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GWAS Study

Common X-Chromosome Variants Are Associated with Parkinson Disease Risk.

Le Guen Y, Napolioni V, Belloy ME et al.

33583074 PubMed ID
GWAS Study Type
304760 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LG
Le Guen Y
NV
Napolioni V
BM
Belloy ME
YE
Yu E
KL
Krohn L
RJ
Ruskey JA
GZ
Gan-Or Z
KG
Kennedy G
ES
Eger SJ
GM
Greicius MD
Chapter II

Abstract

Summary of the research findings

Objective: The objective of this study was to identify genetic variants on the X-chromosome associated with Parkinson disease (PD) risk.

3,500 European ancestry female cases, 1,828 European ancestry female proxy cases, 297,580 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

304760
Total Participants
GWAS
Study Type
Yes
Replicated
535 European ancestry cases, 1,317 European ancestry controls
Replication Participants
European
Ancestry
U.S., 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.