Related references
Note: Only part of the references are listed.Molecular basis and clinical significance of genetic aberrations in B-cell precursor acute lymphoblastic leukemia
Farzaneh Ghazavi et al.
EXPERIMENTAL HEMATOLOGY (2015)
Novel biological insights in T-cell acute lymphoblastic leukemia
Kaat Durinck et al.
EXPERIMENTAL HEMATOLOGY (2015)
Deep sequencing and SNP array analyses of pediatric T-cell acute lymphoblastic leukemia reveal NOTCH1 mutations in minor subclones and a high incidence of uniparental isodisomies affecting CDKN2A
Kristina Karrman et al.
JOURNAL OF HEMATOLOGY & ONCOLOGY (2015)
KRAS and CREBBP mutations: a relapse-linked malicious liaison in childhood high hyperdiploid acute lymphoblastic leukemia
K. Malinowska-Ozdowy et al.
LEUKEMIA (2015)
The landscape of somatic mutations in infant MLL-rearranged acute lymphoblastic leukemias
Anna K. Andersson et al.
NATURE GENETICS (2015)
The genomic landscape of high hyperdiploid childhood acute lymphoblastic leukemia
Kajsa Paulsson et al.
NATURE GENETICS (2015)
Clinical Significance of Previously Cryptic Copy Number Alterations and Loss of Heterozygosity in Pediatric Acute Myeloid Leukemia and Myelodysplastic Syndrome Determined Using Combined Array Comparative Genomic Hybridization plus Single-Nucleotide Polymorphism Microarray Analyses
Kyung-Nam Koh et al.
JOURNAL OF KOREAN MEDICAL SCIENCE (2014)
Translational implications of somatic genomics in acute myeloid leukaemia
Sara C. Meyer et al.
LANCET ONCOLOGY (2014)
Core-binding factor acute myeloid leukemia in pediatric patients enrolled in the AIEOP AML 2002/01 trial: screening and prognostic impact of c-KIT mutations
E. Manara et al.
LEUKEMIA (2014)
Deletions of IKZF1 and SPRED1 are associated with poor prognosis in a population-based series of pediatric B-cell precursor acute lymphoblastic leukemia diagnosed between 1992 and 2011
L. Olsson et al.
LEUKEMIA (2014)
An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions
E. Clappier et al.
LEUKEMIA (2014)
RAG-mediated recombination is the predominant driver of oncogenic rearrangement in ETV6-RUNX1 acute lymphoblastic leukemia
Elli Papaemmanuil et al.
NATURE GENETICS (2014)
Targetable Kinase-Activating Lesions in Ph-like Acute Lymphoblastic Leukemia
K. G. Roberts et al.
NEW ENGLAND JOURNAL OF MEDICINE (2014)
The landscape of somatic mutations in epigenetic regulators across 1,000 paediatric cancer genomes
Robert Huether et al.
NATURE COMMUNICATIONS (2014)
Cooperating gene mutations in childhood acute myeloid leukemia with special reference on mutations of ASXL1, TET2, IDH1, IDH2, and DNMT3A
Der-Cherng Liang et al.
BLOOD (2013)
Use of Single Nucleotide Polymorphism Array Technology to Improve the Identification of Chromosomal Lesions in Leukemia
Ilaria Iacobucci et al.
CURRENT CANCER DRUG TARGETS (2013)
Loss of chromosomes is the primary event in near-haploid and low-hypodiploid acute lymphoblastic leukemia
S. Safavi et al.
LEUKEMIA (2013)
Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia
Kim De Keersmaecker et al.
NATURE GENETICS (2013)
The genomic landscape of hypodiploid acute lymphoblastic leukemia
Linda Holmfeldt et al.
NATURE GENETICS (2013)
Genomic and Epigenomic Landscapes of Adult De Novo Acute Myeloid Leukemia
Timothy J. Ley et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies
Ana Puda et al.
AMERICAN JOURNAL OF HEMATOLOGY (2012)
e-Blood High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations
Michael W. M. Kuehn et al.
