Evidence map›Paper›PMID 34214457›Full record

ArticleAmerican journal of human genetics2021

Genomic partitioning of inbreeding depression in humans.

Loic Yengo, Jian Yang, Matthew C Keller, Michael E Goddard, Naomi R Wray, Peter M Visscher

Open access · bronzeAbstract read
In one paragraph

Article in American journal of human genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Analysis of genetic dominance in the UK Biobank.Science (New York, N.Y.) · 2023
    Article
  5. Article
  6. 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

6 authors at 3 institutions in 3 countries.

Loic YengoInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD 4072, Australia. Electronic address: l.yengodimbou@uq.edu.au.
Jian YangInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD 4072, Australia; School of Life Sciences, Westlake University, Hangzhou, Zhejiang 310024, China; Westlake Laboratory of Life Sciences and Biomedicine, Hangzhou, Zhejiang 310024, China.
Matthew C KellerDepartment of Psychology and Neuroscience, University of Colorado, Boulder, CO 80309, USA; Department of Integrative Physiology, University of Colorado, Boulder, CO 80309, USA.
Michael E GoddardFaculty of Veterinary and Agricultural Science, Na, Parkville, VIC 3010, Australia; Agriculture Victoria Research, Department of Jobs, Precincts and Regions, Bundoora, VIC 3083, Australia.
Naomi R WrayInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD 4072, Australia; Queensland Brain Institute, University of Queensland, Brisbane, QLD 4072, Australia.
Peter M VisscherInstitute for Molecular Bioscience, University of Queensland, Brisbane, QLD 4072, Australia.
The University of Queensland · AUAgriculture Victoria · 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
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NIMH NIH HHS R01 MH100141
6 · The paper itself

Abstract

Across species, offspring of related individuals often exhibit significant reduction in fitness-related traits, known as inbreeding depression (ID), yet the genetic and molecular basis for ID remains elusive. Here, we develop a method to quantify enrichment of ID within specific genomic annotations and apply it to human data. We analyzed the phenomes and genomes of ∼350,000 unrelated participants of the UK Biobank and found, on average of over 11 traits, significant enrichment of ID within genomic regions with high recombination rates (>21-fold; p < 10

Indexed as

Genome-Wide Association StudyLinkage DisequilibriumPhenotypePolymorphism, Single NucleotideFemaleGenomicsHumansInbreeding DepressionMaleMultifactorial Inheritancefunctional annotationgenome-wide association studiesgenomic partitioninginbreeding depression

Identifiers

PMID34214457
PMCPMC8387293
OpenAlexW3176469526

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.