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Author Details

Jean Soulier
University of Paris
1993
181
66
PMIDPaper TitleJournal TitlePublished Year
36054881Clinical and Molecular Determinants of Clonal Evolution in Aplastic Anemia and Paroxysmal Nocturnal Hemoglobinuria.J Clin Oncol2023
37595275Genetic alterations and MRD refine risk assessment for KMT2A-rearranged B-cell precursor ALL in adults: a GRAALL study.Blood2023
36952636The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia.Blood2023
36951151Allogeneic transplantation in acute myelogenous leukemia: a comprehensive single institution's experience.Haematologica2023
37424223Novel precision medicine approaches and treatment strategies in hematological malignancies.J Intern Med2023
37085611UBTF tandem duplications define a distinct subtype of adult de novo acute myeloid leukemia.Leukemia2023
37053552IPSS-M in myelodysplastic neoplasms arising from aplastic anemia and paroxysmal nocturnal hemoglobinuria.Blood2023
37451692Autosomal recessive systemic microangiopathy associated with <i>FANCL</i> Fanconi anaemia.J Neurol Neurosurg Psychiatry2023
37395445A clickable melphalan for monitoring DNA interstrand crosslink accumulation and detecting ICL repair defects in Fanconi anemia patient cells.Nucleic Acids Res2023
36626252Rare germline complement factor H variants in patients with paroxysmal nocturnal hemoglobinuria.Blood2023
36721989A novel cancer risk prediction score for the natural course of FA patients with biallelic BRCA2/FANCD1 mutations.Hum Mol Genet2023
36736290Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.Cell Stem Cell2023
36630200Adult Low-Hypodiploid Acute Lymphoblastic Leukemia Emerges from Preleukemic TP53-Mutant Clonal Hematopoiesis.Blood Cancer Discov2023
33415426Aggressive lymphoma, hemophagocytic lymphohistiocytosis, and G6PD crisis: a lytic cocktail.Ann Hematol2022
35443031Prognostic impact of DDX41 germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study.Blood2022
35316324Concurrent CDX2 cis-deregulation and UBTF::ATXN7L3 fusion define a novel high-risk subtype of B-cell ALL.Blood2022
34751952A new step in understanding stem cell mobilization in patients with Fanconi anemia: A bridge to gene therapy.Transfusion2022
34624096ETV6-NCOA2 fusion induces T/myeloid mixed-phenotype leukemia through transformation of nonthymic hematopoietic progenitor cells.Blood2022
32581253Clonal dominance is an adverse prognostic factor in acute myeloid leukemia treated with intensive chemotherapy.Leukemia2021
34485595Improved collection of hematopoietic stem cells and progenitors from Fanconi anemia patients for gene therapy purposes.Mol Ther Methods Clin Dev2021
34301789Actinomycin D Targets NPM1c-Primed Mitochondria to Restore PML-Driven Senescence in AML Therapy.Cancer Discov2021
34099877Correction to: The long non-coding RNA CRNDE regulates growth of multiple myeloma cells via an effect on IL6 signaling.Leukemia2021
33458694A Tumor Suppressor Enhancer of <i>PTEN</i> in T-cell development and leukemia.Blood Cancer Discov2021
32879426The long non-coding RNA CRNDE regulates growth of multiple myeloma cells via an effect on IL6 signalling.Leukemia2021
32651452FLAG-sequential regimen followed by bone marrow transplantation for myelodysplastic syndrome or acute leukemia in patients with Fanconi anemia: a Franco-Brazilian study.Bone Marrow Transplant2021
32430499Introduction to a review series on secondary leukemia.Blood2020
32007515Outcome and clinicophenotypical features of acute lymphoblastic leukemia/lymphoblastic lymphoma with cutaneous involvement: A multicenter case series.J Am Acad Dermatol2020
33203900XPC deficiency increases risk of hematologic malignancies through mutator phenotype and characteristic mutational signature.Nat Commun2020
32379395A paediatric myelodysplastic syndrome with 5q deletion associated with Fanconi anaemia.Pediatr Blood Cancer2020
30510083<i>PAX5</i> P80R mutation identifies a novel subtype of B-cell precursor acute lymphoblastic leukemia with favorable outcome.Blood2019
31751766BET inhibitors impair leukemic stem cell function only in defined oncogenic subgroups of acute myeloid leukaemias.Leuk Res2019
