Bone progenitor dysfunction induces myelodysplasia and secondary leukaemia von Raaijmakers, Marc H. G. P., Mukherjee, Siddhartha, Guo, Shangqin, Zhang, Siyi, Kobayashi, Tatsuya, Schoonmaker, Jesse A., Ebert, Benjamin L., Al-Shahrour, Fatima, Hasserjian, Robert P., Scadden, Edward O., Aung, Zinmar, Matza, Marc, Merkenschlager, Matthias, Lin, Charles, Rommens, Johanna M., Scadden, David. T.

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Bone marrow inflammation in haematological malignancies von de Jong, Madelon M. E., Chen, Lanpeng, Raaijmakers, Marc H. G. P., Cupedo, Tom

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The mesenchymal niche in MDS von Pronk, Eline, Raaijmakers, Marc H.G.P.

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Quality of life and bariatric surgery: a systematic review of short- and long-term results and comparison with community norms von Raaijmakers, L C H, Pouwels, S, Thomassen, S E M, Nienhuijs, S W

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Specificity in Ras and Rap Signaling von Raaijmakers, Judith H., Bos, Johannes L.

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Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies von Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim

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Niche contributions to oncogenesis: emerging concepts and implications for the hematopoietic system von RAAIJMAKERS, Marc H. G. P

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Additive Value of Semiautomated Quantification of Coronary Artery Disease Using Cardiac Computed Tomographic Angiography to Predict Future Acute Coronary Syndrome von Versteylen, Mathijs O., MD, Kietselaer, Bas L., MD, PhD, Dagnelie, Pieter C., MS, PhD, Joosen, Ivo A., MD, Dedic, Admir, MD, Raaijmakers, Rolf H., RT, Wildberger, Joachim E., MD, PhD, Nieman, Koen, MD, PhD, Crijns, Harry J., MD, PhD, Niessen, Wiro J., MS, PhD, Daemen, Mat J., MD, PhD, Hofstra, Leonard, MD, PhD

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Rps14, Csnk1a1 and miRNA145/miRNA146a deficiency cooperate in the clinical phenotype and activation of the innate immune system in the 5q- syndrome von Ribezzo, Flavia, Snoeren, Inge A. M., Ziegler, Susanne, Stoelben, Jacques, Olofsen, Patricia A., Henic, Almira, Ferreira, Monica Ventura, Chen, Si, Stalmann, Ursula S. A., Buesche, Guntram, Hoogenboezem, Remco M., Kramann, Rafael, Platzbecker, Uwe, Raaijmakers, Marc H. G. P., Ebert, Benjamin L., Schneider, Rebekka K.

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Myeloid cells promote interferon signaling-associated deterioration of the hematopoietic system von Feyen, Jacqueline, Ping, Zhen, Chen, Lanpeng, van Dijk, Claire, van Tienhoven, Tim V. D., van Strien, Paulina M. H., Hoogenboezem, Remco M., Wevers, Michiel J. W., Sanders, Mathijs A., Touw, Ivo P., Raaijmakers, Marc H. G. P.

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Deficiency of the ribosome biogenesis gene Sbds in hematopoietic stem and progenitor cells causes neutropenia in mice by attenuating lineage progression in myelocytes von Zambetti, Noemi A, Bindels, Eric M J, Van Strien, Paulina M H, Valkhof, Marijke G, Adisty, Maria N, Hoogenboezem, Remco M, Sanders, Mathijs A, Rommens, Johanna M, Touw, Ivo P, Raaijmakers, Marc H G P

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ATP-binding-cassette transporters in hematopoietic stem cells and their utility as therapeutical targets in acute and chronic myeloid leukemia von Raaijmakers, M H G P

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Development of a Person-Centred Integrated Care Approach for Chronic Disease Management in Dutch Primary Care: A Mixed-Method Study von Raaijmakers, Lena H A, Schermer, Tjard R, Wijnen, Mandy, van Bommel, Hester E, Michielsen, Leslie, Boone, Floris, Vercoulen, Jan H, Bischoff, Erik W M A

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Myelodysplastic syndromes: revisiting the role of the bone marrow microenvironment in disease pathogenesis von Raaijmakers, Marc H. G. P.

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RUNX1 germline variants in RUNX1-mutant AML: how frequent? von Ernst, Martijn P.T., Kavelaars, François G., Löwenberg, Bob, Valk, Peter J.M., Raaijmakers, Marc H.G.P.

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CRISPR/Cas Applications in Myotonic Dystrophy: Expanding Opportunities von Raaijmakers, Renée H L, Ripken, Lise, Ausems, C Rosanne M, Wansink, Derick G

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Increased survival disparities among children and adolescents & young adults with acute myeloid leukemia: A Dutch population‐based study von Schulpen, Maya, Goemans, Bianca F., Kaspers, Gertjan J. L., Raaijmakers, Marc H. G. P., Zwaan, C. Michel, Karim‐Kos, Henrike E.

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Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies von Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim

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Massive parallel RNA sequencing of highly purified mesenchymal elements in low-risk MDS reveals tissue-context-dependent activation of inflammatory programs von Chen, S, Zambetti, N A, Bindels, E M J, Kenswill, K, Mylona, A M, Adisty, N M, Hoogenboezem, R M, Sanders, M A, Cremers, E M P, Westers, T M, Jansen, J H, van de Loosdrecht, A A, Raaijmakers, M H G P

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How Can a Bundled Payment Model Incentivize the Transition from Single-Disease Management to Person-Centred and Integrated Care for Chronic Diseases in the Netherlands? von Bour, Sterre S, Raaijmakers, Lena H A, Bischoff, Erik W M A, Goossens, Lucas M A, Rutten-van Mölken, Maureen P M H

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