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GWAS Study

3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies.

Hoskens H, Liu D, Naqvi S et al.

33983923 PubMed ID
GWAS Study Type
8246 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

HH
Hoskens H
LD
Liu D
NS
Naqvi S
LM
Lee MK
ER
Eller RJ
IK
Indencleef K
WJ
White JD
LJ
Li J
LM
Larmuseau MHD
HG
Hens G
WJ
Wysocka J
WS
Walsh S
RS
Richmond S
SM
Shriver MD
SJ
Shaffer JR
PH
Peeters H
WS
Weinberg SM
CP
Claes P
Chapter II

Abstract

Summary of the research findings

The analysis of contemporary genomic data typically operates on one-dimensional phenotypic measurements (e.g. standing height). Here we report on a data-driven, family-informed strategy to facial phenotyping that searches for biologically relevant traits and reduces multivariate 3D facial shape variability into amendable univariate measurements, while preserving its structurally complex nature. We performed a biometric identification of siblings in a sample of 424 children, defining 1,048 sib-shared facial traits. Subsequent quantification and analyses in an independent European cohort (n = 8,246) demonstrated significant heritability for a subset of traits (0.17-0.53) and highlighted 218 genome-wide significant loci (38 also study-wide) associated with facial variation shared by siblings. These loci showed preferential enrichment for active chromatin marks in cranial neural crest cells and embryonic craniofacial tissues and several regions harbor putative craniofacial genes, thereby enhancing our knowledge on the genetic architecture of normal-range facial variation.

8,246 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

8246
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., U.K.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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