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Page 1
Collaborative effect of Csnk1a1 haploinsufficiency and mutant p53 in Myc induction can promote leukemic transformation.
Fuchs SNR, Stalmann USA, Snoeren IAM, Bindels E, Schmitz S, Banjanin B, Hoogenboezem RM, van Herk S, Saad M, Walter W, Haferlach T, Seillier L, Saez-Rodriguez J, Dugourd AJF, Lehmann KV, Ben-Neriah Y, Gleitz HFE, Schneider RK. Fuchs SNR, et al. Among authors: haferlach t. Blood Adv. 2024 Feb 13;8(3):766-779. doi: 10.1182/bloodadvances.2022008926. Blood Adv. 2024. PMID: 38147624 Free PMC article.
The E592K variant of SF3B1 creates unique RNA missplicing and associates with high-risk MDS without ring sideroblasts.
Choi IY, Ling JP, Zhang J, Helmenstine E, Walter W, Tsakiroglou P, Bergman RE, Philippe C, Manley JL, Rouault-Pierre K, Li B, Wiseman DH, Batta K, Ouseph M, Bernard E, Dubner B, Li X, Haferlach T, Koget A, Fazal S, Jain T, Gocke CD, DeZern AE, Dalton WB. Choi IY, et al. Among authors: haferlach t. Blood Adv. 2024 Aug 13;8(15):3961-3971. doi: 10.1182/bloodadvances.2023011260. Blood Adv. 2024. PMID: 38759096 Free PMC article.
How I read an article that uses machine learning methods.
Nazha A, Elemento O, McWeeney S, Miles M, Haferlach T. Nazha A, et al. Among authors: haferlach t. Blood Adv. 2023 Aug 22;7(16):4550-4554. doi: 10.1182/bloodadvances.2023010140. Blood Adv. 2023. PMID: 37276509 Free PMC article. No abstract available.
Implementation of Whole-Genome and Transcriptome Sequencing Into Clinical Cancer Care.
Cuppen E, Elemento O, Rosenquist R, Nikic S, IJzerman M, Zaleski ID, Frederix G, Levin LÅ, Mullighan CG, Buettner R, Pugh TJ, Grimmond S, Caldas C, Andre F, Custers I, Campo E, van Snellenberg H, Schuh A, Nakagawa H, von Kalle C, Haferlach T, Fröhling S, Jobanputra V. Cuppen E, et al. Among authors: haferlach t. JCO Precis Oncol. 2022 Dec;6:e2200245. doi: 10.1200/PO.22.00245. JCO Precis Oncol. 2022. PMID: 36480778 Free PMC article. Review.
Explainable AI identifies diagnostic cells of genetic AML subtypes.
Hehr M, Sadafi A, Matek C, Lienemann P, Pohlkamp C, Haferlach T, Spiekermann K, Marr C. Hehr M, et al. Among authors: haferlach t. PLOS Digit Health. 2023 Mar 15;2(3):e0000187. doi: 10.1371/journal.pdig.0000187. eCollection 2023 Mar. PLOS Digit Health. 2023. PMID: 36921004 Free PMC article.
Genetic analysis of myeloid neoplasms with der(1;7)(q10;p10).
Okuda R, Ochi Y, Saiki R, Yamanaka T, Terao C, Yoshizato T, Nakagawa MM, Zhao L, Ohyashiki K, Hiramoto N, Sanada M, Handa H, Kasahara S, Miyazaki Y, Sezaki N, Shih LY, Kern W, Kanemura N, Kitano T, Imashuku S, Watanabe M, Creignou M, Chonabayashi K, Usuki K, Ishikawa T, Gotoh A, Atsuta Y, Shiraishi Y, Mitani K, Chiba S, Takaori-Kondo A, Miyano S, Kamatani Y, Haferlach T, Hellström-Lindberg E, Matsuda K, Yoshida Y, Makishima H, Nannya Y, Ogawa S. Okuda R, et al. Among authors: haferlach t. Leukemia. 2024 Dec 23. doi: 10.1038/s41375-024-02494-2. Online ahead of print. Leukemia. 2024. PMID: 39715854 No abstract available.
Somatic Recombination Between an Ancient and a Recent NOTCH2 Gene Variant Is Associated with the NOTCH2 Gain-of-Function Phenotype in Chronic Lymphocytic Leukemia.
Hubmann R, Hilgarth M, Löwenstern T, Lienhard A, Sima F, Reisinger M, Hobel-Kleisch C, Porpaczy E, Haferlach T, Hoermann G, Laccone F, Jungbauer C, Valent P, Staber PB, Shehata M, Jäger U. Hubmann R, et al. Among authors: haferlach t. Int J Mol Sci. 2024 Nov 22;25(23):12581. doi: 10.3390/ijms252312581. Int J Mol Sci. 2024. PMID: 39684291 Free PMC article.
736 results