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Author Details
Full Name
Claude Preudhomme
Affiliation
Lille University Hospital, INSERM UMR-S7, CNRS UMR9020, Lille University.
ORCID
Career Start Year
1989
Papers
384
H Index
77
Expertise
CM4AI Collaborator
Antoine Forget (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37698981
Three UBA1 clones for a unique VEXAS syndrome.
Rheumatology (Oxford)
2024
37855058
Small myeloid subclones are present at diagnosis of multiple myeloma in patients who develop secondary myelodysplastic syndromes.
Haematologica
2024
36394159
Real-life challenges using personalized prognostic scoring systems in acute myeloid leukemia.
Cancer Med
2023
38093739
Negative Impact of <i>TET2</i> Mutations on Long-Term Survival After Transcatheter Aortic Valve Replacement.
JACC Basic Transl Sci
2023
37637995
Targeted High-throughput Sequencing for Hematological Malignancies: A GBMHM Survey of Practice and Cost Evaluation in France.
Hemasphere
2023
37085611
UBTF tandem duplications define a distinct subtype of adult de novo acute myeloid leukemia.
Leukemia
2023
37205853
LSC17 score complements genetics and measurable residual disease in acute myeloid leukemia: an ALFA study.
Blood Adv
2023
37406166
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41.
Blood Adv
2023
37328541
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group.
Leukemia
2023
34714914
Successful allogeneic hematopoietic stem cell transplantation in patients with VEXAS syndrome: a 2-center experience.
Blood Adv
2022
35443031
Prognostic impact of DDX41 germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study.
Blood
2022
35438802
A randomised phase II study of azacitidine (AZA) alone or with Lenalidomide (LEN), Valproic acid (VPA) or Idarubicin (IDA) in higher-Risk MDS or low blast AML: GFM's "pick a winner" trial, with the impact of somatic mutations.
Br J Haematol
2022
35750691
A multiparametric niche-like drug screening platform in acute myeloid leukemia.
Blood Cancer J
2022
35618837
A cellular hierarchy framework for understanding heterogeneity and predicting drug response in acute myeloid leukemia.
Nat Med
2022
36570694
Relative Mitochondrial Priming Predicts Survival in Older AML Patients Treated Intensively.
Hemasphere
2022
36494771
Publisher Correction: Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
BMC Bioinformatics
2022
36041908
[GATA2 gene mutations: 3 cases].
Rev Med Interne
2022
36307762
Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
BMC Bioinformatics
2022
36151081
Hematopoietic differentiation at single-cell resolution in NPM1-mutated AML.
Blood Cancer J
2022
35256762
Molecular heterogeneity and measurable residual disease of rare NPM1 mutations in acute myeloid leukemia: a nationwide experience from the GBMHM study group.
Leukemia
2022
34983928
Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.
Nat Commun
2022
35008099
Prognostic impact of ABCA3 expression in adult and pediatric acute myeloid leukemia: an ALFA-ELAM02 joint study.
Blood Adv
2022
35176141
Clonal haematopoiesis of indeterminate potential and cardiovascular events in systemic lupus erythematosus (HEMATOPLUS study).
Rheumatology (Oxford)
2022
34615986
Machine learning identifies the independent role of dysplasia in the prediction of response to chemotherapy in AML.
Leukemia
2022
32554555
Germline pathogenic variants in transcription factors predisposing to pediatric acute myeloid leukemia: results from the French ELAM02 trial.
Haematologica
2021
33687433
Transcriptomic and genomic heterogeneity in blastic plasmacytoid dendritic cell neoplasms: from ontogeny to oncogenesis.
Blood Adv
2021
33881523
Prognostic significance of concurrent gene mutations in intensively treated patients with IDH-mutated AML: an ALFA study.
Blood
2021
33906574
Targeting RUNX1 in acute myeloid leukemia: preclinical innovations and therapeutic implications.
Expert Opin Ther Targets
2021
33623140
Genomic landscape of MDS/CMML associated with systemic inflammatory and autoimmune disease.
Leukemia
2021
33778416
Hereditary Predisposition to Acute Myeloid Leukemia in Older Adults.
Hemasphere
2021
34410352
Genetic identification of patients with AML older than 60 years achieving long-term survival with intensive chemotherapy.
Blood
2021
34700215
Standardisation of pathogenicity classification for somatic alterations in solid tumours and haematologic malignancies.
Eur J Cancer
2021
34724563
2021 Update on MRD in acute myeloid leukemia: a consensus document from the European LeukemiaNet MRD Working Party.
Blood
2021
34805765
Improvement of Standardization of Molecular Analyses in Hematology: The 10-year GBMHM French Experience.
Hemasphere
2021
34625784
Early detection of WT1 measurable residual disease identifies high-risk patients, independent of transplantation in AML.
Blood Adv
2021
34344988
Prevalence of UBA1 mutations in MDS/CMML patients with systemic inflammatory and auto-immune disease.
Leukemia
2021
33982372
Optical genome mapping, a promising alternative to gold standard cytogenetic approaches in a series of acute lymphoblastic leukemias.
Genes Chromosomes Cancer
2021
34233450
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy.
Haematologica
2021
33973227
Characterisation of Asp669Tyr Piezo1 cation channel activity in red blood cells: an unexpected phenotype.
Br J Haematol
2021
33054115
Plasmacytoid dendritic cells proliferation associated with acute myeloid leukemia: phenotype profile and mutation landscape
Haematologica
2021
33299234
Minimal residual disease monitoring in acute myeloid leukemia with non-A/B/D-NPM1 mutations by digital polymerase chain reaction: feasibility and clinical use.
Haematologica
2021
33043739
Effects of azacitidine in 93 patients with <i>IDH1/2</i> mutated acute myeloid leukemia/myelodysplastic syndromes: a French retrospective multicenter study.
Leuk Lymphoma
2021
33036026
Germline PAX5 mutation predisposes to familial B-cell precursor acute lymphoblastic leukemia.
Blood
2021
32655144
A transcriptomic continuum of differentiation arrest identifies myeloid interface acute leukemias with poor prognosis.
Leukemia
2021
32871585
A personalized approach to guide allogeneic stem cell transplantation in younger adults with acute myeloid leukemia.
Blood
2021
30987895
Immature platelet fraction (IPF): A reliable tool to predict peripheral thrombocytopenia.
Curr Res Transl Med
2020
31968250
Vitamin D Receptor Controls Cell Stemness in Acute Myeloid Leukemia and in Normal Bone Marrow.
Cell Rep
2020
31988437
Disease escape with the selective loss of the Philadelphia chromosome after tyrosine kinase inhibitor exposure in Ph-positive acute lymphoblastic leukemia.
Leukemia
2020
32098966
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants.
Nat Commun
2020
31827242
Familial myeloid malignancies with germline TET2 mutation.
Leukemia
2020
1 - 50 of 384
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