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Pathologie (Heidelberg, Germany)|August 14, 2024
[Endometrial carcinoma: molecular classification in routine pathology]Udo Siebolts, Birgid Schömig-Markiefka, Janna Siemanowski-Hrach, et al.
Frontiers in Oncology|August 13, 2025
NGS coverage accurately predicts MET and HER2 (ERBB2) gene amplifications in a real-world non-small cell lung cancer cohortAdam Kowalewski, Janna Siemanowski-Hrach, Thomas Stehle, et al.
Human Pathology|September 14, 2025
GNAQ-/GNA14-mutated hepatic vascular malformation with capillary proliferation in adults and childrenAnne Kristin Fischer, Carina Heydt, Janna Siemanowski-Hrach, et al.
Pest Management Science|November 5, 2024
Superior target genes and pathways for RNAi-mediated pest control revealed by genome-wide analysis in the beetle Tribolium castaneumBenjamin Buer, Jürgen Dönitz, Martin Milner, et al.
The Journal of Molecular Diagnostics : JMD|June 5, 2026
Pitfalls in detecting MET exon 14 skipping variants by DNA- and RNA- based next generation sequencing technologies in a large real-world cohort and results of the first multinational EQA schemesCarina Heydt, Michaela Angelika Ihle, Katharina Ilm, et al.
JTO Clinical and Research Reports|March 12, 2026
MET-Driven Resistance to Sotorasib in KRAS G12C-Mutant NSCLC and Response to Combined KRAS and MET InhibitionRichard Riedel, Lea Ruge, Malte Verheyen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|June 10, 2026
Molecular and clinical characteristics of patients with non-small cell lung cancer (NSCLC) harboring KRAS Q61 mutations to assess therapeutic responsesLea Ruge, Felix John, Malte Verheyen, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 19, 2025
Molecular and clinical characteristics of patients with non-small cell lung cancer (NSCLC) harboring KRAS G12V mutationsFelix John, Lea Ruge, Malte Verheyen, et al.
European Journal of Cancer (Oxford, England : 1990)|September 18, 2024
Benchmarking whole exome sequencing in the German network for personalized medicineMichael Menzel, Mihaela Martis-Thiele, Hannah Goldschmid, et al.
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