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Author Details
Full Name
Ivo Buchhalter
Affiliation
German Cancer Research Center (DKFZ) and German Cancer Consortium (DKTK)
ORCID
Career Start Year
2014
Papers
30
H Index
22
Expertise
CM4AI Collaborator
Antoine Forget (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37875569
Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Nat Med
2024
37875569
Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Nat Med
2024
36928815
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Nat Med
2023
36928815
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Nat Med
2023
33405951
Outcomes by Clinical and Molecular Features in Children With Medulloblastoma Treated With Risk-Adapted Therapy: Results of an International Phase III Trial (SJMB03).
J Clin Oncol
2021
34112699
Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers.
Cancer Discov
2021
33405951
Outcomes by Clinical and Molecular Features in Children With Medulloblastoma Treated With Risk-Adapted Therapy: Results of an International Phase III Trial (SJMB03).
J Clin Oncol
2021
34112699
Comprehensive Genomic and Transcriptomic Analysis for Guiding Therapeutic Decisions in Patients with Rare Cancers.
Cancer Discov
2021
32296180
Germline Elongator mutations in Sonic Hedgehog medulloblastoma.
Nature
2020
32296180
Germline Elongator mutations in Sonic Hedgehog medulloblastoma.
Nature
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
33028839
Framework for quality assessment of whole genome cancer sequences.
Nat Commun
2020
30446996
Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels.
Int J Cancer
2019
31802000
The molecular landscape of ETMR at diagnosis and relapse.
Nature
2019
30446996
Measurement of tumor mutational burden (TMB) in routine molecular diagnostics: in silico and real-life analysis of three larger gene panels.
Int J Cancer
2019
30238975
Size matters: Dissecting key parameters for panel-based tumor mutational burden analysis.
Int J Cancer
2019
30653256
Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases.
Int J Cancer
2019
31138115
TelomereHunter - in silico estimation of telomere content and composition from cancer genomes.
BMC Bioinformatics
2019
31802000
The molecular landscape of ETMR at diagnosis and relapse.
Nature
2019
30238975
Size matters: Dissecting key parameters for panel-based tumor mutational burden analysis.
Int J Cancer
2019
31138115
TelomereHunter - in silico estimation of telomere content and composition from cancer genomes.
BMC Bioinformatics
2019
30653256
Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: Analysis of the first 3,000 Heidelberg cases.
Int J Cancer
2019
29269125
Targeted molecular profiling reveals genetic heterogeneity of poromas and porocarcinomas.
Pathology
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
30348504
Genetic profiling of melanoma in routine diagnostics: assay performance and molecular characteristics in a consecutive series of 274 cases.
Pathology
2018
29489754
The landscape of genomic alterations across childhood cancers.
Nature
2018
29269125
Targeted molecular profiling reveals genetic heterogeneity of poromas and porocarcinomas.
Pathology
2018
29753700
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
Lancet Oncol
2018
29435664
Deep sequencing of WNT-activated medulloblastomas reveals secondary SHH pathway activation.
Acta Neuropathol
2018
29363116
EML4-ALK fusion variant V3 is a high-risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK<sup>+</sup> non-small cell lung cancer.
Int J Cancer
2018
29778738
Risk-adapted therapy for young children with medulloblastoma (SJYC07): therapeutic and molecular outcomes from a multicentre, phase 2 trial.
Lancet Oncol
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
30348504
Genetic profiling of melanoma in routine diagnostics: assay performance and molecular characteristics in a consecutive series of 274 cases.
Pathology
2018
29363116
EML4-ALK fusion variant V3 is a high-risk feature conferring accelerated metastatic spread, early treatment failure and worse overall survival in ALK<sup>+</sup> non-small cell lung cancer.
Int J Cancer
2018
29753700
Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
Lancet Oncol
2018
29778738
Risk-adapted therapy for young children with medulloblastoma (SJYC07): therapeutic and molecular outcomes from a multicentre, phase 2 trial.
Lancet Oncol
2018
29489754
The landscape of genomic alterations across childhood cancers.
Nature
2018
29435664
Deep sequencing of WNT-activated medulloblastomas reveals secondary SHH pathway activation.
Acta Neuropathol
2018
28726821
The whole-genome landscape of medulloblastoma subtypes.
Nature
2017
28726821
The whole-genome landscape of medulloblastoma subtypes.
Nature
2017
28572216
Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer.
J Exp Med
2017
28474103
Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature.
Acta Neuropathol
2017
28474103
Meningiomas induced by low-dose radiation carry structural variants of NF2 and a distinct mutational signature.
Acta Neuropathol
2017
28572216
Genetic subclone architecture of tumor clone-initiating cells in colorectal cancer.
J Exp Med
2017
26919435
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs.
Cell
2016
26923874
Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes.
Cancer Cell
2016
26919435
New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs.
Cell
2016
26814967
Active medulloblastoma enhancers reveal subgroup-specific cellular origins.
Nature
2016
26671409
Next-generation sequencing in routine brain tumor diagnostics enables an integrated diagnosis and identifies actionable targets.
Acta Neuropathol
2016
27999735
Identification of immunotherapeutic targets by genomic profiling of rectal NET metastases.
Oncoimmunology
2016
1 - 50 of 60
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