Search Results - "Jansen, Erik A.M."
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Germline MBD4 deficiency causes a multi-tumor predisposition syndrome
Published in American journal of human genetics (05-05-2022)“…We report an autosomal recessive, multi-organ tumor predisposition syndrome, caused by bi-allelic loss-of-function germline variants in the base excision…”
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Clinical Validity of Tumor-Informed Circulating Tumor DNA Analysis in Patients Undergoing Surgery of Colorectal Metastases
Published in Diseases of the colon & rectum (12-07-2022)Get full text
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Evaluation of a Hybrid Capture–Based Pan-Cancer Panel for Analysis of Treatment Stratifying Oncogenic Aberrations and Processes
Published in The Journal of molecular diagnostics : JMD (01-06-2020)“…Stratification of patients for targeted and immune-based therapies requires extensive genomic profiling that enables sensitive detection of clinically relevant…”
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Monoallelic NTHL1 Loss-of-Function Variants and Risk of Polyposis and Colorectal Cancer
Published in Gastroenterology (New York, N.Y. 1943) (01-12-2020)Get full text
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Clinical Validity of Tumor-Informed Circulating Tumor DNA Analysis in Patients Undergoing Surgery of Colorectal Metastases
Published in Diseases of the colon & rectum (01-06-2023)“…Accurate biomarkers to monitor tumor load and response in metastatic colorectal cancer patients undergoing surgery could optimize treatment regimens. This…”
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Mutational signature analysis in non-small cell lung cancer patients with a high tumor mutational burden
Published in Respiratory research (24-11-2021)“…Lung cancer is the leading cause of cancer death worldwide. With the growing number of targeted therapies and the introduction of immuno-oncology (IO),…”
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Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material
Published in BMC cancer (07-04-2020)“…Sensitive and reliable molecular diagnostics is needed to guide therapeutic decisions for cancer patients. Although less material becomes available for…”
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Identification of Fusion Genes and Targets for Genetically Matched Therapies in a Large Cohort of Salivary Gland Cancer Patients
Published in Cancers (27-08-2022)“…Introduction: Salivary gland cancer (SGC) is a rare cancer for which systemic treatment options are limited. Therefore, it is important to characterize its…”
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Comprehensive clinicopathological and genomic profiling of gallbladder cancer reveals actionable targets in half of patients
Published in NPJ precision oncology (05-11-2022)“…Gallbladder cancer (GBC) is a rare, highly aggressive malignancy with a 5-year survival rate of 5–10% in advanced cases, highlighting the need for more…”
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Unraveling Neuroendocrine Gallbladder Cancer: Comprehensive Clinicopathologic and Molecular Characterization
Published in JCO precision oncology (2021)“…Neuroendocrine carcinomas and mixed neuroendocrine non-neuroendocrine neoplasms of the gallbladder (NE GBC) are rare and highly aggressive entities. The cell…”
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