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GWAS Study

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility.

Sorosina M, Barizzone N, Clarelli F et al.

35545683 PubMed ID
GWAS Study Type
17065 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

SM
Sorosina M
BN
Barizzone N
CF
Clarelli F
AS
Anand S
LS
Lupoli S
SE
Salvi E
ME
Mangano E
BR
Bordoni R
RT
Roostaei T
ME
Mascia E
ZM
Zuccalà M
VD
Vecchio D
CP
Cavalla P
SS
Santoro S
FL
Ferrè L
ZA
Zollo A
BC
Barlassina C
CD
Cusi D
MV
Martinelli V
CG
Comi G
LM
Leone M
FM
Filippi M
PN
Patsopoulos NA
DJ
De Jager PL
DB
De Bellis G
EF
Esposito F
DS
D'Alfonso S
MB
Martinelli Boneschi F
Chapter II

Abstract

Summary of the research findings

Over 200 genetic loci have been associated with multiple sclerosis (MS) explaining ~ 50% of its heritability, suggesting that additional mechanisms may account for the "missing heritability" phenomenon.

1,701 Italian ancestry cases, 2,345 Italian ancestry controls

Chapter III

Study Statistics

Key metrics and study information

17065
Total Participants
GWAS
Study Type
Yes
Replicated
4,991 European ancestry cases, 8,028 European ancestry controls
Replication Participants
European
Ancestry
Italy
Recruitment Country
Chapter IV

AI-Generated Summary

AI-generated by DNAGENICS

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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.

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