Author details

Full Name

Bert A van der Reijden

Affiliation

ORCID

Career Start Year

1993

Papers

129

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37190104	Inducible MLL-AF9 Expression Drives an AML Program during Human Pluripotent Stem Cell-Derived Hematopoietic Differentiation.		2023
37731314	BCR::ABL1 kinase domain mutation testing and clinical outcome in a nationwide chronic myeloid leukemia patient population.		2023
37720253	Clonal Hematopoiesis Defined by Somatic Mutations Infrequently Co-occurs With Mosaic Loss of the Y Chromosome in a Population-based Cohort.		2023
37713242	Improvement, Implementation, and Evaluation of the CMyLife Digital Care Platform: Participatory Action Research Approach.		2023
37632778	Clonal hematopoiesis and UBA1 mutations in individuals with biopsy-proven giant cell arteritis and population-based controls.		2023
36713353	Sex Differences in the Spectrum of Clonal Hematopoiesis.		2023
37146604	Evolutionary landscape of clonal hematopoiesis in 3,359 individuals from the general population.	Cancer Cell	2023
36890512	Effectiveness of digital care platform CMyLife for patients with chronic myeloid leukemia: results of a patient-preference trial.		2023
36698617	Abnormal Platelet Counts and Clonal Hematopoiesis in the General Population.		2023
36807648	High expression of an intragenic long noncoding RNA misinterpreted as high FTO oncogene expression in NPM1 mutant acute myeloid leukemia.		2023
35024892	Genetic diversity within leukemia-associated immunophenotype-defined subclones in AML.	Annals of Hematology	2022
35561316	Monocytosis and its association with clonal hematopoiesis in community-dwelling individuals.	Blood Adv	2022
34724563	2021 Update on MRD in acute myeloid leukemia: a consensus document from the European LeukemiaNet MRD Working Party.	Blood	2021
33690840	Specific proteome changes in platelets from individuals with GATA1-, GFI1B-, and RUNX1-linked bleeding disorders.	Blood	2021
33725274	Purging human ovarian cortex of contaminating leukaemic cells by targeting the mitotic catastrophe signalling pathway.		2021
33877299	Prevalence, predictors, and outcomes of clonal hematopoiesis in individuals aged â¿¥80 years.	Blood advances	2021
33496751	Neutrophil specific granule and NETosis defects in gray platelet syndrome.	Blood Adv	2021
33359455	Multicenter Next-Generation Sequencing Studies between Theory and Practice: Harmonization of Data Analysis Using Real-World Myelodysplastic Syndrome Data.	J Mol Diagn	2021
34459888	Peripheral blood cytopenias in the aging general population and risk of incident hematological disease and mortality.	Blood Adv	2021
34450246	Characterization of a genomic region 8Â kb downstream of GFI1B associated with myeloproliferative neoplasms.		2021
33054062	Transcription factor 4 () expression predicts clinical outcome in mutated and translocated acute myeloid leukemia.	Haematologica	2020
32243522	Mutational spectrum and dynamics of clonal hematopoiesis in anemia of older individuals.	Blood	2020
32124467	Platelet CD34 expression in a patient with a partial deletion of transcription factor subunit CBFB.	American Journal of Hematology	2020
32730581	A collapse for venous thromboembolism.	Blood	2020
30673601	Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes.	Cell Rep	2019
31649884	Targeting the GFI1/1B-CoREST Complex in Acute Myeloid Leukemia.	Frontiers in Oncology	2019
30315825	TCF4 promotes erythroid development.	Experimental Hematology	2019
30431218	Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis.	Haemophilia	2019
30573501	Inherited missense variants that affect GFI1B function do not necessarily cause bleeding diatheses.	Haematologica	2019
30655368	Molecular mechanisms of bleeding disorderassociated GFI1B mutation and its affected pathways in megakaryocytes and platelets.	Haematologica	2019
30850577	CBFÎ²-MYH11 interferes with megakaryocyte differentiation via modulating a gene program that includes GATA2 and KLF1.	Blood Cancer Journal	2019
29330221	Minimal/measurable residual disease in AML: a consensus document from the European LeukemiaNet MRD Working Party.	Blood	2018
28983057	Introducing high-throughput sequencing into mainstream genetic diagnosis practice in inherited platelet disorders.	Haematologica	2018
28871137	C-terminal BRE overexpression in 11q23-rearranged and t(8;16) acute myeloid leukemia is caused by intragenic transcription initiation.	Leukemia	2018
29945233	appreci8: a pipeline for precise variant calling integrating 8 tools.	Bioinformatics	2018
29674496	GFI1 is required for <i>RUNX1/ETO</i> positive acute myeloid leukemia.	Haematologica	2018
29311096	Early detection and evolution of preleukemic clones in therapy-related myeloid neoplasms following autologous SCT.	Blood	2018
28114278	MLL-AF9 and MLL-AF4 oncofusion proteins bind a distinct enhancer repertoire and target the RUNX1 program in 11q23 acute myeloid leukemia.	Oncogene	2017
28429724	Clonal evolution in myelodysplastic syndromes.	Nat Commun	2017
29055225	Generation and characterization of a human iPSC line SANi005-A containing the gray platelet associated heterozygous mutation p.Q287* in GFI1B.	Stem Cell Research	2017
28395797	Generation and characterization of human iPSC line MML-6838-Cl2 from mobilized peripheral blood derived megakaryoblasts.	Stem Cell Res	2017
27416910	Comparative value of post-remission treatment in cytogenetically normal AML subclassified by NPM1 and FLT3-ITD allelic ratio.	Leukemia	2017
28280089	Successful Transfer of Umbilical Cord Blood CD34 Hematopoietic Stem and Progenitor-derived NK Cells in Older Acute Myeloid Leukemia Patients.	Clinical Cancer Research	2017
28236351	Genomic array as compared to karyotyping in myelodysplastic syndromes in a prospective clinical trial.	Genes Chromosomes and Cancer	2017
28222155	GLM-based optimization of NGS data analysis: A case study of Roche 454, Ion Torrent PGM and Illumina NextSeq sequencing data.	PLoS ONE	2017
28233799	Evaluating Variant Calling Tools for Non-Matched Next-Generation Sequencing Data.	Scientific Reports	2017
28096094	Platelet CD34 expression and Î±/Î´-granule abnormalities in - and -related familial bleeding disorders.	Blood	2017
27902785	Apoptosis-Related Gene Expression Profiling in Hematopoietic Cell Fractions of MDS Patients.	PLoS One	2016
27080012	GFI1(36N) as a therapeutic and prognostic marker for myelodysplastic syndrome.	Exp Hematol	2016
25579174	5-Hydroxymethylcytosine: An epigenetic mark frequently deregulated in cancer.		2015