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bamSliceR: cross-cohort variant and allelic bias analysis for rare variants and rare diseases.
bioRxiv [Preprint]. 2023 Sep 17:2023.09.15.558026. doi: 10.1101/2023.09.15.558026.
bioRxiv. 2023.
PMID: 37745420
Free PMC article.
Preprint.
Developmental priming of cancer susceptibility.
Panzeri I, Fagnocchi L, Apostle S, Tompkins M, Wolfrum E, Madaj Z, Hostetter G, Liu Y, Schaefer K, Chih-Hsiang Y, Bergsma A, Drougard A, Dror E; PERMUTE; Chandler D, Schramek D, Triche TJ Jr, Pospisilik JA.
Panzeri I, et al.
bioRxiv [Preprint]. 2023 Sep 15:2023.09.12.557446. doi: 10.1101/2023.09.12.557446.
bioRxiv. 2023.
PMID: 37745326
Free PMC article.
Preprint.
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Comprehensive molecular and clinical characterization of NUP98 fusions in pediatric acute myeloid leukemia.
Bertrums EJM, Smith JL, Harmon L, Ries RE, Wang YJ, Alonzo TA, Menssen AJ, Chisholm KM, Leonti AR, Tarlock K, Ostronoff F, Pogosova-Agadjanyan EL, Kaspers GJL, Hasle H, Dworzak M, Walter C, Muhlegger N, Morerio C, Pardo L, Hirsch B, Raimondi S, Cooper TM, Aplenc R, Gamis AS, Kolb EA, Farrar JE, Stirewalt D, Ma X, Shaw TI, Furlan SN, Brodersen LE, Loken MR, Van den Heuvel-Eibrink MM, Zwaan CM, Triche TJ, Goemans BF, Meshinchi S.
Bertrums EJM, et al.
Haematologica. 2023 Aug 1;108(8):2044-2058. doi: 10.3324/haematol.2022.281653.
Haematologica. 2023.
PMID: 36815378
Free PMC article.
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Evolutionary Landscape of SOX Genes to Inform Genotype-to-Phenotype Relationships.
Underwood A, Rasicci DT, Hinds D, Mitchell JT, Zieba JK, Mills J, Arnold NE, Cook TW, Moustaqil M, Gambin Y, Sierecki E, Fontaine F, Vanderweele S, Das AS, Cvammen W, Sirpilla O, Soehnlen X, Bricker K, Alokaili M, Green M, Heeringa S, Wilstermann AM, Freeland TM, Qutob D, Milsted A, Jauch R, Triche TJ Jr, Krawczyk CM, Bupp CP, Rajasekaran S, Francois M, Prokop JW.
Underwood A, et al.
Genes (Basel). 2023 Jan 14;14(1):222. doi: 10.3390/genes14010222.
Genes (Basel). 2023.
PMID: 36672963
Free PMC article.
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