van Ijcken, Wilfred F.J.
Erasmus MC
15 papers on CoChatORCID 0000-0002-0421-8301
Most cited papers
- Verified
Sox2 cooperates with Chd7 to regulate genes that are mutated in human syndromes
Engelen, E., Akinci, U., Bryne, J. C., Hou, J., Gontan, C., Moen, M., Szumska, D., Kockx, C., van IJcken, W., Dekkers, D. H. W., et al. (2011) · Nature Genetics
Congenital Ear and Nasal AnomaliesDevelopmental Biology and Gene Regulation
Cited by 255
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PRC2 Facilitates the Regulatory Topology Required for Poised Enhancer Function during Pluripotent Stem Cell Differentiation
Cruz-Molina, S., Respuela, P., Tebartz, C., Kolovos, P., Nikolic, M., Fueyo, R., van Ijcken, W. F. J., Grosveld, F., Frommolt, P., Bazzi, H., et al. (2017) · Cell Stem Cell
Pluripotent Stem Cells ResearchGenomics and Chromatin Dynamics
Cited by 240
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Delayed and Accelerated Aging Share Common Longevity Assurance Mechanisms
Schumacher, B., van der Pluijm, I., Moorhouse, M. J., Kosteas, T., Robinson, A. R., Suh, Y., Breit, T. M., van Steeg, H., Niedernhofer, L. J., van IJcken, W., et al. (2008) · PLoS Genetics
Genetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence
Cited by 212
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Snail regulates MyoD binding-site occupancy to direct enhancer switching and differentiation-specific transcription in myogenesis
Soleimani, V. D., Yin, H., Jahani-Asl, A., Ming, H., Kockx, C. E. M., van Ijcken, W. F. J., Grosveld, F., & Rudnicki, M. A. (2012) · Molecular Cell
Genomics and Chromatin DynamicsMuscle Physiology and Disorders
Cited by 200
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Two independent transcription initiation codes overlap on vertebrate core promoters
Haberle, V., Li, N., Hadzhiev, Y., Plessy, C., Previti, C., Nepal, C., Gehrig, J., Dong, X., Akalin, A., Suzuki, A. M., et al. (2014) · Nature
Genomics and Chromatin DynamicsDevelopmental Biology and Gene Regulation
Cited by 180
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Colony-Stimulating Factor 1 Receptor (CSF1R) Regulates Microglia Density and Distribution, but Not Microglia Differentiation In Vivo
Oosterhof, N., Kuil, L. E., van der Linde, H. C., Burm, S. M., Berdowski, W., van Ijcken, W. F. J., van Swieten, J. C., Hol, E. M., Verheijen, M. H. G., & van Ham, T. J. (2018) · Cell Reports
Neuroinflammation and Neurodegeneration MechanismsMultiple Sclerosis Research Studies
Cited by 178
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LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
Quadri, M., Mandemakers, W., Grochowska, M. M., Masius, R., Geut, H., Fabrizio, E., Breedveld, G. J., Kuipers, D., Minneboo, M., Vergouw, L. J. M., et al. (2018) · The Lancet Neurology
Parkinson's Disease Mechanisms and TreatmentsNuclear Receptors and Signaling
Cited by 143
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Persistent transcription-blocking DNA lesions trigger somatic growth attenuation associated with longevity
Garinis, G. A., Uittenboogaard, L. M., Stachelscheid, H., Fousteri, M., van Ijcken, W., Breit, T. M., van Steeg, H., Mullenders, L. H. F., van der Horst, G. T. J., Brüning, J. C., et al. (2009) · Nature Cell Biology
Genetics, Aging, and Longevity in Model OrganismsTelomeres, Telomerase, and Senescence
Cited by 138
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Dynamic regulation of the transcription initiation landscape at single nucleotide resolution during vertebrate embryogenesis
Nepal, C., Hadzhiev, Y., Previti, C., Haberle, V., Li, N., Takahashi, H., Suzuki, A. M. M., Sheng, Y., Abdelhamid, R. F., Anand, S., et al. (2013) · Genome Research
Genomics and Chromatin DynamicsGenomics and Phylogenetic Studies
Cited by 127
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Orphan CpG islands amplify poised enhancer regulatory activity and determine target gene responsiveness
Pachano, T., Sánchez-Gaya, V., Ealo, T., Mariner-Faulí, M., Bleckwehl, T., Asenjo, H. G., Respuela, P., Cruz-Molina, S., Muñoz-San Martín, M., Haro, E., et al. (2021) · Nature Genetics
Genomics and Chromatin DynamicsEpigenetics and DNA Methylation
Cited by 116
- Verified
PD-L1 checkpoint blockade promotes regulatory T cell activity that underlies therapy resistance
van Gulijk, M., van Krimpen, A., Schetters, S., Eterman, M., van Elsas, M., Mankor, J., Klaase, L., de Bruijn, M., van Nimwegen, M., van Tienhoven, T., et al. (2023) · Science Immunology
Cancer Immunotherapy and BiomarkersT-cell and B-cell Immunology
Cited by 110
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Discovery of new microRNAs by small RNAome deep sequencing in childhood acute lymphoblastic leukemia
Schotte, D., Moqadam, F. A., Lange-Turenhout, E. A. M., Chen, C., van IJcken, W. F. J., Pieters, R., & den Boer, M. L. (2011) · Leukemia
MicroRNA in disease regulationAcute Lymphoblastic Leukemia research
Cited by 89
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Developmental and activity-dependent miRNA expression profiling in primary hippocampal neuron cultures
van Spronsen, M., van Battum, E. Y., Kuijpers, M., Vangoor, V. R., Rietman, M. L., Pothof, J., Gumy, L. F., van IJcken, W. F. J., Akhmanova, A., Pasterkamp, R. J., et al. (2013) · PLoS ONE
MicroRNA in disease regulationNeurogenesis and neuroplasticity mechanisms
Cited by 82
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A rare missense variant in RCL1 segregates with depression in extended families.
Amin, N., de Vrij, F. M. S., Baghdadi, M., Brouwer, R. W. W., van Rooij, J. G. J., Jovanova, O., Uitterlinden, A. G., Hofman, A., Janssen, H. L. A., Darwish Murad, S., et al. (2018) · Molecular Psychiatry
Genetic Associations and EpidemiologyTreatment of Major Depression
Cited by 37
- Verified
Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome
Visser, W. E., Swagemakers, S. M. A., Őzgűr, Z., Schot, R., Verheijen, F. W., van Ijcken, W. F. J., van der Spek, P. J., & Visser, T. J. (2010) · Human Molecular Genetics
Thyroid Disorders and TreatmentsGenomics and Rare Diseases
Cited by 24
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