Kerstin Wendt
Kerstin Wendt
Erasmus University Medical Center
Verified email at erasmusmc.nl
Title
Cited by
Cited by
Year
Cohesin mediates transcriptional insulation by CCCTC-binding factor
KS Wendt, K Yoshida, T Itoh, M Bando, B Koch, E Schirghuber, ...
Nature 451 (7180), 796-801, 2008
11682008
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells
J Zuin, JR Dixon, MIJA van der Reijden, Z Ye, P Kolovos, RWW Brouwer, ...
Proceedings of the National Academy of Sciences 111 (3), 996-1001, 2014
6722014
Cohesin is required for higher-order chromatin conformation at the imprinted IGF2-H19 locus
R Nativio, KS Wendt, Y Ito, JE Huddleston, S Uribe-Lewis, K Woodfine, ...
PLoS Genet 5 (11), e1000739, 2009
3612009
Dynamic organization of chromatin domains revealed by super-resolution live-cell imaging
T Nozaki, R Imai, M Tanbo, R Nagashima, S Tamura, T Tani, Y Joti, ...
Molecular cell 67 (2), 282-293. e7, 2017
2302017
Multiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions
R Stadhouders, P Kolovos, R Brouwer, J Zuin, A Van Den Heuvel, ...
Nature protocols 8 (3), 509-524, 2013
1532013
How cohesin and CTCF cooperate in regulating gene expression
KS Wendt, JM Peters
Chromosome research 17 (2), 201-214, 2009
1182009
Identification of a subunit of a novel kleisin-β/SMC complex as a potential substrate of protein phosphatase 2A
FM Yeong, H Hombauer, KS Wendt, T Hirota, I Mudrak, K Mechtler, ...
Current Biology 13 (23), 2058-2064, 2003
1122003
A cohesin-independent role for NIPBL at promoters provides insights in CdLS
J Zuin, V Franke, WFJ van IJcken, A Van Der Sloot, ID Krantz, ...
PLoS Genet 10 (2), e1004153, 2014
1042014
Crystal structure of the APC10/DOC1 subunit of the human anaphase-promoting complex
KS Wendt, HC Vodermaier, U Jacob, C Gieffers, M Gmachl, JM Peters, ...
Nature structural biology 8 (9), 784-788, 2001
962001
Targeted Chromatin Capture (T2C): a novel high resolution high throughput method to detect genomic interactions and regulatory elements
P Kolovos, HJG van de Werken, N Kepper, J Zuin, RWW Brouwer, ...
Epigenetics & chromatin 7 (1), 1-17, 2014
712014
The Suv39h–HP1 histone methylation pathway is dispensable for enrichment and protection of cohesin at centromeres in mammalian cells
B Koch, S Kueng, C Ruckenbauer, KS Wendt, JM Peters
Chromosoma 117 (2), 199-210, 2008
682008
Gene regulation and chromatin organization: relevance of cohesin mutations to human disease
E Watrin, FJ Kaiser, KS Wendt
Current opinion in genetics & development 37, 59-66, 2016
632016
Broadening of cohesinopathies: exome sequencing identifies mutations in ANKRD11 in two patients with Cornelia de Lange‐overlapping phenotype
I Parenti, C Gervasini, J Pozojevic, L Graul‐Neumann, J Azzollini, ...
Clinical Genetics 89 (1), 74-81, 2016
632016
Hyperfine structure and isotope shift of the neutron-rich barium isotopes 139–146 Ba and 148 Ba
K Wendt, SA Ahmad, C Ekström, W Klempt, R Neugart, EW Otten
Zeitschrift für Physik A Atomic Nuclei 329 (4), 407-411, 1988
481988
Crystal structure of the carboxyltransferase subunit of the bacterial sodium ion pump glutaconyl‐coenzyme A decarboxylase
KS Wendt, I Schall, R Huber, W Buckel, U Jacob
The EMBO journal 22 (14), 3493-3502, 2003
472003
Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes
I Parenti, ME Teresa-Rodrigo, J Pozojevic, SR Gil, I Bader, D Braunholz, ...
Human genetics 136 (3), 307-320, 2017
462017
Transcription in the context of the 3D nucleus
KS Wendt, FG Grosveld
Current opinion in genetics & development 25, 62-67, 2014
452014
Expanding the clinical spectrum of the ‘HDAC8‐phenotype’ – implications for molecular diagnostics, counseling and risk prediction
I Parenti, C Gervasini, J Pozojevic, KS Wendt, E Watrin, J Azzollini, ...
Clinical genetics 89 (5), 564-573, 2016
382016
Hidden Mutations in C ornelia de L ange Syndrome Limitations of S anger Sequencing in Molecular Diagnostics
D Braunholz, C Obieglo, I Parenti, J Pozojevic, J Eckhold, B Reiz, ...
Human mutation 36 (1), 26-29, 2015
282015
Cohesin complex-associated holoprosencephaly
P Kruszka, SI Berger, V Casa, MR Dekker, J Gaesser, K Weiss, ...
Brain 142 (9), 2631-2643, 2019
242019
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