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Therapy susceptible germline-related BRCA 1-mutation in a case of metastasized mixed adeno-neuroendocrine carcinoma (MANEC) of the small bowel

BMC gastroenterology, 2018-05, Vol.18 (1), p.75-75, Article 75

2018

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Nuclear hBD-1 accumulation in malignant salivary gland tumours

BMC cancer, 2008-10, Vol.8 (1), p.290-290, Article 290

2008

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3125 KEAP1-mutations and NFE2L2-mutations in patients with non-small cell lung cancer (NSCLC)

European journal of cancer (1990), 2015-09, Vol.51, p.S645-S645

2015

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3131 Clinical and molecular characteristics of non-small cell lung cancer in patients harboring CTNNB1 mutations

European journal of cancer (1990), 2015-09, Vol.51, p.S647-S647

2015

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3129 Clinical and genetic presentation of high-level cMET-amplified Non-small cell lung cancer (NSCLC) with adenocarcinoma histology

European journal of cancer (1990), 2015-09, Vol.51, p.S646-S646

2015

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3006 Broad implementation of next generation sequencing based lung cancer genotyping in clinical routine within a nationwide health care provider network in Germany

European journal of cancer (1990), 2015-09, Vol.51, p.S597-S597

2015

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605: Testing cancer related gene panels for high throughput parallel sequencing

European journal of cancer (1990), 2014-07, Vol.50, p.S145-S146

2014

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Improvement of the quality of BRAF testing in melanomas with nationwide external quality assessment, for the BRAF EQA group

BMC cancer, 2013-10, Vol.13 (1), p.472-472, Article 472

2013

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Current diagnostic methods of HER-2/neu detection in breast cancer with special regard to real-time PCR

The American journal of surgical pathology, 2003-12, Vol.27 (12), p.1565-1570

2003

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Associations between polymorphisms in the thymidylate synthase gene, the expression of thymidylate synthase mRNA and the microsatellite instability phenotype of colorectal cancer

Oncology reports, 2004-04, Vol.11 (4), p.839

2004

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Detection of HPV 52, 58 and 87 in cervicovaginal intraepithelial lesions of HIV infected women

International journal of molecular medicine, 2005-11, Vol.16 (5), p.815

2005

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A chymase gene variant is associated with atherosclerosis in venous coronary artery bypass grafts

Coronary artery disease, 2001-09, Vol.12 (6), p.493-497

2001

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Infectious agents in coronary lesions obtained by endatherectomy: pattern of distribution, coinfection, and clinical findings

Coronary artery disease, 2001-02, Vol.12 (1), p.1-6

2001

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High Throughput Genetic Screening for the Detection of Hereditary Nonpolyposis Colon Cancer (HNPCC) Using Capillary Electrophoresis

Combinatorial chemistry & high throughput screening, 2000-12, Vol.3 (6), p.519-524

2000

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High throughput genetic screening for the detection of hereditary non-polyposis colon cancer (HNPCC) using capillary electrophoresis

Combinatorial chemistry & high throughput screening, 2000-12, Vol.3 (6), p.519

2000

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Biomarkers for Homologous Recombination Deficiency in Cancer

Journal of personalized medicine, 2021-06, Vol.11 (7), p.612

2021

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Analysis of tumor mutational burden: correlation of five large gene panels with whole exome sequencing

Scientific reports, 2020-07, Vol.10 (1), p.11387-11387, Article 11387

2020

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Managing Difficulties of Microsatellite Instability Testing in Endometrial Cancer-Limitations and Advantages of Four Different PCR-Based Approaches

Cancers, 2021-03, Vol.13 (6), p.1268

2021

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β-Catenin (CTNNB1) mutations and clinicopathological features of mesenteric desmoid-type fibromatosis

Histopathology, 2013-01, Vol.62 (2), p.294-304

2013

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Mutational spectrum of acquired resistance to reversible versus irreversible EGFR tyrosine kinase inhibitors

