R. Penzel

发表

FXYD3 is overexpressed in pancreatic ductal adenocarcinoma and influences pancreatic cancer cell growth

H. Friess, H. Kayed, J. Kleeff, 2006, International journal of cancer.

Precision oncology based on omics data: The NCT Heidelberg experience

C. von Kalle, S. Fröhling, R. Eils, 2017, International journal of cancer.

Dephosphorylation of cofilin is regulated through Ras and requires the combined activities of the Ras-effectors MEK and PI3K.

R. Penzel, G. Nebl, Y. Samstag, 2004, Cellular signalling.

Automated Universal BRAF State Detection within the Activation Segment in Skin Metastases by Pyrosequencing-Based Assay U-BRAFV600

A. Enk, P. Schirmacher, R. Penzel, 2013, PloS one.

SRC signaling is crucial in the growth of synovial sarcoma cells.

O. Larsson, P. Schirmacher, R. Penzel, 2013, Cancer research.

RNA-Based Detection of Gene Fusions in Formalin-Fixed and Paraffin-Embedded Solid Cancer Samples

P. Schirmacher, A. Stenzinger, D. Kazdal, 2019, Cancers.

Characterization and early embryonic expression of a neural specific transcription factor xSOX3 in Xenopus laevis.

R. Penzel, R. Oschwald, Y. Chen, 1997, The International journal of developmental biology.

Spatial and temporal heterogeneity of panel-based tumor mutational burden (TMB) in pulmonary adenocarcinoma: separating biology from technical artifacts.

S. Fröhling, M. Kriegsmann, A. Warth, 2019, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

KRAS/GNAS‐testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound‐guided workup of suspected mucinous neoplasms of the pancreas

P. Schirmacher, A. Stenzinger, D. Kazdal, 2021, Genes, chromosomes & cancer.

Oligoclonal T-cell populations in an inflammatory pseudotumor of the pancreas possibly related to autoimmune pancreatitis: an immunohistochemical and molecular analysis

H. Friess, R. Penzel, M. Büchler, 2004, Virchows Archiv.

Specific resistance upon lentiviral TRAIL transfer by intracellular retention of TRAIL receptors

R. Penzel, I. Herr, N. Gassler, 2006, Cell Death and Differentiation.

Risk stratification of EGFR+ lung cancer diagnosed with panel-based next-generation sequencing.

M. Kriegsmann, P. Schirmacher, A. Stenzinger, 2020, Lung cancer.

Comparison of molecular abnormalities in vulvar and vaginal melanomas

P. Schirmacher, R. Penzel, C. Gilks, 2014, Modern Pathology.

Mutational activation of the RAS‐RAF‐MAPK and the wnt pathway in small intestinal adenocarcinomas

R. Penzel, B. Helmchen, S. Aulmann, 2004, Scandinavian journal of gastroenterology.

Transitions Between Flat Epithelial Atypia and Low-grade Ductal Carcinoma In Situ of the Breast

P. Schirmacher, R. Penzel, S. Aulmann, 2012, The American journal of surgical pathology.

Genetics of adenocarcinomas of the small intestine: frequent deletions at chromosome 18q and mutations of the SMAD4 gene

R. Penzel, H. Otto, H. Bläker, 2002, Oncogene.

Subclonal evolution of pulmonary adenocarcinomas delineated by spatially distributed somatic mitochondrial mutations.

M. Kriegsmann, R. Longuespée, A. Warth, 2018, Lung cancer.

Histologic classification of thymic epithelial tumors: Comparison of established classification schemes

R. Penzel, A. Morresi‐Hauf, W. Hofmann, 2002, International journal of cancer.

Tubular, lactating, and ductal adenomas are devoid of MED12 Exon2 mutations, and ductal adenomas show recurrent mutations in GNAS and the PI3K–AKT pathway

W. Weichert, P. Schirmacher, A. Stenzinger, 2017, Genes, chromosomes & cancer.

Distribution of MED12 mutations in fibroadenomas and phyllodes tumors of the breast—implications for tumor biology and pathological diagnosis

