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Harmonization of BCR-ABL mRNA quantification using a uniform multifunctional control plasmid in 37 international laboratories

Leukemia, 2008-01, Vol.22 (1), p.96-102

2008

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Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNet

Leukemia, 2011-07, Vol.25 (7), p.1168-1173

2011

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EXPLORING DIFFERENTIAL MUTATIONAL DISTRIBUTION BY TARGETED SEQUENCING IN A R‐CHOP TREATED COHORT OF DIFFUSE LARGE B‐CELL LYMPHOMA PATIENTS

Hematological oncology, 2023-06, Vol.41 (S2), p.654-655

2023

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Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: Biological and clinical implications

Leukemia, 2006-11, Vol.20 (11), p.2051-2054

2006

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P606: META‐ANALYSIS OF LOW ALLELIC BURDEN C481 BTK‐MUTATIONS CALLS FOR CAUTION IN IBRUTINIB RESISTANCE EVALUATION

HemaSphere, 2022-06, Vol.6, p.505-506

2022

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PB2158: EXPLORING THE BIOLOGICAL ROLE OF LILRA4 IN MANTLE CELL LYMPHOMA

HemaSphere, 2022-06, Vol.6 (Suppl), p.2028-2029

2022

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Differential expression levels and methylation status of ROBO1 in mantle cell lymphoma and chronic lymphocytic leukaemia

International journal of laboratory hematology, 2017-06, Vol.39 (3), p.e70-e73

2017

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Measurable residual disease assessment by qPCR in peripheral blood is an informative tool for disease surveillance in childhood acute myeloid leukaemia

British journal of haematology, 2020-07, Vol.190 (2), p.198-208

2020

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Reply to ‘Wilms' tumour 1 mutations are associated with FLT3-ITD and failure of standard induction chemotherapy in patients with normal karyotype AML’ by Summers et al

Leukemia, 2007-03, Vol.21 (3), p.552-552

2007

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Fusion transcript analysis reveals slower response kinetics than multiparameter flow cytometry in childhood acute myeloid leukaemia

International journal of laboratory hematology, 2022-12, Vol.44 (6), p.1094-1101

2022

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Erythropoietin receptor defect: a cause of primary polycythaemia

British journal of haematology, 2004-05, Vol.125 (4), p.537-538

2004

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INTEGRATING DETECTION OF COPY NEUTRAL CHROMOSOMAL LOSSES IN A CLINICAL SETTING IN LEUKEMIA AND LYMPHOMA BY MEANS OF ALLELIC IMBALANCE AND READ DEPTH RATIO COMPARISON: PF528

HemaSphere, 2019-06, Vol.3, p.216-217

2019

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Minimal residual core binding factor AMLs by real time quantitative PCR—Initial response to chemotherapy predicts event free survival and close monitoring of peripheral blood unravels the kinetics of relapse

Leukemia research, 2006-04, Vol.30 (4), p.389-395

2006

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Interleukin-21 mRNA expression during virus infections

Cytokine (Philadelphia, Pa.), 2006-01, Vol.33 (1), p.41-45

2006

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Molecular typing of adult acute myeloid leukaemia: significance of translocations, tandem duplications, methylation, and selective gene expression profiling

British journal of haematology, 2005-11, Vol.131 (4), p.457-467

2005

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Promoter hypermethylation of the retinoic acid receptor β 2 gene is frequent in acute myeloid leukaemia and associated with the presence of CBFβ – MYH11 fusion transcripts

British journal of haematology, 2006-05, Vol.133 (3), p.276-283

2006

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WT1 gene expression in children with Down syndrome and transient myeloproliferative disorder

Leukemia research, 2006-05, Vol.30 (5), p.543-546

2006

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Delineation and molecular characterization of acute myeloid leukemia patients with coduplication of FLT3 and MLL

European journal of haematology, 2005-09, Vol.75 (3), p.185-192

2005

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Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: Biological and clinical implications

Leukemia, 2006, Vol.20 (11), p.2051-2054

2006

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A decade with whole exome sequencing in haematology

British journal of haematology, 2020-02, Vol.188 (3), p.367-382

2020

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Chimeric Antigen Receptor T Cells Targeting CD79b Show Efficacy in Lymphoma with or without Cotargeting CD19

