Lista de obras - Nicolas Duployez - Dominio Público Uruguay

A 17-gene-expression profile to improve prognosis prediction in childhood acute myeloid leukemia

article

A Personalized Approach to Guide Allogeneic Stem Cell Transplantation in Younger Adults with Acute Myeloid Leukemia

scientific article published on 01 September 2020

A novel type of NPM1 mutation characterized by multiple internal tandem repeats in a case of cytogenetically normal acute myeloid leukemia

scholarly article by Nicolas Duployez et al published 14 June 2018 in Haematologica

ASXL2 is essential for haematopoiesis and acts as a haploinsufficient tumour suppressor in leukemia.

artículo científico publicado en 2017

Acquisition of genomic events leading to lymphoblastic transformation in a rare case of myeloproliferative neoplasm with BCR-JAK2 fusion transcript.

artículo científico publicado en 2016

Acute Myeloid Leukemia: The Good, the Bad, and the Ugly

artículo científico publicado en 2018

Added prognostic value of secondary AML-like gene mutations in ELN intermediate-risk older AML: ALFA-1200 study results

scientific article published on 01 May 2020

B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH-Rearranged B-ALL

artículo científico publicado en 2019

Baseline dysmegakaryopoiesis in inherited thrombocytopenia/platelet disorder with predisposition to haematological malignancies

scientific article published on 27 February 2020

Biomarkers of Gemtuzumab Ozogamicin Response for Acute Myeloid Leukemia Treatment

artículo científico publicado en 2020

CDK6 is an essential direct target of NUP98-fusion proteins in acute myeloid leukemia

scientific article published on 28 April 2020

Clinico-Biological Features and Clonal Hematopoiesis in Patients with Severe COVID-19

scientific article published on 21 July 2020

Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype

scientific article published on 30 December 2019

Clonal interference of signaling mutations holds prognostic relevance in core binding factor acute myeloid leukemia.

artículo científico publicado en 2018

Comprehensive molecular landscape in patients older than 80 years old diagnosed with acute myeloid leukemia: a study of the French Hauts-de-France AML observatory

article

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

artículo científico publicado en 2016

Controversies about germline RUNX1 missense variants

scientific article published on 18 October 2019

Cytogenetically masked CBFB-MYH11 fusion and concomitant TP53 deletion in a case of acute myeloid leukemia with a complex karyotype

artículo científico publicado en 2020

Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia

artículo científico publicado en 2017

Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemia

artículo científico publicado en 2015

Disease escape with the selective loss of the Philadelphia chromosome after tyrosine kinase inhibitor exposure in Ph-positive acute lymphoblastic leukemia

scientific article published on 27 January 2020

Efficacy of Tyrosine Kinase Inhibitor Therapy in a Chemotherapy-refractory B-cell Precursor Acute Lymphoblastic Leukemia With ZC3HAV1-ABL2 Fusion

artículo científico publicado en 2019

Efficacy of tyrosine kinase inhibitors in Ph-like acute lymphoblastic leukemia harboring ABL-class rearrangements

artículo científico publicado en 2019

Familial myeloid malignancies with germline TET2 mutation

scientific article published on 11 December 2019

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

artículo científico publicado en 2014

Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia

artículo científico publicado en 2020

Germline RUNX1 Intragenic Deletion: Implications for Accurate Diagnosis of FPD/AML

artículo científico publicado en 2019

Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial

scientific article published on 18 June 2020

High frequency of clonal hematopoiesis in Erdheim-Chester disease

artículo científico publicado en 2020

High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clones.

artículo científico publicado en 2016

IKZF1 Deletions with COBL Breakpoints Are Not Driven by RAG-Mediated Recombination Events in Acute Lymphoblastic Leukemia

artículo científico publicado en 2019

Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.

artículo científico publicado en 2015

Increased risk of adverse acute myeloid leukemia after anti-CD19-targeted immunotherapies in KMT2A-rearranged acute lymphoblastic leukemia: a case report and review of the literature

scientific article published on 07 January 2019

Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia

scientific article published on 01 December 2019

Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy.

artículo científico publicado en 2017

Mature neutrophils with Auer rod bundles in CBFB-MYH11-positive acute myeloid leukemia

scientific article published on 12 November 2019

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

artículo científico publicado en 2014

Mixed phenotype acute leukaemia with Burkitt-like cells and positive peroxidase cytochemistry.

artículo científico publicado en 2013

Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group

artículo científico publicado en 2018

Multi-loci diagnosis of acute lymphoblastic leukaemia with high-throughput sequencing and bioinformatics analysis

artículo científico publicado en 2016

Mutational profile and benefit of gemtuzumab ozogamicin in acute myeloid leukemia

artículo científico publicado en 2020

Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists.

artículo científico publicado en 2016

NUP214-ABL1 fusion defines a rare subtype of B-cell precursor acute lymphoblastic leukemia that could benefit from tyrosine kinase inhibitors

artículo científico publicado en 2015

Polycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemia

artículo científico publicado en 2018

Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors

artículo científico publicado en 2014

Reactive oxygen species levels control NF-κB activation by low dose deferasirox in erythroid progenitors of low risk myelodysplastic syndromes

artículo científico publicado en 2017

SNP-array lesions in core binding factor acute myeloid leukemia

artículo científico publicado en 2018

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

artículo científico publicado en 2015

The homozygous variant p.Gln1311* in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD

artículo científico publicado en 2021

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia

scientific article published on 08 August 2018

Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21)

artículo científico publicado en 2015

When leukocytes bite off more than they can chew

artículo científico publicado en 2020

Lista de obras de Nicolas Duployez

A 17-gene-expression profile to improve prognosis prediction in childhood acute myeloid leukemia

A Personalized Approach to Guide Allogeneic Stem Cell Transplantation in Younger Adults with Acute Myeloid Leukemia

A novel type of NPM1 mutation characterized by multiple internal tandem repeats in a case of cytogenetically normal acute myeloid leukemia

ASXL2 is essential for haematopoiesis and acts as a haploinsufficient tumour suppressor in leukemia.

