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Author Details
Full Name
Daniel Kazdal
Affiliation
Institut fur Pathologie, Universitatsklinikum Heidelberg
ORCID
Career Start Year
2016
Papers
73
H Index
22
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36635225
First proficiency testing for NGS-based and combined NGS- and FISH-based detection of FGFR2 fusions in intrahepatic cholangiocarcinoma.
J Pathol Clin Res
2023
37758351
Response to "NGS, the New Global Standard?"
J Thorac Oncol
2023
37713929
Real-world EGFR testing practices for non-small-cell lung cancer by thoracic pathology laboratories across Europe.
ESMO Open
2023
37586177
Analysis of rare fusions in NSCLC: Genomic architecture and clinical implications.
Lung Cancer
2023
37292089
Is iron deficiency caused by <i>BMPR2</i> mutations or dysfunction in pulmonary arterial hypertension patients?
Pulm Circ
2023
37059713
Homogenous TP53mut-associated tumor biology across mutation and cancer types revealed by transcriptome analysis.
Cell Death Discov
2023
37141769
Spatial profiling of the microenvironment reveals low intratumoral heterogeneity and STK11-associated immune evasion in therapy-naïve lung adenocarcinomas.
Lung Cancer
2023
37327584
Accurate tumor purity determination is critical for the analysis of homologous recombination deficiency (HRD).
Transl Oncol
2023
36852573
Real-world data for precision cancer medicine-A European perspective.
Genes Chromosomes Cancer
2023
36738930
Distribution and Detectability of EGFR Exon 20 Insertion Variants in NSCLC.
J Thorac Oncol
2023
34331337
Assigning evidence to actionability: An introduction to variant interpretation in precision cancer medicine.
Genes Chromosomes Cancer
2022
35384413
Homologous recombination deficiency is inversely correlated with microsatellite instability and identifies immunologically cold tumors in most cancer types.
J Pathol Clin Res
2022
35598358
The impact of TP53 co-mutations and immunologic microenvironment on outcome of lung cancer with EGFR exon 20 insertions.
Eur J Cancer
2022
35681079
Pan-cancer analysis of genomic scar patterns caused by homologous repair deficiency (HRD).
NPJ Precis Oncol
2022
35871236
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing.
Br J Cancer
2022
36207130
Lorlatinib and compound mutations in ALK+ large-cell neuroendocrine lung carcinoma: a case report.
Cold Spring Harb Mol Case Stud
2022
35986087
Precision oncology for intrahepatic cholangiocarcinoma in clinical practice.
Br J Cancer
2022
36387148
Serum cytokines predict efficacy and toxicity, but are not useful for disease monitoring in lung cancer treated with PD-(L)1 inhibitors.
Front Oncol
2022
33631297
Artificial intelligence and pathology: From principles to practice and future applications in histomorphology and molecular profiling.
Semin Cancer Biol
2022
34907344
p53 partial loss-of-function mutations sensitize to chemotherapy.
Oncogene
2022
34997651
Fusion-positive non-small cell lung carcinoma: Biological principles, clinical practice, and diagnostic implications.
Genes Chromosomes Cancer
2022
35058282
Histological and molecular plasticity of ALK-positive non-small-cell lung cancer under targeted therapy: a case report.
Cold Spring Harb Mol Case Stud
2022
34125345
Deciphering the immunosuppressive tumor microenvironment in ALK- and EGFR-positive lung adenocarcinoma.
Cancer Immunol Immunother
2022
34164264
Earlier extracranial progression and shorter survival in ALK-rearranged lung cancer with positive liquid rebiopsies.
Transl Lung Cancer Res
2021
33686791
KRAS/GNAS-testing by highly sensitive deep targeted next generation sequencing improves the endoscopic ultrasound-guided workup of suspected mucinous neoplasms of the pancreas.
Genes Chromosomes Cancer
2021
33520406
A gene expression signature associated with B cells predicts benefit from immune checkpoint blockade in lung adenocarcinoma.
Oncoimmunology
2021
33898315
<i>De Novo</i> Versus Secondary Metastatic <i>EGFR</i>-Mutated Non-Small-Cell Lung Cancer.
Front Oncol
2021
33508231
Strength in numbers: predicting response to checkpoint inhibitors from large clinical datasets.
Cell
2021
33667718
Targeting rare and non-canonical driver variants in NSCLC - An uncharted clinical field.