M. Kriegsmann, W. Weichert, A. Stenzinger, 2015, Genes, chromosomes & cancer.

Recurrent deletions at 6q in early age of onset non‐HNPCC‐ and non‐FAP‐associated intestinal carcinomas. Evidence for a novel cancer susceptibility locus at 6q14‐q22

M. Kloor, P. Schirmacher, R. Penzel, 2008, Genes, chromosomes & cancer.

Synonymous EGFR variant p.Q787Q is neither prognostic nor predictive in patients with lung adenocarcinoma

A. Warth, P. Schirmacher, A. Stenzinger, 2017, Genes, chromosomes & cancer.

KRAS, EGFR, PDGFR-α, KIT and COX-2 status in carcinoma showing thymus-like elements (CASTLE)

P. Schirmacher, R. Penzel, A. Hartmann, 2014, Diagnostic Pathology.

Gains of chromosome region 3q26 in intraepithelial neoplasia and invasive squamous cell carcinoma of the vulva are frequent and independent of HPV status

P. Schirmacher, R. Penzel, S. Aulmann, 2008, Journal of Clinical Pathology.

IDH1 R132H mutation is a rare event in myeloproliferative neoplasms as determined by a mutation specific antibody

R. Penzel, H. Zentgraf, A. von Deimling, 2010, Haematologica.

Somatic mutations in familial adenomatous polyps. Nuclear translocation of beta-catenin requires more than biallelic APC inactivation.

R. Penzel, C. Sutter, H. Otto, 2003, American journal of clinical pathology.

Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers.

C. von Kalle, W. Weichert, P. Schirmacher, 2021, Cancer discovery.

Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity

S. Fröhling, E. Schröck, W. Weichert, 2022, Nature Communications.

Selective downregulation of retinoic acid‐inducible gene I within the intestinal epithelial compartment in crohn's disease

P. Schirmacher, R. Penzel, B. Funke, 2011, Inflammatory bowel diseases.

Comprehensive cancer predisposition testing within the prospective MASTER trial identifies hereditary cancer patients and supports treatment decisions for rare cancers.

C. von Kalle, S. Fröhling, E. Schröck, 2022, Annals of oncology : official journal of the European Society for Medical Oncology.

Non-small cell lung cancer, locally advanced

P. Lambin, S. Kozlov, I. Petersen, 2012 .

Intrauterine onset of acute neuropathic type 2 Gaucher disease: Identification of a novel insertion sequence

R. Penzel, J. Kopitz, U. Felderhoff‐Mueser, 2004, American journal of medical genetics. Part A.

Abnormal crosstalk between pancreatic acini and macrophages during the clearance of apoptotic cells in chronic pancreatitis

H. Friess, K. Ketterer, T. Giese, 2008, The Journal of pathology.

TERT promoter hotspot mutations are recurrent in myxoid liposarcomas but rare in other soft tissue sarcoma entities

P. Schirmacher, R. Penzel, E. Wardelmann, 2014, Journal of Experimental & Clinical Cancer Research.

Chromosomal imbalances in sporadic neuroendocrine tumours of the thymus.

H. Dienemann, P. Schirmacher, R. Penzel, 2005, Cancer letters.

Discovered on gastrointestinal stromal tumor 1 (DOG1) is expressed in pancreatic centroacinar cells and in solid-pseudopapillary neoplasms--novel evidence for a histogenetic relationship.

P. Schirmacher, R. Penzel, E. Herpel, 2011, Human pathology.

Invasive ductal breast cancer within a malignant phyllodes tumor: case report and assessment of clonality.

P. Schirmacher, R. Penzel, F. Marmé, 2010, Human pathology.

NUT carcinoma of the thorax: Case report and review of the literature.

A. Warth, H. Dienemann, W. Weichert, 2015, Lung cancer.

Elevated expression of c-kit in small venous malformations of blue rubber bleb nevus syndrome

P. Schirmacher, R. Penzel, A. Kulozik, 2010, Rare tumors.

NRG1 Fusions in KRAS Wild-Type Pancreatic Cancer.

David Bonekamp, Kortine Kleinheinz, Matthias Schlesner, 2018, Cancer discovery.

