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GWAS Study

Genetic Variants in the 9p21.3 Locus Associated with Glioma Risk in Children, Adolescents, and Young Adults: a Case-control Study.

Dahlin AM, Wibom C, Andersson U et al.

31040135 PubMed ID
GWAS Study Type
4543 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DA
Dahlin AM
WC
Wibom C
AU
Andersson U
HD
Hougaard DM
BJ
Bybjerg-Grauholm J
DI
Deltour I
HC
Hultman CM
KA
Kähler AK
KR
Karlsson R
HU
Hjalmars U
MB
Melin B
Chapter II

Abstract

Summary of the research findings

Genome-wide association studies have identified germline genetic variants in 25 genetic loci that increase the risk of developing glioma in adulthood. It is not known if these variants increase the risk of developing glioma in children and adolescents and young adults (AYA). To date, no studies have performed genome-wide analyses to find novel genetic variants associated with glioma risk in children and AYA.

854 European ancestry cases, 3,689 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

4543
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, Denmark
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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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.