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Reiner Siebert (1968-)

Genetiker

Name	Reiner Siebert
Zeit	1968- (Lebensdaten)
Ort	Kiel (Wirkungsort) Deutschland
Geschlecht	männlich
Akademischer Grad bzw. Titel	Prof. Dr. med.
Beruf	Genetiker (charakteristischer Beruf) Hochschullehrer
Variante	R. Siebert
Beziehung	Universitätsklinikum Schleswig-Holstein. Campus Kiel
Weitere Angaben	Diss. Fachbereich Humanmedizin; Direktor des Instituts für Humangenetik der Univ. Kiel
Datensatztyp	Person
GND-Nummer	115859845
Datensatz-ID	115859845
Beteiligt an alle anzeigen Transcriptional reprogramming by mutated IRF4 in lymphoma Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker Modified risk-stratified sequential treatment (subcutaneous rituximab with or without chemotherapy) in B-cell Post-transplant lymphoproliferative disorder (PTLD) after Solid organ transplantation (SOT): the prospective multicentre phase II PTLD-2 trial The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms J wave syndromes in patients with spinal and bulbar muscular atrophy ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age Identifying blood-specific biomarkers for therapy-related clonal hematopoiesis in patients with hereditary or non-hereditary ovarian cancer J wave syndromes in patients with spinal and bulbar muscular atrophy LINC00892 is an lncRNA induced by T cell activation and expressed by follicular lymphoma-resident T helper cells LINC00892 Is an lncRNA Induced by T Cell Activation and Expressed by Follicular Lymphoma-Resident T Helper Cells Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma Epigenetic Activation of SOX11 in Lymphoid Neoplasms by Histone Modifications Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma Family-based germline sequencing in children with cancer Alterations of microRNA and microRNA-regulated messenger RNA expression in germinal center B-cell lymphomas determined by integrative sequencing analysis Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control MINCR is a MYC-induced lncRNA able to modulate MYC's transcriptional network in Burkitt lymphoma cells The PCBP1 gene encoding poly(rc) binding protein i is recurrently mutated in Burkitt lymphoma Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levels A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols Hodgkin-Reed-Sternberg cells in classical Hodgkin lymphoma show alterations of genes encoding the NADPH oxidase complex and impaired reactive oxygen species synthesis capacity Hypermutation of the inactive X chromosome is a frequent event in cancer Signatures of mutational processes in human cancer Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation Fast Approach for Clarification of Chromosomal Aberrations by Using LM-PCR and FT-CGH in Leukaemic Sample Array-based DNA methylation profiling of primary lymphomas of the central nervous system TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma Molekulargenetische Analysen der humanen Chromosomenregion 3p14.2-p21.1 bei Lungen- und Nierenzellkarzinomen zur Identifizierung putativer Tumorsuppressorgenloci

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Katalog der Deutschen Nationalbibliothek

Reiner Siebert (1968-)

Transcriptional reprogramming by mutated IRF4 in lymphoma

Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker

Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age

Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker

Modified risk-stratified sequential treatment (subcutaneous rituximab with or without chemotherapy) in B-cell Post-transplant lymphoproliferative disorder (PTLD) after Solid organ transplantation (SOT): the prospective multicentre phase II PTLD-2 trial

The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms

J wave syndromes in patients with spinal and bulbar muscular atrophy

ATRT–SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance

Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age

Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age

Identifying blood-specific biomarkers for therapy-related clonal hematopoiesis in patients with hereditary or non-hereditary ovarian cancer

J wave syndromes in patients with spinal and bulbar muscular atrophy

LINC00892 is an lncRNA induced by T cell activation and expressed by follicular lymphoma-resident T helper cells

LINC00892 Is an lncRNA Induced by T Cell Activation and Expressed by Follicular Lymphoma-Resident T Helper Cells

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas

Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma

Epigenetic Activation of SOX11 in Lymphoid Neoplasms by Histone Modifications

Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma

Family-based germline sequencing in children with cancer

Alterations of microRNA and microRNA-regulated messenger RNA expression in germinal center B-cell lymphomas determined by integrative sequencing analysis

Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer

Changes of bivalent chromatin coincide with increased expression of developmental genes in cancer

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control

MINCR is a MYC-induced lncRNA able to modulate MYC's transcriptional network in Burkitt lymphoma cells

The PCBP1 gene encoding poly(rc) binding protein i is recurrently mutated in Burkitt lymphoma

Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levels

A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma

Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols

Hodgkin-Reed-Sternberg cells in classical Hodgkin lymphoma show alterations of genes encoding the NADPH oxidase complex and impaired reactive oxygen species synthesis capacity

Hypermutation of the inactive X chromosome is a frequent event in cancer

Signatures of mutational processes in human cancer

Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma

Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing

A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms

Androgen receptor mutations are associated with altered epigenomic programming as evidenced by HOXA5 methylation

Fast Approach for Clarification of Chromosomal Aberrations by Using LM-PCR and FT-CGH in Leukaemic Sample

Array-based DNA methylation profiling of primary lymphomas of the central nervous system

TNFAIP3 (A20) is a tumor suppressor gene in Hodgkin lymphoma and primary mediastinal B cell lymphoma

Molekulargenetische Analysen der humanen Chromosomenregion 3p14.2-p21.1 bei Lungen- und Nierenzellkarzinomen zur Identifizierung putativer Tumorsuppressorgenloci