Evidence map›Paper›PMID 34952928›Full record

ArticleEuropean journal of human genetics : EJHG2022

Correction to: 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 9 more

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PubMed Full text at PMC Publisher
In one paragraph

Article in European journal of human genetics : EJHG, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Begoña Martínez-Cruz *Departament de Ciències Experimentals i de la Salut, Institut de Biologia Evolutiva (CSIC-UPF), Universitat Pompeu Fabra, Barcelona, Spain.
Isabel Mendizabal *Departament 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.
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. david.comas@upf.edu.
Genographic Consortium

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID34952928
PMCPMC8989938

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.