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Imaging Characteristics of Wingless Pathway Subgroup Medulloblastomas: Results from the German HIT/SIOP-Trial Cohort

American journal of neuroradiology : AJNR, 2019-11, Vol.40 (11), p.1811-1817

2019

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Minimal methylation classifier (MIMIC): A novel method for derivation and rapid diagnostic detection of disease-associated DNA methylation signatures

Scientific reports, 2017-10, Vol.7 (1), p.13421-8, Article 13421

2017

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Gliosarcoma with extensive extracranial metastatic spread and familial coincidence: A case report

Pathology, research and practice, 2023-04, Vol.244, p.154399, Article 154399

2023

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Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial

The lancet oncology, 2018-12, Vol.19 (12), p.1602-1616

2018

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JS04.4.A Beyond β-catenin: Genetic alterations of TP53 and OTX2 and older age indicate increased risk of relapse in WNT medulloblastomas

Neuro-oncology (Charlottesville, Va.), 2022-09, Vol.24 (Supplement_2), p.ii6-ii7

2022

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JS04.4.A Beyond β-catenin: Genetic alterations ofTP53 andOTX2 and older age indicate increased risk of relapse in WNT medulloblastomas

Neuro-oncology (Charlottesville, Va.), 2022-09, Vol.24 (Suppl 2), p.ii6-ii7

2022

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OS9.8 Genomic landscape of medulloblastoma in adults

Neuro-oncology (Charlottesville, Va.), 2019-09, Vol.21 (Supplement_3), p.iii20-iii20

2019

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Molecular stratification of medulloblastoma: comparison of histological and genetic methods to detect Wnt activated tumours

Neuropathology and applied neurobiology, 2015-02, Vol.41 (2), p.135-144

2015

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Biomarker-driven stratification of disease-risk in non-metastatic medulloblastoma: Results from the multi-center HIT-SIOP-PNET4 clinical trial

Oncotarget, 2015-11, Vol.6 (36), p.38827-38839

2015

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Molecular stratification of medulloblastoma: Comparison of histological and genetical methods to detect Wnt activated tumors

Klinische Pädiatrie, 2013, Vol.225 (3)

2013

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A WHOLE CHROMOSOME ABERRATION PHENOTYPE IN NON-WNT/NON-SHH TUMORS PREDICTS OUTCOME WITHIN STANDARD-RISK MEDULLOBLASTOMAS FROM THE HIT-SIOP-PNET4 CLINICAL TRIAL

NEURO-ONCOLOGY, 2018, Vol.20, p.123

2018

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Supratentorial ependymomas of childhood carry C11orf95-RELA fusions leading to activation of the NF-kB signalling pathway

Klinische Pädiatrie, 2014, Vol.226 (3)

2014

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PROGNOSTIC SIGNIFICANCE OF CLINICAL, HISTOPATHOLOGICAL, AND MOLECULAR CHARACTERISTICS OF MEDULLOBLASTOMAS IN THE PROSPECTIVE HIT2000 MULTICENTER CLINICAL TRIAL COHORT

Neuro-oncology (Charlottesville, Va.), 2014-07, Vol.16 (suppl 3), p.iii24-iii25

2014

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Genetic analysis of adamantinomatous craniopharyngioma (ACP)

Klinische Pädiatrie, 2014-05, Vol.226 (3)

2014

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Chromosomal aberrations of M0 versus M+ non-WNT/non-SHH medulloblastomas

Klinische Pädiatrie, 2016-05, Vol.228 (3)

2016

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Gliosarcoma with extensive extracranial metastatic spread and familial coincidence: A case report

Pathology, research and practice, 2023, Vol.244, p.154399-154399

2023

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MDB-25. LARGE CELL/ANAPLASTIC MEDULLOBLASTOMA REPRESENTS MORE THAN ONE DISEASE ENTITY

Neuro-oncology (Charlottesville, Va.), 2023-06, Vol.25 (Supplement_1), p.i67-i67

2023

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FH-mutant glioma displaying the epigenetic signature of IDH-mutant astrocytomas

Journal of neuropathology and experimental neurology, 2024-10, Vol.83 (10), p.887-889

2024

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PTEN Mutations and Activation of the PI3K/Akt/mTOR Signaling Pathway in Papillary Tumors of the Pineal Region

Journal of neuropathology and experimental neurology, 2014-08, Vol.73 (8), p.747-751

