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Genotype-Specific Minimal Residual Disease Interpretation Improves Stratification in Pediatric Acute Lymphoblastic Leukemia

Journal of clinical oncology, 2018-01, Vol.36 (1), p.34-43

2018

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Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features

Haematologica (Roma), 2013-07, Vol.98 (7), p.1081-1088

2013

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A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia

Blood, 2014-08, Vol.124 (9), p.1434-1444

2014

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Advances in B‐cell Precursor Acute Lymphoblastic Leukemia Genomics

HemaSphere, 2018-08, Vol.2 (4), p.e53-n/a

2018

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Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia

Leukemia, 2023-03, Vol.37 (3), p.518-528

2023

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EBF1-PDGFRB fusion in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL): genetic profile and clinical implications

Blood, 2016-05, Vol.127 (18), p.2214-2218

2016

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Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial

The lancet oncology, 2010-05, Vol.11 (5), p.429-438

2010

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Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2015-10, Vol.100 (10), p.1301-1310

2015

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Use of Minimal Residual Disease Assessment to Redefine Induction Failure in Pediatric Acute Lymphoblastic Leukemia

Journal of clinical oncology, 2017-02, Vol.35 (6), p.660-667

2017

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Genetic characterisation of childhood B‐other‐acute lymphoblastic leukaemia in UK patients by fluorescence in situ hybridisation and Multiplex Ligation‐dependent Probe Amplification

British journal of haematology, 2022-02, Vol.196 (3), p.753-763

2022

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Hyperactive CREB subpopulations increase during therapy in pediatric B-lineage acute lymphoblastic leukemia

Haematologica (Roma), 2023-04, Vol.108 (4), p.981-992

2023

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Risk-Directed Treatment Intensification Significantly Reduces the Risk of Relapse Among Children and Adolescents With Acute Lymphoblastic Leukemia and Intrachromosomal Amplification of Chromosome 21: A Comparison of the MRC ALL97/99 and UKALL2003 Trials

Journal of clinical oncology, 2013-09, Vol.31 (27), p.3389-3396

2013

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SH2B3 inactivation through CN-LOH 12q is uniquely associated with B-cell precursor ALL with iAMP21 or other chromosome 21 gain

Leukemia, 2019-08, Vol.33 (8), p.1881-1894

2019

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Concordance of copy number abnormality detection using SNP arrays and Multiplex Ligation-dependent Probe Amplification (MLPA) in acute lymphoblastic leukaemia

Scientific reports, 2020-01, Vol.10 (1), p.45-45, Article 45

2020

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Characterization of leukemias with ETV6-ABL1 fusion

Haematologica (Roma), 2016-09, Vol.101 (9), p.1082-1093

2016

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IGH@ Translocations, CRLF2 Deregulation, and Microdeletions in Adolescents and Adults With Acute Lymphoblastic Leukemia

Journal of clinical oncology, 2012-09, Vol.30 (25), p.3100-3108

2012

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Dynamic clonal progression in xenografts of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21

Haematologica (Roma), 2018-04, Vol.103 (4), p.634-644

2018

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Advances in acute lymphoblastic leukemia genomics

HemaSphere, 2018-06, Vol.2 (S2), p.5-7

2018

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Genomic characterization implicates iAMP21 as a likely primary genetic event in childhood B-cell precursor acute lymphoblastic leukemia

Blood, 2011-06, Vol.117 (25), p.6848-6855

2011

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Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia

Haematologica (Roma), 2016-08, Vol.101 (8), p.951-958

2016

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Episomal amplification of NUP214-ABL1 fusion gene in B-cell acute lymphoblastic leukemia

Blood, 2012-11, Vol.120 (22), p.4441-4443

2012

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Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia

Genes chromosomes & cancer, 2013-02, Vol.52 (2), p.202-213

2013

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Treating childhood acute lymphoblastic leukemia in Malawi

Haematologica (Roma), 2013-01, Vol.98 (1), p.e1-e3

2013

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Whole Genome Sequencing for Detection of Prognostically Relevant Genetic Abnormalities in Paediatric Acute Myeloid Leukaemia

Blood, 2022-11, Vol.140 (Supplement 1), p.3204-3205

2022

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Genotype-Specific Minimal Residual Disease Interpretation Improves Stratification in Pediatric Acute Lymphoblastic Leukemia

Genes commonly deleted in childhood B-cell precursor acute lymphoblastic leukemia: association with cytogenetics and clinical features

A novel integrated cytogenetic and genomic classification refines risk stratification in pediatric acute lymphoblastic leukemia

Advances in B‐cell Precursor Acute Lymphoblastic Leukemia Genomics

Whole genome sequencing provides comprehensive genetic testing in childhood B-cell acute lymphoblastic leukaemia

EBF1-PDGFRB fusion in pediatric B-cell precursor acute lymphoblastic leukemia (BCP-ALL): genetic profile and clinical implications

Prognostic effect of chromosomal abnormalities in childhood B-cell precursor acute lymphoblastic leukaemia: results from the UK Medical Research Council ALL97/99 randomised trial

Targeted sequencing identifies associations between IL7R-JAK mutations and epigenetic modulators in T-cell acute lymphoblastic leukemia

Use of Minimal Residual Disease Assessment to Redefine Induction Failure in Pediatric Acute Lymphoblastic Leukemia

Integration of genetic and clinical risk factors improves prognostication in relapsed childhood B-cell precursor acute lymphoblastic leukemia

Genetic characterisation of childhood B‐other‐acute lymphoblastic leukaemia in UK patients by fluorescence in situ hybridisation and Multiplex Ligation‐dependent Probe Amplification

Hyperactive CREB subpopulations increase during therapy in pediatric B-lineage acute lymphoblastic leukemia

Risk-Directed Treatment Intensification Significantly Reduces the Risk of Relapse Among Children and Adolescents With Acute Lymphoblastic Leukemia and Intrachromosomal Amplification of Chromosome 21: A Comparison of the MRC ALL97/99 and UKALL2003 Trials

SH2B3 inactivation through CN-LOH 12q is uniquely associated with B-cell precursor ALL with iAMP21 or other chromosome 21 gain

Concordance of copy number abnormality detection using SNP arrays and Multiplex Ligation-dependent Probe Amplification (MLPA) in acute lymphoblastic leukaemia

Characterization of leukemias with ETV6-ABL1 fusion

IGH@ Translocations, CRLF2 Deregulation, and Microdeletions in Adolescents and Adults With Acute Lymphoblastic Leukemia

Dynamic clonal progression in xenografts of acute lymphoblastic leukemia with intrachromosomal amplification of chromosome 21

Advances in acute lymphoblastic leukemia genomics

Genomic characterization implicates iAMP21 as a likely primary genetic event in childhood B-cell precursor acute lymphoblastic leukemia

Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia

Episomal amplification of NUP214-ABL1 fusion gene in B-cell acute lymphoblastic leukemia

Abnormalities of the der(12)t(12;21) in ETV6-RUNX1 acute lymphoblastic leukemia

Treating childhood acute lymphoblastic leukemia in Malawi

Whole Genome Sequencing for Detection of Prognostically Relevant Genetic Abnormalities in Paediatric Acute Myeloid Leukaemia

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