Evidence map›Paper›PMID 32502155›Full record

ArticlePloS one2020

Facial shape and allometry quantitative trait locus intervals in the Diversity Outbred mouse are enriched for known skeletal and facial development genes.

David C Katz, J David Aponte, Wei Liu, Rebecca M Green, Jessica M Mayeux, K Michael Pollard, Daniel Pomp, Steven C Munger, Stephen A Murray, Charles C Roseman and 4 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Fifteen years of the Diversity Outbred mouse model: a review.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  9. Genome research · 2022
    Article
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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

14 authors at 8 institutions in 2 countries.

David C KatzDepartment of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.ORCID 0000-0002-0827-5602
J David AponteDepartment of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.ORCID 0000-0002-1608-8612
Wei LiuDepartment of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.
Rebecca M GreenDepartment of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.
Jessica M MayeuxDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States of America.
K Michael PollardDepartment of Molecular Medicine, The Scripps Research Institute, La Jolla, CA, United States of America.
Daniel PompDepartment of Genetics, University of North Carolina School of Medicine, Chapel Hill, NC, United States of America.ORCID 0000-0001-6609-9195
Steven C MungerThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Stephen A MurrayThe Jackson Laboratory, Bar Harbor, ME, United States of America.
Charles C RosemanDepartment of Evolution, Ecology, and Behavior, University of Illinois Urbana Champaign, Urbana, IL, United States of America.
Christopher J PercivalDepartment of Anthropology, Stony Brook University, Stony Brook, NY, United States of America.ORCID 0000-0002-8883-9737
James CheverudDepartment of Biology, Loyola University Chicago, Chicago, IL, United States of America.ORCID 0000-0001-7651-863X
Ralph S MarcucioDepartment of Orthopaedic Surgery, School of Medicine, University of California San Francisco, San Francisco, CA, United States of America.
Benedikt HallgrímssonDepartment of Cell Biology & Anatomy, Alberta Children's Hospital Research Institute and McCaig Bone and Joint Institute, Cumming School of Medicine, University of Calgary, AB, Canada.ORCID 0000-0002-7192-9103
University of Calgary · CAJackson Laboratory · USScripps Research Institute · USLoyola University Chicago · USStony Brook University · USUniversity of California, San Francisco · USUniversity of Illinois Urbana-Champaign · USUniversity of North Carolina at Chapel Hill · US

Funding

The role of continuous phenotypic variation in structural defects of the faceR01DE019638 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Benedikt Hallgrimsson, Ralph S Marcucio · 2010 to 2026
$7.3M
Genetic Determinants of Orofacial Shape and Relationship to Cleft Lip/PalateU01DE020054 · NIDCR · UNIVERSITY OF COLORADO DENVER · PI SPRITZ, RICHARD ANDREW · 2009 to 2014
$2.4M
Leveraging Natural Genetic Diversity and Systems Genetics to Elucidate the Complex Hierarchy of Gene Regulation Underlying Ground State Pluripotency, Cell Fate Decisions and Tissue HomeostasisR35GM133495 · NIGMS · JACKSON LABORATORY · PI MUNGER, STEVEN CARMEN · 2019 to 2023
$2.0M
Developmental mechanisms underlying genotype-phenotype correlationsR01DE021708 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HALLGRIMSSON, BENEDIKT, MARCUCIO, RALPH S · 2011 to 2015
$1.9M
The Diversity Outbred Mouse as a Model of Silica-induced AutoimmunityR21ES024485 · NIEHS · SCRIPPS RESEARCH INSTITUTE, THE · PI POLLARD, KENNETH MICHAEL · 2014 to 2015
$521k
NIDCR NIH HHS R01 DE019638NIDCR NIH HHS R01 DE021708NIDCR NIH HHS U01 DE020054NIEHS NIH HHS R21 ES024485NIGMS NIH HHS R35 GM133495
6 · The paper itself

Abstract

The biology of how faces are built and come to differ from one another is complex. Discovering normal variants that contribute to differences in facial morphology is one key to untangling this complexity, with important implications for medicine and evolutionary biology. This study maps quantitative trait loci (QTL) for skeletal facial shape using Diversity Outbred (DO) mice. The DO is a randomly outcrossed population with high heterozygosity that captures the allelic diversity of eight inbred mouse lines from three subspecies. The study uses a sample of 1147 DO animals (the largest sample yet employed for a shape QTL study in mouse), each characterized by 22 three-dimensional landmarks, 56,885 autosomal and X-chromosome markers, and sex and age classifiers. We identified 37 facial shape QTL across 20 shape principal components (PCs) using a mixed effects regression that accounts for kinship among observations. The QTL include some previously identified intervals as well as new regions that expand the list of potential targets for future experimental study. Three QTL characterized shape associations with size (allometry). Median support interval size was 3.5 Mb. Narrowing additional analysis to QTL for the five largest magnitude shape PCs, we found significant overrepresentation of genes with known roles in growth, skeletal and facial development, and sensory organ development. For most intervals, one or more of these genes lies within 0.25 Mb of the QTL's peak. QTL effect sizes were small, with none explaining more than 0.5% of facial shape variation. Thus, our results are consistent with a model of facial diversity that is influenced by key genes in skeletal and facial development and, simultaneously, is highly polygenic.

Indexed as

AllelesAnimalsBone and BonesBone DevelopmentChromosome MappingCollaborative Cross MiceFaceFacial BonesFemaleGenetic VariationGenotypeMaleMaxillofacial DevelopmentMicePhenotypePolymorphism, Single Nucleotide

Identifiers

PMID32502155
PMCPMC7274373
OpenAlexW3034146909

What Socratic 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 Socratic graph.