BLOOD (2012)
Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing
Anna Dolnik et al.
BLOOD (2012)
An Inv(16)(p13.3q24.3)-Encoded CBFA2T3-GLIS2 Fusion Protein Defines an Aggressive Subtype of Pediatric Acute Megakaryoblastic Leukemia
Tanja A. Gruber et al.
CANCER CELL (2012)
Whole-exome sequencing of pediatric acute lymphoblastic leukemia
H. Lilljebjorn et al.
LEUKEMIA (2012)
Genetic and epigenetic similarities and differences between childhood and adult AML
Caroline Juhl-Christensen et al.
PEDIATRIC BLOOD & CANCER (2012)
Whole-exome sequencing identifies somatic mutations of BCOR in acute myeloid leukemia with normal karyotype
Vera Grossmann et al.
BLOOD (2011)
Response-Guided Induction Therapy in Pediatric Acute Myeloid Leukemia With Excellent Remission Rate
Jonas Abrahamsson et al.
JOURNAL OF CLINICAL ONCOLOGY (2011)
PHF6 mutations in adult acute myeloid leukemia
P. Van Vlierberghe et al.
LEUKEMIA (2011)
IDH1 and IDH2 mutations in pediatric acute leukemia
A. K. Andersson et al.
LEUKEMIA (2011)
Uniparental Disomy and Human Disease: An Overview
Kazuki Yamazawa et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2010)
PHF6 mutations in T-cell acute lymphoblastic leukemia
Pieter Van Vlierberghe et al.
NATURE GENETICS (2010)
Fast and accurate short read alignment with Burrows-Wheeler transform
Heng Li et al.
BIOINFORMATICS (2009)
Identification and molecular characterization of recurrent genomic deletions on 7p12 in the IKZF1 gene in a large cohort of BCR-ABL1-positive acute lymphoblastic leukemia patients: on behalf of Gruppo Italiano Malattie Ematologiche dell'Adulto Acute Leukemia Working Party (GIMEMAALWP)
Ilaria Iacobucci et al.
BLOOD (2009)
New Lesions Detected by Single Nucleotide Polymorphism Array-Based Chromosomal Analysis Have Important Clinical Impact in Acute Myeloid Leukemia
Ramon V. Tiu et al.
JOURNAL OF CLINICAL ONCOLOGY (2009)
A subtype of childhood acute lymphoblastic leukaemia with poor treatment outcome: a genome-wide classification study
Monique L. Den Boer et al.
LANCET ONCOLOGY (2009)
Genomic analysis reveals few genetic alterations in pediatric acute myeloid leukemia
Ina Radtke et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
Acquired copy number alterations in adult acute myeloid leukemia genomes
Matthew J. Walter et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2009)
250K Single Nucleotide Polymorphism Array Karyotyping Identifies Acquired Uniparental Disomy and Homozygous Mutations, Including Novel Missense Substitutions of c-Cbl, in Myeloid Malignancies
Andrew J. Dunbar et al.
CANCER RESEARCH (2008)
Novel regions of acquired uniparental disomy discovered in acute myeloid leukemia
Manu Gupta et al.
GENES CHROMOSOMES & CANCER (2008)
BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros
Charles G. Mullighan et al.
NATURE (2008)
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
Charles G. Mullighan et al.
NATURE (2007)
Rapid and sensitive typing of NPM1 mutations using LNA-mediated PCR clamping
C. Thiede et al.
LEUKEMIA (2006)
Long-term results in children with AML: NOPHO-AML Study Group - report of three consecutive trials
SO Lie et al.
LEUKEMIA (2005)
Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias
J Fitzgibbon et al.
CANCER RESEARCH (2005)
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients
A Andersson et al.
EUROPEAN JOURNAL OF HAEMATOLOGY (2004)
Fusion gene transcripts and Ig/TCR gene rearrangements are complementary but infrequent targets for PCR-based detection of minimal residual disease in acute myeloid leukemia
N Boeckx et al.
LEUKEMIA (2002)