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Annekathrin Reinhardt (1986-)

Neuropathologin

Name	Annekathrin Reinhardt
Zeit	1986- (Lebensdaten)
Ort	Wittenberg (Geburtsort) Deutschland
Geschlecht	weiblich
Akademischer Grad bzw. Titel	Dr. med. (Berlin, Univ.-Medizin) (2015)
Beruf	Neuropathologin (charakteristischer Beruf) Ärztin
Variante	Annekathrin Kratz (früherer Name)
Beziehung	Universitätsklinikum Heidelberg
Quelle	https://www.klinikum.uni-heidelberg.de/fileadmin/neurologie/neuroonkologie/CV_Reinhardt_oProjektbeschr.pdf (Stand: 21.07.2023)
Datensatztyp	Person
GND-Nummer	1078930309
Datensatz-ID	1078930309
Beteiligt an alle anzeigen Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology Analysing cerebrospinal fluid with explainable deep learning: From diagnostics to insights Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology Pleomorphic xanthoastrocytoma is a heterogeneous entity with pTERT mutations prognosticating shorter survival Genetic and epigenetic characterization of posterior pituitary tumors Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1 Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1 Accurate calling of KIAA1549‐BRAF fusions from DNA of human brain tumours using methylation array‐based copy number and gene panel sequencing data Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis Comparative molecular analysis of primary and recurrent oligodendroglioma that acquired imbalanced 1p/19q codeletion and TP53 mutation: a case report Infratentorial IDH-mutant astrocytoma is a distinct subtype Diffuse midline glioma of the cervical spinal cord with H3 K27M genotype phenotypically mimicking anaplastic ganglioglioma: a case report and review of the literature 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 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 Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities 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 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 Gain of 12p encompassing CCND2 is associated with gemistocytic histology in IDH mutant astrocytomas Methylation-based classification of benign and malignant peripheral nerve sheath tumors Next-generation sequencing in routine brain tumor diagnostics enables an integrated diagnosis and identifies actionable targets Adult IDH wild type astrocytomas biologically and clinically resolve into other tumor entities Kombinationseffekte von TRAIL und Retinoiden an Zellkulturmodellen des Mammakarzinoms und des Osteosarkoms

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Annekathrin Reinhardt (1986-)

Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

Analysing cerebrospinal fluid with explainable deep learning: From diagnostics to insights

Multiomic neuropathology improves diagnostic accuracy in pediatric neuro-oncology

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

Genetic and epigenetic characterization of posterior pituitary tumors

Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1

Glioblastomas with primitive neuronal component harbor a distinct methylation and copy-number profile with inactivation of TP53, PTEN, and RB1

Accurate calling of KIAA1549‐BRAF fusions from DNA of human brain tumours using methylation array‐based copy number and gene panel sequencing data

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

Comparative molecular analysis of primary and recurrent oligodendroglioma that acquired imbalanced 1p/19q codeletion and TP53 mutation: a case report

Infratentorial IDH-mutant astrocytoma is a distinct subtype

Diffuse midline glioma of the cervical spinal cord with H3 K27M genotype phenotypically mimicking anaplastic ganglioglioma: a case report and review of the literature

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

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

Tumors diagnosed as cerebellar glioblastoma comprise distinct molecular entities

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

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

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

Methylation-based classification of benign and malignant peripheral nerve sheath tumors

Next-generation sequencing in routine brain tumor diagnostics enables an integrated diagnosis and identifies actionable targets

Adult IDH wild type astrocytomas biologically and clinically resolve into other tumor entities

Kombinationseffekte von TRAIL und Retinoiden an Zellkulturmodellen des Mammakarzinoms und des Osteosarkoms