R.W.W. Brouwer
R.W.W. Brouwer
ErasmusMC
Verified email at erasmusmc.nl
Title
Cited by
Cited by
Year
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
6762014
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
1542013
Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome
MEC Meuwissen, R Schot, S Buta, G Oudesluijs, S Tinschert, SD Speer, ...
Journal of Experimental Medicine 213 (7), 1163-1174, 2016
1532016
Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma
AE Koopmans, RM Verdijk, RWW Brouwer, TPP Van Den Bosch, ...
Modern pathology 27 (10), 1321-1330, 2014
1522014
Contribution of rare and common variants determine complex diseases—Hirschsprung disease as a model
MM Alves, Y Sribudiani, RWW Brouwer, J Amiel, G Antiņolo, S Borrego, ...
Developmental biology 382 (1), 320-329, 2013
1192013
The relative value of operon predictions
RWW Brouwer, OP Kuipers, SAFT van Hijum
Briefings in bioinformatics 9 (5), 367-375, 2008
1182008
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
Loss of LMOD1 impairs smooth muscle cytocontractility and causes megacystis microcolon intestinal hypoperistalsis syndrome in humans and mice
D Halim, MP Wilson, D Oliver, E Brosens, JBGM Verheij, Y Han, V Nanda, ...
Proceedings of the National Academy of Sciences 114 (13), E2739-E2747, 2017
692017
Genome-wide DNA methylation profiling of non-small cell lung carcinomas
RH Carvalho, V Haberle, J Hou, T van Gent, S Thongjuea, W van IJcken, ...
Epigenetics & chromatin 5 (1), 1-18, 2012
692012
LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
M Quadri, W Mandemakers, MM Grochowska, R Masius, H Geut, ...
The Lancet Neurology 17 (7), 597-608, 2018
622018
Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study
D Van Opstal, MC Van Maarle, K Lichtenbelt, MM Weiss, ...
Genetics in Medicine 20 (5), 480-485, 2018
602018
Targeted Next Generation Sequencing reveals previously unidentified TSC1 and TSC2 mutations
M Nellist, RWW Brouwer, CEM Kockx, M van Veghel-Plandsoen, ...
BMC medical genetics 16 (1), 1-11, 2015
582015
NARWHAL, a primary analysis pipeline for NGS data
RWW Brouwer, M van den Hout, FG Grosveld, WFJ van IJcken
Bioinformatics 28 (2), 284-285, 2012
582012
Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes
H Gui, D Schriemer, WW Cheng, RK Chauhan, G Antiňolo, C Berrios, ...
Genome biology 18 (1), 1-13, 2017
552017
PLD3 variants in population studies
SJ Van der Lee, H Holstege, TH Wong, J Jakobsdottir, JC Bis, V Chouraki, ...
Nature 520 (7545), E2-E3, 2015
552015
Loss-of-function variants in MYLK cause recessive megacystis microcolon intestinal hypoperistalsis syndrome
D Halim, E Brosens, F Muller, MF Wangler, AL Beaudet, JR Lupski, ...
The American Journal of Human Genetics 101 (1), 123-129, 2017
482017
Sp1/Sp3 transcription factors regulate hallmarks of megakaryocyte maturation and platelet formation and function
M Meinders, DI Kulu, HJG van de Werken, M Hoogenboezem, H Janssen, ...
Blood, The Journal of the American Society of Hematology 125 (12), 1957-1967, 2015
482015
ACTG2 variants impair actin polymerization in sporadic Megacystis Microcolon Intestinal Hypoperistalsis Syndrome
D Halim, RMW Hofstra, L Signorile, RM Verdijk, CS van der Werf, ...
Human molecular genetics 25 (3), 571-583, 2016
472016
Exome-sequencing in a large population-based study reveals a rare Asn396Ser variant in the LIPG gene associated with depressive symptoms
N Amin, O Jovanova, HHH Adams, A Dehghan, M Kavousi, MW Vernooij, ...
Molecular Psychiatry 22 (4), 537-543, 2017
422017
A novel complex, RUNX1-MYEF2, represses hematopoietic genes in erythroid cells
B van Riel, T Pakozdi, R Brouwer, R Monteiro, K Tuladhar, V Franke, ...
Molecular and cellular biology 32 (19), 3814-3822, 2012
352012
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