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GWAS Study

Role of the X Chromosome in Alzheimer Disease Genetics.

Belloy ME, Le Guen Y, Stewart I et al.

39250132 PubMed ID
GWAS Study Type
1152284 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BM
Belloy ME
LG
Le Guen Y
SI
Stewart I
WK
Williams K
HJ
Herz J
SR
Sherva R
ZR
Zhang R
MV
Merritt V
PM
Panizzon MS
HR
Hauger RL
GJ
Gaziano JM
LM
Logue M
NV
Napolioni V
GM
Greicius MD
Chapter II

Abstract

Summary of the research findings

Importance: The X chromosome has remained enigmatic in Alzheimer disease (AD), yet it makes up 5% of the genome and carries a high proportion of genes expressed in the brain, making it particularly appealing as a potential source of unexplored genetic variation in AD.

138,558 European ancestry cases, 1,013,726 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1152284
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S., Finland
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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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.