Evidence map›Paper›PMID 20691402›Full record

ArticleAmerican journal of human genetics2010

Whole-genome genetic diversity in a sample of Australians with deep Aboriginal ancestry.

Brian P McEvoy, Joanne M Lind, Eric T Wang, Robert K Moyzis, Peter M Visscher, Sheila M van Holst Pellekaan, Alan N Wilton

Abstract read
In one paragraph

Article in American journal of human genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

  1. Article
  2. Ancestral Origins and Admixture History of Kazakhs.Molecular biology and evolution · 2024
    Article
  3. Article
  4. Review
  5. TheCancers · 2020
    Article
  6. Analysis of theFrontiers in genetics · 2020
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Genome-wide data substantiate Holocene gene flow from India to Australia.Proceedings of the National Academy of Sciences of the United States of America · 2013
    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

7 authors.

Brian P McEvoyQueensland Institute of Medical Research, Brisbane, Queensland 4006, Australia. brian.mcevoy@qimr.edu.au
Joanne M Lind
Eric T Wang
Robert K Moyzis
Peter M Visscher
Sheila M van Holst Pellekaan
Alan N Wilton

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Australia was probably settled soon after modern humans left Africa, but details of this ancient migration are not well understood. Debate centers on whether the Pleistocene Sahul continent (composed of New Guinea, Australia, and Tasmania) was first settled by a single wave followed by regional divergence into Aboriginal Australian and New Guinean populations (common origin) or whether different parts of the continent were initially populated independently. Australia has been the subject of relatively few DNA studies even though understanding regional variation in genomic structure and diversity will be important if disease-association mapping methods are to be successfully evaluated and applied across populations. We report on a genome-wide investigation of Australian Aboriginal SNP diversity in a sample of participants from the Riverine region. The phylogenetic relationship of these Aboriginal Australians to a range of other global populations demonstrates a deep common origin with Papuan New Guineans and Melanesians, with little evidence of substantial later migration until the very recent arrival of European colonists. The study provides valuable and robust insights into an early and important phase of human colonization of the globe. A broader survey of Australia, including diverse geographic sample populations, will be required to fully appreciate the continent's unique population history and consequent genetic heritage, as well as the importance of both to the understanding of health issues.

Indexed as

Genetic VariationPhylogenyAustraliaGenetic MarkersGenetics, PopulationGenome, HumanGeographyHumansPolymorphism, Single NucleotidePrincipal Component AnalysisGenetic Markers

Identifiers

PMID20691402
PMCPMC2917718

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.