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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2006 1
2007 1
2008 2
2009 3
2010 5
2011 8
2012 2
2013 4
2014 6
2015 7
2016 10
2017 7
2018 2
2019 6
2020 3
2021 6
2022 6
2023 1
2024 3
2025 1

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70 results

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Page 1
Real-World Validation of Molecular International Prognostic Scoring System for Myelodysplastic Syndromes.
Sauta E, Robin M, Bersanelli M, Travaglino E, Meggendorfer M, Zhao LP, Caballero Berrocal JC, Sala C, Maggioni G, Bernardi M, Di Grazia C, Vago L, Rivoli G, Borin L, D'Amico S, Tentori CA, Ubezio M, Campagna A, Russo A, Mannina D, Lanino L, Chiusolo P, Giaccone L, Voso MT, Riva M, Oliva EN, Zampini M, Riva E, Nibourel O, Bicchieri M, Bolli N, Rambaldi A, Passamonti F, Savevski V, Santoro A, Germing U, Kordasti S, Santini V, Diez-Campelo M, Sanz G, Sole F, Kern W, Platzbecker U, Ades L, Fenaux P, Haferlach T, Castellani G, Della Porta MG. Sauta E, et al. Among authors: nibourel o. J Clin Oncol. 2023 May 20;41(15):2827-2842. doi: 10.1200/JCO.22.01784. Epub 2023 Mar 17. J Clin Oncol. 2023. PMID: 36930857 Free PMC article.
Clinical and Genomic-Based Decision Support System to Define the Optimal Timing of Allogeneic Hematopoietic Stem-Cell Transplantation in Patients With Myelodysplastic Syndromes.
Tentori CA, Gregorio C, Robin M, Gagelmann N, Gurnari C, Ball S, Caballero Berrocal JC, Lanino L, D'Amico S, Spreafico M, Maggioni G, Travaglino E, Sauta E, Meggendorfer M, Zhao LP, Campagna A; GenoMed4All, Synthema, GESMD, FISIM, and EuroBloodNET; Savevski V, Santoro A, Al Ali N, Sallman D, Sole F, Garcia-Manero G, Germing U, Kroger N, Kordasti S, Santini V, Sanz G, Kern W, Platzbecker U, Diez-Campelo M, Maciejewski JP, Ades L, Fenaux P, Haferlach T, Zeidan AM, Castellani G, Komrokji R, Ieva F, Della Porta MG; GenoMed4all and Synthema Consortiums. Tentori CA, et al. J Clin Oncol. 2024 Aug 20;42(24):2873-2886. doi: 10.1200/JCO.23.02175. Epub 2024 May 9. J Clin Oncol. 2024. PMID: 38723212 Free PMC article.
High-throughput genomic analysis in Waldenström's macroglobulinemia.
Poulain S, Braggio E, Roumier C, Aijjou R, Broucqsault N, Galiègue-Zouitina S, Manier S, Soenen V, Nibourel O, Duthilleul P, Fonseca R, Leleu X. Poulain S, et al. Among authors: nibourel o. Clin Lymphoma Myeloma Leuk. 2011 Feb;11(1):106-8. doi: 10.3816/CLML.2011.n.021. Clin Lymphoma Myeloma Leuk. 2011. PMID: 21454205 Review.
Chronic myeloid leukaemia presenting with monocytosis.
Podvin B, Goursaud L, Roynard P, Nibourel O, Duployez N, Fenwarth L. Podvin B, et al. Among authors: nibourel o. 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.
Absence of CALR mutations in JAK2-negative polycythemia.
Chauveau A, Nibourel O, Tondeur S, Luque Paz D, Mansier O, Paul F, Wemeau M, Preudhomme C, Lippert E, Ugo V; French Intergroup of Myeloproliferative Neoplasms. Chauveau A, et al. Among authors: nibourel o. Haematologica. 2017 Jan;102(1):e15-e16. doi: 10.3324/haematol.2016.154799. Epub 2016 Oct 6. Haematologica. 2017. PMID: 27758825 Free PMC article. No abstract available.
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: nibourel o. BMC Bioinformatics. 2022 Oct 28;23(1):448. doi: 10.1186/s12859-022-04983-6. BMC Bioinformatics. 2022. PMID: 36307762 Free PMC article.
MYD88 L265P mutation in Waldenstrom macroglobulinemia.
Poulain S, Roumier C, Decambron A, Renneville A, Herbaux C, Bertrand E, Tricot S, Daudignon A, Galiègue-Zouitina S, Soenen V, Theisen O, Grardel N, Nibourel O, Roche-Lestienne C, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: nibourel o. Blood. 2013 May 30;121(22):4504-11. doi: 10.1182/blood-2012-06-436329. Epub 2013 Mar 26. Blood. 2013. PMID: 23532735 Free article.
Three UBA1 clones for a unique VEXAS syndrome.
Podvin B, Cleenewerck N, Nibourel O, Marceau-Renaut A, Roynard P, Preudhomme C, Duployez N, Terriou L. Podvin B, et al. Among authors: nibourel o. Rheumatology (Oxford). 2024 Feb 1;63(2):e48-e50. doi: 10.1093/rheumatology/kead472. Rheumatology (Oxford). 2024. PMID: 37698981 No abstract available.
Genomic Landscape of CXCR4 Mutations in Waldenström Macroglobulinemia.
Poulain S, Roumier C, Venet-Caillault A, Figeac M, Herbaux C, Marot G, Doye E, Bertrand E, Geffroy S, Lepretre F, Nibourel O, Decambron A, Boyle EM, Renneville A, Tricot S, Daudignon A, Quesnel B, Duthilleul P, Preudhomme C, Leleu X. Poulain S, et al. Among authors: nibourel o. Clin Cancer Res. 2016 Mar 15;22(6):1480-8. doi: 10.1158/1078-0432.CCR-15-0646. Epub 2015 Oct 21. Clin Cancer Res. 2016. PMID: 26490317
70 results