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GWAS Study

Association of GATA3 polymorphisms with minimal residual disease and relapse risk in childhood acute lymphoblastic leukemia.

Zhang H, Liu AP, Devidas M et al.

32894760 PubMed ID
GWAS Study Type
3088 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ZH
Zhang H
LA
Liu AP
DM
Devidas M
LS
Lee SH
CX
Cao X
PD
Pei D
BM
Borowitz M
WB
Wood B
GJ
Gastier-Foster JM
DY
Dai Y
RE
Raetz E
LE
Larsen E
WN
Winick N
BW
Bowman WP
KS
Karol S
YW
Yang W
MP
Martin PL
CW
Carroll WL
PC
Pui CH
MC
Mullighan CG
EW
Evans WE
CC
Cheng C
HS
Hunger SP
RM
Relling MV
LM
Loh ML
YJ
Yang JJ
Chapter II

Abstract

Summary of the research findings

Minimal residual disease (MRD) after induction therapy is one of the strongest prognostic factors in childhood acute lymphoblastic leukemia (ALL), and MRD-directed treatment intensification improves survival. Little is known about the effects of inherited genetic variants on interpatient variability in MRD.

243 European ancestry cases, 1,181 European ancestry controls, 18 Black cases, 110 Black controls, 141 Hispanic cases, 531 Hispanic controls, 16 Asian ancestry cases, 54 Asian ancestry controls, 54 cases, 249 controls

Chapter III

Study Statistics

Key metrics and study information

3088
Total Participants
GWAS
Study Type
Yes
Replicated
49 European ancestry cases, 248 European ancestry controls, 4 Black cases, 29 Black controls, 23 Hispanic cases, 82 Hispanic controls, 3 Asian ancestry cases, 9 Asian ancestry controls, 3 cases, 41 controls
Replication Participants
European, African unspecified, Hispanic or Latin American, Asian unspecified
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.