Author details

Full Name

Reiner Siebert

Affiliation

ORCID

Career Start Year

1959

Papers

640

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34740919	Bi-allelic loss-of-function variants in <i>KIF21A</i> cause severe fetal akinesia with arthrogryposis multiplex.	J Med Genet	2023
35522148	Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas.	Haematologica	2023
35708139	Monomorphic epitheliotropic intestinal T-cell lymphoma comprises morphologic and genomic heterogeneity impacting outcome.	Haematologica	2023
35856126	Molecular characterization of an embryonal rhabdomyosarcoma occurring in a patient with Kabuki syndrome: report and literature review in the light of tumor predisposition syndromes.	Familial Cancer	2023
37647808	PI3K/AKT inhibitor BEZ-235 targets CCND2 and induces G1 arrest in breast implant-associated anaplastic large cell lymphoma.		2023
37993930	Targeting oncogenic TERT promoter variants by allele-specific epigenome editing.		2023
37555362	DNA methylation-associated allelic inactivation regulates Keratin 19 gene expression during pancreatic development and carcinogenesis.		2023
37553222	Rhabdoid tumors in patients conceived following ART: is there an association?		2023
37684676	A quantum physics layer of epigenetics: a hypothesis deduced from charge transfer and chirality-induced spin selectivity of DNA.		2023
36973349	Response to the Comments from the Groupe Francophone de CytogÃ©nÃ©tique HÃ©matologique (GFCH) on the 5th edition of the World Health Organization classification of haematolymphoid tumors.	Leukemia	2023
36907637	Biopathology of childhood, adolescent and young adult non-Hodgkin lymphoma.		2023
37468552	Correction: "The 5th edition of The World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms" Leukemia. 2022 Jul;36(7):1720-1748.	Leukemia	2023
36961799	Identification of two unannotated miRNAs in classic Hodgkin lymphoma cell lines.		2023
37196929	AMD3100-Mediated CXCR4 Inhibition Impairs Development of Primary Lymphoma of the Central Nervous System.		2023
37450044	Recurrent atypical teratoid/rhabdoid tumors (AT/RT) reveal discrete features of progression on histology, epigenetics, copy number profiling, and transcriptomics.	Acta Neuropathol	2023
36697831	Author Correction: Genomic basis for RNA alterations in cancer.	Nature	2023
36997001	Proteogenomic Profiling of High-Grade B-Cell Lymphoma With 11q Aberrations and Burkitt Lymphoma Reveals Lymphoid Enhancer Binding Factor 1 as a Novel Biomarker.		2023
37365157	The DNA methylation status of the TERT promoter differs between subtypes of mature B-cell lymphomas.		2023
36858027	Combined Heterozygous Genetic Variations in Complement C2 and C8B: An Explanation for Multidimensional Immune Imbalance?		2023
36609404	Publisher Correction: Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker.	Clin Epigenetics	2023
36786840	SMARCA4-associated schwannomatosis.	Acta Neuropathol	2023
37223130	Spectrum and frequency of genetic variants in sporadic amyotrophic lateral sclerosis.		2023
36658118	Molecular characterization of Richter syndrome identifies de novo diffuse large B-cell lymphomas with poor prognosis.	Nat Commun	2023
35325565	Auditing the Editor: A Review of Key Translational Issues in Epigenetic Editing.	CRISPR J	2022
35974101	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.	Leukemia	2022
35913887	Germline Missense Variants in CDC20 Result in Aberrant Mitotic Progression and Familial Cancer.	Cancer Research	2022
35524550	Human activation-induced deaminase lacks strong replicative strand bias or preference for cytosines in hairpin loops.	Nucleic Acids Research	2022
35446794	SMARCB1-deficient and SMARCA4-deficient Malignant Brain Tumors With Complex Copy Number Alterations and TP53 Mutations May Represent the First Clinical Manifestation of Li-Fraumeni Syndrome.	Am J Surg Pathol	2022
35884496	Classifying Germinal Center Derived Lymphomas-Navigate a Complex Transcriptional Landscape.	Cancers	2022
36083597	Exploration of whole genome and transcriptome sequencing data lacks evidence for oncogenic viral elements to drive the pathogenesis of T-cell prolymphocytic leukemia.	Leuk Lymphoma	2022
35501487	ATRT-SHH comprises three molecular subgroups with characteristic clinical and histopathological features and prognostic significance.	Acta Neuropathol	2022
35565313	Infants and Newborns with Atypical Teratoid Rhabdoid Tumors (ATRT) and Extracranial Malignant Rhabdoid Tumors (eMRT) in the EU-RHAB Registry: A Unique and Challenging Population.	Cancers (Basel)	2022
35935612	Successful Retreatment With Venetoclax in a Patient With Chronic Lymphocytic Leukemia.	HemaSphere	2022
35737900	Detection of Few Hydrogen Peroxide Molecules Using Self-Reporting Fluorescent Nanodiamond Quantum Sensors.	Journal of the American Chemical Society	2022
35736637	LINC00892 Is an lncRNA Induced by T Cell Activation and Expressed by Follicular Lymphoma-Resident T Helper Cells.	Non-coding RNA	2022
35732831	The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/DendriticÂ Neoplasms.	Leukemia	2022
35732829	The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms.	Leukemia	2022
35986215	20 Years with SGBS cells - a versatile in vitro model of human adipocyte biology.	International Journal of Obesity	2022
35794096	Clinical relevance of molecular characteristics in Burkitt lymphoma differs according to age.	Nat Commun	2022
35609565	A unifying hypothesis for PNMZL and PTFL: morphological variants with a common molecular profile.	Blood Adv	2022
36056446	Researcher perspectives on ethics considerations in epigenetics: an international survey.	Clin Epigenetics	2022
36260299	Expression of Cas9 in a Syngeneic Model of Primary Central Nervous System Lymphoma Induces Intracerebral NK and CD8 T Cell-Mediated Lymphoma Cell Lysis Via Perforin.	CRISPR Journal	2022
35405042	Congenital generalized lipodystrophy type 4 due to a novel PTRF/CAVIN1 pathogenic variant in a child: effects of metreleptin substitution.	Journal of Pediatric Endocrinology and Metabolism	2022
36376973	Epigenome-wide analysis of T-cell large granular lymphocytic leukemia identifies BCL11B as a potential biomarker.	Clin Epigenetics	2022
36051037	B-cell receptors of EBV-negative Burkitt lymphoma bind modified isoforms of autoantigens.		2022
36522349	Burkitt lymphoma.		2022
34689140	Genetic Obesity in Children: Overview of Possible Diagnoses with a Focus on SH2B1 Deletion.	Hormone Research in Paediatrics	2022
34617271	Epstein-Barr virus status of sporadic Burkitt lymphoma is associated with patient age and mutational features.	Br J Haematol	2022
35218115	T-cell prolymphocytic leukemia is associated with deregulation of oncogenic microRNAs on transcriptional and epigenetic level.	Genes Chromosomes Cancer	2022
35173482	Current and Emerging Therapeutic Approaches for Extracranial Malignant Rhabdoid Tumors.	Cancer Management and Research	2022