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GWAS Study

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Stambolian D, Wojciechowski R, Oexle K et al.

23474815 PubMed ID
GWAS Study Type
27043 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SD
Stambolian D
WR
Wojciechowski R
OK
Oexle K
PM
Pirastu M
LX
Li X
RL
Raffel LJ
CM
Cotch MF
CE
Chew EY
KB
Klein B
KR
Klein R
WT
Wong TY
SC
Simpson CL
KC
Klaver CC
VD
van Duijn CM
VV
Verhoeven VJ
BP
Baird PN
VV
Vitart V
PA
Paterson AD
MP
Mitchell P
SS
Saw SM
FM
Fossarello M
KK
Kazmierkiewicz K
MF
Murgia F
PL
Portas L
SM
Schache M
RA
Richardson A
XJ
Xie J
WJ
Wang JJ
RE
Rochtchina E
VA
Viswanathan AC
HC
Hayward C
WA
Wright AF
PO
Polasek O
CH
Campbell H
RI
Rudan I
OB
Oostra BA
UA
Uitterlinden AG
HA
Hofman A
RF
Rivadeneira F
AN
Amin N
KL
Karssen LC
VJ
Vingerling JR
HS
Hosseini SM
DA
Döring A
BT
Bettecken T
VZ
Vatavuk Z
GC
Gieger C
WH
Wichmann HE
WJ
Wilson JF
FB
Fleck B
FP
Foster PJ
TF
Topouzis F
MP
McGuffin P
SX
Sim X
IM
Inouye M
HE
Holliday EG
AJ
Attia J
SR
Scott RJ
RJ
Rotter JI
MT
Meitinger T
BJ
Bailey-Wilson JE
Chapter II

Abstract

Summary of the research findings

Visual refractive errors (REs) are complex genetic traits with a largely unknown etiology. To date, genome-wide association studies (GWASs) of moderate size have identified several novel risk markers for RE, measured here as mean spherical equivalent (MSE). We performed a GWAS using a total of 7280 samples from five cohorts: the Age-Related Eye Disease Study (AREDS); the KORA study ('Cooperative Health Research in the Region of Augsburg'); the Framingham Eye Study (FES); the Ogliastra Genetic Park-Talana (OGP-Talana) Study and the Multiethnic Study of Atherosclerosis (MESA). Genotyping was performed on Illumina and Affymetrix platforms with additional markers imputed to the HapMap II reference panel. We identified a new genome-wide significant locus on chromosome 16 (rs10500355, P = 3.9 × 10(-9)) in a combined discovery and replication set (26 953 samples). This single nucleotide polymorphism (SNP) is located within the RBFOX1 gene which is a neuron-specific splicing factor regulating a wide range of alternative splicing events implicated in neuronal development and maturation, including transcription factors, other splicing factors and synaptic proteins.

6,597 European ancestry and Erasmus Rucphen individuals, 683 Sardinian inidividuals

Chapter III

Study Statistics

Key metrics and study information

27043
Total Participants
GWAS
Study Type
Yes
Replicated
19,763 European ancestry individuals
Replication Participants
European
Ancestry
U.S., Australia, Netherlands, Canada, U.K., Croatia, Italy, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.