Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

E. van Drunen · SciRah

Researcher profile · Semantic Scholar

E. van Drunen

Share profile

E. van Drunen — researcher profile on SciRah

h-index: 27
Works: 39
Citations: 4,832

Most-cited papers

Growth inhibition and DNA damage induced by Cre recombinase in mammalian cells
Ate Loonstra, M. Vooijs, H. Beverloo, Bushra Al Allak +4 more
2001Proceedings of the National Academy of Sciences of the United States of America634 citations Open access
Semantic Scholar
The Structure-Specific Endonuclease Ercc1-Xpf Is Required To Resolve DNA Interstrand Cross-Link-Induced Double-Strand Breaks
L. Niedernhofer, H. Odijk, Magda Budzowska, E. van Drunen +7 more
2004Molecular and Cellular Biology502 citations Open access
Semantic Scholar
The structure-specific endonuclease Mus81 contributes to replication restart by generating double-strand DNA breaks
K. Hanada, Magda Budzowska, S. Davies, E. van Drunen +6 more
2007Nature Structural &Molecular Biology421 citations
Semantic Scholar
A functional role for tumor cell heterogeneity in a mouse model of small cell lung cancer.
J. Calbó, E. van Montfort, N. Proost, E. van Drunen +3 more
2011Cancer Cell377 citations Open access
Semantic Scholar
Selective Inhibition of BRCA2-Deficient Mammary Tumor Cell Growth by AZD2281 and Cisplatin
B. Evers, R. Drost, Eva Schut, M. de Bruin +11 more
2008Clinical Cancer Research333 citations Open access
Semantic Scholar
ERCC1-XPF Endonuclease Facilitates DNA Double-Strand Break Repair
Anwaar Ahmad, A. Robinson, A. Duensing, E. van Drunen +5 more
2008Molecular and Cellular Biology308 citations Open access
Semantic Scholar
High EVI1 levels predict adverse outcome in acute myeloid leukemia: prevalence of EVI1 overexpression and chromosome 3q26 abnormalities underestimated.
S. Lugthart, E. van Drunen, Y. van Norden, A. V. van Hoven +5 more
2008Blood297 citations
Semantic Scholar
Genomic and expression profiling of human spermatocytic seminomas: primary spermatocyte as tumorigenic precursor and DMRT1 as candidate chromosome 9 gene.
L. Looijenga, R. Hersmus, Ad J. M. Gillis, R. Pfundt +14 more
2006Cancer Research225 citations
Semantic Scholar
TEL/AML1 gene fusion is related to in vitro drug sensitivity for L-asparaginase in childhood acute lymphoblastic leukemia.
N. L. Ramakers-van Woerden, R. Pieters, A. Loonen, I. Hubeek +10 more
2000Blood160 citations
Semantic Scholar
Further characterization of the first seminoma cell line TCam‐2
J. de Jong, H. Stoop, Ad J. M. Gillis, R. Hersmus +12 more
2008Genes, Chromosomes and Cancer148 citations
Semantic Scholar
Identification of NUP98 abnormalities in acute leukemia: JARID1A (12p13) as a new partner gene
L. V. van Zutven, Emine Önen, S. C. Velthuizen, E. van Drunen +7 more
2006Genes, Chromosomes and Cancer138 citations
Semantic Scholar
Molecular cytogenetic and clinical findings in ETV6/ABL1‐positive leukemia
H. Van Limbergen, H. Beverloo, E. van Drunen, A. Janssens +7 more
2001Genes, Chromosomes and Cancer125 citations
Semantic Scholar
Establishment and characterization of primary and metastatic uveal melanoma cell lines
G. Luyten, N. Naus, C. Mooy, A. Hagemeijer +5 more
1996International Journal of Cancer120 citations Open access
Semantic Scholar
Increased genomic instability is not a prerequisite for shortened lifespan in DNA repair deficient mice.
M. Dollé, R. Busuttil, A. García, S. Wijnhoven +6 more
2006Mutation research116 citations
Semantic Scholar
High incidence of t(7;12)(q36;p13) in infant AML but not in infant ALL, with a dismal outcome and ectopic expression of HLXB9
A. V. von Bergh, E. van Drunen, E. V. van Wering, L. V. van Zutven +5 more
2006Genes, Chromosomes and Cancer94 citations
Semantic Scholar
Detection of genetic prognostic markers in uveal melanoma biopsies using fluorescence in situ hybridization.
N. Naus, Anette C A Verhoeven, E. van Drunen, R. Slater +4 more
2002Clinical Cancer Research77 citations
Semantic Scholar
Fusion of the homeobox gene HLXB9 and the ETV6 gene in infant acute myeloid leukemias with the t(7;12)(q36;p13).
H. Beverloo, I. Panagopoulos, M. Isaksson, E. V. van Wering +4 more
2001Cancer Research75 citations
Semantic Scholar
Mutation of the mouse Rad17 gene leads to embryonic lethality and reveals a role in DNA damage‐dependent recombination
Magda Budzowska, Iris Jaspers, J. Essers, H. de Waard +8 more
2004EMBO Journal70 citations Open access
Semantic Scholar
Characterization of complex chromosomal abnormalities in uveal melanoma by fluorescence in situ hybridization, spectral karyotyping, and comparative genomic hybridization
N. Naus, E. van Drunen, A. de Klein, G. Luyten +5 more
2001Genes, Chromosomes and Cancer69 citations
Semantic Scholar
Dynamics of relative chromosome position during the cell cycle.
J. Essers, W. V. van Cappellen, A. Theil, E. van Drunen +5 more
