Menu
GWAS Study

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans: A Genome-Wide Association Study.

Foo JN, Chew EGY, Chung SJ et al.

32310270 PubMed ID
GWAS Study Type
1961445 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FJ
Foo JN
CE
Chew EGY
CS
Chung SJ
PR
Peng R
BC
Blauwendraat C
NM
Nalls MA
MK
Mok KY
SW
Satake W
TT
Toda T
CY
Chao Y
TL
Tan LCS
TM
Tandiono M
LM
Lian MM
NE
Ng EY
PK
Prakash KM
AW
Au WL
MW
Meah WY
MS
Mok SQ
AA
Annuar AA
CA
Chan AYY
CL
Chen L
CY
Chen Y
JB
Jeon BS
JL
Jiang L
LJ
Lim JL
LJ
Lin JJ
LC
Liu C
MC
Mao C
MV
Mok V
PZ
Pei Z
SH
Shang HF
SC
Shi CH
SK
Song K
TA
Tan AH
WY
Wu YR
XY
Xu YM
XR
Xu R
YY
Yan Y
YJ
Yang J
ZB
Zhang B
KW
Koh WP
LS
Lim SY
KC
Khor CC
LJ
Liu J
TE
Tan EK
Chapter II

Abstract

Summary of the research findings

Importance: Large-scale genome-wide association studies in the European population have identified 90 risk variants associated with Parkinson disease (PD); however, there are limited studies in the largest population worldwide (ie, Asian).

6,724 East Asian ancestry cases, 24,851 East Asian ancestry controls

Chapter III

Study Statistics

Key metrics and study information

1961445
Total Participants
GWAS
Study Type
Yes
Replicated
57,545 European ancestry cases, 1,868,816 European ancestry controls, 988 Japanese ancestry cases, 2,521 Japanese ancestry controls
Replication Participants
East Asian, European
Ancestry
China, Hong Kong SAR, Malaysia, Republic of Korea, Singapore, Taiwan, Australia, Japan
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.