Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in…
By D. Grimwade, R. Hills, A. Moorman, H. Walker, S. Chatters, A. Goldstone, K. Wheatley, C. Harrison, A. Burnett. Blood, 2010
1,914 citations recorded by the source corpus.
Subfields: Hematology, Molecular Biology, Public Health, Environmental and Occupational Health
View Paper: https://www.semanticscholar.org/paper/a0d61d52574cbd949ad1cace39073240444b671a
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Citations in the corpus
- TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome. (2012, methodology): “3 INTRODUCTION Chromosomal abnormalities are found in about 55% of adult patients with acute myeloid leukemia (AML) and are among the most important independent prognostic factors(1-3).”
- Diagnosis and management of AML in adults: 2017 ELN recommendations from an international expert panel. (2017, background): “Other rare balanced rearrangements are recognized.(49,50) Although considered diseaseinitiating events, they do not formally define disease categories.”