Evidence map›Paper›PMID 28747529›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Detection and quantification of inbreeding depression for complex traits from SNP data.

Loic Yengo, Zhihong Zhu, Naomi R Wray, Bruce S Weir, Jian Yang, Matthew R Robinson, Peter M Visscher

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 3 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

33 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Bony fish genomes: Status and gaps.Journal of fish biology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Detecting inbreeding depression in structured populations.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  10. Article
  11. Article
  12. Article
  13. Article
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  17. Article
  18. Review
  19. Article
  20. Genomic partitioning of inbreeding depression in humans.American journal of human genetics · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Loic YengoInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; l.yengodimbou@uq.edu.au peter.visscher@uq.edu.au.ORCID 0000-0002-4272-9305
Zhihong ZhuInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Naomi R WrayInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Bruce S WeirDepartment of Biostatistics, University of Washington, Seattle, WA 98195.
Jian YangInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Matthew R RobinsonInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.
Peter M VisscherInstitute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia; l.yengodimbou@uq.edu.au peter.visscher@uq.edu.au.

Funding

Statistical Methods for X-Chromosome Genetic DataP01GM099568 · NIGMS · UNIVERSITY OF WASHINGTON · PI WEIR, BRUCE S. · 2012 to 2016
$7.3M
Theoretical Population Genetics SupplementR01GM075091 · NIGMS · UNIVERSITY OF WASHINGTON · PI WEIR, BRUCE S. · 2006 to 2020
$4.7M
Genome-Wide Analyses of Health and Well-Being PhenotypesR01AG042568 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BENJAMIN, DANIEL J · 2015 to 2021
$2.8M
Medical Research Council MC_QA137853NIA NIH HHS R01 AG042568NIGMS NIH HHS P01 GM099568NIGMS NIH HHS R01 GM075091
6 · The paper itself

Abstract

Quantifying the effects of inbreeding is critical to characterizing the genetic architecture of complex traits. This study highlights through theory and simulations the strengths and shortcomings of three SNP-based inbreeding measures commonly used to estimate inbreeding depression (ID). We demonstrate that heterogeneity in linkage disequilibrium (LD) between causal variants and SNPs biases ID estimates, and we develop an approach to correct this bias using LD and minor allele frequency stratified inference (LDMS). We quantified ID in 25 traits measured in [Formula: see text] participants of the UK Biobank, using LDMS, and confirmed previously published ID for 4 traits. We find unique evidence of ID for handgrip strength, waist/hip ratio, and visual and auditory acuity (ID between -2.3 and -5.2 phenotypic SDs for complete inbreeding; [Formula: see text]). Our results illustrate that a careful choice of the measure of inbreeding combined with LDMS stratification improves both detection and quantification of ID using SNP data.

Indexed as

ConsanguinityDatabases, Nucleic AcidLinkage DisequilibriumModels, GeneticPolymorphism, Single NucleotideQuantitative Trait, HeritableFemaleHumansMaledirectional dominancehomozygosityinbreeding depressionquantitative geneticssingle-nucleotide polymorphism

Identifiers

PMID28747529
PMCPMC5558994

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.