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Annika K. Wefers (1982-)

Ärztin

Name	Annika K. Wefers
Zeit	1982- (Lebensdaten)
Ort	München (Wirkungsort) Heidelberg (Wirkungsort) Deutschland
Beruf	Ärztin (charakteristischer Beruf)
Variante	Annika Wefers A. K. Wefers Annika Kristina Wefers (vollständiger Name)
Beziehung	Ludolf-Krehl-Klinik Universität Heidelberg. Pathologisches Institut
Datensatztyp	Person
GND-Nummer	1110221673
Datensatz-ID	1110221673
Beteiligt an alle anzeigen Integrated analyses reveal two molecularly and clinically distinct subtypes of H3 K27M-mutant diffuse midline gliomas with prognostic significance A prognostic neural epigenetic signature in high-grade glioma Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology 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 Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification ACTH-secreting pituitary carcinoma with TP53, NF1, ATRX and PTEN mutations Case report and review of the literature Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survival DNA methylation-based classification of sinonasal tumors Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation — High-Grade PitNET or PitNEC? Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course IDH-wildtype glioblastomas and grade III/IV IDH-mutant gliomas show elevated tracer uptake in fibroblast activation protein–specific PET/CT Routine RNA sequencing of formalin-fixed paraffin-embedded specimens in neuropathology diagnostics identifies diagnostically and therapeutically relevant gene fusions Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1 Mutational patterns and regulatory networks in epigenetic subgroups of meningioma Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCA Mutational patterns and regulatory networks in epigenetic subgroups of meningioma Chordoid meningiomas can be sub-stratified into prognostically distinct DNA methylation classes and are enriched for heterozygous deletions of chromosomal arm 2p FGFR1:TACC1 fusion is a frequent event in molecularly defined extraventricular neurocytoma Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience DNA methylation-based reclassification of olfactory neuroblastoma Novel, improved grading system(s) for IDH-mutant astrocytic gliomas Anaplastic astrocytoma with piloid features, a novel molecular class of IDH wildtype glioma with recurrent MAPK pathway, CDKN2A/B and ATRX alterations Rapid detection of 2-hydroxyglutarate in frozen sections of IDH mutant tumors by MALDI-TOF mass spectrometry Migration of Interneuron Precursors in the Nascent Cerebellar Cortex Neurogenesis from Sox2 expressing cells in the adult cerebellar cortex Gain of 12p encompassing CCND2 is associated with gemistocytic histology in IDH mutant astrocytomas Overexpression of Lin28b in Neural Stem Cells is Insufficient for Brain Tumor Formation, but Induces Pathological Lobulation of the Developing Cerebellum Canonical Wnt Signaling Drives Tumor-Like Lesions from Sox2-Positive Precursors of the Murine Olfactory Epithelium Synaptische Innervation als Richtungsgeber für migrierende Vorläufer zentralnervöser Interneurone

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Katalog der Deutschen Nationalbibliothek

Annika K. Wefers (1982-)

Integrated analyses reveal two molecularly and clinically distinct subtypes of H3 K27M-mutant diffuse midline gliomas with prognostic significance

A prognostic neural epigenetic signature in high-grade glioma

Author Correction: Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

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

Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability

Epigenetic neural glioblastoma enhances synaptic integration and predicts therapeutic vulnerability

Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

Amplification of the PLAG-family genes—PLAGL1 and PLAGL2—is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification

ACTH-secreting pituitary carcinoma with TP53, NF1, ATRX and PTEN mutations Case report and review of the literature

Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survival

DNA methylation-based classification of sinonasal tumors

Two Pituitary Neuroendocrine Tumors (PitNETs) with Very High Proliferation and TP53 Mutation — High-Grade PitNET or PitNEC?

Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis

Desmoplastic myxoid tumor, SMARCB1-mutant: clinical, histopathological and molecular characterization of a pineal region tumor encountered in adolescents and adults

Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities

Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course

IDH-wildtype glioblastomas and grade III/IV IDH-mutant gliomas show elevated tracer uptake in fibroblast activation protein–specific PET/CT

Routine RNA sequencing of formalin-fixed paraffin-embedded specimens in neuropathology diagnostics identifies diagnostically and therapeutically relevant gene fusions

Rosette-forming glioneuronal tumors share a distinct DNA methylation profile and mutations in FGFR1, with recurrent co-mutation of PIK3CA and NF1

Mutational patterns and regulatory networks in epigenetic subgroups of meningioma

Papillary glioneuronal tumor (PGNT) exhibits a characteristic methylation profile and fusions involving PRKCA

Mutational patterns and regulatory networks in epigenetic subgroups of meningioma

Chordoid meningiomas can be sub-stratified into prognostically distinct DNA methylation classes and are enriched for heterozygous deletions of chromosomal arm 2p

FGFR1:TACC1 fusion is a frequent event in molecularly defined extraventricular neurocytoma

Practical implementation of DNA methylation and copy-number-based CNS tumor diagnostics: the Heidelberg experience

DNA methylation-based reclassification of olfactory neuroblastoma

Novel, improved grading system(s) for IDH-mutant astrocytic gliomas

Anaplastic astrocytoma with piloid features, a novel molecular class of IDH wildtype glioma with recurrent MAPK pathway, CDKN2A/B and ATRX alterations

Rapid detection of 2-hydroxyglutarate in frozen sections of IDH mutant tumors by MALDI-TOF mass spectrometry

Migration of Interneuron Precursors in the Nascent Cerebellar Cortex

Neurogenesis from Sox2 expressing cells in the adult cerebellar cortex

Gain of 12p encompassing CCND2 is associated with gemistocytic histology in IDH mutant astrocytomas

Overexpression of Lin28b in Neural Stem Cells is Insufficient for Brain Tumor Formation, but Induces Pathological Lobulation of the Developing Cerebellum

Canonical Wnt Signaling Drives Tumor-Like Lesions from Sox2-Positive Precursors of the Murine Olfactory Epithelium

Synaptische Innervation als Richtungsgeber für migrierende Vorläufer zentralnervöser Interneurone