Genetic heterogeneity in synchronous colorectal cancers impacts genotyping approaches and therapeutic strategies

Nicole Pfarr, Volker Endris, Wilko Weichert, 2016, Genes, chromosomes & cancer.

Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases

Olaf Neumann, Michael Thomas, Ivo Buchhalter, 2019, International journal of cancer.

Detection of the ASPSCR1–TFE3 gene fusion in paraffin‐embedded alveolar soft part sarcomas

P. Schirmacher, R. Penzel, S. Aulmann, 2007, Histopathology.

Poly(ADP-ribose) polymerase inhibition reverses vascular dysfunction after γ-irradiation

R. Penzel, S. Hagl, I. Berger, 2006 .

Poly(ADP-ribose) polymerase inhibition reverses vascular dysfunction after gamma-irradiation.

R. Penzel, S. Hagl, I. Berger, 2006, International Journal of Radiation Oncology, Biology, Physics.

Stimulation of the calcium-sensing receptor stabilizes the podocyte cytoskeleton, improves cell survival, and reduces toxin-induced glomerulosclerosis.

R. Penzel, F. Schaefer, M. Gross, 2011, Kidney international.

β‐catenin accumulation and mutation of the CTNNB1 gene in hepatoblastoma

R. Penzel, W. Hofmann, H. Otto, 1999, Genes, chromosomes & cancer.

Comparative analysis of cell populations involved in the proliferative and inflammatory processes in diffuse and localised pigmented villonodular synovitis.

R. Penzel, H. Weckauf, B. Helmchen, 2004, Histology and histopathology.

Rheumatoid arthritis and pigmented villonodular synovitis: comparative analysis of cell polyploidy, cell cycle phases and expression of macrophage and fibroblast markers in proliferating synovial cells

R. Penzel, F. Autschbach, H. Weckauf, 2005, Histopathology.

Molecular characterisation of pancreatic ductal adenocarcinoma in patients under 40

H. Friess, P. Schirmacher, J. Kleeff, 2006, Journal of Clinical Pathology.

Follicle‐stimulating hormone receptor expression in soft tissue sarcomas

A. Warth, W. Weichert, P. Schirmacher, 2013, Histopathology.

Identification of a CTL4/Neu1 fusion transcript in a sialidosis patient

R. Penzel, H. Otto, J. Kopitz, 2002, FEBS letters.

Splice donor site mutation in the lysosomal neuraminidase gene causing exon skipping and complete loss of enzyme activity in a sialidosis patient

R. Penzel, H. Otto, J. Kopitz, 2001, FEBS letters.

Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine

S. Fröhling, P. Schirmacher, A. Stenzinger, 2021, Genes, chromosomes & cancer.

TERT promoter hotspot mutations are recurrent in myxoid liposarcomas but rare in other soft tissue sarcoma entities

P. Schirmacher, R. Penzel, E. Wardelmann, 2014, Journal of experimental & clinical cancer research : CR.

Integrative DNA methylation and gene expression analysis in high-grade soft tissue sarcomas

Roland Eils, Thomas Wolf, Volker Hovestadt, 2013, Genome Biology.

MicroRNA profiling of primary high‐grade soft tissue sarcomas

R. Eils, P. Schirmacher, R. Penzel, 2012, Genes, chromosomes & cancer.

Microcystic tubulopapillary carcinoma of the pancreas: a new tumor entity?

Frank Bergmann, Jörg D. Hoheisel, Roland Penzel, 2004, Virchows Archiv.

Targeted next‐generation sequencing enables reliable detection of HER2 (ERBB2) status in breast cancer and provides ancillary information of clinical relevance

Jan Budczies, Nicole Pfarr, Volker Endris, 2017, Genes, chromosomes & cancer.

EGFR, KRAS, BRAF and ALK gene alterations in lung adenocarcinomas: patient outcome, interplay with morphology and immunophenotype

A. Warth, H. Dienemann, W. Weichert, 2013, European Respiratory Journal.

Anti‐programmed cell death‐1 therapy in nonmelanoma skin cancer

R. Schneiderbauer, A. Enk, S. Fröhling, 2017, The British journal of dermatology.

Variant classification in precision oncology

Melanie Boerries, Olaf Neumann, Michael Thomas, 2019, International journal of cancer.

Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real‐life analysis of three larger gene panels

Olaf Neumann, Michael Thomas, Ivo Buchhalter, 2019, International journal of cancer.

Size matters: Dissecting key parameters for panel‐based tumor mutational burden analysis

Olaf Neumann, Michael Thomas, Ivo Buchhalter, 2018, International journal of cancer.

Implementing tumor mutational burden (TMB) analysis in routine diagnostics-a primer for molecular pathologists and clinicians.

Olaf Neumann, Michael Thomas, Jan Budczies, 2018, Translational lung cancer research.

Genetic profiling of melanoma in routine diagnostics: assay performance and molecular characteristics in a consecutive series of 274 cases.

A. Enk, S. Fröhling, P. Schirmacher, 2018, Pathology.

PD-L1 (CD274) copy number gain, expression, and immune cell infiltration as candidate predictors for response to immune checkpoint inhibitors in soft-tissue sarcoma

S. Fröhling, P. Schirmacher, A. Stenzinger, 2017, Oncoimmunology.

Erlotinib and bevacizumab versus cisplatin, gemcitabine and bevacizumab in unselected nonsquamous nonsmall cell lung cancer

N. Reinmuth, A. Reuss, R. Penzel, 2015, European Respiratory Journal.

Colorectal mixed adenoneuroendocrine carcinomas and neuroendocrine carcinomas are genetically closely related to colorectal adenocarcinomas

M. Kloor, W. Weichert, A. Stenzinger, 2017, Modern Pathology.

Genotyping of colorectal cancer for cancer precision medicine: Results from the IPH Center for Molecular Pathology

M. Kloor, W. Weichert, P. Schirmacher, 2016, Genes, chromosomes & cancer.

Expression and mutation analysis of EGFR, c-KIT, and β-catenin in pulmonary blastoma

H. Dienemann, P. Schirmacher, R. Penzel, 2011, Journal of Clinical Pathology.

Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

C. von Kalle, S. Fröhling, R. Eils, 2019, Nature Communications.

Mutations in POLE and survival of colorectal cancer patients – link to disease stage and treatment

M. Kloor, H. Brenner, J. Chang-Claude, 2014, Cancer medicine.

Copy number changes of clinically actionable genes in melanoma, non‐small cell lung cancer and colorectal cancer—A survey across 822 routine diagnostic cases

Daniel Heim, Nicole Pfarr, Volker Endris, 2016, Genes, chromosomes & cancer.

Targeting rare and non-canonical driver variants in NSCLC - An uncharted clinical field.

S. Fröhling, M. Kriegsmann, P. Schirmacher, 2021, Lung cancer.

Analysis of the proliferative activity in lung adenocarcinomas with specific driver mutations.

M. Kriegsmann, R. Longuespée, A. Warth, 2018, Pathology, research and practice.

MET expression and copy number status in clear-cell renal cell carcinoma: prognostic value and potential predictive marker

P. Schirmacher, R. Penzel, V. Endris, 2016, Oncotarget.

Next-generation sequencing facilitates detection of the classic E13-A20 EML4-ALK fusion in an ALK-FISH/IHC inconclusive biopsy of a stage IV lung cancer patient: a case report

A. Warth, P. Schirmacher, A. Stenzinger, 2016, Diagnostic Pathology.

Response to olaparib in a PALB2 germline mutated prostate cancer and genetic events associated with resistance

S. Fröhling, R. Eils, E. Schröck, 2019, Cold Spring Harbor molecular case studies.

Down‐regulation of tumor suppressor a kinase anchor protein 12 in human hepatocarcinogenesis by epigenetic mechanisms

C. Plass, A. Warth, P. Schirmacher, 2010, Hepatology.

Glypican-1 antisense transfection modulates TGF-beta-dependent signaling in Colo-357 pancreatic cancer cells.

