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GWAS Study

Genome-wide analyses of non-syndromic cleft lip with palate identify 14 novel loci and genetic heterogeneity.

Yu Y, Zuo X, He M et al.

28232668 PubMed ID
GWAS Study Type
11972 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

YY
Yu Y
ZX
Zuo X
HM
He M
GJ
Gao J
FY
Fu Y
QC
Qin C
ML
Meng L
WW
Wang W
SY
Song Y
CY
Cheng Y
ZF
Zhou F
CG
Chen G
ZX
Zheng X
WX
Wang X
LB
Liang B
ZZ
Zhu Z
FX
Fu X
SY
Sheng Y
HJ
Hao J
LZ
Liu Z
YH
Yan H
ME
Mangold E
RI
Ruczinski I
LJ
Liu J
MM
Marazita ML
LK
Ludwig KU
BT
Beaty TH
ZX
Zhang X
SL
Sun L
BZ
Bian Z
Chapter II

Abstract

Summary of the research findings

Non-syndromic cleft lip with palate (NSCLP) is the most serious sub-phenotype of non-syndromic orofacial clefts (NSOFC), which are the most common craniofacial birth defects in humans. Here we conduct a GWAS of NSCLP with multiple independent replications, totalling 7,404 NSOFC cases and 16,059 controls from several ethnicities, to identify new NSCLP risk loci, and explore the genetic heterogeneity between sub-phenotypes of NSOFC. We identify 41 SNPs within 26 loci that achieve genome-wide significance, 14 of which are novel (RAD54B, TMEM19, KRT18, WNT9B, GSC/DICER1, PTCH1, RPS26, OFCC1/TFAP2A, TAF1B, FGF10, MSX1, LINC00640, FGFR1 and SPRY1). These 26 loci collectively account for 10.94% of the heritability for NSCLP in Chinese population. We find evidence of genetic heterogeneity between the sub-phenotypes of NSOFC and among different populations. This study substantially increases the number of genetic susceptibility loci for NSCLP and provides important insights into the genetic aetiology of this common craniofacial malformation.

2,033 Han Chinese ancestry cases, 4,051 Han Chinese ancestry controls

Chapter III

Study Statistics

Key metrics and study information

11972
Total Participants
GWAS
Study Type
Yes
Replicated
1,346 Han Chinese ancestry cases, 4,542 Han Chinese ancestry controls
Replication Participants
East Asian
Ancestry
China
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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