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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Journal of clinical oncology, 2010-06, Vol.28 (16), p.2682-2689

2010

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Treatment and outcome of IG-MYC + neoplasms with precursor B-cell phenotype in childhood and adolescence

Leukemia, 2020-03, Vol.34 (3), p.942-946

2020

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Acute leukaemias of ambiguous lineage in children: characterization, prognosis and therapy recommendations

British journal of haematology, 2010-04, Vol.149 (1), p.84-92

2010

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MicroRNAs distinguish cytogenetic subgroups in pediatric AML and contribute to complex regulatory networks in AML-relevant pathways

PloS one, 2013-02, Vol.8 (2), p.e56334-e56334

2013

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Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia

Genes chromosomes & cancer, 2013-06, Vol.52 (6), p.564-579

2013

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Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

PloS one, 2011-06, Vol.6 (6), p.e20607-e20607

2011

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Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups

Cancer, 2016-12, Vol.122 (24), p.3821-3830

2016

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Characterization of IG-MYC-breakpoints and their application for quantitative minimal disease monitoring in high-risk pediatric Burkitt-lymphoma and -leukemia

Leukemia, 2022-09, Vol.36 (9), p.2343-2346

2022

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Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR)

Experimental hematology & oncology, 2012-11, Vol.1 (1), p.33-33, Article 33

2012

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Imatinib treatment of paediatric Philadelphia chromosome-positive acute lymphoblastic leukaemia (EsPhALL2010): a prospective, intergroup, open-label, single-arm clinical trial

The Lancet. Haematology, 2018-12, Vol.5 (12), p.e641-e652

2018

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Long-term follow up of pediatric Philadelphia positive acute lymphoblastic leukemia treated with the EsPhALL2004 study: high white blood cell count at diagnosis is the strongest prognostic factor

Haematologica (Roma), 2019-01, Vol.104 (1), p.e13-e16

2019

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Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse

British journal of haematology, 2019-04, Vol.185 (2), p.266-283

2019

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Molecular characterization and clinical outcome of B-cell precursor acute lymphoblastic leukemia with IG-MYC rearrangement

Haematologica (Roma), 2023-03, Vol.108 (3), p.717-731

2023

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Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations

British journal of haematology, 2015-09, Vol.170 (6), p.814-825

2015

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Distribution of NPM1‐ALK and X‐ALK fusion transcripts in paediatric anaplastic large cell lymphoma: a molecular–histological correlation

British journal of haematology, 2009-08, Vol.146 (3), p.306-309

2009

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PAX5-AUTS2 : A recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia

Leukemia research, 2012-08, Vol.36 (8), p.e178-e181

2012

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Response monitoring of infant acute myeloid leukemia treatment by quantification of the tumor specific MLL-FNBP1 fusion gene

Leukemia & lymphoma, 2015-03, Vol.56 (3), p.793-796

2015

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Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients

Leukemia research, 2015-09, Vol.39 (9), p.990-1001

2015

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Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

British journal of haematology, 2012-09, Vol.158 (6), p.772-777

2012

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Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notation

BMC bioinformatics, 2003-01, Vol.4 (1), p.4-4, Article 4

2003

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CyDAS: a cytogenetic data analysis system

Bioinformatics, 2005-04, Vol.21 (7), p.1282-1283

2005

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miRNAs Function As Biomarker in Pediatric AML and Regulate Gene-Silencing in AML-Relevant Pathways

Blood, 2011-11, Vol.118 (21), p.570-570

2011

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PAX5 fusion genes in t(7;9)(q11.2;p13) leukemia: a case report and review of the literature

Molecular cytogenetics, 2014-02, Vol.7 (1), p.13-13, Article 13

2014

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Chromothripsis-Mediated Structural Variations and Clonal Evolution In Recurrent Childhood High Hyperdiploid Acute Lymphoblastic Leukemia

Blood, 2013-11, Vol.122 (21), p.233-233

2013

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Prognostic Impact of Specific Chromosomal Aberrations in a Large Group of Pediatric Patients With Acute Myeloid Leukemia Treated Uniformly According to Trial AML-BFM 98

Treatment and outcome of IG-MYC + neoplasms with precursor B-cell phenotype in childhood and adolescence

Acute leukaemias of ambiguous lineage in children: characterization, prognosis and therapy recommendations

MicroRNAs distinguish cytogenetic subgroups in pediatric AML and contribute to complex regulatory networks in AML-relevant pathways

Next-generation-sequencing-based risk stratification and identification of new genes involved in structural and sequence variations in near haploid lymphoblastic leukemia

Genomic imbalances are confined to non-proliferating cells in paediatric patients with acute myeloid leukaemia and a normal or incomplete karyotype

Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups

Molecular response to treatment redefines all prognostic factors in children and adolescents with B-cell precursor acute lymphoblastic leukemia: results in 3184 patients of the AIEOP-BFM ALL 2000 study

Characterization of IG-MYC-breakpoints and their application for quantitative minimal disease monitoring in high-risk pediatric Burkitt-lymphoma and -leukemia

Quantification of minimal residual disease (MRD) in acute lymphoblastic leukemia (ALL) using amplicon-fusion-site polymerase chain reaction (AFS-PCR)

Imatinib treatment of paediatric Philadelphia chromosome-positive acute lymphoblastic leukaemia (EsPhALL2010): a prospective, intergroup, open-label, single-arm clinical trial

Long-term follow up of pediatric Philadelphia positive acute lymphoblastic leukemia treated with the EsPhALL2004 study: high white blood cell count at diagnosis is the strongest prognostic factor

Aneuploidy in children with relapsed B‐cell precursor acute lymphoblastic leukaemia: clinical importance of detecting a hypodiploid origin of relapse

Molecular characterization and clinical outcome of B-cell precursor acute lymphoblastic leukemia with IG-MYC rearrangement

Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations

Distribution of NPM1‐ALK and X‐ALK fusion transcripts in paediatric anaplastic large cell lymphoma: a molecular–histological correlation

PAX5-AUTS2 : A recurrent fusion gene in childhood B-cell precursor acute lymphoblastic leukemia

Response monitoring of infant acute myeloid leukemia treatment by quantification of the tumor specific MLL-FNBP1 fusion gene

Next-generation-sequencing of recurrent childhood high hyperdiploid acute lymphoblastic leukemia reveals mutations typically associated with high risk patients

Treatment outcome of CRLF2-rearranged childhood acute lymphoblastic leukaemia: a comparative analysis of the AIEOP-BFM and UK NCRI-CCLG study groups

Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notation

CyDAS: a cytogenetic data analysis system

miRNAs Function As Biomarker in Pediatric AML and Regulate Gene-Silencing in AML-Relevant Pathways

PAX5 fusion genes in t(7;9)(q11.2;p13) leukemia: a case report and review of the literature

Chromothripsis-Mediated Structural Variations and Clonal Evolution In Recurrent Childhood High Hyperdiploid Acute Lymphoblastic Leukemia

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