List of works - André Baruchel

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

scientific article published on 16 November 2017

Activating mutations in human acute megakaryoblastic leukemia.

scientific article

Acute lymphoblastic leukemia in adolescent and young adults: treat as adults or as children?

scientific article published on 12 June 2018

An effective modestly intensive re-induction regimen with bortezomib in relapsed or refractory paediatric acute lymphoblastic leukaemia

scientific article published on 20 April 2018

Biallelic inactivation of REV7 is associated with Fanconi anemia

scientific article published on 8 August 2016

Biallelic inactivation of REV7 is associated with Fanconi anemia

scientific article published on March 2017

Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005.

scientific article

Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child

scientific article published on 24 September 2020

Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia

scientific article

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

scientific article published on 19 October 2010

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

scientific article published on 8 April 2009

Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling.

scholarly article

Juvenile myelomonocytic leukaemia and Noonan syndrome.

scientific article published on 5 August 2014

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network.

scientific article published on 12 October 2015

MicroRNA-106b~25 cluster is upregulated in relapsed MLL-rearranged pediatric acute myeloid leukemia

scientific article published on 24 June 2016

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

scientific article published on 16 February 2011

Nelarabine for T Cell Acute Lymphoblastic Leukemia Relapsing after Allogeneic Hematopoietic Stem Cell Transplantation: An Opportunity to Improve Survival ⬇️

scientific article published on May 3, 2013

Outcome of acute promyelocytic leukemia (APL) in children and adolescents: an analysis in two consecutive trials of the European APL Group.

scientific article published on 2 April 2012

Outcomes after induction failure in childhood acute lymphoblastic leukemia

scientific article

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

scientific article published on 08 August 2018

When can real-time quantitative RT-PCR effectively define molecular relapse in acute promyelocytic leukemia patients? (Results of the French Belgian Swiss APL Group).

scientific article

List of works by André Baruchel

A landscape of germline mutations in a cohort of inherited bone marrow failure patients

Activating mutations in human acute megakaryoblastic leukemia.

Acute lymphoblastic leukemia in adolescent and young adults: treat as adults or as children?

An effective modestly intensive re-induction regimen with bortezomib in relapsed or refractory paediatric acute lymphoblastic leukaemia

Biallelic inactivation of REV7 is associated with Fanconi anemia

Biallelic inactivation of REV7 is associated with Fanconi anemia

Clinical outcome of children with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia treated between 1995 and 2005.

Cranial polyneuropathy as the first manifestation of a severe COVID-19 in a child

Criteria for evaluating response and outcome in clinical trials for children with juvenile myelomonocytic leukemia

Genetic typing of CBL, ASXL1, RUNX1, TET2 and JAK2 in juvenile myelomonocytic leukaemia reveals a genetic profile distinct from chronic myelomonocytic leukaemia

High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder.

Identification of distinct molecular phenotypes in acute megakaryoblastic leukemia by gene expression profiling.

Juvenile myelomonocytic leukaemia and Noonan syndrome.

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network.

MicroRNA-106b~25 cluster is upregulated in relapsed MLL-rearranged pediatric acute myeloid leukemia

Myelodysplasia and leukemia of Fanconi anemia are associated with a specific pattern of genomic abnormalities that includes cryptic RUNX1/AML1 lesions

Nelarabine for T Cell Acute Lymphoblastic Leukemia Relapsing after Allogeneic Hematopoietic Stem Cell Transplantation: An Opportunity to Improve Survival ⬇️

Outcome of acute promyelocytic leukemia (APL) in children and adolescents: an analysis in two consecutive trials of the European APL Group.

Outcomes after induction failure in childhood acute lymphoblastic leukemia

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

When can real-time quantitative RT-PCR effectively define molecular relapse in acute promyelocytic leukemia patients? (Results of the French Belgian Swiss APL Group).