H. Friess, H. Kayed, J. Kleeff, 2004, Biochemical and biophysical research communications.

Optimized algorithm for Sanger sequencing-based EGFR mutation analyses in NSCLC biopsies

A. Warth, P. Schirmacher, M. Dietel, 2012, Virchows Archiv.

EGFR mutation detection in NSCLC—assessment of diagnostic application and recommendations of the German Panel for Mutation Testing in NSCLC

I. Petersen, P. Schirmacher, M. Dietel, 2010, Virchows Archiv.

Adrenomedullin is induced by hypoxia and enhances pancreatic cancer cell invasion

H. Friess, H. Kayed, J. Kleeff, 2007, International journal of cancer.

Heat Shock Protein 90-Sheltered Overexpression of Insulin-Like Growth Factor 1 Receptor Contributes to Malignancy of Thymic Epithelial Tumors

G. Giaccone, H. Dienemann, P. Schirmacher, 2011, Clinical Cancer Research.

Gastrointestinal stromal tumours and their response to treatment with the tyrosine kinase inhibitor imatinib

T. Lehnert, R. Penzel, M. Libicher, 2004, Virchows Archiv.

EGFR T790M mutation testing of non-small cell lung cancer tissue and blood samples artificially spiked with circulating cell-free tumor DNA: results of a round robin trial

P. Schirmacher, A. Stenzinger, M. Dietel, 2017, Virchows Archiv.

Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma

C. von Kalle, S. Fröhling, R. Eils, 2016, Annals of oncology : official journal of the European Society for Medical Oncology.

Phosphatidylinositol‐3′‐kinase/AKT signaling is essential in synovial sarcoma

O. Larsson, P. Schirmacher, R. Penzel, 2011, International journal of cancer.

Clonality of lobular carcinoma in situ (LCIS) and metachronous invasive breast cancer

P. Schirmacher, R. Penzel, B. Funke, 2008, Breast Cancer Research and Treatment.

Visceral leishmaniasis in a patient with relapsed multiple myeloma receiving high-dose melphalan and autologous stem cell transplant

H. Goldschmidt, R. Penzel, T. Luft, 2014, Leukemia & lymphoma.

SS18-SSX fusion protein-induced Wnt/β-catenin signaling is a therapeutic target in synovial sarcoma

O. Larsson, P. Schirmacher, R. Penzel, 2014, Oncogene.

Moesin-dependent cytoskeleton remodelling is associated with an anaplastic phenotype of pancreatic cancer

H. Friess, J. Kleeff, K. Felix, 2009, Journal of cellular and molecular medicine.

Mutational profiles of Brenner tumors show distinctive features uncoupling urothelial carcinomas and ovarian carcinoma with transitional cell histology

W. Weichert, P. Schirmacher, A. Stenzinger, 2017, Genes, chromosomes & cancer.

Molecular diagnostic profiling of lung cancer specimens with a semiconductor-based massive parallel sequencing approach: feasibility, costs, and performance compared with conventional sequencing.

Volker Endris, Wilko Weichert, Arne Warth, 2013, The Journal of molecular diagnostics : JMD.

Genome-wide analysis of pediatric-type follicular lymphoma reveals low genetic complexity and recurrent alterations of TNFRSF14 gene.

J. D. van der Walt, A. Rosenwald, E. Campo, 2016, Blood.

Anaplastic lymphoma kinase (ALK) gene rearrangement in non-small cell lung cancer (NSCLC): results of a multi-centre ALK-testing.

I. Petersen, A. Warth, P. Schirmacher, 2013, Lung cancer.

A Novel EML4-ALK Variant: Exon 6 of EML4 Fused to Exon 19 of ALK

A. Warth, P. Schirmacher, R. Penzel, 2012, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Pitfalls in mutational testing and reporting of common KIT and PDGFRA mutations in gastrointestinal stromal tumors

R. Penzel, E. Wardelmann, R. Simon, 2010, BMC Medical Genetics.

Targeting the BRAF V600E mutation in multiple myeloma.

