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Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

Nature communications, 2016-06, Vol.7 (1), p.11790-11790, Article 11790

2016

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Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing

Leukemia, 2021-05, Vol.35 (5), p.1485-1489

2021

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Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Proceedings of the National Academy of Sciences - PNAS, 2010-12, Vol.107 (50), p.21719-21724

2010

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Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

PloS one, 2013-06, Vol.8 (6), p.e65373-e65373

2013

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Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

Blood, 2009-06, Vol.113 (24), p.6077-6084

2009

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Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia

Blood cancer journal (New York), 2020-05, Vol.10 (5), p.51-51, Article 51

2020

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Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia

Genes chromosomes & cancer, 2008-01, Vol.47 (1), p.26-33

2008

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Molecular Signatures in Childhood Acute Leukemia and Their Correlations to Expression Patterns in Normal Hematopoietic Subpopulations

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (52), p.19069-19074

2005

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Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1

Genes chromosomes & cancer, 2015-05, Vol.54 (5), p.315-325

2015

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The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

British journal of haematology, 2016-07, Vol.174 (2), p.292-301

2016

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SFPQ‐ABL1‐positive B‐cell precursor acute lymphoblastic leukemias

Genes chromosomes & cancer, 2020-09, Vol.59 (9), p.540-543

2020

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The DNA methylome of pediatric acute lymphoblastic leukemia

Human molecular genetics, 2009-11, Vol.18 (21), p.4054-4065

2009

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Parental origin of monosomy 7 in acute leukaemia

British journal of haematology, 2021-03, Vol.192 (5), p.e132-e135

2021

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Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status

Leukemia, 2007-06, Vol.21 (6), p.1198-1203

2007

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Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases

Genes chromosomes & cancer, 2018-11, Vol.57 (11), p.604-607

2018

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Insulin‐dependent diabetes: A chronic complication to acute pancreatitis in childhood acute lymphoblastic leukemia

Pediatric blood & cancer, 2019-01, Vol.66 (1), p.e27437-n/a

2019

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Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

Leukemia, 2018-09, Vol.32 (9), p.2058-2062

2018

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Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

Oncotarget, 2015-12, Vol.6 (40), p.42793-42802

2015

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Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia

Leukemia, 2018-10, Vol.32 (10), p.2117-2125

2018

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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

Journal of hematology and oncology, 2015-04, Vol.8 (1), p.42-42, Article 42

2015

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Comprehensive Genetic Characterization of Pediatric T-Cell Acute Lymphoblastic Leukemia

56th Annual Meeting of the American Society of Hematology,San Francisco, United States,2014-12-06 - 2014-12-09, 2014-12, Vol.124 (21), p.1084-1084

2014

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The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias

Human molecular genetics, 2010-08, Vol.19 (16), p.3150-3158

2010

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Identification of ETV6-RUNX1-like and DUX4-rearranged subtypes in paediatric B-cell precursor acute lymphoblastic leukaemia

Single base substitution mutational signatures in pediatric acute myeloid leukemia based on whole genome sequencing

Flow cytometric detection of leukemic blasts in cerebrospinal fluid predicts risk of relapse in childhood acute lymphoblastic leukemia: a Nordic Society of Pediatric Hematology and Oncology study

Genetic landscape of high hyperdiploid childhood acute lymphoblastic leukemia

Promoter DNA methylation pattern identifies prognostic subgroups in childhood T-cell acute lymphoblastic leukemia

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

Parental origin of monosomic chromosomes in near-haploid acute lymphoblastic leukemia

Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia

Molecular Signatures in Childhood Acute Leukemia and Their Correlations to Expression Patterns in Normal Hematopoietic Subpopulations

Correction: Flow cytometric detection of leukemic blasts in cerebrospinal fluid predicts risk of relapse in childhood acute lymphoblastic leukemia: a Nordic Society of Pediatric Hematology and Oncology study

Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1

The genetic landscape of paediatric de novo acute myeloid leukaemia as defined by single nucleotide polymorphism array and exon sequencing of 100 candidate genes

SFPQ‐ABL1‐positive B‐cell precursor acute lymphoblastic leukemias

The DNA methylome of pediatric acute lymphoblastic leukemia

Parental origin of monosomy 7 in acute leukaemia

Microarray-based classification of a consecutive series of 121 childhood acute leukemias: prediction of leukemic and genetic subtype as well as of minimal residual disease status

Improved cytogenetic characterization and risk stratification of pediatric acute lymphoblastic leukemia using single nucleotide polymorphism array analysis: A single center experience of 296 cases

Insulin‐dependent diabetes: A chronic complication to acute pancreatitis in childhood acute lymphoblastic leukemia

Whole-exome sequencing exploration of acquired uniparental disomies in B-cell precursor acute lymphoblastic leukemia

Genetic and epigenetic characterization of hypodiploid acute lymphoblastic leukemia

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia

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

Comprehensive Genetic Characterization of Pediatric T-Cell Acute Lymphoblastic Leukemia

The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias

Minimal residual disease assessment in childhood acute lymphoblastic leukaemia: a Swedish multi‐centre study comparing real‐time polymerase chain reaction and multicolour flow cytometry

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