Wils, Hans
Janssen (Belgium)
3 papers on CoChatORCID 0009-0006-5697-9600
Most cited papers
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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
Cruts, M., Gijselinck, I., van der Zee, J., Engelborghs, S., Wils, H., Pirici, D., Rademakers, R., Vandenberghe, R., Dermaut, B., Martin, J.-J., et al. (2006) · Nature
Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments
Cited by 1,512
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Intraneuronal amyloid β and reduced brain volume in a novel APP T714I mouse model for Alzheimer's disease
Van Broeck, B., Vanhoutte, G., Pirici, D., Van Dam, D., Wils, H., Cuijt, I., Vennekens, K., Zabielski, M., Michalik, A., Theuns, J., et al. (2008) · Neurobiology of Aging
Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research
Cited by 60
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Comparative analysis of antibody- and lipid-based multiplexing methods for single-cell RNA-seq
Mylka, V., Matetovici, I., Poovathingal, S., Aerts, J., Vandamme, N., Seurinck, R., Verstaen, K., Hulselmans, G., Van den Hoecke, S., Scheyltjens, I., et al. (2022) · Genome Biology
Single-cell and spatial transcriptomicsGenomics and Phylogenetic Studies
Cited by 53
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