H. Goldschmidt, P. Schirmacher, R. Penzel, 2013, Cancer discovery.

Decentral gene expression analysis for ER+/Her2− breast cancer: results of a proficiency testing program for the EndoPredict assay

H. Höfler, P. Schirmacher, C. Denkert, 2012, Virchows Archiv.

Identification of a highly lethal V3+TP53+ subset in ALK+ lung adenocarcinoma

P. Schirmacher, A. Stenzinger, R. Penzel, 2018, International journal of cancer.

Utility of different massive parallel sequencing platforms for mutation profiling in clinical samples and identification of pitfalls using FFPE tissue

R. Penzel, V. Endris, F. Haller, 2015, International journal of molecular medicine.

[Molecular diagnostics of non-small cell lung cancer: New markers and technologies].

M. Kriegsmann, A. Warth, W. Weichert, 2015, Der Pathologe.

Molecular signaling in multiple myeloma: association of RAS/RAF mutations and MEK/ERK pathway activation

H. Goldschmidt, P. Schirmacher, R. Penzel, 2017, Oncogenesis.

CT characteristics in pulmonary adenocarcinoma with epidermal growth factor receptor mutation

H. Kauczor, A. Warth, N. Reinmuth, 2017, PloS one.

The gefitinib long-term responder (LTR)--a cancer stem-like cell story? Insights from molecular analyses of German long-term responders treated in the IRESSA expanded access program (EAP).

R. Penzel, Michael Thomas, P. Schnabel, 2012, Lung cancer.

Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal α-N-acetyl-neuraminidase (sialidase) gene

R. Penzel, H. Otto, C. Sergi, 2001, Human Genetics.

Unmasked: when a clinically malignant disease turns out infectious. A rare case of tularemia.

W. Weichert, A. Stenzinger, R. Penzel, 2013, International journal of surgical pathology.

Tenascin C and annexin II expression in the process of pancreatic carcinogenesis

H. Friess, P. Schirmacher, H. Kayed, 2006, The Journal of pathology.

Prognostic Value of Tumor Necrosis Factor–Related Apoptosis-Inducing Ligand (TRAIL) and TRAIL Receptors in Renal Cell Cancer

P. Schirmacher, R. Penzel, B. Teh, 2009, Clinical Cancer Research.

Correlation of glypican-1 expression with TGF-beta, BMP, and activin receptors in pancreatic ductal adenocarcinoma.

H. Friess, H. Kayed, J. Kleeff, 2006, International journal of oncology.

Microsatellite instability in pulmonary adenocarcinomas: a comprehensive study of 480 cases

M. Kloor, A. Warth, H. Dienemann, 2016, Virchows Archiv.

Molecular heterogeneity of TFE3 activation in renal cell carcinomas

P. Schirmacher, R. Penzel, S. Aulmann, 2012, Modern Pathology.

Gastrointestinale Stromatumoren

T. Lehnert, R. Penzel, S. Joos, 2003, Der Pathologe.

Gastrointestinale Stromatumoren

T. Lehnert, R. Penzel, S. Joos, 2003 .

EML4‐ALK fusion variant V3 is a high‐risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK+ non‐small cell lung cancer

A. Warth, P. Schirmacher, A. Stenzinger, 2018, International journal of cancer.

High‐throughput diagnostic profiling of clinically actionable gene fusions in lung cancer

A. Warth, H. Dienemann, W. Weichert, 2016, Genes, chromosomes & cancer.

A current perspective on the pathological assessment of FOXL2 in adult‐type granulosa cell tumours of the ovary

P. Schirmacher, R. Penzel, D. Huntsman, 2014, Histopathology.

CTCF Gene Mutations in Invasive Ductal Breast Cancer

R. Penzel, S. Aulmann, H. Otto, 2003, Breast Cancer Research and Treatment.

Semiconductor-based sequencing of formalin-fixed, paraffin-embedded colorectal cancer samples.

W. Weichert, R. Penzel, V. Endris, 2015, The oncologist.

NGS-based BRCA1/2 mutation testing of high-grade serous ovarian cancer tissue: results and conclusions of the first international round robin trial

Michael Hummel, Ulrich Lehmann, Nicole Pfarr, 2016, Virchows Archiv.