2014

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MEDB-61. Genetic alterations ofTP53 andOTX2 indicate increased risk of relapse in WNT medulloblastomas

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (Suppl 1), p.i120-i120

2022

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MEDB-61. Genetic alterations of TP53 and OTX2 indicate increased risk of relapse in WNT medulloblastomas

Neuro-oncology (Charlottesville, Va.), 2022-06, Vol.24 (Supplement_1), p.i120-i120

2022

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Genomic Alterations of Adamantinomatous and Papillary Craniopharyngioma

Journal of neuropathology and experimental neurology, 2017-02, Vol.76 (2), p.126-134

2017

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FGFR1 Mutations in Rosette-Forming Glioneuronal Tumors of the Fourth Ventricle

Journal of neuropathology and experimental neurology, 2014-06, Vol.73 (6), p.580-584

2014

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Supratentorial ependymomas of childhood carry C11orf95–RELA fusions leading to pathological activation of the NF-κB signaling pathway

Acta neuropathologica, 2014-04, Vol.127 (4), p.609-611

2014

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Imaging Characteristics of Wingless Pathway Subgroup Medulloblastomas: Results from the German HIT/SIOP-Trial Cohort

Minimal methylation classifier (MIMIC): A novel method for derivation and rapid diagnostic detection of disease-associated DNA methylation signatures

Gliosarcoma with extensive extracranial metastatic spread and familial coincidence: A case report

Prognostic effect of whole chromosomal aberration signatures in standard-risk, non-WNT/non-SHH medulloblastoma: a retrospective, molecular analysis of the HIT-SIOP PNET 4 trial

JS04.4.A Beyond β-catenin: Genetic alterations of TP53 and OTX2 and older age indicate increased risk of relapse in WNT medulloblastomas

JS04.4.A Beyond β-catenin: Genetic alterations ofTP53 andOTX2 and older age indicate increased risk of relapse in WNT medulloblastomas

OS9.8 Genomic landscape of medulloblastoma in adults

Molecular stratification of medulloblastoma: comparison of histological and genetic methods to detect Wnt activated tumours

Biomarker-driven stratification of disease-risk in non-metastatic medulloblastoma: Results from the multi-center HIT-SIOP-PNET4 clinical trial

Molecular stratification of medulloblastoma: Comparison of histological and genetical methods to detect Wnt activated tumors

A WHOLE CHROMOSOME ABERRATION PHENOTYPE IN NON-WNT/NON-SHH TUMORS PREDICTS OUTCOME WITHIN STANDARD-RISK MEDULLOBLASTOMAS FROM THE HIT-SIOP-PNET4 CLINICAL TRIAL

Supratentorial ependymomas of childhood carry C11orf95-RELA fusions leading to activation of the NF-kB signalling pathway

PROGNOSTIC SIGNIFICANCE OF CLINICAL, HISTOPATHOLOGICAL, AND MOLECULAR CHARACTERISTICS OF MEDULLOBLASTOMAS IN THE PROSPECTIVE HIT2000 MULTICENTER CLINICAL TRIAL COHORT

Genetic analysis of adamantinomatous craniopharyngioma (ACP)

Chromosomal aberrations of M0 versus M+ non-WNT/non-SHH medulloblastomas

Gliosarcoma with extensive extracranial metastatic spread and familial coincidence: A case report

MDB-25. LARGE CELL/ANAPLASTIC MEDULLOBLASTOMA REPRESENTS MORE THAN ONE DISEASE ENTITY

FH-mutant glioma displaying the epigenetic signature of IDH-mutant astrocytomas

Prognostic significance of clinical, histopathological, and molecular characteristics of medulloblastomas in the prospective HIT2000 multicenter clinical trial cohort

PTEN Mutations and Activation of the PI3K/Akt/mTOR Signaling Pathway in Papillary Tumors of the Pineal Region

MEDB-61. Genetic alterations ofTP53 andOTX2 indicate increased risk of relapse in WNT medulloblastomas

MEDB-61. Genetic alterations of TP53 and OTX2 indicate increased risk of relapse in WNT medulloblastomas

Genomic Alterations of Adamantinomatous and Papillary Craniopharyngioma

FGFR1 Mutations in Rosette-Forming Glioneuronal Tumors of the Fourth Ventricle

Supratentorial ependymomas of childhood carry C11orf95–RELA fusions leading to pathological activation of the NF-κB signaling pathway

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