Lung Cancer
2021
34408792
Real-world implementation of sequential targeted therapies for EGFR-mutated lung cancer.
Ther Adv Med Oncol
2021
34487971
The immune microenvironment in EGFR- and ERBB2-mutated lung adenocarcinoma.
ESMO Open
2021
34536122
GOPC:ROS1 and other ROS1 fusions represent a rare but recurrent drug target in a variety of glioma types.
Acta Neuropathol
2021
33938987
[Variant interpretation in molecular pathology and oncology : An introduction].
Pathologe
2021
34012783
Conventional and semi-automatic histopathological analysis of tumor cell content for multigene sequencing of lung adenocarcinoma.
Transl Lung Cancer Res
2021
33959513
Feasibility and Challenges for Sequential Treatments in ALK-Rearranged Non-Small-Cell Lung Cancer.
Front Oncol
2021
34090172
Effect of timing, technique and molecular features on brain control with local therapies in oncogene-driven lung cancer.
ESMO Open
2021
33976623
Combination of Crizotinib and Osimertinib in T790M+ EGFR-Mutant Non-Small Cell Lung Cancer with Emerging MET Amplification Post-Osimertinib Progression in a 10-Year Survivor: A Case Report.
Case Rep Oncol
2021
34307143
Comprehensive Dissection of Treatment Patterns and Outcome for Patients With Metastatic Large-Cell Neuroendocrine Lung Carcinoma.
Front Oncol
2021
30358615
Insulinoma-associated Protein 1 (INSM1) in Thoracic Tumors is Less Sensitive but More Specific Compared With Synaptophysin, Chromogranin A, and CD56.
Appl Immunohistochem Mol Morphol
2020
31970771
Integrated clinicomolecular characterization identifies RAS activation and CDKN2A deletion as independent adverse prognostic factors in cancer of unknown primary.
Int J Cancer
2020
31652375
Testing NTRK testing: Wet-lab and in silico comparison of RNA-based targeted sequencing assays.
Genes Chromosomes Cancer
2020
32003543
Microproteomics and Immunohistochemistry Reveal Differences in Aldo-Keto Reductase Family 1 Member C3 in Tissue Specimens of Ulcerative Colitis and Crohn's Disease.
Proteomics Clin Appl
2020
33087321
YAP Orchestrates Heterotypic Endothelial Cell Communication via HGF/c-MET Signaling in Liver Tumorigenesis.
Cancer Res
2020
33161228
Longitudinal therapy monitoring of ALK-positive lung cancer by combined copy number and targeted mutation profiling of cell-free DNA.
EBioMedicine
2020
32119917
Harmonization and Standardization of Panel-Based Tumor Mutational Burden Measurement: Real-World Results and Recommendations of the Quality in Pathology Study.
J Thorac Oncol
2020
32212351
Immuno-oncology gene expression profiling of formalin-fixed and paraffin-embedded clear cell renal cell carcinoma: Performance comparison of the NanoString nCounter technology with targeted RNA sequencing.
Genes Chromosomes Cancer
2020
32143116
Quantifying potential confounders of panel-based tumor mutational burden (TMB) measurement.
Lung Cancer
2020
32319699
NTRK testing: First results of the QuiP-EQA scheme and a comprehensive map of NTRK fusion variants and their diagnostic coverage by targeted RNA-based NGS assays.
Genes Chromosomes Cancer
2020
32129943
Automated sample preparation with SP3 for low-input clinical proteomics.
Mol Syst Biol
2020
31601699
Patients Resistant Against PSMA-Targeting α-Radiation Therapy Often Harbor Mutations in DNA Damage-Repair-Associated Genes.
J Nucl Med
2020
1 - 50 of 73
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Institute of Pathology, University Hospital Heidelberg
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Co-authored papers
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Olaf Neumann
Institute of Pathology, University Hospital Heidelberg
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Stefan Fr??hling
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Holger S??ltmann
German Cancer Research Center (DKFZ)
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Markus Ball
Institute of Pathology, Heidelberg University Hospital
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Huriye Seker-Cin
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Peter Horak
German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT)
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Frederick Klauschen
Institute of Pathology, Ludwig-Maximilians-Universitat Munchen
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Susanne Beck
Vrije Universiteit Brussel (VUB)
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Thomas Longerich
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Hannah Goldschmid
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