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GWAS Study

Genome Wide Association Study Identifies Risk Loci For Cluster Headache.

O'Connor E, Fourier C, Ran C et al.

34184781 PubMed ID
GWAS Study Type
8191 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

OE
O'Connor E
FC
Fourier C
RC
Ran C
SP
Sivakumar P
LF
Liesecke F
SL
Southgate L
HA
Harder AVE
VL
Vijfhuizen LS
YJ
Yip J
GN
Giffin N
SN
Silver N
AF
Ahmed F
HI
Hostettler IC
DB
Davies B
CM
Cader MZ
SB
Simpson BS
SR
Sullivan R
ES
Efthymiou S
AJ
Adebimpe J
QO
Quinn O
CC
Campbell C
CG
Cavalleri GL
VM
Vikelis M
KT
Kelderman T
PK
Paemeleire K
KE
Kilbride E
GL
Grangeon L
LS
Lagrata S
DD
Danno D
TR
Trembath R
WN
Wood NW
KI
Kockum I
WB
Winsvold BS
SA
Steinberg A
SC
Sjöstrand C
WE
Waldenlind E
VJ
Vandrovcova J
HH
Houlden H
MM
Matharu M
BA
Belin AC
Chapter II

Abstract

Summary of the research findings

Objective: This study was undertaken to identify susceptibility loci for cluster headache and obtain insights into relevant disease pathways.

1,443 European ancestry cases, 6,748 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

8191
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, U.K.
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.