Evidence map›Paper›PMID 30838127›Full record

ReviewEvolution, medicine, and public health2019

Interpreting polygenic scores, polygenic adaptation, and human phenotypic differences.

Noah A Rosenberg, Michael D Edge, Jonathan K Pritchard, Marcus W Feldman

Abstract readReview
In one paragraph

Review in Evolution, medicine, and public health, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed, 2 pooled it
–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

69 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Article
  6. The Multiethnic Cohort: A Resource for the Study of Genetic and Nongenetic Cancer Risk across Populations.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2026
    Article
  7. Article
  8. Article
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  10. Review
  11. The risk of biological race.History and philosophy of the life sciences · 2025
    Article
  12. Article
  13. Article
  14. Article
  15. Genes, culture, and scientific racism.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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

4 authors.

Noah A RosenbergDepartment of Biology, Stanford University, Stanford, CA, USA.
Michael D EdgeDepartment of Evolution and Ecology, University of California, Davis, CA, USA.
Jonathan K PritchardDepartment of Biology, Stanford University, Stanford, CA, USA.
Marcus W FeldmanDepartment of Biology, Stanford University, Stanford, CA, USA.

Funding

Population genetics for large-scale sequencing studies of diverse populationsR01HG005855 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Noah Rosenberg, Paul A Scheet · 2010 to 2026
$5.8M
Genome-wide approaches to polygenic adaptationR01GM108779 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI COOP, GRAHAM · 2014 to 2019
$1.0M
Reconstructing the history of polygenic adaptation using ancestral recombimation graphsF32GM130050 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI EDGE, MICHAEL DONALD · 2018 to 2020
$101k
NHGRI NIH HHS R01 HG005855NIGMS NIH HHS F32 GM130050NIGMS NIH HHS R01 GM108779
6 · The paper itself

Abstract

Recent analyses of polygenic scores have opened new discussions concerning the genetic basis and evolutionary significance of differences among populations in distributions of phenotypes. Here, we highlight limitations in research on polygenic scores, polygenic adaptation and population differences. We show how genetic contributions to traits, as estimated by polygenic scores, combine with environmental contributions so that differences among populations in trait distributions need not reflect corresponding differences in genetic propensity. Under a null model in which phenotypes are selectively neutral, genetic propensity differences contributing to phenotypic differences among populations are predicted to be small. We illustrate this null hypothesis in relation to health disparities between African Americans and European Americans, discussing alternative hypotheses with selective and environmental effects. Close attention to the limitations of research on polygenic phenomena is important for the interpretation of their relationship to human population differences.

Indexed as

adaptationhealth disparitieshuman variationpolygenic scorespopulation genetics

Identifiers

PMID30838127
PMCPMC6393779

What OpenQuestion holds

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Registered trials

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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.