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GWAS Study

Genome-wide Association Study points to novel locus for Gilles de la Tourette Syndrome.

Tsetsos F, Topaloudi A, Jain P et al.

36738982 PubMed ID
GWAS Study Type
19698 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TF
Tsetsos F
TA
Topaloudi A
JP
Jain P
YZ
Yang Z
YD
Yu D
KP
Kolovos P
TZ
Tumer Z
RR
Rizzo R
HA
Hartmann A
DC
Depienne C
WY
Worbe Y
MK
Müller-Vahl KR
CD
Cath DC
BD
Boomsma DI
WT
Wolanczyk T
ZC
Zekanowski C
BC
Barta C
NZ
Nemoda Z
TZ
Tarnok Z
PS
Padmanabhuni SS
BJ
Buxbaum JD
GD
Grice D
GJ
Glennon J
SH
Stefansson H
HB
Hengerer B
YE
Yannaki E
SJ
Stamatoyannopoulos JA
BN
Benaroya-Milshtein N
CF
Cardona F
HT
Hedderly T
HI
Heyman I
HC
Huyser C
MP
Mir P
MA
Morer A
MN
Mueller N
MA
Munchau A
PK
Plessen KJ
PC
Porcelli C
RV
Roessner V
WS
Walitza S
SA
Schrag A
MD
Martino D
TJ
Tischfield JA
HG
Heiman GA
WA
Willsey AJ
DA
Dietrich A
DL
Davis LK
CJ
Crowley JJ
MC
Mathews CA
SJ
Scharf JM
GM
Georgitsi M
HP
Hoekstra PJ
PP
Paschou P
Chapter II

Abstract

Summary of the research findings

Tourette syndrome (TS) is a childhood-onset neurodevelopmental disorder of complex genetic architecture and is characterized by multiple motor tics and at least one vocal tic persisting for more than 1 year.

6,133 European ancestry cases, 13,565 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

19698
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, France, Germany, Spain
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.