Marie Loosveld

Centre National de la Recherche Scientifique — France

Medicine · Health Sciences

18h-index1.5kcitations84works0.82yr avg
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Research Topics

Acute Lymphoblastic Leukemia research(21), Acute Myeloid Leukemia Research(19), Hemoglobinopathies and Related Disorders(11), CAR-T cell therapy research(11), Immune Cell Function and Interaction(10)

Publications83 total

Expanded clinical, genetic, and biological spectrum of filaminopathies with hematological involvement.
Haematologica·2025Open Access
Ras‐Associated Autoimmune Leukoproliferative Disorder With Cutaneous and Ocular Involvement
Pediatric Blood & Cancer·2025
Ectopic expression of <i>BEX</i> genes in T-cell acute lymphoblastic leukemia
Blood Advances·2025· 1 citedOpen Access
Leucémies aiguës de lignée ambiguë1
Hématologie·2025
High Proportion of PNH Type II Neutrophils, I.e. Relative Percentage ≥3%, Is Associated with Thrombosis in Patients Displaying a PNH Clone &amp;gt;1%: Evidence from Analysis of the 5-Year French Nation-Wide Multicenter Observational Study
Blood·2024Open Access
How to diagnose acid sphingomyelinase deficiency (ASMD) and Niemann–Pick disease type C from bone marrow and peripheral blood smears
HemaSphere·2024· 1 citedOpen Access
Reactive oxygen species and aldehyde dehydrogenase <scp>1A</scp> as prognosis and theragnostic biomarker in acute myeloid leukaemia patients
Journal of Cellular and Molecular Medicine·2024· 6 citedOpen Access
MYC deficiency impairs the development of effector/memory T lymphocytes
Zenodo (CERN European Organization for Nuclear Research)·2024Open Access
MYC deficiency impairs the development of effector/memory T lymphocytes
2024Open Access
Suspicion d’anomalie constitutionnelle au diagnostic de leucémie chez l’enfant : mise au point du comité leucémies de la Société française des cancers de l’enfant
Bulletin du Cancer·2024
<i>CBFB</i>::<i>MYH11</i> fusion in a nonmonocytic acute myeloid leukemia
Blood·2023· 1 citedOpen Access
Syndrome leucoprolifératif auto-immun associé à une mutation du gène RAS
Annales de Dermatologie et de Vénéréologie - FMC·2023
Neutrophil PNH Type II Cells Are Associated with Thrombosis and Bone Marrow Failure without Hemolysis: Evidence from Analysis of the 5-Year French Nation-Wide Multicenter Observational Study
Blood·2023
Primary central nervous system lymphoma with initial spinal cord involvement (PCNSL-SC) is a rare entity: 4 case reports and review of literature
Revue Neurologique·2023· 2 cited
Dramatic response to intravenous immunoglobulin in erythroblastic synartesis
British Journal of Haematology·2023Open Access
Diagnostic challenge in a case of ambiguous lineage acute leukemia with <i>PICALM::MLLT10</i> rearrangement
Pediatric Blood & Cancer·2023· 1 citedOpen Access
Single-cell analysis of megakaryopoiesis in peripheral CD34+ cells: insights into ETV6-related thrombocytopenia
Journal of Thrombosis and Haemostasis·2023· 9 citedOpen Access
Cytological Diagnosis of Classic Myeloproliferative Neoplasms at the Age of Molecular Biology
Cells·2023· 7 citedOpen Access
SARS-CoV-2 spike protein induces a differential monocyte activation that may contribute to age bias in COVID-19 severity
Scientific Reports·2022· 11 citedOpen Access
Rare PNH Cells May be Considered As Genuine PNH Clone: Insights from Analysis of the 5-Year French Nation-Wide Multicenter Observational Study
Blood·2022
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Frequent Co-authors

Dominique Payet‐Bornet(13), Pierre‐Emmanuel Morange(11), Isabelle Arnoux(11), Marie‐Christine Alessi(9), Vanessa Nivaggioni(8), Julie Quessada(8), Delphine Potier(7), Denis Bernot(7), Jacques Quilici(6), Paul Saultier(6), Gérard Michel(6), Bertrand Nadel(6), Mathis Nozais(5), Thomas Cuisset(5), Jean‐Louis Bonnet(5), Mårina Lafage‐Pochitaloff(5), Chantal Fossat(5), Gérard Michel(5), Saran Pankaew(4), Pierre Julien Moro(4)