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GNAQ and GNA11 mutant nonuveal melanoma: a subtype distinct from both cutaneous and uveal melanoma

British journal of dermatology (1951), 2020-11, Vol.183 (5), p.928-939

2020

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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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Assessment of clinical parameters associated with mutational status in metastatic malignant melanoma: a single-centre investigation of 141 patients

British journal of dermatology (1951), 2013-04, Vol.168 (4), p.708-716

2013

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Differences in genetic alterations between primary lobular and ductal breast cancers detected by comparative genomic hybridization

The Journal of pathology, 2001-01, Vol.193 (1), p.40-47

2001

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Deletion of Trp‐557 and Lys‐558 in the juxtamembrane domain of the c‐kit protooncogene is associated with metastatic behavior of gastrointestinal stromal tumors

International journal of cancer, 2003-10, Vol.106 (6), p.887-895

2003

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Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining

The Journal of pathology, 2005-12, Vol.207 (4), p.385-395

2005

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HR23b expression is a potential predictive biomarker for HDAC inhibitor treatment in mesenchymal tumours and is associated with response to vorinostat

The journal of pathology. Clinical research, 2016-04, Vol.2 (2), p.59-71

2016

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Benign metastasizing leiomyoma: A cytogenetically balanced but clonal disease

Human pathology, 2000, Vol.31 (1), p.126-128

2000

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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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c-KIT codon 816 mutation in a recurrent and metastatic dysgerminoma of a 14-year-old girl: case study

Virchows Archiv : an international journal of pathology, 2004-12, Vol.445 (6), p.651-654

2004

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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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NOTCH, ASCL1, p53 and RB alterations define an alternative pathway driving neuroendocrine and small cell lung carcinomas

International journal of cancer, 2016-02, Vol.138 (4), p.927-938

2016

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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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Genetic instability and recurrent MYC amplification in ALK‐translocated NSCLC: a central role of TP53 mutations

The Journal of pathology, 2018-09, Vol.246 (1), p.67-76

2018

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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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Prevalence and potential biological role of TERT amplifications in ALK translocated adenocarcinoma of the lung

Histopathology, 2021-03, Vol.78 (4), p.578-585

2021

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Comparative proteomics reveals a diagnostic signature for pulmonary head‐and‐neck cancer metastasis

EMBO molecular medicine, 2018-09, Vol.10 (9), p.1-n/a

2018

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Detection of gene fusions using targeted next-generation sequencing: a comparative evaluation

BMC medical genomics, 2021-02, Vol.14 (1), p.62-14, Article 62

2021

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Clinicopathological and molecular features of a large cohort of gastrointestinal stromal tumors (GISTs) and review of the literature: BRAF mutations in KIT/PDGFRA wild-type GISTs are rare events

Human pathology, 2017-04, Vol.62, p.206-214

2017

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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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Immune profile and immunosurveillance in treatment-naive and neoadjuvantly treated esophageal adenocarcinoma

Cancer Immunology, Immunotherapy, 2020-04, Vol.69 (4), p.523-533

2020

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Comparison of the genomic background of MET-altered carcinomas of the lung: biological differences and analogies

Modern pathology, 2019-05, Vol.32 (5), p.627-638

2019

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Activating PDGFRA mutations in inflammatory fibroid polyps occur in exons 12, 14 and 18 and are associated with tumour localization

Histopathology, 2012-07, Vol.61 (1), p.59-68

2012

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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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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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GNAQ and GNA11 mutant nonuveal melanoma: a subtype distinct from both cutaneous and uveal melanoma

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

Assessment of clinical parameters associated with mutational status in metastatic malignant melanoma: a single-centre investigation of 141 patients

Differences in genetic alterations between primary lobular and ductal breast cancers detected by comparative genomic hybridization

Deletion of Trp‐557 and Lys‐558 in the juxtamembrane domain of the c‐kit protooncogene is associated with metastatic behavior of gastrointestinal stromal tumors

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining

HR23b expression is a potential predictive biomarker for HDAC inhibitor treatment in mesenchymal tumours and is associated with response to vorinostat

Benign metastasizing leiomyoma: A cytogenetically balanced but clonal disease

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

c-KIT codon 816 mutation in a recurrent and metastatic dysgerminoma of a 14-year-old girl: case study

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

NOTCH, ASCL1, p53 and RB alterations define an alternative pathway driving neuroendocrine and small cell lung carcinomas

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

Genetic instability and recurrent MYC amplification in ALK‐translocated NSCLC: a central role of TP53 mutations

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

Prevalence and potential biological role of TERT amplifications in ALK translocated adenocarcinoma of the lung

Comparative proteomics reveals a diagnostic signature for pulmonary head‐and‐neck cancer metastasis

Detection of gene fusions using targeted next-generation sequencing: a comparative evaluation

Clinicopathological and molecular features of a large cohort of gastrointestinal stromal tumors (GISTs) and review of the literature: BRAF mutations in KIT/PDGFRA wild-type GISTs are rare events

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

Immune profile and immunosurveillance in treatment-naive and neoadjuvantly treated esophageal adenocarcinoma

Comparison of the genomic background of MET-altered carcinomas of the lung: biological differences and analogies

Activating PDGFRA mutations in inflammatory fibroid polyps occur in exons 12, 14 and 18 and are associated with tumour localization

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

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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