Evidence map›Paper›PMID 29100086›Full record

ArticleAmerican journal of human genetics2017

Genome-wide Ancestry and Demographic History of African-Descendant Maroon Communities from French Guiana and Suriname.

Cesar Fortes-Lima, Antoine Gessain, Andres Ruiz-Linares, Maria-Cátira Bortolini, Florence Migot-Nabias, Gil Bellis, J Víctor Moreno-Mayar, Berta Nelly Restrepo, Winston Rojas, Efren Avendaño-Tamayo and 8 more

Abstract read
In one paragraph

Article in American journal of human genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

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  7. Genomic ancestry,Haematologica · 2026
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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

18 authors.

Cesar Fortes-LimaLaboratoire d'Anthropologie Moléculaire et Imagerie de Synthèse, AMIS UMR5288, Centre National de la Recherche Scientifique (CNRS) -Université Paul Sabatier Toulouse III, Toulouse 31000, France; Laboratory Eco-Anthropology and Ethno-Biology, UMR7206, CNRS-MNHN-University Paris Diderot, Musée de l'Homme, 17 Place du Trocadéro, 75016 Paris, France.
Antoine GessainOncogenic Virus Epidemiology and Pathophysiology Group, Department of Virology, CNRS UMR3569, Pasteur Institute, Paris 75015, France.
Andres Ruiz-LinaresDepartment of Genetics, Evolution, and Environment, University College London, London WC1E 6BT, United Kingdom; Ministry of Education Key Laboratory of Contemporary Anthropology and Collaborative Innovation Center of Genetics and Development, Fudan University, Shanghai 200438, China; Laboratory of Biocultural Anthropology, Law, Ethics, and Health, CNRS/EFS ADES UMR7268, Aix-Marseille University, Marseille 13824, France.
Maria-Cátira BortoliniDepartment of Genetics, Federal University of Rio Grande do Sul, Porto Alegre 91501-970, Brazil.
Florence Migot-NabiasMother and Child Facing Tropical Infections (MERIT), Research Institute for Development, Paris 5 University, Sorbonne Paris Cité, Paris 75006, France.
Gil BellisFrench Institute for Demographic Studies, Paris 75020, France.
J Víctor Moreno-MayarNatural History Museum of Denmark, University of Copenhagen, Copenhagen 1350, Denmark.
Berta Nelly RestrepoInstituto Colombiano de Medicina Tropical, Universidad CES, Sabaneta, Antioquia 055450, Colombia.
Winston RojasLaboratory of Molecular Genetics, Institute of Biology, University of Antioquia, Medellín 050010, Colombia.
Efren Avendaño-TamayoLaboratory of Molecular Genetics, Institute of Biology, University of Antioquia, Medellín 050010, Colombia; Grupo de Ciencias Básicas Aplicadas del Tecnológico de Antioquia, Tecnológico de Antioquia - Institución Universitaria, Medellín 050034, Colombia.
Gabriel BedoyaLaboratory of Molecular Genetics, Institute of Biology, University of Antioquia, Medellín 050010, Colombia.
Ludovic OrlandoLaboratoire d'Anthropologie Moléculaire et Imagerie de Synthèse, AMIS UMR5288, Centre National de la Recherche Scientifique (CNRS) -Université Paul Sabatier Toulouse III, Toulouse 31000, France; Natural History Museum of Denmark, University of Copenhagen, Copenhagen 1350, Denmark.
Antonio SalasUnidade de Xenética, Departamento de Anatomía Patolóxica e Ciencias Forenses, Instituto de Ciencias Forenses, Facultade de Medicina, Universidade de Santiago de Compostela, Galicia 15782, Spain; GenPoB Research Group, Instituto de Investigaciones Sanitarias, Hospital Clínico Universitario de Santiago, Galicia 15782, Spain.
Agnar HelgasonDeCode Genetics, Reykjavik IS-101, Iceland.
M Thomas P GilbertNatural History Museum of Denmark, University of Copenhagen, Copenhagen 1350, Denmark; Norwegian University of Science and Technology, University Museum, Trondheim 7491, Norway.
Martin SikoraNatural History Museum of Denmark, University of Copenhagen, Copenhagen 1350, Denmark.
Hannes SchroederNatural History Museum of Denmark, University of Copenhagen, Copenhagen 1350, Denmark; Faculty of Archaeology, Leiden University, Leiden 2333, the Netherlands. Electronic address: hschroeder@snm.ku.dk.
Jean-Michel DugoujonLaboratoire d'Anthropologie Moléculaire et Imagerie de Synthèse, AMIS UMR5288, Centre National de la Recherche Scientifique (CNRS) -Université Paul Sabatier Toulouse III, Toulouse 31000, France. Electronic address: jean-michel.dugoujon@univ-tlse3.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The transatlantic slave trade was the largest forced migration in world history. However, the origins of the enslaved Africans and their admixture dynamics remain unclear. To investigate the demographic history of African-descendant Marron populations, we generated genome-wide data (4.3 million markers) from 107 individuals from three African-descendant populations in South America, as well as 124 individuals from six west African populations. Throughout the Americas, thousands of enslaved Africans managed to escape captivity and establish lasting communities, such as the Noir Marron. We find that this population has the highest proportion of African ancestry (∼98%) of any African-descendant population analyzed to date, presumably because of centuries of genetic isolation. By contrast, African-descendant populations in Brazil and Colombia harbor substantially more European and Native American ancestry as a result of their complex admixture histories. Using ancestry tract-length analysis, we detect different dates for the European admixture events in the African-Colombian (1749 CE; confidence interval [CI]: 1737-1764) and African-Brazilian (1796 CE; CI: 1789-1804) populations in our dataset, consistent with the historically attested earlier influx of Africans into Colombia. Furthermore, we find evidence for sex-specific admixture patterns, resulting from predominantly European paternal gene flow. Finally, we detect strong genetic links between the African-descendant populations and specific source populations in Africa on the basis of haplotype sharing patterns. Although the Noir Marron and African-Colombians show stronger affinities with African populations from the Bight of Benin and the Gold Coast, the African-Brazilian population from Rio de Janeiro has greater genetic affinity with Bantu-speaking populations from the Bight of Biafra and west central Africa.

Indexed as

AfricaBlack PeopleBrazilFemaleFrench GuianaGene FlowGenetics, PopulationGenome-Wide Association StudyHaplotypesHispanic or LatinoHumansMalePolymorphism, Single NucleotideSurinameWhite Peopleadmixture timingAfrican-descendant populationancestral originancestry inferencegenome-wide SNP datahaplotype-based methodNoir Marron communitiessex-specific admixture patternsslave tradeSouth America

Identifiers

PMID29100086
PMCPMC5673667

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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.