Clinical cancer research, 2019-12, Vol.25 (23), p.7046-7057

2019

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Germline GATA1s-generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype

Blood, 2022-05, Vol.139 (21), p.3159-3165

2022

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Quantification of Fusion Transcripts Reveals Slower Treatment Kinetics As Compared with Multiparameter Flow Cytometry during Induction Treatment of Acute Myeloid Leukemia in Children

Blood, 2018-11, Vol.132 (Supplement 1), p.2814-2814

2018

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Nature and nurture: a case of transcending haematological pre‐malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B‐cell proliferations

British journal of haematology, 2015-05, Vol.169 (3), p.391-400

2015

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Precise quantification of minimal residual disease at day 29 allows identification of children with acute lymphoblastic leukemia and an excellent outcome

Blood, 2002-02, Vol.99 (4), p.1253-1258

2002

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Harmonization of BCR-ABL mRNA quantification using a uniform multifunctional control plasmid in 37 international laboratories

Development of standardized approaches to reporting of minimal residual disease data using a reporting software package designed within the European LeukemiaNet

EXPLORING DIFFERENTIAL MUTATIONAL DISTRIBUTION BY TARGETED SEQUENCING IN A R‐CHOP TREATED COHORT OF DIFFUSE LARGE B‐CELL LYMPHOMA PATIENTS

Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: Biological and clinical implications

P606: META‐ANALYSIS OF LOW ALLELIC BURDEN C481 BTK‐MUTATIONS CALLS FOR CAUTION IN IBRUTINIB RESISTANCE EVALUATION

PB2158: EXPLORING THE BIOLOGICAL ROLE OF LILRA4 IN MANTLE CELL LYMPHOMA

Differential expression levels and methylation status of ROBO1 in mantle cell lymphoma and chronic lymphocytic leukaemia

Measurable residual disease assessment by qPCR in peripheral blood is an informative tool for disease surveillance in childhood acute myeloid leukaemia

Reply to ‘Wilms' tumour 1 mutations are associated with FLT3-ITD and failure of standard induction chemotherapy in patients with normal karyotype AML’ by Summers et al

Fusion transcript analysis reveals slower response kinetics than multiparameter flow cytometry in childhood acute myeloid leukaemia

Erythropoietin receptor defect: a cause of primary polycythaemia

INTEGRATING DETECTION OF COPY NEUTRAL CHROMOSOMAL LOSSES IN A CLINICAL SETTING IN LEUKEMIA AND LYMPHOMA BY MEANS OF ALLELIC IMBALANCE AND READ DEPTH RATIO COMPARISON: PF528

Minimal residual core binding factor AMLs by real time quantitative PCR—Initial response to chemotherapy predicts event free survival and close monitoring of peripheral blood unravels the kinetics of relapse

Interleukin-21 mRNA expression during virus infections

Molecular typing of adult acute myeloid leukaemia: significance of translocations, tandem duplications, methylation, and selective gene expression profiling

Promoter hypermethylation of the retinoic acid receptor β 2 gene is frequent in acute myeloid leukaemia and associated with the presence of CBFβ – MYH11 fusion transcripts

WT1 gene expression in children with Down syndrome and transient myeloproliferative disorder

Delineation and molecular characterization of acute myeloid leukemia patients with coduplication of FLT3 and MLL

Wilms' tumor 1 mutation accumulated during therapy in acute myeloid leukemia: Biological and clinical implications

A decade with whole exome sequencing in haematology

Chimeric Antigen Receptor T Cells Targeting CD79b Show Efficacy in Lymphoma with or without Cotargeting CD19

Germline GATA1s-generating mutations predispose to leukemia with acquired trisomy 21 and Down syndrome-like phenotype

Quantification of Fusion Transcripts Reveals Slower Treatment Kinetics As Compared with Multiparameter Flow Cytometry during Induction Treatment of Acute Myeloid Leukemia in Children

Nature and nurture: a case of transcending haematological pre‐malignancies in a pair of monozygotic twins adding possible clues on the pathogenesis of B‐cell proliferations

Precise quantification of minimal residual disease at day 29 allows identification of children with acute lymphoblastic leukemia and an excellent outcome

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