Menu
Currency
GWAS Study

Multiomics analysis of rheumatoid arthritis yields sequence variants that have large effects on risk of the seropositive subset.

Saevarsdottir S, Stefansdottir L, Sulem P et al.

35470158 PubMed ID
GWAS Study Type
1026690 Participants
97 Views
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SS
Saevarsdottir S
SL
Stefansdottir L
SP
Sulem P
TG
Thorleifsson G
FE
Ferkingstad E
RG
Rutsdottir G
GB
Glintborg B
WH
Westerlind H
GG
Grondal G
LI
Loft IC
SS
Sorensen SB
LB
Lie BA
BM
Brink M
ÄL
Ärlestig L
AA
Arnthorsson AO
BE
Baecklund E
BK
Banasik K
BS
Bank S
BL
Bjorkman LI
ET
Ellingsen T
EC
Erikstrup C
FO
Frei O
GI
Gjertsson I
GD
Gudbjartsson DF
GS
Gudjonsson SA
HG
Halldorsson GH
HO
Hendricks O
HJ
Hillert J
HE
Hogdall E
JS
Jacobsen S
JD
Jensen DV
JH
Jonsson H
KA
Kastbom A
KI
Kockum I
KS
Kristensen S
KH
Kristjansdottir H
LM
Larsen MH
LA
Linauskas A
HE
Hauge EM
LA
Loft AG
LB
Ludviksson BR
LS
Lund SH
MT
Markusson T
MG
Masson G
MP
Melsted P
MK
Moore KHS
MH
Munk H
NK
Nielsen KR
NG
Norddahl GL
OA
Oddsson A
OT
Olafsdottir TA
OP
Olason PI
OT
Olsson T
OS
Ostrowski SR
HK
Hørslev-Petersen K
RS
Rognvaldsson S
SH
Sanner H
SG
Silberberg GN
SH
Stefansson H
SE
Sørensen E
SI
Sørensen IJ
TC
Turesson C
BT
Bergman T
AL
Alfredsson L
KT
Kvien TK
BS
Brunak S
SK
Steinsson K
AV
Andersen V
AO
Andreassen OA
RS
Rantapää-Dahlqvist S
HM
Hetland ML
KL
Klareskog L
AJ
Askling J
PL
Padyukov L
PO
Pedersen OB
TU
Thorsteinsdottir U
JI
Jonsdottir I
SK
Stefansson K
Chapter II

Abstract

Summary of the research findings

Objectives: To find causal genes for rheumatoid arthritis (RA) and its seropositive (RF and/or ACPA positive) and seronegative subsets.

26,612 European ancestry cases, 869,454 European ancestry controls, 4,701 cases, 125,923 controls

Chapter III

Study Statistics

Key metrics and study information

1026690
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, Norway, Denmark, U.K., Iceland
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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

Important: This summary is AI-generated by DNAGENICS for informational purposes only. It was not created by, affiliated with, or endorsed by the researchers behind the original publication, and is based solely on that published research. It may contain errors or omissions. DNAGENICS disclaims all liability for any inaccuracies or consequences arising from use of this information. Verify all information against the original publication. This is not professional scientific review or medical advice.

AI Summary In Progress

Our AI-generated summary of this publication is being prepared. Please check back soon.