Acquisition of genomic events leading to lymphoblastic transformation in a rare case of myeloproliferative neoplasm with BCR-JAK2 fusion transcript.

Acute Myeloid Leukemia: The Good, the Bad, and the Ugly

Added prognostic value of secondary AML-like gene mutations in ELN intermediate-risk older AML: ALFA-1200 study results

B-ALL With t(5;14)(q31;q32); IGH-IL3 Rearrangement and Eosinophilia: A Comprehensive Analysis of a Peculiar IGH-Rearranged B-ALL

Baseline dysmegakaryopoiesis in inherited thrombocytopenia/platelet disorder with predisposition to haematological malignancies

Biomarkers of Gemtuzumab Ozogamicin Response for Acute Myeloid Leukemia Treatment

CDK6 is an essential direct target of NUP98-fusion proteins in acute myeloid leukemia

Clinico-Biological Features and Clonal Hematopoiesis in Patients with Severe COVID-19

Clofarabine Improves Relapse-Free Survival of Acute Myeloid Leukemia in Younger Adults with Micro-Complex Karyotype

Clonal interference of signaling mutations holds prognostic relevance in core binding factor acute myeloid leukemia.

Comprehensive molecular landscape in patients older than 80 years old diagnosed with acute myeloid leukemia: a study of the French Hauts-de-France AML observatory

Comprehensive mutational profiling of core binding factor acute myeloid leukemia

Controversies about germline RUNX1 missense variants

Cytogenetically masked CBFB-MYH11 fusion and concomitant TP53 deletion in a case of acute myeloid leukemia with a complex karyotype

Detection of a new heterozygous germline ETV6 mutation in a case with hyperdiploid acute lymphoblastic leukemia

Diagnosis of intrachromosomal amplification of chromosome 21 (iAMP21) by molecular cytogenetics in pediatric acute lymphoblastic leukemia

Disease escape with the selective loss of the Philadelphia chromosome after tyrosine kinase inhibitor exposure in Ph-positive acute lymphoblastic leukemia

Efficacy of Tyrosine Kinase Inhibitor Therapy in a Chemotherapy-refractory B-cell Precursor Acute Lymphoblastic Leukemia With ZC3HAV1-ABL2 Fusion

Efficacy of tyrosine kinase inhibitors in Ph-like acute lymphoblastic leukemia harboring ABL-class rearrangements

Familial myeloid malignancies with germline TET2 mutation

Frequent ASXL2 mutations in acute myeloid leukemia patients with t(8;21)/RUNX1-RUNX1T1 chromosomal translocations.

Germline PAX5 mutation predisposes to familial B acute lymphoblastic leukemia

Germline RUNX1 Intragenic Deletion: Implications for Accurate Diagnosis of FPD/AML

Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial

High frequency of clonal hematopoiesis in Erdheim-Chester disease

High-throughput sequencing in acute lymphoblastic leukemia: Follow-up of minimal residual disease and emergence of new clones.

IKZF1 Deletions with COBL Breakpoints Are Not Driven by RAG-Mediated Recombination Events in Acute Lymphoblastic Leukemia

Incidence of ATRX mutations in myelodysplastic syndromes, the value of microcytosis.

Increased risk of adverse acute myeloid leukemia after anti-CD19-targeted immunotherapies in KMT2A-rearranged acute lymphoblastic leukemia: a case report and review of the literature

Inherited transmission of the CSF3R T618I mutational hotspot in familial chronic neutrophilic leukemia

Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy.

Mature neutrophils with Auer rod bundles in CBFB-MYH11-positive acute myeloid leukemia

Minimal residual disease monitoring in t(8;21) acute myeloid leukemia based on RUNX1-RUNX1T1 fusion quantification on genomic DNA

Mixed phenotype acute leukaemia with Burkitt-like cells and positive peroxidase cytochemistry.

Molecular Profiling Defines Distinct Prognostic Subgroups in Childhood AML: A Report From the French ELAM02 Study Group

Multi-loci diagnosis of acute lymphoblastic leukaemia with high-throughput sequencing and bioinformatics analysis

Mutational profile and benefit of gemtuzumab ozogamicin in acute myeloid leukemia

Myelodysplastic syndromes and acute leukemia with genetic predispositions: a new challenge for hematologists.

NUP214-ABL1 fusion defines a rare subtype of B-cell precursor acute lymphoblastic leukemia that could benefit from tyrosine kinase inhibitors

Polycomb repressive complex 2 haploinsufficiency identifies a high-risk subgroup of pediatric acute myeloid leukemia

Prognosis and monitoring of core-binding factor acute myeloid leukemia: current and emerging factors

Reactive oxygen species levels control NF-κB activation by low dose deferasirox in erythroid progenitors of low risk myelodysplastic syndromes

SNP-array lesions in core binding factor acute myeloid leukemia

Somatic mutations associated with leukemic progression of familial platelet disorder with predisposition to acute myeloid leukemia

The homozygous variant p.Gln1311* in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD

The stem cell-associated gene expression signature allows risk stratification in pediatric acute myeloid leukemia

Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21)

When leukocytes bite off more than they can chew