List of works - Thierry Leblanc

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

scientific article published on 16 November 2017

Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group

scientific article published in January 2005

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

Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

scientific article published on 24 August 2017

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells

scientific article

Bone marrow sites differently imprint dormancy and chemoresistance to T-cell acute lymphoblastic leukemia

scientific article published on 08 September 2017

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome

scientific article

Diagnosis of Fanconi anemia in patients with bone marrow failure

scientific article published on 10 March 2009

Fanconi anemia and solid malignancies in childhood: a national retrospective study

scientific article published on 8 November 2014

Interleukin-18 produced by bone marrow-derived stromal cells supports T-cell acute leukaemia progression

scientific article

Is pegfilgrastim safe and effective in congenital neutropenia? An analysis of the French Severe Chronic Neutropenia registry

scientific article

Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register.

scientific article published on 12 February 2004

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome

scientific article published on 18 June 2018

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

Nationwide Survey on the Use of Horse Antithymocyte Globulins (ATGAM) in Patients with Acquired Aplastic Anemia: A Report on Behalf of the French Reference Center for Aplastic Anemia

scientific article

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients

article

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

PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects

scientific article published on 12 June 2018

Sequential treatment for allogeneic hematopoietic stem cell transplantation in Fanconi anemia with acute myeloid leukemia

scientific article published on August 2014

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients

scientific article

List of works by Thierry Leblanc

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

Analysis of risk factors for myelodysplasias, leukemias and death from infection among patients with congenital neutropenia. Experience of the French Severe Chronic Neutropenia Study Group

Biallelic inactivation of REV7 is associated with Fanconi anemia

Biallelic inactivation of REV7 is associated with Fanconi anemia

Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia

Bone marrow failure in Fanconi anemia is triggered by an exacerbated p53/p21 DNA damage response that impairs hematopoietic stem and progenitor cells

Bone marrow sites differently imprint dormancy and chemoresistance to T-cell acute lymphoblastic leukemia

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome

Diagnosis of Fanconi anemia in patients with bone marrow failure

Fanconi anemia and solid malignancies in childhood: a national retrospective study

Interleukin-18 produced by bone marrow-derived stromal cells supports T-cell acute leukaemia progression

Is pegfilgrastim safe and effective in congenital neutropenia? An analysis of the French Severe Chronic Neutropenia registry

Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register.

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome

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

Nationwide Survey on the Use of Horse Antithymocyte Globulins (ATGAM) in Patients with Acquired Aplastic Anemia: A Report on Behalf of the French Reference Center for Aplastic Anemia

Natural history of GATA2 deficiency in a survey of 79 French and Belgian patients

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

PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects

Sequential treatment for allogeneic hematopoietic stem cell transplantation in Fanconi anemia with acute myeloid leukemia

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients