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GWAS Study

A Genome-Wide Association Study Finds Genetic Associations with Broadly-Defined Headache in UK Biobank (N=223,773).

Meng W, Adams MJ, Hebert HL et al.

29397368 PubMed ID
GWAS Study Type
223782 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

MW
Meng W
AM
Adams MJ
HH
Hebert HL
DI
Deary IJ
MA
McIntosh AM
SB
Smith BH
Chapter II

Abstract

Summary of the research findings

Headache is the most common neurological symptom and a leading cause of years lived with disability. We sought to identify the genetic variants associated with a broadly-defined headache phenotype in 223,773 subjects from the UK Biobank cohort.

74,461 British ancestry cases, 149,321 British ancestry controls

Chapter III

Study Statistics

Key metrics and study information

223782
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.K.
Recruitment Country
Chapter IV

AI-Generated Summary

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