Selelcted publications

  1. Hu Z, Kovach AE, Yelapantulla V, Ostrow D, Doan A, Ji J, Schmidt RJ, Gu Z*, Bhojwani D and Raca G*. Transcriptome Sequencing Allows Comprehensive Genomic Characterization of Pediatric B-Cell Acute Lymphoblastic Leukemia in an Academic Clinical Laboratory. J Mol Diagn.. Epub 2023 Nov 18. (*co-corresponding)
  2. Gu Z & Izraeli S. All about Down syndrome ALL. Blood. 142, 126-128. 2023
  3. Hu Z, Jia Z, Liu J, Mao A, Han H, Gu Z. MD-ALL: an Integrative Platform for Molecular Diagnosis of B-Acute Lymphoblastic Leukemia. Haematologica. [Online ahead of print] 2023. (corresponding)
  4. Jia Z, Gu Z. PAX5 alterations in B-cell acute lymphoblastic leukemia. Frontiers in Oncology. 2022. (corresponding)
  5. Bařinka J, Hu Z, Wang L, ..., Gu Z*, Mullighan CG*. RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data. Leukemia. 2022; 36(6): 1492-1498. (*co-corresponding)
  6. Montefiori LE*, Bendig S*, Gu Z*, Dobson SM*, ..., Klco JM, Haferlach C, Mullighan CG. Enhancer hijacking drives oncogenic BCL11B expression in lineage ambiguous stem cell leukemia Cancer Discovery. 2021; 11(11): 2846-2867 (*co-first)
  7. Waanders E*, Gu Z*, Chen X*, ..., Dick JE, Kuiper RP, Mullighan CG. Mutational landscape and patterns of clonal evolution in relapsed pediatric acute lymphoblastic leukemia. Blood Cancer Discovery. 2020; 21:1-16 (*co-first)
  8. Gu Z*, Churchman ML*, Roberts KG*, ..., Loh ML, Hunger SP, Mullighan CG. PAX5-driven Subtypes of B-cell Acute Lymphoblastic Leukemia. Nature Genetics. 2019; 51(2):296-307 (*co-first)
  9. Alexander TB*, Gu Z*, Iacobucci I*, ..., Hunger SP, Inaba H, Mullighan CG. The genetic basis and cell of origin of mixed phenotype acute leukemia. Nature. 2018; 562(7727):373-379 (*co-first)
  10. Gu Z, Mullighan CG. ShinyCNV: a Shiny/R application to view and annotate DNA copy number variations. Bioinformatics. 2018; 35(1):126-129. doi: 10.1093/bioinformatics/bty546.
  11. Gu Z, Churchman M, Roberts K, ..., L. Loh M, P. Hunger SP, Mullighan CG. Genomic analyses identify recurrent MEF2D fusions in acute lymphoblastic leukaemia. Nature Communications. 2016; 7:13331
  12. Jiang L*, Gu Z*, Yan ZX*, Zhao X*, ..., Zhao WL, Chen Z, Chen SJ. Exome sequencing identifies somatic mutations of DDX3X in natural killer/T-cell lymphoma. Nature Genetics. 2015; 47(9):1061-6 (*co-first)
  13. Yan XJ*, Xu J*, Gu Z*, Pan CM*, Lu G*, ..., Li KQ, Chen Z, Chen SJ. Exome sequencing identifies somatic mutations of DNA methyltransferase gene DNMT3A in acute monocytic leukemia. Nature Genetics. 2011; 43(4):309-15 (*co-first)
  14. Xu L*, Gu Z*, Li Y*, Zhang JL*, Chang CK*, ..., Li X, Chen Z & Chen SJ. Genomic Landscape of CD34+ Hematopoietic Cells in Myelodysplastic Syndrome and Gene Mutation Profiles as Prognostic Markers. Proc Natl Acad Sci U S A. 2014; 111(23):8589-94 (*co-first)