Rutger W. W. Brouwer

Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells

Jessica Zuin, Jesse R. Dixon, Michael I. J. A. van der Reijden et al. · Proceedings of the National Academy of Sciences · 2013 · 813 citations · Full text

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

Marije Meuwissen, Rachel Schot, Sofija Buta et al. · The Journal of Experimental Medicine · 2016 · 278 citations · Full text

Disease Etiology, Genetics, Pseudo-torch Syndrome +17

Clinical significance of immunohistochemistry for detection of BAP1 mutations in uveal melanoma

Anna E. Koopmans, Robert M. Verdijk, Rutger W. W. Brouwer et al. · Modern Pathology · 2014 · 219 citations

Uveal Melanoma, Photocarcinogenesis, Melanoma +6

LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

Marialuisa Quadri, Wim Mandemakers, Martyna M. Grochowska et al. · The Lancet Neurology · 2018 · 159 citations

Neurodegenerative Diseases, Genetic Disorder, Genetics +9

Multiplexed chromosome conformation capture sequencing for rapid genome-scale high-resolution detection of long-range chromatin interactions

Ralph Stadhouders, Petros Kolovos, Rutger W. W. Brouwer et al. · Nature Protocols · 2013 · 150 citations

Long-read Sequencing, Chromatin, Chromatin Remodeling +9