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Paper Details

The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions.
Nat Med
468
2018
-, AML, CBL, Children, Children's Oncology, DNA variants, DNMT3A, ELF1, FLT3, GATA2, ITD, KMT2A, KRAS, MBNL1, MYC, MYC-, NRAS, Polycomb, TP53, WT1, Wnt, ZEB2, innate immune cell, mRNA, microRNA, participants, pediatric AML, pediatric acute myeloid leukemia, zinc, zinc finger-encoding genes
Author NameAffiliation
Timothy J TricheUniversity of Southern California Norris Comprehensive Cancer Center
Timothy J TricheUniversity of Southern California Norris Comprehensive Cancer Center
Rhonda E RiesClinical Research Division, Fred Hutchinson Cancer Research Center
Rhonda E RiesClinical Research Division, Fred Hutchinson Cancer Research Center
Todd A AlonzoKeck School of Medicine, University of Southern California
Todd A Alonzo
Todd A AlonzoKeck School of Medicine, University of Southern California
Todd A Alonzo
Yussanne Ma
Richard A Moore
Andrew J Mungall
Marco A Marra
Marco A Marra
Jinghui ZhangSt. Jude Children's Research Hospital
Jinghui ZhangSt. Jude Children's Research Hospital
Xiaotu MaSt. Jude Children's Research Hospital
Xiaotu MaSt. Jude Children's Research Hospital
Yu LiuSt. Jude Children's Research Hospital
Yu LiuSt. Jude Children's Research Hospital
Yanling LiuSt. Jude Children's Research Hospital
Yanling LiuSt. Jude Children's Research Hospital
Jaime M Guidry AuvilNational Cancer Institute
Jaime M Guidry AuvilNational Cancer Institute
Tanja M DavidsenNational Cancer Institute
Leandro C HermidaNational Cancer Institute
Leandro C HermidaNational Cancer Institute
Stephen CaponeUniversity of Southern California Norris Comprehensive Cancer Center
Stephen R PiccoloBrigham Young University
Stephen R PiccoloUniversity of Utah
Edward A KolbNemours Center for Cancer and Blood Disorders, Alfred I. DuPont Hospital for Children
Malcolm A SmithNational Cancer Institute
Malcolm A SmithNational Cancer Institute
Daniela S GerhardNational Cancer Institute
Daniela S GerhardNational Cancer Institute
Soheil MeshinchiClinical Research Division, Fred Hutchinson Cancer Research Center
Soheil MeshinchiClinical Research Division, Fred Hutchinson Cancer Research Center
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