BMC cancer, 2020-05, Vol.20 (1), p.408-408, Article 408

2020

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Deep learning for sensitive detection of Helicobacter Pylori in gastric biopsies

BMC gastroenterology, 2020-12, Vol.20 (1), p.417-417, Article 417

2020

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Expression of cell cycle regulators and frequency of TP53 mutations in high risk gastrointestinal stromal tumors prior to adjuvant imatinib treatment

PloS one, 2018-02, Vol.13 (2), p.e0193048-e0193048

2018

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Comparison of pre-analytical FFPE sample preparation methods and their impact on massively parallel sequencing in routine diagnostics

PloS one, 2014-08, Vol.9 (8), p.e104566-e104566

2014

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Mismatch Repair Deficiency and Somatic Mutations in Human Sinonasal Tumors

Cancers, 2021-12, Vol.13 (23), p.6081

2021

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Teenage-Onset Colorectal Cancers in a Digenic Cancer Predisposition Syndrome Provide Clues for the Interaction between Mismatch Repair and Polymerase δ Proofreading Deficiency in Tumorigenesis

Biomolecules (Basel, Switzerland), 2022-09, Vol.12 (10), p.1350

2022

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Therapy susceptible germline-related BRCA 1-mutation in a case of metastasized mixed adeno-neuroendocrine carcinoma (MANEC) of the small bowel

Nuclear hBD-1 accumulation in malignant salivary gland tumours

3125 KEAP1-mutations and NFE2L2-mutations in patients with non-small cell lung cancer (NSCLC)

3131 Clinical and molecular characteristics of non-small cell lung cancer in patients harboring CTNNB1 mutations

3129 Clinical and genetic presentation of high-level cMET-amplified Non-small cell lung cancer (NSCLC) with adenocarcinoma histology

3006 Broad implementation of next generation sequencing based lung cancer genotyping in clinical routine within a nationwide health care provider network in Germany

605: Testing cancer related gene panels for high throughput parallel sequencing

Improvement of the quality of BRAF testing in melanomas with nationwide external quality assessment, for the BRAF EQA group

Current diagnostic methods of HER-2/neu detection in breast cancer with special regard to real-time PCR

Associations between polymorphisms in the thymidylate synthase gene, the expression of thymidylate synthase mRNA and the microsatellite instability phenotype of colorectal cancer

Detection of HPV 52, 58 and 87 in cervicovaginal intraepithelial lesions of HIV infected women

A chymase gene variant is associated with atherosclerosis in venous coronary artery bypass grafts

Infectious agents in coronary lesions obtained by endatherectomy: pattern of distribution, coinfection, and clinical findings

High Throughput Genetic Screening for the Detection of Hereditary Nonpolyposis Colon Cancer (HNPCC) Using Capillary Electrophoresis

High throughput genetic screening for the detection of hereditary non-polyposis colon cancer (HNPCC) using capillary electrophoresis

Biomarkers for Homologous Recombination Deficiency in Cancer

Analysis of tumor mutational burden: correlation of five large gene panels with whole exome sequencing

Managing Difficulties of Microsatellite Instability Testing in Endometrial Cancer-Limitations and Advantages of Four Different PCR-Based Approaches

β-Catenin (CTNNB1) mutations and clinicopathological features of mesenteric desmoid-type fibromatosis

Mutational spectrum of acquired resistance to reversible versus irreversible EGFR tyrosine kinase inhibitors

Deep learning for sensitive detection of Helicobacter Pylori in gastric biopsies

Expression of cell cycle regulators and frequency of TP53 mutations in high risk gastrointestinal stromal tumors prior to adjuvant imatinib treatment

Comparison of pre-analytical FFPE sample preparation methods and their impact on massively parallel sequencing in routine diagnostics

Mismatch Repair Deficiency and Somatic Mutations in Human Sinonasal Tumors

Teenage-Onset Colorectal Cancers in a Digenic Cancer Predisposition Syndrome Provide Clues for the Interaction between Mismatch Repair and Polymerase δ Proofreading Deficiency in Tumorigenesis

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