Page 107 - Read Online
P. 107

Page 237                   Xu et al. J Transl Genet Genom 2021;5:218-39  https://dx.doi.org/10.20517/jtgg.2021.20

                    PubMed
               130.      Sawalha Y, Advani AS. Management of older adults with acute lymphoblastic leukemia: challenges & current approaches. Int J
                    Hematol Oncol 2018;7:IJH02.  DOI  PubMed  PMC
               131.      Kozlowski P, Lennmyr E, Ahlberg L, et al; Swedish Adult Acute Lymphoblastic Leukemia Group (SVALL). Age but not
                    Philadelphia positivity impairs outcome in older/elderly patients with acute lymphoblastic leukemia in Sweden. Eur J Haematol
                    2017;99:141-9.  DOI  PubMed
               132.      Harvey RC, Mullighan CG, Chen IM, et al. Rearrangement of CRLF2 is associated with mutation of JAK kinases, alteration of
                    IKZF1,  Hispanic/Latino  ethnicity,  and  a  poor  outcome  in  pediatric  B-progenitor  acute  lymphoblastic  leukemia.  Blood
                    2010;115:5312-21.  DOI  PubMed  PMC
               133.      Yang H, Zhang H, Luan Y, et al. Non-coding germline GATA3 variants alter chromatin topology and contribute to pathogenesis of
                    acute lymphoblastic leukemia. Cancer Biology 2020.  DOI
               134.      Herold T, Schneider S, Metzeler KH, et al. Adults with Philadelphia chromosome-like acute lymphoblastic leukemia frequently have
                    IGH-CRLF2 and JAK2 mutations, persistence of minimal residual disease and poor prognosis. Haematologica 2017;102:130-8.  DOI
                    PubMed  PMC
               135.      Perez-Andreu V, Roberts KG, Xu H, et al. A genome-wide association study of susceptibility to acute lymphoblastic leukemia in
                    adolescents and young adults. Blood 2015;125:680-6.  DOI  PubMed  PMC
               136.      Evans TJ, Milne E, Anderson D, et al. Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and
                    interaction with parental environmental exposures. PLoS One 2014;9:e110255.  DOI  PubMed  PMC
               137.      Walsh KM, Chokkalingam AP, Hsu LI, et al. Associations between genome-wide Native American ancestry, known risk alleles and
                    B-cell ALL risk in Hispanic children. Leukemia 2013;27:2416-9.  DOI  PubMed  PMC
               138.      Walsh KM, de Smith AJ, Chokkalingam AP, et al. GATA3 risk alleles are associated with ancestral components in Hispanic children
                    with ALL. Blood 2013;122:3385-7.  DOI  PubMed  PMC
               139.      Xu H, Cheng C, Devidas M, et al. ARID5B genetic polymorphisms contribute to racial disparities in the incidence and treatment
                    outcome of childhood acute lymphoblastic leukemia. J Clin Oncol 2012;30:751-7.  DOI  PubMed  PMC
               140.      Wolfe D, Dudek S, Ritchie MD, Pendergrass SA. Visualizing genomic information across chromosomes with PhenoGram. BioData
                    Min 2013;6:18.  DOI  PubMed  PMC
               141.      Buniello A, MacArthur JAL, Cerezo M, et al. The NHGRI-EBI GWAS Catalog of published genome-wide association studies,
                    targeted arrays and summary statistics 2019. Nucleic Acids Res 2019;47:D1005-12.  DOI  PubMed  PMC
               142.      Yang JJ, Landier W, Yang W, et al. Inherited NUDT15 variant is a genetic determinant of mercaptopurine intolerance in children
                    with acute lymphoblastic leukemia. J Clin Oncol 2015;33:1235-42.  DOI  PubMed  PMC
               143.      Diouf B, Crews KR, Lew G, et al. Association of an inherited genetic variant with vincristine-related peripheral neuropathy in
                    children with acute lymphoblastic leukemia. JAMA 2015;313:815-23.  DOI  PubMed  PMC
               144.      Fernandez CA, Smith C, Yang W, et al. Genome-wide analysis links NFATC2 with asparaginase hypersensitivity. Blood
                    2015;126:69-75.  DOI  PubMed  PMC
               145.      Liu C, Yang W, Devidas M, et al. Clinical and genetic risk factors for acute pancreatitis in patients with acute lymphoblastic
                    leukemia. J Clin Oncol 2016;34:2133-40.  DOI  PubMed  PMC
               146.      Liu Y, Fernandez CA, Smith C, et al. Genome-wide study links PNPLA3 variant with elevated hepatic transaminase after acute
                    lymphoblastic leukemia therapy. Clin Pharmacol Ther 2017;102:131-40.  DOI  PubMed  PMC
               147.      Højfeldt SG, Wolthers BO, Tulstrup M, et al; Nordic Society of Paediatric Haematology Oncology (NOPHO) group. Genetic
                    predisposition  to  PEG-asparaginase  hypersensitivity  in  children  treated  according  to  NOPHO  ALL2008.  Br  J  Haematol
                    2019;184:405-17.  DOI  PubMed
               148.      Liu C, Yang W, Pei D, et al. Genomewide approach validates thiopurine methyltransferase activity is a monogenic pharmacogenomic
                    trait. Clin Pharmacol Ther 2017;101:373-81.  DOI  PubMed  PMC
               149.      Tulstrup M, Grosjean M, Nielsen SN, et al. NT5C2 germline variants alter thiopurine metabolism and are associated with acquired
                    NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. Leukemia 2018;32:2527-35.  DOI  PubMed
               150.      Yang JJ, Cheng C, Devidas M, et al. Genome-wide association study identifies germline polymorphisms associated with relapse of
                    childhood acute lymphoblastic leukemia. Blood 2012;120:4197-204.  DOI  PubMed  PMC
               151.      Spear ML, Diaz-Papkovich A, Ziv E, et al. Recent shifts in the genomic ancestry of Mexican Americans may alter the genetic
                    architecture of biomedical traits. Elife 2020;9:e56029.  DOI  PubMed  PMC
               152.      Karol SE, Larsen E, Cheng C, et al. Genetics of ancestry-specific risk for relapse in acute lymphoblastic leukemia. Leukemia
                    2017;31:1325-32.  DOI  PubMed  PMC
               153.      Yang JJ, Cheng C, Devidas M, et al. Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Nat Genet
                    2011;43:237-41.  DOI  PubMed  PMC
               154.      Zhang H, Liu AP, Devidas M, et al. Association of GATA3 polymorphisms with minimal residual disease and relapse risk in
                    childhood acute lymphoblastic leukemia. J Natl Cancer Inst 2021;113:408-17.  DOI  PubMed
               155.      Jain N, Zhang H, Roberts K G, et al. GATA3 rs3824662A allele is overrepresented in adult patients with Ph-like ALL, especially in
                    patients with CRLF2 abnormalities. Blood 2017;130:1430.
               156.      Moriyama T, Nishii R, Perez-Andreu V, et al. NUDT15 polymorphisms alter thiopurine metabolism and hematopoietic toxicity. Nat
                    Genet 2016;48:367-73.  DOI  PubMed  PMC
               157.      Greaves M. Childhood leukaemia. BMJ 2002;324:283-7.  DOI  PubMed  PMC
               158.      Wiemels J, Cazzaniga G, Daniotti M, et al. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet 1999;354:1499-503.
   102   103   104   105   106   107   108   109   110   111   112