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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
63 Views
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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

AI-Generated Summary

AI-generated by DNAGENICS

Independent AI summary of health and genetic findings from the published study

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