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dr. A. Buijs

dr. A. Buijs

Research Analyst
  • Section genome diagnostics

Research Programs

Strategic Program Cancer

Research Output (85)

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

van Engelen N., van Dijk F., Waanders E., Buijs A., Vermeulen M. A., Loeffen J. L.C., Kuiper R. P., Jongmans M. C.J. okt 2021, In: Familial cancer. 20 , p. 349-354 6 p.

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

van der Veken Lars T., Maiburg Merel C., Groenendaal Floris, van Gijn Mariëlle E., Bloem Andries C., Erpelinck Claudia, Gröschel Stefan, Sanders Mathijs A., Delwel Ruud, Bierings Marc B., Buijs Arjan 8 feb 2018, In: Haematologica. 103 , p. e173-e176

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

Hochstenbach Ron, van Binsbergen Ellen, Schuring-Blom Heleen, Buijs Arjan, Ploos van Amstel Hans Kristian 1 jan 2018, In: European Journal of Medical Genetics. 62

Lymphoblastic lymphoma with a triple-hit profile:a rare but distinct and relevant entity

Hiemcke-Jiwa Laura S., Leguit RJ, van der Veken Lars T., Buijs A, Leeuwis JW, de Boer Mirthe, Jiwa Mehdi, Bloem AC, Clevers-Petersen E.J., de Weger Roel A., Huibers Manon M.H. mei 2017, In: Human Pathology. 63 , p. 171-176 6 p.

A neonate with a unique non-Down syndrome transient proliferative megakaryoblastic disease

Bertrums Eline J M, Buijs Arjan, van Grotel Martine, Dors Natasja, de Rooij Jasmijn D E, de Haas Valerie, Hopman Sanne, Jongmans Marjolijn C J, Zwaan C M, van den Heuvel-Eibrink Marry M 2017, In: Pediatric Blood & Cancer. 64

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

Franssen Laurens E, Raijmakers Reinier A P, Buijs Arjan, Schmitz Marian F, van Dorp Suzanne, Mutis Tuna, Lokhorst Henk M, van de Donk Niels W C J 2016, In: European Journal of Haematology. 97 , p. 479–488

Sequential cancer mutations in cultured human intestinal stem cells

Drost Jarno, van Jaarsveld Richard H. , Ponsioen Bas, Zimberlin Cheryl, van Boxtel Ruben, Buijs Arjan, Sachs Norman, Overmeer Rene M., Offerhaus G. Johan, Begthel Harry, Korving Jeroen, van de Wetering Marc, Schwank Gerald, Logtenberg Meike, Cuppen Edwin, Snippert Hugo J., Medema Jan Paul, Kops Geert J. P. L., Clevers Hans 7 mei 2015, In: Nature. 521 , p. 43-U329 23 p.

Novel 3q26 EVI1/MECOM deletion syndrome in a newborn with multiple severe congenital abnormalities and bone marrow failure

van der Veken L.T.J.N., Bierings M.B., Maiburg M.C., Groenendaal F., Bloem A.C., Knoers N.V.A.M., Buijs A. 13 jun 2013,

A ZMYM2-FGFR1 8p11 myeloproliferative neoplasm with a novel nonsense RUNX1 mutation and tumor lysis upon imatinib treatment

Buijs A., van Wijnen M., van den Blink D., van Gijn M.E., Klein S.K. 2013, In: Cancer Genetics and Cytogenetics. 206 , p. 140-144 5 p.

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

Broyl A., Kuiper R., van Duin M., van der Holt B., el Jarari L., Bertsch U., Zweegman S., Buijs A., Hose D., Lokhorst H.M., Goldschmidt H., HOVON Dutch-Belgian Hematology-Oncology Group x, Sonneveld P. 2013, In: Blood. 121 , p. 624-627 4 p.

All research output

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