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Author Details
Full Name
Dominik Sturm
Affiliation
Hopp Children's Cancer Center Heidelberg (KiTZ)
ORCID
Career Start Year
2008
Papers
99
H Index
46
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
36437415
Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
Acta Neuropathol
2023
37851269
Clinical, genomic, and epigenomic analyses of H3K27M-mutant diffuse midline glioma long-term survivors reveal a distinct group of tumors with MAPK pathway alterations.
Acta Neuropathol
2023
36715306
Risk prediction in early childhood sonic hedgehog medulloblastoma treated with radiation-avoiding chemotherapy: Evidence for more than 2 subgroups.
Neuro Oncol
2023
36959034
Corrigendum to 'Molecular diagnostics enables detection of actionable targets: the Pediatric Targeted Therapy 2.0 registry' [Eur J Cancer 180 (2023) 71-84].
Eur J Cancer
2023
37188167
Clinical outcome following surgical resection and radiotherapy in adult patients with pleomorphic xanthoastrocytoma as defined by DNA methylation profiling.
Neurooncol Pract
2023
37379234
Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome.
Neuro Oncol
2023
36542877
Molecular diagnostics enables detection of actionable targets: the Pediatric Targeted Therapy 2.0 registry.
Eur J Cancer
2023
36928815
Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology.
Nat Med
2023
36459208
Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohorts.
Acta Neuropathol
2023
36786841
Correction to: Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
Acta Neuropathol
2023
37517472
Implementation of DNA Methylation Array Profiling in Pediatric Central Nervous System Tumors: The AIM BRAIN Project: An Australian and New Zealand Children's Haematology/Oncology Group Study.
J Mol Diagn
2023
37851269
Clinical, genomic, and epigenomic analyses of H3K27M-mutant diffuse midline glioma long-term survivors reveal a distinct group of tumors with MAPK pathway alterations.
Acta Neuropathol
2023
37517472
Implementation of DNA Methylation Array Profiling in Pediatric Central Nervous System Tumors: The AIM BRAIN Project: An Australian and New Zealand Children's Haematology/Oncology Group Study.
J Mol Diagn
2023
36959034
Corrigendum to 'Molecular diagnostics enables detection of actionable targets: the Pediatric Targeted Therapy 2.0 registry' [Eur J Cancer 180 (2023) 71-84].
Eur J Cancer
2023
37188167
Clinical outcome following surgical resection and radiotherapy in adult patients with pleomorphic xanthoastrocytoma as defined by DNA methylation profiling.
Neurooncol Pract
2023
37379234
Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome.
Neuro Oncol
2023
36786841
Correction to: Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
Acta Neuropathol
2023
36715306
Risk prediction in early childhood sonic hedgehog medulloblastoma treated with radiation-avoiding chemotherapy: Evidence for more than 2 subgroups.
Neuro Oncol
2023
36542877
Molecular diagnostics enables detection of actionable targets: the Pediatric Targeted Therapy 2.0 registry.
Eur J Cancer
2023
36437415
Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification.
Acta Neuropathol
2023
36459208
Identification of low and very high-risk patients with non-WNT/non-SHH medulloblastoma by improved clinico-molecular stratification of the HIT2000 and I-HIT-MED cohorts.
Acta Neuropathol
2023
34699462
Cui Bono? Identifying Patient Groups That May Benefit From Granulocyte Transfusions in Pediatric Hematology and Oncology.
J Pediatr Hematol Oncol
2022
36070143
Epigenetic profiling reveals a subset of pediatric-type glioneuronal tumors characterized by oncogenic gene fusions involving several targetable kinases.
Acta Neuropathol
2022
35603902
Changing paradigms in oncology: Toward noncytotoxic treatments for advanced gliomas.
Int J Cancer
2022
35660939
DNA-methylome-assisted classification of patients with poor prognostic subventricular zone associated IDH-wildtype glioblastoma.
Acta Neuropathol
2022
34674226
Primary central nervous system sarcoma with DICER1 mutation-treatment results of a novel molecular entity in pediatric Peruvian patients.
