Cytogenetics and molecular genetics of acute lymphoblastic leukemia

K Mrózek, DP Harper, PD Aplan - Hematology/Oncology …, 2009 - hemonc.theclinics.com
Acute lymphoblastic leukemia (ALL) is a neoplastic disease characterized by clonal
expansion of leukemic cells in the bone marrow (BM), lymph nodes, thymus, or spleen. ALL …

Diagnostic and prognostic value of cytogenetics in acute myeloid leukemia

D Grimwade, K Mrózek - Hematology/Oncology Clinics, 2011 - hemonc.theclinics.com
The last 4 decades have seen major advances in understanding the genetic basis of acute
myeloid leukemia (AML), paralleled by substantial improvements in survival of children and …

IDH1 and IDH2 Gene Mutations Identify Novel Molecular Subsets Within De Novo Cytogenetically Normal Acute Myeloid Leukemia: A Cancer and Leukemia Group …

G Marcucci, K Maharry, YZ Wu… - Journal of clinical …, 2010 - ascopubs.org
Purpose To analyze the frequency and associations with prognostic markers and outcome of
mutations in IDH genes encoding isocitrate dehydrogenases in adult de novo …

Prognostic significance of the European LeukemiaNet standardized system for reporting cytogenetic and molecular alterations in adults with acute myeloid leukemia

K Mrózek, G Marcucci, D Nicolet, KS Maharry… - Journal of clinical …, 2012 - ascopubs.org
Purpose To evaluate the prognostic significance of the international European LeukemiaNet
(ELN) guidelines for reporting genetic alterations in acute myeloid leukemia (AML). Patients …

[HTML][HTML] Outcome prediction by the 2022 European LeukemiaNet genetic-risk classification for adults with acute myeloid leukemia: an Alliance study

K Mrózek, J Kohlschmidt, JS Blachly, D Nicolet… - Leukemia, 2023 - nature.com
Abstract Recently, the European LeukemiaNet (ELN) revised its genetic-risk classification of
acute myeloid leukemia (AML). We categorized 1637 adults with AML treated with …

RUNX1 Mutations Are Associated With Poor Outcome in Younger and Older Patients With Cytogenetically Normal Acute Myeloid Leukemia and With Distinct Gene …

JH Mendler, K Maharry, MD Radmacher… - Journal of clinical …, 2012 - ascopubs.org
Purpose To determine the association of RUNX1 mutations with therapeutic outcome in
younger and older patients with primary cytogenetically normal acute myeloid leukemia (CN …

TET2 Mutations Improve the New European LeukemiaNet Risk Classification of Acute Myeloid Leukemia: A Cancer and Leukemia Group B Study

KH Metzeler, K Maharry, MD Radmacher… - Journal of clinical …, 2011 - ascopubs.org
Purpose To determine the frequency of TET2 mutations, their associations with clinical and
molecular characteristics and outcome, and the associated gene-and microRNA-expression …

ASXL1 mutations identify a high-risk subgroup of older patients with primary cytogenetically normal AML within the ELN Favorable genetic category

KH Metzeler, H Becker, K Maharry… - Blood, The Journal …, 2011 - ashpublications.org
The associations of mutations in the enhancer of trithorax and polycomb family gene ASXL1
with pretreatment patient characteristics, outcomes, and gene-/microRNA-expression …

Expression and prognostic impact of lncRNAs in acute myeloid leukemia

R Garzon, S Volinia, D Papaioannou… - Proceedings of the …, 2014 - National Acad Sciences
Long noncoding RNAs (lncRNAs) are transcripts longer than 200 nucleotides, located within
the intergenic stretches or overlapping antisense transcripts of protein coding genes …

Age-Related Prognostic Impact of Different Types of DNMT3A Mutations in Adults With Primary Cytogenetically Normal Acute Myeloid Leukemia

G Marcucci, KH Metzeler, S Schwind… - Journal of clinical …, 2012 - ascopubs.org
Purpose To determine the frequency of DNMT3A mutations, their associations with clinical
and molecular characteristics and outcome, and the associated gene-and microRNA …