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Recurrent CTNNB1 mutations in craniofacial osteomas.
Baumhoer D, Berthold R, Isfort I, Heinst L, Ameline B, Grünewald I, Thieringer FM, Rudack C, Wardelmann E, Vieth V, Sperveslage J, Trautmann M, Hartmann W. Baumhoer D, et al. Among authors: ameline b. Mod Pathol. 2022 Apr;35(4):489-494. doi: 10.1038/s41379-021-00956-x. Epub 2021 Nov 1. Mod Pathol. 2022. PMID: 34725446 Free PMC article.
Activating mutations in the MAP-kinase pathway define non-ossifying fibroma of bone.
Baumhoer D, Kovac M, Sperveslage J, Ameline B, Strobl AC, Krause A, Trautmann M, Wardelmann E, Nathrath M, Höller S, Hardes J, Gosheger G, Krieg AH, Vieth V, Tirabosco R, Amary F, Flanagan AM, Hartmann W. Baumhoer D, et al. Among authors: ameline b. J Pathol. 2019 May;248(1):116-122. doi: 10.1002/path.5216. Epub 2019 Jan 24. J Pathol. 2019. PMID: 30549028
NTRK fusions in osteosarcoma are rare and non-functional events.
Ameline B, Saba KH, Kovac M, Magnusson L, Witt O, Bielack S, Nathrath M, Nord KH, Baumhoer D. Ameline B, et al. J Pathol Clin Res. 2020 Apr;6(2):107-112. doi: 10.1002/cjp2.158. Epub 2020 Feb 5. J Pathol Clin Res. 2020. PMID: 32022484 Free PMC article.
Germline RET variants underlie a subset of paediatric osteosarcoma.
Kovac M, Woolley C, Ribi S, Blattmann C, Roth E, Morini M, Kovacova M, Ameline B, Kulozik A, Bielack S, Hartmann W, Ballinger ML, Thomas DM, Tomlinson I, Nathrath M, Heinimann K, Baumhoer D. Kovac M, et al. Among authors: ameline b. J Med Genet. 2021 Jan;58(1):20-24. doi: 10.1136/jmedgenet-2019-106734. Epub 2020 Mar 16. J Med Genet. 2021. PMID: 32179705
46 results