| 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 | 1405 | 2008 |
| 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 | 917 | 2014 |
| 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 | 442 | 2017 |
| 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 genetics 5 (11), e1000739, 2009 | 404 | 2009 |
| 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 | 179 | 2013 |
| 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 genetics 10 (2), e1004153, 2014 | 153 | 2014 |
| How cohesin and CTCF cooperate in regulating gene expression KS Wendt, JM Peters Chromosome research 17, 201-214, 2009 | 129 | 2009 |
| 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 | 123 | 2003 |
| 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 | 104 | 2001 |
| 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, 1-17, 2014 | 96 | 2014 |
| 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 | 95 | 2016 |
| RNA polymerase II is required for spatial chromatin reorganization following exit from mitosis S Zhang, N Übelmesser, N Josipovic, G Forte, JA Slotman, M Chiang, ... Science advances 7 (43), eabg8205, 2021 | 92 | 2021 |
| Mutations in chromatin regulators functionally link Cornelia de Lange syndrome and clinically overlapping phenotypes I Parenti, ME Teresa-Rodrigo, J Pozojevic, S Ruiz Gil, I Bader, ... Human genetics 136, 307-320, 2017 | 85 | 2017 |
| 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 | 82 | 2016 |
| Redundant and specific roles of cohesin STAG subunits in chromatin looping and transcriptional control V Casa, MM Gines, EG Gusmao, JA Slotman, A Zirkel, N Josipovic, E Oole, ... Genome Research 30 (4), 515-527, 2020 | 77 | 2020 |
| 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, 199-210, 2008 | 74 | 2008 |
| Cohesin complex-associated holoprosencephaly P Kruszka, SI Berger, V Casa, MR Dekker, J Gaesser, K Weiss, ... Brain 142 (9), 2631-2643, 2019 | 59 | 2019 |
| 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 | 53 | 2016 |
| MAU2 and NIPBL variants impair the heterodimerization of the cohesin loader subunits and cause Cornelia de Lange syndrome I Parenti, F Diab, SR Gil, E Mulugeta, V Casa, R Berutti, RWW Brouwer, ... Cell reports 31 (7), 2020 | 52 | 2020 |
| Transcription in the context of the 3D nucleus KS Wendt, FG Grosveld Current opinion in genetics & development 25, 62-67, 2014 | 47 | 2014 |
