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Author Details
Full Name
Sebastian Uhrig
Affiliation
National Center for Tumor Diseases (NCT), German Cancer Research Center (DKFZ)
ORCID
Career Start Year
2016
Papers
39
H Index
16
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36789265
aRgus: Multilevel visualization of non-synonymous single nucleotide variants & advanced pathogenicity score modeling for genetic vulnerability assessment.
Comput Struct Biotechnol J
2023
37884744
NCT/DKFZ MASTER handbook of interpreting whole-genome, transcriptome, and methylome data for precision oncology.
NPJ Precis Oncol
2023
37734378
Signaling-induced systematic repression of miRNAs uncovers cancer vulnerabilities and targeted therapy sensitivity.
Cell Rep Med
2023
37532709
Proteogenomic analysis reveals RNA as a source for tumor-agnostic neoantigen identification.
Nat Commun
2023
35045690
Comprehensive genomic analysis of refractory multiple myeloma reveals a complex mutational landscape associated with drug resistance and novel therapeutic vulnerabilities.
Haematologica
2022
35668118
MCL1 as putative target in pancreatoblastoma.
Virchows Arch
2022
35366909
Correction to: Deconvolution of sarcoma methylomes reveals varying degrees of immune cell infiltrates with association to genomic aberrations.
J Transl Med
2022
35871236
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing.
Br J Cancer
2022
35983950
Bcl-x<sub>L</sub> as prognostic marker and potential therapeutic target in cholangiocarcinoma.
Liver Int
2022
35918329
Comprehensive genomic and epigenomic analysis in cancer of unknown primary guides molecularly-informed therapies despite heterogeneity.
Nat Commun
2022
36252999
IgE type multiple myeloma exhibits hypermutated phenotype and tumor reactive T cells.
J Immunother Cancer
2022
32949162
Integrating proteomics into precision oncology.
Int J Cancer
2021
34785797
Publisher Correction: Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia.
Leukemia
2021
34808524
Rationale and design of the CRAFT (Continuous ReAssessment with Flexible ExTension in Rare Malignancies) multicenter phase II trial.
ESMO Open
2021
34250401
Response to Cabozantinib Following Acquired Entrectinib Resistance in a Patient With <i>ETV6-NTRK3</i> Fusion-Positive Carcinoma Harboring the <i>NTRK3</i> <sup>G623R</sup> Solvent-Front Mutation.
JCO Precis Oncol
2021
34146471
A community challenge to evaluate RNA-seq, fusion detection, and isoform quantification methods for cancer discovery.
Cell Syst
2021
33980253
Deconvolution of sarcoma methylomes reveals varying degrees of immune cell infiltrates with association to genomic aberrations.
J Transl Med
2021
34112699
Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers.
Cancer Discov
2021
33441414
Accurate and efficient detection of gene fusions from RNA sequencing data.
Genome Res
2021
31558800
Identification and characterization of a BRAF fusion oncoprotein with retained autoinhibitory domains.
Oncogene
2020
33442346
Prolonged Survival of a Patient with Advanced-Stage Combined Hepatocellular-Cholangiocarcinoma.
Case Rep Gastroenterol
2020
32913197
MCL-1 gains occur with high frequency in lung adenocarcinoma and can be targeted therapeutically.
Nat Commun
2020
32843432
Successful BRAF/MEK inhibition in a patient with <i>BRAF</i><sup>V600E</sup>-mutated extrapancreatic acinar cell carcinoma.
Cold Spring Harb Mol Case Stud
2020
32476062
An optimized workflow to improve reliability of detection of KIAA1549:BRAF fusions from RNA sequencing data.
Acta Neuropathol
2020
32501622
Germline SDHB-inactivating mutation in gastric spindle cell sarcoma.
Genes Chromosomes Cancer
2020
32385320
The landscape of chromothripsis across adult cancer types.
Nat Commun
2020
32127638
Comprehensive genomic characterization of gene therapy-induced T-cell acute lymphoblastic leukemia.
Leukemia
2020
30901310
<i>RSPO2</i> gene rearrangement: a powerful driver of β-catenin activation in liver tumours.
Gut
2019
29985981
PingPongPro: a tool for the detection of piRNA-mediated transposon-silencing in small RNA-Seq data.
Bioinformatics
2019
31069492
Mutational patterns and regulatory networks in epigenetic subgroups of meningioma.
Acta Neuropathol
2019
30833416
Response to olaparib in a <i>PALB2</i> germline mutated prostate cancer and genetic events associated with resistance.
Cold Spring Harb Mol Case Stud
2019
31008532
Variant classification in precision oncology.
Int J Cancer
2019
30967556
Defective homologous recombination DNA repair as therapeutic target in advanced chordoma.
Nat Commun
2019
29802158
<i>NRG1</i> Fusions in <i>KRAS</i> Wild-Type Pancreatic Cancer.
Cancer Discov
2018
35135162
Validating Comprehensive Next-Generation Sequencing Results for Precision Oncology: The NCT/DKTK Molecularly Aided Stratification for Tumor Eradication Research Experience.
JCO Precis Oncol
2018
28619747
Successful immune checkpoint blockade in a patient with advanced stage microsatellite-unstable biliary tract cancer.
Cold Spring Harb Mol Case Stud
2017
28122742
Ex vivo drug response profiling detects recurrent sensitivity patterns in drug-resistant acute lymphoblastic leukemia.
Blood
2017
28597939
Precision oncology based on omics data: The NCT Heidelberg experience.
Int J Cancer
2017
27900363
Integration of genomics and histology revises diagnosis and enables effective therapy of refractory cancer of unknown primary with <i>PDL1</i> amplification.
Cold Spring Harb Mol Case Stud
2016
1 - 39 of 39
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Stephan Wolf
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Michael Allg??uer
Institute of Pathology, Heidelberg University Hospital
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Martina Kirchner
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