2004Molecular Biology of the Cell66 citations Open access
Semantic Scholar
CDKN2 deletions have no prognostic value in childhood precursor-B acute lymphoblastic leukaemia
L. van Zutven, E. van Drunen, J. D. de Bont, M. M. Wattel +5 more
2005Leukemia64 citations Open access
Semantic Scholar
Rapid and sensitive detection of all types of MLL gene translocations with a single FISH probe set
M. V. D. van der Burg, H. Beverloo, A. Langerak, J. Wijsman +3 more
1999Leukemia62 citations Open access
Semantic Scholar
Segmental uniparental disomy as a recurrent mechanism for homozygous CEBPA mutations in acute myeloid leukemia
Bas J. Wouters, M. Sanders, S. Lugthart, W. Geertsma-Kleinekoort +5 more
2007Leukemia40 citations Open access
Semantic Scholar
Mutation analysis of the PTEN gene in uveal melanoma cell lines
N. Naus, W. Zuidervaart, Nazik Rayman, R. Slater +4 more
2000International Journal of Cancer39 citations Open access
Semantic Scholar
Integrated genome-wide genotyping and gene expression profiling reveals BCL11B as a putative oncogene in acute myeloid leukemia with 14q32 aberrations
Saman Abbas, M. Sanders, A. Zeilemaker, W. Geertsma-Kleinekoort +12 more
2014Haematologica31 citations Open access
Semantic Scholar
Selective Inhibition of BRCA 2-Deficient MammaryTumor Cell Growth byAZD 2281 and Cisplatin
B. Evers, R. Drost, Eva Schut, M. de Bruin +11 more
200831 citations
Semantic Scholar
ERCC 1-XPF Endonuclease Facilitates DNA Double-Strand Break Repair †
Anwaar Ahmad, A. Robinson, A. Duensing, E. van Drunen +5 more
200828 citations
Semantic Scholar
The response of mammalian cells to UV-light reveals Rad54-dependent and independent pathways of homologous recombination.
Berina Eppink, Agnieszka A. Tafel, K. Hanada, E. van Drunen +3 more
2011DNA Repair27 citations Open access
Semantic Scholar
Generation of a tightly regulated doxycycline‐inducible model for studying mouse intestinal biology
Sabrina Roth, P. Franken, W. van Veelen, L. Blonden +7 more
2009Genesis26 citations
Semantic Scholar
JKT-1 is not a human seminoma cell line.
J. de Jong, H. Stoop, A. Gillis, R. V. van Gurp +10 more
2007International Journal of Andrology26 citations Open access
Semantic Scholar
Specific cytogenetic aberrations in two novel human prostatic cell lines immortalized by human papillomavirus type 18 DNA.
P. Weijerman, E. van Drunen, Josée J. König, Wilma Teubel +3 more
1997Cancer Genetics and Cytogenetics24 citations Open access
Semantic Scholar
Novel murine B‐cell lymphoma/leukemia model to study BCL2‐driven oncogenesis
J. Meijerink, E. V. Van Lieshout, H. Beverloo, E. van Drunen +3 more
2005International Journal of Cancer21 citations Open access
Semantic Scholar
Gene expression profiling and gene copy‐number changes in malignant mesothelioma cell lines
C. Zanazzi, R. Hersmus, I. Veltman, Ad J. M. Gillis +7 more
2007Genes, Chromosomes and Cancer18 citations
Semantic Scholar
Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183)
M. Mulder, M. Wilke, A. Langeveld, L. Wilming +8 more
1995Human Genetics15 citations Open access
Semantic Scholar
Constitutional DNA‐level aberrations in chromosome 22 in a patient with multiple meningiomas
R. L. Lekanne Deprez, N. Groen, D. Louz, T. van der Kwast +6 more
1994Genes, Chromosomes and Cancer13 citations
Semantic Scholar
NBS1 cooperates with homologous recombination to counteract chromosome breakage during replication
L. Brugmans, Nicole S. Verkaik, M. Kunen, E. van Drunen +5 more
2009DNA Repair11 citations Open access
Semantic Scholar
High Incidence of t(7;12)(q36;p13) with Involvement of HLXB9 in Infant AML.
A. V. von Bergh, E. van Drunen, E. V. van Wering, J. Meijerink +2 more
20051 citations
Semantic Scholar
Positional mapping of loci in the DiGeorge critical region at chromosome 22 q l l using a new marker ( D 22 S 183 )
M. Mulder, M. Wilke, L. Wilming, A. Hagemeijer +8 more
20031 citations
Semantic Scholar
T1768 Generation of a Tightly Regulated Doxycycline-Inducible Model for Studying Mouse Intestinal Biology
Sabrina Roth, P. Franken, W. van Veelen, L. Blonden +7 more
20090 citations
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

H. Beverloo×18
Invite
H. Beverloo — researcher profile on SciRah
R. Kanaar×7
Invite
R. Kanaar — researcher profile on SciRah
A. Hagemeijer×7
Invite
A. Hagemeijer — researcher profile on SciRah
J. Hoeijmakers×6
Invite
J. Hoeijmakers — researcher profile on SciRah

×5

Invite

J. Essers — researcher profile on SciRah

Invite

R. Slater — researcher profile on SciRah

L. Niedernhofer×4

Invite

L. Niedernhofer — researcher profile on SciRah

H. B. Beverloo×4

Invite

H. B. Beverloo — researcher profile on SciRah

L. Looijenga×4

Invite

L. Looijenga — researcher profile on SciRah

E. V. van Wering×4

Invite

E. V. van Wering — researcher profile on SciRah

Invite

N. Naus — researcher profile on SciRah

Invite

A. de Klein — researcher profile on SciRah