Evidence map›Paper›PMID 26374132›Full record

ArticleEuropean journal of human genetics : EJHG2016

Origins, admixture and founder lineages in European Roma.

Begoña Martínez-Cruz, Isabel Mendizabal, Christine Harmant, Rosario de Pablo, Mihai Ioana, Dora Angelicheva, Anastasia Kouvatsi, Halyna Makukh, Mihai G Netea, Horolma Pamjav and 8 more

Erratum issuedAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

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  11. Pathogenic Variants ofInternational journal of molecular sciences · 2023
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  19. Phylogeographic review of Y chromosome haplogroups in Europe.International journal of legal medicine · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors.

Begoña Martínez-CruzDepartament de Ciències Experimentals i de la Salut, Institut de Biologia Evolutiva (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain.
Isabel MendizabalDepartament de Ciències Experimentals i de la Salut, Institut de Biologia Evolutiva (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain.
Christine HarmantUnit of Human Evolutionary Genetics, Department of Genomes and Genetics, Institut Pasteur, Paris, France.
Rosario de PabloServicio de Inmunología, Hospital Universitario Puerta de Hierro, Madrid, Spain.
Mihai IoanaUniversity of Medicine and Pharmacy Craiova, Craiova, Romania.
Dora AngelichevaHarry Perkins Institute of Medical Research and Centre for Medical Research, University of Western Australia, Perth, WA, Australia.
Anastasia KouvatsiDepartment of Genetics, Development and Molecular Biology, School of Biology, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Halyna MakukhInstitute of Hereditary Pathology of the Ukrainian Academy of Medical Sciences, Lviv, Ukraine.
Mihai G NeteaDepartment of Medicine, Radboud Institute for Molecular Life Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
Horolma PamjavInstitute of Forensic Medicine, Network of Forensic Science Institutes, Budapest, Hungary.
Andrea ZalánInstitute of Forensic Medicine, Network of Forensic Science Institutes, Budapest, Hungary.
Ivailo TournevDepartment of Neurology, Medical University-Sofia, Sofia, Bulgaria.
Elena MarushiakovaInstitute of Ethnology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Vesselin PopovInstitute of Ethnology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Jaume BertranpetitDepartament de Ciències Experimentals i de la Salut, Institut de Biologia Evolutiva (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain.ORCID 0000-0003-0100-0590
Luba KalaydjievaHarry Perkins Institute of Medical Research and Centre for Medical Research, University of Western Australia, Perth, WA, Australia.
Lluis Quintana-MurciUnit of Human Evolutionary Genetics, Department of Genomes and Genetics, Institut Pasteur, Paris, France.
David ComasDepartament de Ciències Experimentals i de la Salut, Institut de Biologia Evolutiva (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The Roma, also known as 'Gypsies', represent the largest and the most widespread ethnic minority of Europe. There is increasing evidence, based on linguistic, anthropological and genetic data, to suggest that they originated from the Indian subcontinent, with subsequent bottlenecks and undetermined gene flow from/to hosting populations during their diaspora. Further support comes from the presence of Indian uniparentally inherited lineages, such as mitochondrial DNA M and Y-chromosome H haplogroups, in a significant number of Roma individuals. However, the limited resolution of most genetic studies so far, together with the restriction of the samples used, have prevented the detection of other non-Indian founder lineages that might have been present in the proto-Roma population. We performed a high-resolution study of the uniparental genomes of 753 Roma and 984 non-Roma hosting European individuals. Roma groups show lower genetic diversity and high heterogeneity compared with non-Roma samples as a result of lower effective population size and extensive drift, consistent with a series of bottlenecks during their diaspora. We found a set of founder lineages, present in the Roma and virtually absent in the non-Roma, for the maternal (H7, J1b3, J1c1, M18, M35b, M5a1, U3, and X2d) and paternal (I-P259, J-M92, and J-M67) genomes. This lineage classification allows us to identify extensive gene flow from non-Roma to Roma groups, whereas the opposite pattern, although not negligible, is substantially lower (up to 6.3%). Finally, the exact haplotype matching analysis of both uniparental lineages consistently points to a Northwestern origin of the proto-Roma population within the Indian subcontinent.

Indexed as

Founder EffectPedigreeChromosomes, Human, YDNA, MitochondrialEuropeGenetic HeterogeneityGenome, HumanHuman MigrationHumansPolymorphism, GeneticRomani PeopleDNA, Mitochondrial

Identifiers

PMID26374132
PMCPMC4867443

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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.