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GWAS Study

Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis.

Fogh I, Lin K, Tiloca C et al.

27244217 PubMed ID
GWAS Study Type
4256 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

FI
Fogh I
LK
Lin K
TC
Tiloca C
RJ
Rooney J
GC
Gellera C
DF
Diekstra FP
RA
Ratti A
SA
Shatunov A
VE
van Es MA
PP
Proitsi P
JA
Jones A
SW
Sproviero W
CA
Chiò A
MR
McLaughlin RL
SG
Sorarù G
CL
Corrado L
SD
Stahl D
DB
Del Bo R
CC
Cereda C
CB
Castellotti B
GJ
Glass JD
NS
Newhouse S
DR
Dobson R
SB
Smith BN
TS
Topp S
VR
van Rheenen W
MV
Meininger V
MJ
Melki J
MK
Morrison KE
SP
Shaw PJ
LP
Leigh PN
AP
Andersen PM
CG
Comi GP
TN
Ticozzi N
ML
Mazzini L
DS
D'Alfonso S
TB
Traynor BJ
VD
Van Damme P
RW
Robberecht W
BR
Brown RH
LJ
Landers JE
HO
Hardiman O
LC
Lewis CM
VD
van den Berg LH
SC
Shaw CE
VJ
Veldink JH
SV
Silani V
AA
Al-Chalabi A
PJ
Powell J
Chapter II

Abstract

Summary of the research findings

Importance: Amyotrophic lateral sclerosis (ALS) is a devastating adult-onset neurodegenerative disorder with a poor prognosis and a median survival of 3 years. However, a significant proportion of patients survive more than 10 years from symptom onset.

4,256 European ancestry cases

Chapter III

Study Statistics

Key metrics and study information

4256
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, U.S., Italy, Netherlands, Belgium, U.K., France, Republic of Ireland
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.