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Arjan Buijs

Utrecht University

33

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567

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Elevated Enhancer-Oncogene Contacts and Higher Oncogene Expression Levels by Recurrent CTCF Inactivating Mutations in Acute T Cell Leukemia

2021 Social Science Research Network
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Constitutional 2p16.3 deletion including MSH6 and FBXO11 in a boy with developmental delay and diffuse large B-cell lymphoma.

2021 Familial Cancer
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Guideline for management of non-Down syndrome neonates with a myeloproliferative disease on behalf of the I-BFM AML Study Group and EWOG-MDS.

2020 Haematologica
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Lethal neonatal bone marrow failure syndrome with multiple congenital abnormalities, including limb defects, due to a constitutional deletion of 3’ MECOM

2018 Haematologica
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A survey of undetected, clinically relevant chromosome abnormalities when replacing postnatal karyotyping by Whole Genome Sequencing

2018 European Journal of Medical Genetics
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A neonate with a unique non-Down syndrome transient proliferative megakaryoblastic disease

2017 Pediatric Blood & Cancer
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Lymphoblastic lymphoma with a triple-hit profile: a rare but distinct and relevant entity

2017 Human Pathology
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Outcome of allogeneic transplantation in newly diagnosed and relapsed/refractory multiple myeloma: long-term follow-up in a single institution

2016 European Journal of Haematology
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Paired Analyses of Diagnostic and Relapse Samples of MLL rearranged Infant Acute Lymphoblastic Leukemia Reveals Potential Therapy-Resistant Genomic Alterations

2014 Blood
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High cereblon expression is associated with better survival in patients with newly diagnosed multiple myeloma treated with thalidomide maintenance

2013 Blood
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Citations (102)