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Gene|November 19, 2023
Frequency and functional characterization of fusion genes in squamous cell carcinoma of the lungChristina Alidousty, Arvid Becker, Elke Binot, et al.
Cancer Immunology, Immunotherapy : CII|January 22, 2020
Immune profile and immunosurveillance in treatment-naive and neoadjuvantly treated esophageal adenocarcinomaSvenja Wagener-Ryczek, Max Schoemmel, Max Kraemer, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer|July 20, 2023
KEAP1/NFE2L2 Pathway Signature Outperforms KEAP1/NFE2L2 Mutation Status and Reveals Alternative Pathway-Activating Mutations in NSCLCChristoph Arolt, Margaret Dugan, Robert Wild, et al.
NPJ Precision Oncology|November 11, 2024
Benchmark of screening markers for KEAP1/NFE2L2 mutations and joint analysis with the K1N2-scoreChristoph Arolt, Andreas H Scheel, Margaret Dugan, et al.
Lung Cancer (Amsterdam, Netherlands)|March 29, 2014
Sensitive and specific detection of EML4-ALK rearrangements in non-small cell lung cancer (NSCLC) specimens by multiplex amplicon RNA massive parallel sequencingEvgeny A Moskalev, Judith Frohnauer, Sabine Merkelbach-Bruse, et al.
Lung Cancer (Amsterdam, Netherlands)|September 30, 2025
Evaluating docetaxel effectiveness in KRAS G12C-mutated NSCLC: insights from a Real-World cohortMatthias Scheffler, Lia Tzala, Karly Louie, et al.
Human Pathology|August 22, 2008
KIT codon 558 insertions in gastrointestinal stromal tumors. Analysis of 17 rare KIT mutantsJerzy Lasota, Wojciech Kuban, Eva Wardelmann, et al.
Histopathology|September 18, 2020
Prevalence and potential biological role of TERT amplifications in ALK translocated adenocarcinoma of the lungChristina Alidousty, Nicolai Duerbaum, Svenja Wagener-Ryczek, et al.
Lung Cancer (Amsterdam, Netherlands)|June 16, 2019
Acquired KRAS mutation and loss of low-level MET amplification after durable response to crizotinib in a patient with lung adenocarcinomaRichard Riedel, Sebastian Michels, Carina Heydt, 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.
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