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Corrigendum.
Burns MA, Place AE, Stevenson KE, Gutiérrez A, Forrest S, Pikman Y, Vrooman LM, Harris MH, Weinberg OK, Hunt SK, O'Brien JE, Asselin BL, Athale UH, Clavell LA, Cole PD, Gennarini LM, Kahn J, Kelly KM, Laverdiere C, Leclerc JM, Michon B, Schorin MA, Sulis ML, Welch JJG, Neuberg DS, Sallan SE, Silverman LB. Burns MA, et al. Among authors: weinberg ok. Pediatr Blood Cancer. 2021 Mar;68(3):e28885. doi: 10.1002/pbc.28885. Epub 2020 Dec 31. Pediatr Blood Cancer. 2021. PMID: 33506554 No abstract available.
Genomic and clinical characterization of B/T mixed phenotype acute leukemia reveals recurrent features and T-ALL like mutations.
Mi X, Griffin G, Lee W, Patel S, Ohgami R, Ok CY, Wang S, Geyer JT, Xiao W, Roshal M, Garcia JS, Silverman LB, Sallan SE, Aster JC, Harris MH, Weinberg OK. Mi X, et al. Among authors: ok cy, weinberg ok. Am J Hematol. 2018 Nov;93(11):1358-1367. doi: 10.1002/ajh.25256. Epub 2018 Sep 26. Am J Hematol. 2018. PMID: 30117174 Free PMC article.
NPM1 mutation but not RUNX1 mutation or multilineage dysplasia defines a prognostic subgroup within de novo acute myeloid leukemia lacking recurrent cytogenetic abnormalities in the revised 2016 WHO classification.
Weinberg OK, Gibson CJ, Blonquist TM, Neuberg D, Pozdnyakova O, Kuo F, Ebert BL, Hasserjian RP. Weinberg OK, et al. Am J Hematol. 2017 Jul;92(7):E123-E124. doi: 10.1002/ajh.24739. Epub 2017 May 26. Am J Hematol. 2017. PMID: 28370403 Free PMC article. No abstract available.
Diagnostic work-up of acute myeloid leukemia.
Weinberg OK, Sohani AR, Bhargava P, Nardi V. Weinberg OK, et al. Am J Hematol. 2017 Mar;92(3):317-321. doi: 10.1002/ajh.24648. Epub 2017 Feb 3. Am J Hematol. 2017. PMID: 28066929 Free article. Review.
116 results