including population-specific deleterious alleles, highlighting the need for broader African genomic representation. Notably, local ancestry inference reveals a strong signal of adaptive admixture on chromosome 1 in Sudanese Copts, marked by a peak of Nilo-Saharan ancestry introduced via genetic admixture 1,000 to 1,500 y ago. At this locus, we estimate a remarkably strong selection coefficient (s = 0.0996) for SNP rs2814778 within the

Indexed as

Adaptation, PhysiologicalBlack PeopleMalariaDuffy Blood-Group SystemGenetics, PopulationHumansNorth African PeoplePolymorphism, Single NucleotideSudanWhole Genome SequencingDuffy Blood-Group Systemadmixturelocal adaptationpopulation geneticssudan

Identifiers

PMID41493817
PMCPMC12818401

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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.