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Page 1
Genetic characterization and mutational profiling of foramen magnum meningiomas: a multi-institutional study.
Hua L, Alkhatib M, Fujio S, Alhasan B, Herold S, Zeugner S, Zolal A, Hijazi MM, Clark VE, Wakimoto H, Shankar GM, Brastianos PK, Barker FG, Cahill DP, Ren L, Eyüpoglu IY, Gong Y, Schackert G, Juratli TA. Hua L, et al. Among authors: zeugner s. J Neurosurg. 2024 Jan 26:1-7. doi: 10.3171/2023.11.JNS231936. Online ahead of print. J Neurosurg. 2024. PMID: 38277657
Sporadic multiple meningiomas harbor distinct driver mutations.
Juratli TA, Prilop I, Saalfeld FC, Herold S, Meinhardt M, Wenzel C, Zeugner S, Aust DE, Barker FG 2nd, Cahill DP, Brastianos PK, Santagata S, Schackert G, Pinzer T. Juratli TA, et al. Among authors: zeugner s. Acta Neuropathol Commun. 2021 Jan 6;9(1):8. doi: 10.1186/s40478-020-01113-2. Acta Neuropathol Commun. 2021. PMID: 33407897 Free PMC article. No abstract available.
Two predominant molecular subtypes of spinal meningioma: thoracic NF2-mutant tumors strongly associated with female sex, and cervical AKT1-mutant tumors originating ventral to the spinal cord.
Hua L, Alkhatib M, Podlesek D, Günther L, Pinzer T, Meinhardt M, Zeugner S, Herold S, Cahill DP, Brastianos PK, Williams EA, E Clark V, Shankar GM, Wakimoto H, Ren L, Chen J, Gong Y, Schackert G, Juratli TA. Hua L, et al. Among authors: zeugner s. Acta Neuropathol. 2022 Nov;144(5):1053-1055. doi: 10.1007/s00401-022-02474-9. Epub 2022 Aug 9. Acta Neuropathol. 2022. PMID: 35943573 Free PMC article. No abstract available.
Targeted capture-based NGS is superior to multiplex PCR-based NGS for hereditary BRCA1 and BRCA2 gene analysis in FFPE tumor samples.
Zakrzewski F, Gieldon L, Rump A, Seifert M, Grützmann K, Krüger A, Loos S, Zeugner S, Hackmann K, Porrmann J, Wagner J, Kast K, Wimberger P, Baretton G, Schröck E, Aust D, Klink B. Zakrzewski F, et al. Among authors: zeugner s. BMC Cancer. 2019 Apr 27;19(1):396. doi: 10.1186/s12885-019-5584-6. BMC Cancer. 2019. PMID: 31029168 Free PMC article.
Next-generation panel sequencing identifies NF1 germline mutations in three patients with pheochromocytoma but no clinical diagnosis of neurofibromatosis type 1.
Gieldon L, Masjkur JR, Richter S, Därr R, Lahera M, Aust D, Zeugner S, Rump A, Hackmann K, Tzschach A, Januszewicz A, Prejbisz A, Eisenhofer G, Schrock E, Robledo M, Klink B. Gieldon L, et al. Among authors: zeugner s. Eur J Endocrinol. 2018 Feb;178(2):K1-K9. doi: 10.1530/EJE-17-0714. Epub 2017 Nov 20. Eur J Endocrinol. 2018. PMID: 29158289
DNA copy number changes define spatial patterns of heterogeneity in colorectal cancer.
Mamlouk S, Childs LH, Aust D, Heim D, Melching F, Oliveira C, Wolf T, Durek P, Schumacher D, Bläker H, von Winterfeld M, Gastl B, Möhr K, Menne A, Zeugner S, Redmer T, Lenze D, Tierling S, Möbs M, Weichert W, Folprecht G, Blanc E, Beule D, Schäfer R, Morkel M, Klauschen F, Leser U, Sers C. Mamlouk S, et al. Among authors: zeugner s. Nat Commun. 2017 Jan 25;8:14093. doi: 10.1038/ncomms14093. Nat Commun. 2017. PMID: 28120820 Free PMC article.
EGFR T790M mutation testing of non-small cell lung cancer tissue and blood samples artificially spiked with circulating cell-free tumor DNA: results of a round robin trial.
Fassunke J, Ihle MA, Lenze D, Lehmann A, Hummel M, Vollbrecht C, Penzel R, Volckmar AL, Stenzinger A, Endris V, Jung A, Lehmann U, Zeugner S, Baretton G, Kreipe H, Schirmacher P, Kirchner T, Dietel M, Büttner R, Merkelbach-Bruse S. Fassunke J, et al. Among authors: zeugner s. Virchows Arch. 2017 Oct;471(4):509-520. doi: 10.1007/s00428-017-2226-8. Epub 2017 Sep 8. Virchows Arch. 2017. PMID: 28884371 Clinical Trial.
14 results