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Author Details

Anna Raimbault
CHU La Miletrie University Hospital Poitiers France.
2012
24
12
PMIDPaper TitleJournal TitlePublished Year
36736290Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemia.Cell Stem Cell2023
37207087Hairy cell leukemia with isolated bone lesions.Clin Case Rep2023
32327500Integrated analyses of translatome and proteome identify the rules of translation selectivity in RPS14-deficient cells.Haematologica2021
34399652Identification and genetic characterization of a <i>NUP98-HHEX</i> molecular rearrangement in a pediatric acute myeloid leukemia.Leuk Lymphoma2021
32818241p53 activation during ribosome biogenesis regulates normal erythroid differentiation.Blood2021
32581253Clonal dominance is an adverse prognostic factor in acute myeloid leukemia treated with intensive chemotherapy.Leukemia2021
31498561Phenotypic landscape of granulocytes and monocytes by multiparametric flow cytometry: A prospective study of a 1-tube panel strategy for diagnosis and prognosis of patients with MDS.Cytometry B Clin Cytom2020
32627184De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia.Clin Genet2020
32557566Holding on to the Matutes score while dropping FMC7: new opportunity from standardised approaches in multiparameter flow cytometry.Br J Haematol2020
30545930Downregulation of TREM-like transcript-1 and collagen receptor α2 subunit, two novel RUNX1-targets, contributes to platelet dysfunction in familial platelet disorder with predisposition to acute myelogenous leukemia.Haematologica2019
31648317ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.Blood Adv2019
30198568CD13 expression in B cell malignancies is a hallmark of plasmacytic differentiation.Br J Haematol2019
31501599Successful engraftment of gene-corrected hematopoietic stem cells in non-conditioned patients with Fanconi anemia.Nat Med2019
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
30963682The fraction of CD117/c-KIT-expressing erythroid precursors predicts ESA response in low-risk myelodysplastic syndromes.Cytometry B Clin Cytom2019
29146883A landscape of germ line mutations in a cohort of inherited bone marrow failure patients.Blood2018
26910909APG101 efficiently rescues erythropoiesis in lower risk myelodysplastic syndromes with severe impairment of hematopoiesis.Oncotarget2016
26626993Effect of lenalidomide treatment on clonal architecture of myelodysplastic syndromes without 5q deletion.Blood2016
28034875Plasma cell leukemia revealing a G6PD deficiency.Blood2016
27452463Comprehensive Proteomic Analysis of Human Erythropoiesis.Cell Rep2016
23432206Flow cytometry thresholds of myeloperoxidase detection to discriminate between acute lymphoblastic or myeloblastic leukaemia.Br J Haematol2013
22898599Dysmegakaryopoiesis of FPD/AML pedigrees with constitutional RUNX1 mutations is linked to myosin II deregulated expression.Blood2012
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Co-authored papers 5
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Lille University Hospital, INSERM UMR-S7, CNRS UMR9020, Lille University.
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The University of Chicago
Co-authored papers 1
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Co-authored papers 1
Emory University School of Medicine
Co-authored papers 1
Hannover Medical School
Co-authored papers 1
Knight Cancer Institute, Oregon Health & Science University
Co-authored papers 1
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Universite Paris Cite, CNRS
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Houston Methodist Hospital
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