Multicenter Immunohistochemical ALK-Testing of Non–Small-Cell Lung Cancer Shows High Concordance after Harmonization of Techniques and Interpretation Criteria

H. Höfler, D. Aust, A. Warth, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Application of a BRAF V600E Mutation-specific Antibody for the Diagnosis of Hairy Cell Leukemia

W. Weichert, R. Penzel, A. von Deimling, 2012, The American journal of surgical pathology.

A primary malignant ependymoma of the abdominal cavity: a case report and review of the literature

P. Schirmacher, R. Penzel, L. Grenacher, 2009, Virchows Archiv.

Screening for Helicobacter pylori in Idiopathic Pulmonary Fibrosis Lung Biopsies

A. Warth, R. Penzel, K. Rabe, 2015, Respiration.

Structure and content of the EU-IVDR

W. Weichert, D. Kazdal, R. Penzel, 2023, Pathologie.

Mutations in genes encoding PI3K‐AKT and MAPK signaling define anogenital papillary hidradenoma

A. Warth, W. Weichert, A. Stenzinger, 2016, Genes, chromosomes & cancer.

Reduction of CD44(+)/CD24(-) breast cancer cells by conventional cytotoxic chemotherapy.

P. Schirmacher, R. Penzel, S. Aulmann, 2010, Human pathology.

Temporary changes of the AP-1 transcription factor binding activity in the gerbil hippocampus after transient global ischemia, and ischemic tolerance induction 1 1 Published on the World Wide Web on 22 June 2000.

C. Sommer, R. Penzel, M. Kiessling, 2000, Brain Research.

[Pleomorphic high-grade soft tissue sarcomas: is the subclassification up to date?].

P. Schirmacher, R. Penzel, G. Mechtersheimer, 2011, Der Pathologe.

Status quo of ALK testing in lung cancer: results of an EQA scheme based on in-situ hybridization, immunohistochemistry, and RNA/DNA sequencing

D. Aust, P. Schirmacher, A. Stenzinger, 2021, Virchows Archiv.

ALK-FISH borderline cases in non-small cell lung cancer: Implications for diagnostics and clinical decision making.

A. Warth, W. Weichert, P. Schirmacher, 2015, Lung cancer.

Validating Comprehensive Next-Generation Sequencing Results for Precision Oncology: The NCT/DKTK Molecularly Aided Stratification for Tumor Eradication Research Experience.

Melanie Boerries, Mario Lamping, Damian T. Rieke, 2018, JCO precision oncology.

Invasive Tubular Carcinoma of the Breast Frequently is Clonally Related to Flat Epithelial Atypia and Low-grade Ductal Carcinoma In Situ

P. Schirmacher, R. Penzel, S. Aulmann, 2009, The American journal of surgical pathology.

Mutant KIT as imatinib-sensitive target in metastatic sinonasal carcinoma.

C. von Kalle, S. Fröhling, R. Eils, 2017 .

Recurrent herpes simplex virus hepatitis after liver retransplantation despite acyclovir therapy

P. Schirmacher, R. Penzel, J. Encke, 2005, Liver transplantation : official publication of the American Association for the Study of Liver Diseases and the International Liver Transplantation Society.

The HMGB1 protein induces a metabolic type of tumour cell death by blocking aerobic respiration

Jonathan C. Fuller, H. Brenner, J. Chang-Claude, 2016, Nature Communications.

The immune microenvironment in EGFR- and ERBB2-mutated lung adenocarcinoma

S. Fröhling, M. Kriegsmann, P. Schirmacher, 2021, ESMO open.

Next generation sequencing of the cellular and liquid fraction of pancreatic cyst fluid supports discrimination of IPMN from pseudocysts and reveals cases with multiple mutated driver clones: First findings from the prospective ZYSTEUS biomarker study

P. Schirmacher, A. Stenzinger, R. Penzel, 2018, Genes, chromosomes & cancer.

The location of KIT and PDGFRA gene mutations in gastrointestinal stromal tumours is site and phenotype associated

R. Penzel, S. Aulmann, R. Rieker, 2005, Journal of Clinical Pathology.

Clusters of chromosomal imbalances in thymic epithelial tumours are associated with the WHO classification and the staging system according to Masaoka

R. Penzel, A. Morresi‐Hauf, S. Aulmann, 2003, International journal of cancer.

Regulation of enterocyte apoptosis by acyl-CoA synthetase 5 splicing.

