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Year Number of Results
2019 5
2020 6
2021 9
2022 9
2023 5
2024 3

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31 results

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Page 1
Prognostic impact of DDX41 germline mutations in intensively treated acute myeloid leukemia patients: an ALFA-FILO study.
Duployez N, Largeaud L, Duchmann M, Kim R, Rieunier J, Lambert J, Bidet A, Larcher L, Lemoine J, Delhommeau F, Hirsch P, Fenwarth L, Kosmider O, Decroocq J, Bouvier A, Le Bris Y, Ochmann M, Santagostino A, Adès L, Fenaux P, Thomas X, Micol JB, Gardin C, Itzykson R, Soulier J, Clappier E, Recher C, Preudhomme C, Pigneux A, Dombret H, Delabesse E, Sébert M. Duployez N, et al. Among authors: fenwarth l. Blood. 2022 Aug 18;140(7):756-768. doi: 10.1182/blood.2021015328. Blood. 2022. PMID: 35443031 Free PMC article.
Prognostic impact of CEBPA mutational subgroups in adult AML.
Georgi JA, Stasik S, Kramer M, Meggendorfer M, Röllig C, Haferlach T, Valk P, Linch D, Herold T, Duployez N, Taube F, Middeke JM, Platzbecker U, Serve H, Baldus CD, Muller-Tidow C, Haferlach C, Koch S, Berdel WE, Woermann BJ, Krug U, Braess J, Hiddemann W, Spiekermann K, Boertjes EL, Hills RK, Burnett A, Ehninger G, Metzeler K, Rothenberg-Thurley M, Dufour A, Dombret H, Pautas C, Preudhomme C, Fenwarth L, Bornhäuser M, Gale R, Thiede C. Georgi JA, et al. Among authors: fenwarth l. Leukemia. 2024 Feb;38(2):281-290. doi: 10.1038/s41375-024-02140-x. Epub 2024 Jan 16. Leukemia. 2024. PMID: 38228680 Free PMC article.
UBTF tandem duplications define a distinct subtype of adult de novo acute myeloid leukemia.
Duployez N, Vasseur L, Kim R, Largeaud L, Passet M, L'Haridon A, Lemaire P, Fenwarth L, Geffroy S, Helevaut N, Celli-Lebras K, Adès L, Lebon D, Berthon C, Marceau-Renaut A, Cheok M, Lambert J, Récher C, Raffoux E, Micol JB, Pigneux A, Gardin C, Delabesse E, Soulier J, Hunault M, Dombret H, Itzykson R, Clappier E, Preudhomme C. Duployez N, et al. Among authors: fenwarth l. Leukemia. 2023 Jun;37(6):1245-1253. doi: 10.1038/s41375-023-01906-z. Epub 2023 Apr 21. Leukemia. 2023. PMID: 37085611 Free PMC article.
Chronic myeloid leukaemia presenting with monocytosis.
Podvin B, Goursaud L, Roynard P, Nibourel O, Duployez N, Fenwarth L. Podvin B, et al. Among authors: fenwarth l. Br J Haematol. 2022 Jan;196(1):8. doi: 10.1111/bjh.17725. Epub 2021 Aug 19. Br J Haematol. 2022. PMID: 34409591 No abstract available.
[GATA2 gene mutations: 3 cases].
Perrard N, Pokeerbux MR, Quesnel B, Duployez N, Fenwarth L, Preudhomme C, Lefèvre G, Baillet C, Launay D, Terriou L. Perrard N, et al. Among authors: fenwarth l. Rev Med Interne. 2022 Nov;43(11):677-682. doi: 10.1016/j.revmed.2022.08.007. Epub 2022 Aug 28. Rev Med Interne. 2022. PMID: 36041908 French.
Controversies about germline RUNX1 missense variants.
Duployez N, Fenwarth L. Duployez N, et al. Among authors: fenwarth l. Leuk Lymphoma. 2020 Feb;61(2):497-499. doi: 10.1080/10428194.2019.1675882. Epub 2019 Oct 18. Leuk Lymphoma. 2020. PMID: 31623479 No abstract available.
LSC17 score complements genetics and measurable residual disease in acute myeloid leukemia: an ALFA study.
Vasseur L, Fenwarth L, Lambert J, de Botton S, Figeac M, Villenet C, Heiblig M, Dumas PY, Récher C, Berthon C, Lemasle E, Lebon D, Lambert J, Terré C, Celli-Lebras K, Dombret H, Preudhomme C, Cheok M, Itzykson R, Duployez N. Vasseur L, et al. Among authors: fenwarth l. Blood Adv. 2023 Aug 8;7(15):4024-4034. doi: 10.1182/bloodadvances.2023010155. Blood Adv. 2023. PMID: 37205853 Free PMC article.
Frugal alignment-free identification of FLT3-internal tandem duplications with FiLT3r.
Boudry A, Darmon S, Duployez N, Figeac M, Geffroy S, Bucci M, Celli-Lebras K, Duchmann M, Joudinaud R, Fenwarth L, Nibourel O, Goursaud L, Itzykson R, Dombret H, Hunault M, Preudhomme C, Salson M. Boudry A, et al. Among authors: fenwarth l. BMC Bioinformatics. 2022 Oct 28;23(1):448. doi: 10.1186/s12859-022-04983-6. BMC Bioinformatics. 2022. PMID: 36307762 Free PMC article.
31 results