Evidence map›Paper›PMID 33594080›Full record

ArticleNature communications2021

Phenotypic covariance across the entire spectrum of relatedness for 86 billion pairs of individuals.

Kathryn E Kemper, Loic Yengo, Zhili Zheng, Abdel Abdellaoui, Matthew C Keller, Michael E Goddard, Naomi R Wray, Jian Yang, Peter M Visscher

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 5% of its field
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 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Family history of fracture and fracture risk: a meta-analysis to update the FRAX® risk assessment tool.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2025
    Pooled it
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  6. Polygenic prediction of human complex traits using ancient DNA.Current opinion in genetics & development · 2025
    Review
  7. Family-GWAS reveals effects of environment and mating on genetic associations.medRxiv : the preprint server for health sciences · 2025
    Article
  8. Article
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  12. Review
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  15. Article
  16. Article
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  18. Article
  19. How to estimate heritability: a guide for genetic epidemiologists.International journal of epidemiology · 2023
    Article
  20. 15 years of GWAS discovery: Realizing the promise.American journal of human genetics · 2023
    Review
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

9 authors at 4 institutions in 3 countries.

Kathryn E KemperInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia. k.kemper@uq.edu.au.ORCID 0000-0002-9288-4522
Loic YengoInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0002-4272-9305
Zhili ZhengInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
Abdel AbdellaouiDepartment of Psychiatry, Amsterdam UMC, University of Amsterdam, Amsterdam, the Netherlands.
Matthew C KellerDepartment of Psychology & Neuroscience, University of Colorado at Boulder, Boulder, CO, USA.
Michael E GoddardFaculty of Veterinary and Agricultural Science, University of Melbourne, Parkville, VIC, Australia.
Naomi R WrayInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0001-7421-3357
Jian YangInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.ORCID 0000-0003-2001-2474
Peter M VisscherInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia. peter.visscher@uq.edu.au.ORCID 0000-0002-2143-8760
The University of Queensland · AUAmsterdam University Medical Centers · NLThe University of Melbourne · AUUniversity of Colorado Boulder · US

Funding

Estimating the genetic and environmental architecture of psychiatric disordersR01MH100141 · NIMH · UNIVERSITY OF COLORADO · PI KELLER, MATTHEW CHARLES · 2013 to 2022
$5.3M
Genome-Wide Analyses of Health and Well-Being PhenotypesR01AG042568 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI BENJAMIN, DANIEL J · 2015 to 2021
$2.8M
NIA NIH HHS R01 AG042568NIMH NIH HHS R01 MH100141
6 · The paper itself

Abstract

Attributing the similarity between individuals to genetic and non-genetic factors is central to genetic analyses. In this paper we use the genomic relationship ([Formula: see text]) among 417,060 individuals to investigate the phenotypic covariance between pairs of individuals for 32 traits across the spectrum of relatedness, from unrelated pairs through to identical twins. We find linear relationships between phenotypic covariance and [Formula: see text] that agree with the SNP-based heritability ([Formula: see text]) in unrelated pairs ([Formula: see text]), and with pedigree-estimated heritability in close relatives ([Formula: see text]). The covariance increases faster than [Formula: see text] in distant relatives ([Formula: see text]), and we attribute this to imperfect linkage disequilibrium between causal variants and the common variants used to construct [Formula: see text]. We also examine the effect of assortative mating on heritability estimates from different experimental designs. We find that full-sib identity-by-descent regression estimates for height (0.66 s.e. 0.07) are consistent with estimates from close relatives (0.82 s.e. 0.04) after accounting for the effect of assortative mating.

Indexed as

Genome, HumanPhylogenyAdultAgedBiological Specimen BanksBody Mass IndexEducational StatusHumansInheritance PatternsLinkage DisequilibriumMiddle AgedModels, GeneticPhenotypePolymorphism, Single NucleotideQuantitative Trait, HeritableRegression Analysis

Identifiers

PMID33594080
PMCPMC7886899
OpenAlexW3131877806

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.