Menu
GWAS Study

Genome-wide association analysis reveals the associations of NPHP4, TYW1-AUTS2 and SEMA6D for Behçet's disease and HLA-B*46:01 for its intestinal involvement.

Jung ES, Ellinghaus D, Degenhardt F et al.

37977914 PubMed ID
GWAS Study Type
5346 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

JE
Jung ES
ED
Ellinghaus D
DF
Degenhardt F
MA
Meguro A
KS
Khor SS
MS
Mucha S
WM
Wendorff M
JS
Juzenas S
MN
Mizuki N
TK
Tokunaga K
KS
Kim SW
LM
Lee MG
SS
Schreiber S
KW
Kim WH
FA
Franke A
CJ
Cheon JH
Chapter II

Abstract

Summary of the research findings

Intestinal involvement in Behçet's disease (BD) is associated with poor prognosis and is more prevalent in East Asian than in Mediterranean populations. Identifying the genetic causes of intestinal BD is important for understanding the pathogenesis and for appropriate treatment of BD patients.

1,689 Korean ancestry cases, 2,327 Korean ancestry controls

Chapter III

Study Statistics

Key metrics and study information

5346
Total Participants
GWAS
Study Type
Yes
Replicated
593 Japanese ancestry cases, 737 Japanese ancestry controls
Replication Participants
East Asian
Ancestry
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.