Reiner Siebert

Albert Einstein Allee 11
Ulm, BW 89081, Germany

Last Updated: 09/26/2026

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Found 376 publications

Correction: A rare missense variant impacting NEK1 kinase function is associated with ALS.

Correction: A rare missense variant impacting NEK1 kinase function is associated with ALS.

Journal: Acta neuropathologica communications

Published: July 21, 2026

Analysis of Surface Immunoglobulin Expression in Burkitt Lymphoma Reveals a Subset of IgA-Expressing Cases Enriched at Mucosal Sites and Surface Immunoglobulin-Undetectable Cases: Insights into the Mutational Landscape.

Analysis of Surface Immunoglobulin Expression in Burkitt Lymphoma Reveals a Subset of IgA-Expressing Cases Enriched at Mucosal Sites and Surface Immunoglobulin-Undetectable Cases: Insights into the Mutational Landscape.

Journal: Cancers

Published: June 11, 2026

Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism.

Discrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism.

Journal: Molecular cytogenetics

Published: March 03, 2026

A rare missense variant impacting NEK1 kinase function is associated with ALS.

A rare missense variant impacting NEK1 kinase function is associated with ALS.

Journal: Acta neuropathologica communications

Published: February 25, 2026

Genomic loss of MLH1/PMS2 loci defines a mismatch repair deficient subgroup in monomorphic epitheliotropic intestinal T-cell lymphoma.

Genomic loss of MLH1/PMS2 loci defines a mismatch repair deficient subgroup in monomorphic epitheliotropic intestinal T-cell lymphoma.

Journal: Blood cancer journal

Published: January 23, 2026

Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testing.

Protein-truncating variants in APBA1 in minors with severe, early-onset obesity: implications for genetic testing.

Journal: Molecular and cellular pediatrics

Published: January 15, 2026

DNA methylation signatures distinguish extranodal NK/T-cell lymphoma and EBV-positive nodal T/NK-cell lymphoma and identify prognostic subgroups.

DNA methylation signatures distinguish extranodal NK/T-cell lymphoma and EBV-positive nodal T/NK-cell lymphoma and identify prognostic subgroups.

Journal: Leukemia

Published: January 02, 2026

Correction: Divergent molecular pathways drive monomorphic epitheliotropic and enteropathy-associated intestinal T-cell lymphoma.

Correction: Divergent molecular pathways drive monomorphic epitheliotropic and enteropathy-associated intestinal T-cell lymphoma.

Journal: Leukemia

Published: November 20, 2025

PLCG2 exon-skipped variants: insights into their potential role in chronic lymphocytic leukemia.

PLCG2 exon-skipped variants: insights into their potential role in chronic lymphocytic leukemia.

Journal: Blood advances

Published: November 13, 2025

Towards a WHO classification of genetic tumour syndromes.

Towards a WHO classification of genetic tumour syndromes.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: November 10, 2025

Genetic tumor syndromes - It's time for action.

Genetic tumor syndromes - It's time for action.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: November 10, 2025

The spectrum of immunoglobulin heavy chain enhancer hijacking in chronic lymphocytic leukemia.

The spectrum of immunoglobulin heavy chain enhancer hijacking in chronic lymphocytic leukemia.

Journal: Leukemia

Published: October 27, 2025

Showing 1-12 of 376

Last Updated: 09/26/2026