Rabea J. Wagener

Kiel, SH, Germany

Last Updated: 09/26/2026

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Found 60 publications

Comparative DNA Methylation Profiling of Human and Murine ALK-Positive B-Cell Neoplasms.

Comparative DNA Methylation Profiling of Human and Murine ALK-Positive B-Cell Neoplasms.

Journal: Genes, chromosomes & cancer
Published: February 24, 2025

Subtyping Burkitt Lymphoma by DNA Methylation.

Subtyping Burkitt Lymphoma by DNA Methylation.

Journal: Genes, chromosomes & cancer
Published: February 06, 2025

MicroRNA Expression in High-Grade B-Cell Lymphoma With 11q Aberration.

MicroRNA Expression in High-Grade B-Cell Lymphoma With 11q Aberration.

Journal: Genes, chromosomes & cancer
Published: November 11, 2024

Subgrouping germinal center-derived B-cell lymphomas based on machine learning-deduced DNA methylation modules.

Subgrouping germinal center-derived B-cell lymphomas based on machine learning-deduced DNA methylation modules.

Journal: Leukemia
Published: September 13, 2024

H1-0 is a specific mediator of the repressive ETV6::RUNX1 transcriptional landscape in preleukemia and B cell acute lymphoblastic leukemia.

H1-0 is a specific mediator of the repressive ETV6::RUNX1 transcriptional landscape in preleukemia and B cell acute lymphoblastic leukemia.

Journal: HemaSphere
Published: July 04, 2024

Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants.

Hyperdiploid acute lymphoblastic leukemia in children with LZTR1 germline variants.

Journal: HemaSphere
Published: October 12, 2023

Co-targeting HSP90 alpha and CDK7 overcomes resistance against HSP90 inhibitors in BCR-ABL1+ leukemia cells.

Co-targeting HSP90 alpha and CDK7 overcomes resistance against HSP90 inhibitors in BCR-ABL1+ leukemia cells.

Journal: Cell death & disease
Published: June 06, 2023

Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas.

Lack of SMARCB1 expression characterizes a subset of human and murine peripheral T-cell lymphomas.

Journal: Nature communications
Published: May 04, 2023

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.

Optical Genome Mapping Identifies Novel Recurrent Structural Alterations in Childhood ETV6::RUNX1+ and High Hyperdiploid Acute Lymphoblastic Leukemia.

Journal: HemaSphere
Published: January 31, 2023

Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients.

Optical genome mapping identifies structural variants in potentially new cancer predisposition candidate genes in pediatric cancer patients.

Journal: International journal of cancer
Published: January 29, 2023

Reply to: Comments on "The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients".

Reply to: Comments on "The CHK2 kinase is recurrently mutated and functionally impaired in the germline of pediatric cancer patients".

Journal: International journal of cancer
Published: December 21, 2022

A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children.

A clinical screening tool to detect genetic cancer predisposition in pediatric oncology shows high sensitivity but can miss a substantial percentage of affected children.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 18, 2022
Showing 1-12 of 60

Last Updated: 09/26/2026