Menu
GWAS Study

ExomeChip-based rare variant association study in restless legs syndrome.

Tilch E, Schormair B, Zhao C et al.

35489115 PubMed ID
GWAS Study Type
9012 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

TE
Tilch E
SB
Schormair B
ZC
Zhao C
HB
Högl B
SA
Stefani A
BK
Berger K
TC
Trenkwalder C
BC
Bachmann CG
HM
Hornyak M
FI
Fietze I
MM
Müller-Nurasyid M
PA
Peters A
HS
Herms S
NM
Nöthen MM
MB
Müller-Myhsok B
OK
Oexle K
WJ
Winkelmann J
Chapter II

Abstract

Summary of the research findings

Restless legs syndrome (RLS) is a common sleep-related movement disorder in populations of European descent and disease risk is strongly influenced by genetic factors. Common variants have been assessed extensively in several genome-wide association studies, but the contribution of rarer genetic variation has not been investigated at this scale. We therefore genotyped a case-control set of 9246 individuals for mainly rare and low frequency exonic variants using the Illumina ExomeChip. However, standard single variant and gene-level association tests were negative. This does not preclude a role of rare variants in RLS, but is likely due to the small sample size and the limited selection of rare genetic variation captured on the array. Therefore, exome or whole genome sequencing should be performed rather than increasing the sample size of ExomeChip studies in order to identify rare risk variants for RLS.

3,652 European ancestry cases, 5,360 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

9012
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Germany
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.