Robert Meyer
Aachen, NW, Germany
Last Updated: 09/26/2026
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Found 51 publications
JAK2V617F-positive clonal hematopoiesis in germline BRCA1 versus BRCA2 mutation carriers.
Journal: Leukemia
Published: March 24, 2026
Exome and Genome Sequencing for the Diagnosis of Rare Diseases.
Journal: Deutsches Arzteblatt international
Published: March 19, 2026
Tagungsbericht GfH-Juniorakademie 2025: Junge Humangenetik auf Schloss Buchenau: Austausch, Vernetzung und neue Perspektiven.
Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V
Published: February 19, 2026
RTEL1 mutation modifies dyskeratosis congenita caused by a telomerase RNA template mutation.
Journal: Nature communications
Published: February 16, 2026
Machine learning-based prediction of one-year mortality after alloHCT identifies the impact of pre-transplant immunity and inflammation.
Journal: Frontiers in immunology
Published: November 13, 2025
Allogeneic stem cell transplantation from variant-carrying family donors leads to long-term engraftment in Telomere Biology Disorders.
Journal: Blood cancer journal
Published: May 16, 2025
Application of machine learning in the diagnostic work-up of telomere biology disorders.
Journal: HemaSphere
Published: February 12, 2025
MDM4 haploinsufficiency leads to p53-mediated bone marrow failure.
Journal: Blood
Published: October 18, 2024
MDM4 HAPLOINSUFFICIENCY LEADS TO P53-MEDIATED BONE MARROW FAILURE.
Journal: Blood
Published: October 18, 2024
Late-onset telomere biology disorders in adults: clinical insights and treatment outcomes from a retrospective registry cohort.
Journal: Blood advances
Published: September 04, 2024
Benchmarking whole exome sequencing in the German network for personalized medicine.
Journal: European journal of cancer (Oxford, England : 1990)
Published: June 20, 2024
Last Updated: 09/26/2026