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Page 1
Somatic variant profiling in chronic phase pediatric chronic myeloid leukemia.
Behrens YL, Gaschler L, Nienhold R, Reinkens T, Schirmer E, Knöß S, Strasser R, Sembill S, Wotschofsky Z, Suttorp M, Krumbholz M, Schlegelberger B, Metzler M, Göhring G, Karow A. Behrens YL, et al. Among authors: schlegelberger b. Haematologica. 2024 Mar 1;109(3):942-947. doi: 10.3324/haematol.2023.283800. Haematologica. 2024. PMID: 37706343 Free PMC article. No abstract available.
An artificial intelligence-assisted clinical framework to facilitate diagnostics and translational discovery in hematologic neoplasia.
Tang M, Antić Ž, Fardzadeh P, Pietzsch S, Schröder C, Eberhardt A, van Bömmel A, Escherich G, Hofmann W, Horstmann MA, Illig T, McCrary JM, Lentes J, Metzler M, Nejdl W, Schlegelberger B, Schrappe M, Zimmermann M, Miarka-Walczyk K, Pastorczak A, Cario G, Renard BY, Stanulla M, Bergmann AK. Tang M, et al. Among authors: schlegelberger b. EBioMedicine. 2024 Jun;104:105171. doi: 10.1016/j.ebiom.2024.105171. Epub 2024 May 28. EBioMedicine. 2024. PMID: 38810562 Free PMC article.
Genomic variant profiling in blast-phase paediatric chronic myeloid leukaemia: Predisposing and driving alterations.
Behrens YL, Reinkens T, Hofmann W, Gumann A, Förster A, Gaschler L, Ghete T, Strasser R, Espenkötter J, Haermeyer B, Losch M, Sembill S, Wotschofsky Z, von Hörsten S, Schuh W, Di Donato N, Suttorp M, Krumbholz M, Ripperger T, Schlegelberger B, Göhring G, Metzler M, Karow A. Behrens YL, et al. Among authors: schlegelberger b. Br J Haematol. 2025 Jul;207(1):141-150. doi: 10.1111/bjh.20133. Epub 2025 May 8. Br J Haematol. 2025. PMID: 40344211 Free PMC article.
Rare and potentially fatal - Cytogenetically cryptic TNIP1::PDGFRB and PCM1::FGFR1 fusion leading to myeloid/lymphoid neoplasms with eosinophilia in children.
Berking AC, Flaadt T, Behrens YL, Yoshimi A, Leipold A, Holzer U, Lang P, Quintanilla-Martinez L, Schlegelberger B, Reiter A, Niemeyer C, Strahm B, Göhring G. Berking AC, et al. Among authors: schlegelberger b. Cancer Genet. 2023 Apr;272-273:29-34. doi: 10.1016/j.cancergen.2023.01.002. Epub 2023 Jan 7. Cancer Genet. 2023. PMID: 36657267
European standard clinical practice - Key issues for the medical care of individuals with familial leukemia.
Förster A, Davenport C, Duployez N, Erlacher M, Ferster A, Fitzgibbon J, Göhring G, Hasle H, Jongmans MC, Kolenova A, Kronnie G, Lammens T, Mecucci C, Mlynarski W, Niemeyer CM, Sole F, Szczepanski T, Waanders E, Biondi A, Wlodarski M, Schlegelberger B, Ripperger T. Förster A, et al. Among authors: schlegelberger b. Eur J Med Genet. 2023 Apr;66(4):104727. doi: 10.1016/j.ejmg.2023.104727. Epub 2023 Feb 10. Eur J Med Genet. 2023. PMID: 36775010
Deciphering the needs of patients with hereditary breast and ovarian Cancer in the Process of Genetic Counseling to Inform the Development of a Mobile Support App: a qualitative study in Germany.
Ammon N, Reichert C, Kupka T, Oeltze-Jafra S, Bergmann AK, Schlegelberger B, Wolff D, Vajen B. Ammon N, et al. Among authors: schlegelberger b. J Community Genet. 2024 Dec;15(6):603-613. doi: 10.1007/s12687-024-00727-6. Epub 2024 Aug 19. J Community Genet. 2024. PMID: 39158769 Free PMC article.
468 results