Concepedia

Author

Arjan Buijs

University Medical Center Utrecht

Also Known As

A Buijs, A. Buijs, A.‐M. Buijs, Arjan Buijs

63

Publications

4.4K

Citations

23

H-Index

38

Concepts

All Affiliations

University Medical Center UtrechtSt. Jude Children's Research HospitalErasmus University RotterdamUtrecht UniversityAmsterdam UMC Location University of Amsterdam
AB

About

Arjan Buijs is an author at University Medical Center Utrecht specializing in medicine, cell biology, and gene expression.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

10

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2K

2

Cell Biology

8

8

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3

Natural Sciences

4

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473

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Molecular Biology

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473

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Immunology

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278

Arjan Buijs

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27

Publications

4.2K

Citations

21

H-Index

YearCitations

Sequential cancer mutations in cultured human intestinal stem cells

Jarno Drost, Richard H. van Jaarsveld, Bas Ponsioen,

Nature

2015

1.1K

TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis.

Sheila Shurtleff, Arjan Buijs, F G Behm,

PubMed

1995

561

The translocation (6;9), associated with a specific subtype of acute myeloid leukemia, results in the fusion of two genes, dek and can, and the expression of a chimeric, leukemia-specific dek-can mRNA.

Marieke von Lindern, Maarten Fornerod, Sjozèf van Baal,

Molecular and Cellular Biology

1992

377

Gene expression profiling for molecular classification of multiple myeloma in newly diagnosed patients

Annemiek Broyl, Dirk Hose, Henk M. Lokhorst,

Blood

2010

336

The t(12;21) Translocation Converts AML-1B from an Activator to a Repressor of Transcription

Scott W. Hiebert, Wuhua Sun, J. Nathan Davis,

Molecular and Cellular Biology

1996

278

TEL gene rearrangement in acute lymphoblastic leukemia: a new genetic marker with prognostic significance.

Jeffrey E. Rubnitz, James R. Downing, C-H Pui,

Journal of Clinical Oncology

1997

205

Relocation of the carboxyterminal part of CAN from the nuclear envelope to the nucleus as a result of leukemia-specific chromosome rearrangements.

Maarten Fornerod, Judith M. Boer, Sjozèf van Baal,

PubMed

1995

160

A novel CBFA2 single-nucleotide mutation in familial platelet disorder with propensity to develop myeloid malignancies

Arjan Buijs, Pino J. Poddighe, Richard van Wijk,

Blood

2001

132

Reconstructing the human hematopoietic niche in immunodeficient mice: opportunities for studying primary multiple myeloma

Richard W.J. Groen, Willy A. Noort, Reinier Raymakers,

Blood

2012

129

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

Annemiek Broyl, Rowan Kuiper, Mark van Duin,

Blood

2012

128

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