31648317ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.Blood Adv2019
31501599Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia.Nat Med2019
31434701Efficacy of tyrosine kinase inhibitors in Ph-like acute lymphoblastic leukemia harboring ABL-class rearrangements.Blood2019
31570891Germline NPM1 mutations lead to altered rRNA 2'-O-methylation and cause dyskeratosis congenita.Nat Genet2019
31484648Germline DDX41 mutations define a significant entity within adult MDS/AML patients.Blood2019
30779244A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis.Genes Chromosomes Cancer2019
30914417Familial predisposition to TP53/complex karyotype MDS and leukemia in DNA repair-deficient xeroderma pigmentosum.Blood2019
30514801T-cell acute lymphoblastic leukemias express a unique truncated FAT1 isoform that cooperates with NOTCH1 in leukemia development.Haematologica2019
30390009Creatine kinase pathway inhibition alters GSK3 and WNT signaling in EVI1-positive AML.Leukemia2019
28837157Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia.Genet Med2018
29954933A comprehensive inventory of TLX1 controlled long non-coding RNAs in T-cell acute lymphoblastic leukemia through polyA+ and total RNA sequencing.Haematologica2018
30266814Deletion 6q Drives T-cell Leukemia Progression by Ribosome Modulation.Cancer Discov2018
30449320Studies in an Early Development Window Unveils a Severe HSC Defect in both Murine and Human Fanconi Anemia.Stem Cell Reports2018
29496663HOXA9 Cooperates with Activated JAK/STAT Signaling to Drive Leukemia Development.Cancer Discov2018
29535430Granulomonocytic progenitors are key target cells of azacytidine in higher risk myelodysplastic syndromes and acute myeloid leukemia.Leukemia2018
29051182Oncogenetic mutations combined with MRD improve outcome prediction in pediatric T-cell acute lymphoblastic leukemia.Blood2018
29146883A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.Blood2018
29187379Mutant JAK3 signaling is increased by loss of wild-type JAK3 or by acquisition of secondary JAK3 mutations in T-ALL.Blood2018
28073829dUTPase (<i>DUT</i>) Is Mutated in a Novel Monogenic Syndrome With Diabetes and Bone Marrow Failure.Diabetes2017
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Collaborators

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Saint-Louis Hospital
Co-authored papers 41
Herv?? Dombret
Institut de Recherche Saint-Louis, Universite de Paris
Co-authored papers 27
Raphael Itzykson
Universite Paris Cite, INSERM, CNRS
Co-authored papers 12
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Universite Paris Diderot
Co-authored papers 12
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Assistance Publique des Hopitaux de Paris (AP-HP)
Co-authored papers 11
Claude Preudhomme
Lille University Hospital, INSERM UMR-S7, CNRS UMR9020, Lille University.
Co-authored papers 9
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CHU La Miletrie University Hospital Poitiers France.
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Curie Institute Hospital Group
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Location Vrije Universiteit Amsterdam
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Claude Gardin
Avicenne Hospital
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Tom Vulliamy
Blizard Institute, Queen Mary University of London
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Alexandre Puissant
Universite de Paris, INSERM, CNRS
Co-authored papers 3
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
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Pieter Mestdagh
Co-authored papers 3
Ruud H Brakenhoff
Vrije Universiteit Amsterdam
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Charles G Mullighan
St Jude Children's Research Hospital
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Richard B Lock
Children's Cancer Institute, Lowy Cancer Research Centre, School of Clinical Medicine
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Frederic D Bushman
Perelman School of Medicine, University of Pennsylvania
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Meenakshi Devidas
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Release 1.2