Citation Impact
Citing Papers
The Spatial Organization of the Human Genome
2013
Co-incidence of RCC-susceptibility polymorphisms with HIF cis-acting sequences supports a pathway tuning model of cancer
2019 StandoutNobel
Capture‐C reveals preformed chromatin interactions between HIF ‐binding sites and distant promoters
2016 StandoutNobel
Genetic variation at the 8q24.21 renal cancer susceptibility locus affects HIF binding to a MYC enhancer
2016 StandoutNobel
A decade of 3C technologies: insights into nuclear organization
2012
The molecular hallmarks of epigenetic control
2016 Standout
Transcriptional architecture of the mammalian circadian clock
2016 Standout
Long-Range Chromatin Interactions
2015
Multiplexed analysis of chromosome conformation at vastly improved sensitivity
2015
Epigenetic modulators, modifiers and mediators in cancer aetiology and progression
2016
Chromatin regulation at the frontier of synthetic biology
2015
Chromatin-Driven Behavior of Topologically Associating Domains
2014
The complex transcription regulatory landscape of our genome: control in three dimensions
2011
Cancer Epigenetics: From Mechanism to Therapy
2012 Standout
Mutation profile of theGAA gene in 40 Italian patients with late onset glycogen storage disease type II
2006
Single-Molecule Dynamics of Enhanceosome Assembly in Embryonic Stem Cells
2014 StandoutNobel
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Hypoxia drives glucose transporter 3 expression through hypoxia-inducible transcription factor (HIF)–mediated induction of the long noncoding RNA NICI
2019 StandoutNobel
The Hierarchy of the 3D Genome
2013
The 3D Genome as Moderator of Chromosomal Communication
2016
A misplaced lncRNA causes brachydactyly in humans
2012
Transcription factors: from enhancer binding to developmental control
2012 Standout
Higher-order chromatin structure: bridging physics and biology
2012
Frequency of glycogen storage disease type II in The Netherlands: implications for diagnosis and genetic counselling
1999
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
2016 Standout
Three-Dimensional Folding and Functional Organization Principles of the Drosophila Genome
2012
Click-EM for imaging metabolically tagged nonprotein biomolecules
2016 StandoutNobel
Topological domains in mammalian genomes identified by analysis of chromatin interactions
2012 StandoutNature
22q11.2 deletion syndrome
2015 Standout
TNFα signals through specialized factories where responsive coding and miRNA genes are transcribed
2012
ATAC-see reveals the accessible genome by transposase-mediated imaging and sequencing
2016 StandoutNobel
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
2014 Standout
Long Noncoding RNAs: Cellular Address Codes in Development and Disease
2013 Standout
Spatial partitioning of the regulatory landscape of the X-inactivation centre
2012 StandoutNature
Multiple renal cancer susceptibility polymorphisms modulate the HIF pathway
2017 StandoutNobel
Genome Architecture: Domain Organization of Interphase Chromosomes
2013
The 11q terminal deletion disorder: A prospective study of 110 cases
2004
Transcription Factories: Genome Organization and Gene Regulation
2013
The Natural Course of Infantile Pompe’s Disease: 20 Original Cases Compared With 133 Cases From the Literature
2003
2011 ACCF/AHA Guideline for the Diagnosis and Treatment of Hypertrophic Cardiomyopathy
2011 Standout
Combination therapy in combating cancer
2017 Standout
3D imaging of Sox2 enhancer clusters in embryonic stem cells
2014 StandoutNobel
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Works of Bert Eussen being referenced
Variegated gene expression caused by cell-specific long-range DNA interactions
2011
Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome
1992
The effect of a single base pair deletion (ΔT525) and a C1634T missense mutation (pro545leu) on the expression of lysosomal α-glucosidase in patients with glycogen storage disease type II
1994