P. Schirmacher, R. Penzel, H. Zentgraf, 2007, Gastroenterology.

Coordinated expression of stathmin family members by far upstream sequence element-binding protein-1 increases motility in non-small cell lung cancer.

Arne Warth, Kai Breuhahn, Peter Schirmacher, 2009, Cancer research.

Clonality of multifocal nonsmall cell lung cancer: implications for staging and therapy

A. Warth, P. Schirmacher, R. Penzel, 2011, European Respiratory Journal.

Oncogenetic tree models based on cytogenetic data: new insights into the development of epithelial tumors of the thymus.

Roland Penzel, Herwart F Otto, Gunhild Mechtersheimer, 2005, Cancer genetics and cytogenetics.

FAM96A is a novel pro‐apoptotic tumor suppressor in gastrointestinal stromal tumors

R. Penzel, K. Zatloukal, V. Dötsch, 2015, International journal of cancer.

Targeted molecular profiling reveals genetic heterogeneity of poromas and porocarcinomas.

P. Schirmacher, A. Stenzinger, R. Penzel, 2017, Pathology.

ROS1 expression and translocations in non‐small‐cell lung cancer: clinicopathological analysis of 1478 cases

A. Warth, H. Dienemann, W. Weichert, 2014, Histopathology.

Prevalence of somatic mitochondrial mutations and spatial distribution of mitochondria in non-small cell lung cancer

M. Kriegsmann, A. Warth, W. Weichert, 2017, British Journal of Cancer.

Targeted deep sequencing of effusion cytology samples is feasible, informs spatiotemporal tumor evolution, and has clinical and diagnostic utility

M. Kriegsmann, A. Warth, P. Schirmacher, 2018, Genes, chromosomes & cancer.

[Lobular carcinoma in situ (LCIS): risk factor and precursor of invasive lobular breast cancer].

P. Schirmacher, R. Penzel, S. Aulmann, 2007, Verhandlungen der Deutschen Gesellschaft fur Pathologie.

[Molecular pathology of sarcomas. Update on the research group "Molecular Diagnosis of Sarcomas"].

A. Marx, P. Schirmacher, R. Penzel, 2010, Der Pathologe.

Impaired expression of acyl‐CoA synthetase 5 in sporadic colorectal adenocarcinomas

P. Schirmacher, R. Penzel, I. Herr, 2005, The Journal of pathology.

Differential diagnosis of non-epithelial tumors of the pancreas: malignant non-epithelial pancreatic tumor with focal pigmentation

R. Penzel, M. Büchler, I. Esposito, 2004, Virchows Archiv.

Multicenter ALK Testing in Non–Small-Cell Lung Cancer: Results of a Round Robin Test

A. Warth, P. Schirmacher, M. Dietel, 2014, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

[Clonal association of flat epithelial atypia and tubular breast cancer].

P. Schirmacher, R. Penzel, S. Aulmann, 2008, Der Pathologe.

Loss of SMAD4 function in small intestinal adenocarcinomas: comparison of genetic and immunohistochemical findings.

R. Penzel, B. Helmchen, S. Aulmann, 2004, Pathology, research and practice.

Genetic changes of non-small cell lung cancer under neoadjuvant therapy

Nicole Pfarr, Volker Endris, Wilko Weichert, 2016, Oncotarget.

KRAS-mutation positive, metastatic tonsil carcinoma with cancer stem-like cell features and long-term response to gefitinib: a case report and review of the literature.

R. Penzel, Michael Thomas, P. Schnabel, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Defective homologous recombination DNA repair as therapeutic target in advanced chordoma

Roland Eils, David Bonekamp, Kortine Kleinheinz, 2019, Nature Communications.

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Genome-wide analysis of pediatric-type follicular lymphoma reveals low genetic complexity and recurrent alterations of TNFRSF14 gene.

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LYMPHOID NEOPLASIA Genome-wide analysis of pediatric-type follicular lymphoma reveals low genetic complexity and recurrent alterations of TNFRSF14 gene