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Page 1
Genotyping circulating tumor DNA of pediatric Hodgkin lymphoma.
Desch AK, Hartung K, Botzen A, Brobeil A, Rummel M, Kurch L, Georgi T, Jox T, Bielack S, Burdach S, Classen CF, Claviez A, Debatin KM, Ebinger M, Eggert A, Faber J, Flotho C, Frühwald M, Graf N, Jorch N, Kontny U, Kramm C, Kulozik A, Kühr J, Sykora KW, Metzler M, Müller HL, Nathrath M, Nüßlein T, Paulussen M, Pekrun A, Reinhardt D, Reinhard H, Rössig C, Sauerbrey A, Schlegel PG, Schneider DT, Scheurlen W, Schweigerer L, Simon T, Suttorp M, Vorwerk P, Schmitz R, Kluge R, Mauz-Körholz C, Körholz D, Gattenlöhner S, Bräuninger A. Desch AK, et al. Among authors: brauninger a. Leukemia. 2020 Jan;34(1):151-166. doi: 10.1038/s41375-019-0541-6. Epub 2019 Aug 20. Leukemia. 2020. PMID: 31431735
Pathogenesis of Hodgkin's lymphoma.
Küppers R, Schmitz R, Distler V, Renné C, Bräuninger A, Hansmann ML. Küppers R, et al. Among authors: brauninger a. Eur J Haematol Suppl. 2005 Jul;(66):26-33. doi: 10.1111/j.1600-0609.2005.00451.x. Eur J Haematol Suppl. 2005. PMID: 16007865 Review.
Targeted Next-Generation Sequencing Is a Sensitive Tool for Differential Diagnosis of Myelodysplastic Syndromes in Bone Marrow Trephines.
Bräuninger A, Blau W, Kunze K, Desch AK, Brobeil A, Tur MK, Etschmann B, Günther U, Körholz D, Schliesser G, Käbisch A, Kiehl M, Rummel M, Gattenlöhner S. Bräuninger A, et al. J Mol Diagn. 2018 May;20(3):344-354. doi: 10.1016/j.jmoldx.2018.01.006. Epub 2018 Feb 19. J Mol Diagn. 2018. PMID: 29471115 Free article.
Insights into the multistep transformation process of lymphomas: IgH-associated translocations and tumor suppressor gene mutations in clonally related composite Hodgkin's and non-Hodgkin's lymphomas.
Schmitz R, Renné C, Rosenquist R, Tinguely M, Distler V, Menestrina F, Lestani M, Stankovic T, Austen B, Bräuninger A, Hansmann ML, Küppers R. Schmitz R, et al. Among authors: brauninger a. Leukemia. 2005 Aug;19(8):1452-8. doi: 10.1038/sj.leu.2403841. Leukemia. 2005. PMID: 15973455
Detection of an activated JAK3 variant and a Xq26.3 microdeletion causing loss of PHF6 and miR-424 expression in myelodysplastic syndromes by combined targeted next generation sequencing and SNP array analysis.
Kunze K, Gamerdinger U, Leßig-Owlanj J, Sorokina M, Brobeil A, Tur MK, Blau W, Burchardt A, Käbisch A, Schliesser G, Kiehl M, Rosenwald A, Rummel M, Grimminger F, Hain T, Chakraborty T, Bräuninger A, Gattenlöhner S. Kunze K, et al. Among authors: brauninger a. Pathol Res Pract. 2014 Jun;210(6):369-76. doi: 10.1016/j.prp.2014.02.006. Epub 2014 Feb 23. Pathol Res Pract. 2014. PMID: 24674452
79 results