Evidence map›Paper›PMID 33958743›Full record

ArticleEuropean journal of human genetics : EJHG2021

Phylogenetic history of patrilineages rare in northern and eastern Europe from large-scale re-sequencing of human Y-chromosomes.

Anne-Mai Ilumäe, Helen Post, Rodrigo Flores, Monika Karmin, Hovhannes Sahakyan, Mayukh Mondal, Francesco Montinaro, Lauri Saag, Concetta Bormans, Luisa Fernanda Sanchez and 8 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. On the Edge of Empire: Paleogenomic Insights into Roman Dacia.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. 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

18 authors.

Anne-Mai Ilumäe *Estonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia. annemai.ilumae@ut.ee.ORCID http://orcid.org/0000-0001-6920-1335
Helen Post *Estonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Rodrigo FloresEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0002-0965-5973
Monika KarminEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0001-9827-5579
Hovhannes SahakyanEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0003-1596-2838
Mayukh MondalEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Francesco MontinaroEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Lauri SaagEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Concetta BormansGenomic Research Center, Gene by Gene, Houston, TX, USA.
Luisa Fernanda SanchezGenomic Research Center, Gene by Gene, Houston, TX, USA.
Adam AmeurScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-6085-6749
Ulf GyllenstenScience for Life Laboratory, Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden.
Mart KalsEstonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Reedik MägiEstonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Luca PaganiEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.ORCID http://orcid.org/0000-0002-6639-524X
Doron M BeharEstonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Siiri Rootsi *Estonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.
Richard Villems *Estonian Biocentre, Institute of Genomics, University of Tartu, Tartu, Estonia.

Funding

New York Center for Collaborative Research In Common Disease Genomics: Genome Aggregation and Joint Variant Calling for CCDG Freeze2UM1HG008901 · NHGRI · NEW YORK GENOME CENTER · PI MANIATIS, THOMAS P, WIGLER, MICHAEL H · 2016 to 2020
$56.6M
NHGRI NIH HHS UM1 HG008901
6 · The paper itself

Abstract

The most frequent Y-chromosomal (chrY) haplogroups in northern and eastern Europe (NEE) are well-known and thoroughly characterised. Yet a considerable number of men in every population carry rare paternal lineages with estimated frequencies around 5%. So far, limited sample-sizes and insufficient resolution of genotyping have obstructed a truly comprehensive look into the variety of rare paternal lineages segregating within populations and potential signals of population history that such lineages might convey. Here we harness the power of massive re-sequencing of human Y chromosomes to identify previously unknown population-specific clusters among rare paternal lineages in NEE. We construct dated phylogenies for haplogroups E2-M215, J2-M172, G-M201 and Q-M242 on the basis of 421 (of them 282 novel) high-coverage chrY sequences collected from large-scale databases focusing on populations of NEE. Within these otherwise rare haplogroups we disclose lineages that began to radiate ~1-3 thousand years ago in Estonia and Sweden and reveal male phylogenetic patterns testifying of comparatively recent local demographic expansions. Conversely, haplogroup Q lineages bear evidence of ancient Siberian influence lingering in the modern paternal gene pool of northern Europe. We assess the possible direction of influx of ancestral carriers for some of these male lineages. In addition, we demonstrate the congruency of paternal haplogroup composition of our dataset with two independent population-based cohorts from Estonia and Sweden.

Indexed as

PhylogenyPolymorphism, GeneticChromosomes, Human, YEstoniaHaplotypesHuman MigrationHumansMalePedigreeSweden

Identifiers

PMID33958743
PMCPMC8484622

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.