Cancer
2022
35195346
ALK inhibition as a salvage therapy for a relapsed unclassifiable sarcomatous CNS tumor with EML4/ALK fusion in an infant.
Pediatr Blood Cancer
2022
35190934
Clinical and molecular characterization of isolated M1 disease in pediatric medulloblastoma: experience from the German HIT-MED studies.
J Neurooncol
2022
35012690
Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survival.
Acta Neuropathol Commun
2022
34699462
Cui Bono? Identifying Patient Groups That May Benefit From Granulocyte Transfusions in Pediatric Hematology and Oncology.
J Pediatr Hematol Oncol
2022
35053437
A Systematic Review and Meta-Analysis of Malignant Rhabdoid and Small Cell Undifferentiated Liver Tumors: A Rational for a Uniform Classification.
Cancers (Basel)
2022
35603902
Changing paradigms in oncology: Toward noncytotoxic treatments for advanced gliomas.
Int J Cancer
2022
35660939
DNA-methylome-assisted classification of patients with poor prognostic subventricular zone associated IDH-wildtype glioblastoma.
Acta Neuropathol
2022
36070143
Epigenetic profiling reveals a subset of pediatric-type glioneuronal tumors characterized by oncogenic gene fusions involving several targetable kinases.
Acta Neuropathol
2022
35190934
Clinical and molecular characterization of isolated M1 disease in pediatric medulloblastoma: experience from the German HIT-MED studies.
J Neurooncol
2022
35012690
Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survival.
Acta Neuropathol Commun
2022
35053437
A Systematic Review and Meta-Analysis of Malignant Rhabdoid and Small Cell Undifferentiated Liver Tumors: A Rational for a Uniform Classification.
Cancers (Basel)
2022
35195346
ALK inhibition as a salvage therapy for a relapsed unclassifiable sarcomatous CNS tumor with EML4/ALK fusion in an infant.
Pediatr Blood Cancer
2022
34674226
Primary central nervous system sarcoma with DICER1 mutation-treatment results of a novel molecular entity in pediatric Peruvian patients.
Cancer
2022
33479225
Sarcoma classification by DNA methylation profiling.
Nat Commun
2021
34077956
Therapeutic implications of improved molecular diagnostics for rare CNS embryonal tumor entities: results of an international, retrospective study.
Neuro Oncol
2021
33479225
Sarcoma classification by DNA methylation profiling.
Nat Commun
2021
33879448
Cross-Species Genomics Reveals Oncogenic Dependencies in ZFTA/C11orf95 Fusion-Positive Supratentorial Ependymomas.
Cancer Discov
2021
34355256
Recurrent fusions in PLAGL1 define a distinct subset of pediatric-type supratentorial neuroepithelial tumors.
Acta Neuropathol
2021
33130881
A subset of pediatric-type thalamic gliomas share a distinct DNA methylation profile, H3K27me3 loss and frequent alteration of EGFR.
Neuro Oncol
2021
33336421
Accurate calling of KIAA1549-BRAF fusions from DNA of human brain tumours using methylation array-based copy number and gene panel sequencing data.
Neuropathol Appl Neurobiol
2021
33216206
Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis.
Acta Neuropathol
2021
1 - 50 of 198
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Andreas von Deimling
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44
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33
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Martin Sill
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30
David Capper
Charite University Medicine Berlin
Co-authored papers
28
Peter Lichter
German Cancer Research Center (DKFZ)
Co-authored papers
28
Christof M Kramm
Co-authored papers
27
Stefan Rutkowski
University Medical Center Hamburg-Eppendorf
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26
Ulrich Sch??ller
University Medical Center Hamburg-Eppendorf
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24
Torsten Pietsch
Co-authored papers
24
Marina Ryzhova
N.N. Burdenko Neurosurgical Institute
Co-authored papers
23
Nada Jabado
McGill University Health Centre (MUHC), Montreal Children's Hospital (MCH)
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23
Christel Herold-Mende
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Paul A Northcott
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Andreas E Kulozik
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Guido Reifenberger
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